Item | Value |
---|---|
geneid | 23061 |
ensemblid | ENSG00000197226.13 |
hgncid | 29097 |
symbol | TBC1D9B |
name | TBC1 domain family member 9B |
refseq_nuc | NM_015043.4 |
refseq_prot | NP_055858.2 |
ensembl_nuc | ENST00000355235.8 |
ensembl_prot | ENSP00000347375.3 |
mane_status | MANE Select |
chr | chr5 |
start | 179862071 |
end | 179907897 |
strand | - |
ver | v1.2 |
region | chr5:179862071-179907897 |
region5000 | chr5:179857071-179912897 |
regionname0 | TBC1D9B_chr5_179862071_179907897 |
regionname5000 | TBC1D9B_chr5_179857071_179912897 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1233 | 212 | 30 | 41 | 108 | 3 | 29 | 79 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0002 | 1/0 | 1233 | 114 | 36 | 23 | 33 | 9 | 12 | 22 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0003 | 0/0 | 1233 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0004 | 0/0 | 1233 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0005 | 0/0 | 1233 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0006 | 0/0 | 1233 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0007 | 0/0 | 1233 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0008 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0009 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0010 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0011 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0012 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0013 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0014 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0015 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1222): Show |
chr5 | 179857071 | 179912897 |
a0016 | 0/0 | 145 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(140): Show |
chr5 | 179857071 | 179912897 |
a0017 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
a0018 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | MWLSP others(1228): Show |
chr5 | 179857071 | 179912897 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3699 | 195 | 19 | 41 | 103 | 2 | 29 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0005 | 0/0 | 3699 | 8 | 8 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0011 | 0/0 | 3699 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0016 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0017 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0022 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0026 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0028 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0029 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0001c0030 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0002 | 1/0 | 3699 | 82 | 12 | 20 | 29 | 9 | 11 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0003 | 0/0 | 3699 | 16 | 15 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0006 | 0/0 | 3699 | 7 | 7 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0007 | 0/0 | 3699 | 6 | 1 | 2 | 3 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0012 | 0/0 | 3699 | 2 | 0 | 0 | 1 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0002c0025 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0003c0004 | 0/0 | 3699 | 9 | 9 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0004c0009 | 0/0 | 3699 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0004c0024 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0005c0008 | 0/0 | 3699 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0006c0010 | 0/0 | 3699 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0007c0013 | 0/0 | 3699 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0008c0027 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0009c0015 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0010c0014 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0011c0020 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0012c0023 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0013c0019 | 0/0 | 3699 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0014c0021 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0015c0018 | 0/0 | 3681 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3676): Show |
chr5 | 179857071 | 179912897 | ||
a0016c0033 | 0/0 | 3710 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3705): Show |
chr5 | 179857071 | 179912897 | ||
a0017c0031 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 | ||
a0018c0032 | 0/0 | 3699 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ATGTG others(3694): Show |
chr5 | 179857071 | 179912897 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5155 | 69 | 8 | 15 | 41 | 1 | 4 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0002 | 0/0 | 5155 | 8 | 0 | 3 | 5 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0003 | 0/0 | 5155 | 52 | 1 | 11 | 26 | 0 | 14 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0004 | 0/1 | 5155 | 48 | 3 | 12 | 22 | 1 | 9 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0006 | 0/0 | 5142 | 2 | 1 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | GGACG others(5137): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0008 | 0/0 | 5155 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0010 | 0/0 | 5155 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0011 | 0/0 | 5155 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0012 | 0/0 | 5183 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5178): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0013 | 0/0 | 5169 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5164): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0014 | 0/0 | 5169 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5164): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0018 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0019 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0020 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0001t0022 | 0/0 | 5142 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | GGACG others(5137): Show |
chr5 | 179857071 | 179912897 |
a0001c0005t0001 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0005t0005 | 0/0 | 5155 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0005t0006 | 0/0 | 5142 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | GGACG others(5137): Show |
chr5 | 179857071 | 179912897 |
a0001c0011t0001 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0016t0004 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0017t0003 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0022t0004 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0026t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0028t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0029t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0001c0030t0004 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0001 | 0/0 | 5155 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0002 | 0/0 | 5155 | 58 | 4 | 12 | 25 | 7 | 10 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0003 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0004 | 0/0 | 5155 | 5 | 2 | 2 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0005 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0007 | 1/0 | 5155 | 9 | 0 | 6 | 0 | 2 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0009 | 0/0 | 5169 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5164): Show |
chr5 | 179857071 | 179912897 |
a0002c0002t0016 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0003t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0003t0005 | 0/0 | 5155 | 6 | 5 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0003t0006 | 0/0 | 5142 | 9 | 9 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | GGACG others(5137): Show |
chr5 | 179857071 | 179912897 |
a0002c0006t0001 | 0/0 | 5155 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0006t0005 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0006t0015 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0006t0021 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0007t0001 | 0/0 | 5155 | 4 | 1 | 1 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0007t0003 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0007t0017 | 0/0 | 5155 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0012t0002 | 0/0 | 5155 | 2 | 0 | 0 | 1 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0002c0025t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0003c0004t0005 | 0/0 | 5155 | 9 | 9 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0004c0009t0005 | 0/0 | 5155 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0004c0024t0005 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0005c0008t0001 | 0/0 | 5155 | 5 | 5 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0006c0010t0005 | 0/0 | 5155 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0007c0013t0002 | 0/0 | 5155 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0008c0027t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0009c0015t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0010c0014t0002 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0011c0020t0002 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0012c0023t0007 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0013c0019t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0014c0021t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0015c0018t0003 | 0/0 | 5137 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5132): Show |
chr5 | 179857071 | 179912897 |
a0016c0033t0002 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5161): Show |
chr5 | 179857071 | 179912897 |
a0017c0031t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
a0018c0032t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | ACGCT others(5150): Show |
chr5 | 179857071 | 179912897 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0008g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0011g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0014g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0019g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0020g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0001t0022g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0005t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0011t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0011t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0016t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0017t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0022t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0026t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0028t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0029t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0001c0030t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0012 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0007g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0009g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0002t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0003t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0015g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0006t0021g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0007t0017g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0012t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0012t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0002c0025t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0003c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0009t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0009t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0009t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0009t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0009t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0004c0024t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0005c0008t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0005c0008t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0005c0008t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0005c0008t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0005c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0006c0010t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0006c0010t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0006c0010t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0007c0013t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0008c0027t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0009c0015t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0010c0014t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0011c0020t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0012c0023t0007g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0013c0019t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0014c0021t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0015c0018t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0016c0033t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0017c0031t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
a0018c0032t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0058 | EUR | GBR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00099 | hp2 | a0002 | c0002 | t0007 | g0297 | EUR | GBR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | GBR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00140 | hp2 | a0001 | c0030 | t0004 | g0107 | EUR | GBR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0071 | EUR | FIN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00408 | hp1 | a0001 | c0017 | t0003 | g0218 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00423 | hp1 | a0001 | c0001 | t0012 | g0031 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00642 | hp2 | a0002 | c0002 | t0007 | g0294 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00733 | hp2 | a0002 | c0002 | t0007 | g0012 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00738 | hp2 | a0002 | c0002 | t0007 | g0292 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG00741 | hp2 | a0002 | c0002 | t0007 | g0295 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0165 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0166 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01106 | hp1 | a0002 | c0002 | t0007 | g0012 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01243 | hp1 | a0002 | c0007 | t0001 | g0191 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01243 | hp2 | a0002 | c0003 | t0005 | g0122 | AMR | PUR | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01261 | hp1 | a0002 | c0007 | t0017 | g0266 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01515 | hp1 | a0002 | c0002 | t0007 | g0293 | EUR | IBS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0092 | EUR | IBS | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0113 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01884 | hp2 | a0002 | c0002 | t0005 | g0050 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02015 | hp2 | a0001 | c0029 | t0001 | g0263 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02055 | hp1 | a0002 | c0003 | t0005 | g0118 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02055 | hp2 | a0006 | c0010 | t0005 | g0128 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02074 | hp1 | a0002 | c0002 | t0009 | g0013 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02083 | hp2 | a0002 | c0007 | t0003 | g0175 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02135 | hp2 | a0001 | c0001 | t0013 | g0032 | EAS | KHV | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02145 | hp1 | a0001 | c0005 | t0006 | g0305 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02145 | hp2 | a0002 | c0007 | t0001 | g0190 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02155 | hp1 | a0002 | c0002 | t0009 | g0013 | EAS | CDX | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | CDX | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02165 | hp1 | a0001 | c0001 | t0010 | g0193 | EAS | CDX | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02257 | hp1 | a0002 | c0006 | t0005 | g0133 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0060 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0117 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02280 | hp2 | a0001 | c0011 | t0001 | g0145 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0200 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02451 | hp2 | a0001 | c0005 | t0006 | g0300 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02572 | hp1 | a0009 | c0015 | t0001 | g0034 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02622 | hp1 | a0002 | c0003 | t0005 | g0119 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02630 | hp1 | a0002 | c0002 | t0004 | g0170 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02630 | hp2 | a0002 | c0006 | t0001 | g0144 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02647 | hp1 | a0002 | c0025 | t0001 | g0127 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02647 | hp2 | a0002 | c0002 | t0004 | g0149 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02683 | hp1 | a0001 | c0001 | t0014 | g0033 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0260 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0186 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02717 | hp1 | a0003 | c0004 | t0005 | g0138 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02723 | hp1 | a0003 | c0004 | t0005 | g0008 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02723 | hp2 | a0001 | c0011 | t0001 | g0134 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0280 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02738 | hp1 | a0010 | c0014 | t0002 | g0042 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0052 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02809 | hp1 | a0003 | c0004 | t0005 | g0008 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02818 | hp2 | a0001 | c0005 | t0005 | g0112 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02886 | hp1 | a0002 | c0006 | t0001 | g0142 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02895 | hp2 | a0003 | c0004 | t0005 | g0008 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02896 | hp1 | a0004 | c0009 | t0005 | g0125 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02897 | hp2 | a0003 | c0004 | t0005 | g0109 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02922 | hp1 | a0005 | c0008 | t0001 | g0040 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02970 | hp1 | a0001 | c0028 | t0001 | g0171 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02970 | hp2 | a0004 | c0009 | t0005 | g0126 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02976 | hp1 | a0002 | c0006 | t0001 | g0141 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02976 | hp2 | a0006 | c0010 | t0005 | g0130 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03041 | hp1 | a0001 | c0005 | t0005 | g0111 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03041 | hp2 | a0002 | c0003 | t0006 | g0030 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03098 | hp1 | a0002 | c0003 | t0005 | g0120 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03098 | hp2 | a0003 | c0004 | t0005 | g0139 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03139 | hp1 | a0005 | c0008 | t0001 | g0041 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03139 | hp2 | a0006 | c0010 | t0005 | g0129 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03195 | hp1 | a0002 | c0003 | t0006 | g0307 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03209 | hp2 | a0002 | c0006 | t0015 | g0143 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03225 | hp1 | a0004 | c0009 | t0005 | g0123 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03225 | hp2 | a0005 | c0008 | t0001 | g0038 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03453 | hp1 | a0002 | c0003 | t0005 | g0121 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03486 | hp1 | a0002 | c0006 | t0005 | g0132 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03486 | hp2 | a0004 | c0009 | t0005 | g0131 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03490 | hp2 | a0007 | c0013 | t0002 | g0018 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03492 | hp1 | a0007 | c0013 | t0002 | g0018 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03516 | hp1 | a0001 | c0005 | t0005 | g0114 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03516 | hp2 | a0002 | c0003 | t0006 | g0304 | AFR | ESN | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03540 | hp1 | a0001 | c0005 | t0005 | g0135 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03540 | hp2 | a0002 | c0003 | t0006 | g0306 | AFR | GWD | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03579 | hp2 | a0004 | c0024 | t0005 | g0136 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0169 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03688 | hp1 | a0002 | c0002 | t0004 | g0167 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0290 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03834 | hp1 | a0002 | c0012 | t0002 | g0094 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03927 | hp1 | a0011 | c0020 | t0002 | g0066 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0101 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0043 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03942 | hp2 | a0012 | c0023 | t0007 | g0296 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0160 | SAS | BEB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04199 | hp1 | a0001 | c0001 | t0022 | g0309 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | STU | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18522 | hp2 | a0005 | c0008 | t0001 | g0039 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CHB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18906 | hp1 | a0013 | c0019 | t0001 | g0140 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18906 | hp2 | a0002 | c0003 | t0006 | g0299 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18944 | hp1 | a0001 | c0001 | t0010 | g0192 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0310 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18949 | hp2 | a0014 | c0021 | t0001 | g0282 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18962 | hp2 | a0001 | c0026 | t0001 | g0272 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18972 | hp1 | a0001 | c0001 | t0019 | g0285 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18972 | hp2 | a0002 | c0002 | t0016 | g0097 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18984 | hp2 | a0001 | c0001 | t0018 | g0281 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18985 | hp2 | a0001 | c0001 | t0011 | g0219 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18989 | hp1 | a0015 | c0018 | t0003 | g0213 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0220 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19010 | hp2 | a0002 | c0012 | t0002 | g0093 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19030 | hp1 | a0002 | c0003 | t0006 | g0302 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19030 | hp2 | a0002 | c0003 | t0006 | g0303 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19043 | hp1 | a0002 | c0003 | t0006 | g0301 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19043 | hp2 | a0003 | c0004 | t0005 | g0115 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19062 | hp2 | a0016 | c0033 | t0002 | g0106 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19065 | hp1 | a0002 | c0007 | t0001 | g0238 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19066 | hp2 | a0001 | c0022 | t0004 | g0181 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19068 | hp2 | a0001 | c0016 | t0004 | g0164 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19070 | hp1 | a0017 | c0031 | t0001 | g0250 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19076 | hp1 | a0018 | c0032 | t0001 | g0222 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19079 | hp2 | a0002 | c0007 | t0001 | g0173 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA19240 | hp2 | a0002 | c0003 | t0005 | g0116 | AFR | YRI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20129 | hp1 | a0002 | c0003 | t0006 | g0030 | AFR | ASW | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | ASW | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0099 | EUR | TSI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0084 | EUR | TSI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0063 | EUR | TSI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0180 | EUR | TSI | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | GIH | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | GIH | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01123 | hp1 | a0002 | c0002 | t0007 | g0291 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02109 | hp2 | a0003 | c0004 | t0005 | g0110 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG02486 | hp2 | a0008 | c0027 | t0001 | g0108 | AFR | ACB | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03471 | hp1 | a0002 | c0006 | t0021 | g0298 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG03471 | hp2 | a0001 | c0001 | t0020 | g0147 | AFR | MSL | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG06807 | hp1 | a0004 | c0009 | t0005 | g0124 | AFR | USA | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
HG06807 | hp2 | a0003 | c0004 | t0005 | g0137 | AFR | USA | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | USA | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
NA21309 | hp2 | a0005 | c0008 | t0001 | g0037 | AFR | LWK | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0161 | REF | REF | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
homoSapiens | grch38p0 | a0002 | c0002 | t0007 | g0012 | REF | REF | TBC1D9B_chr5_179857071_179912897 | TBC1D9B | chr5 | 179857071 | 179912897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179863803 | C | T | 1 | a0014 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.3347G>A | p.Gly1116Asp | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 3423/5155 | 3347/3702 | 1116/1233 | chr5 | 179863803 | |||
chr5:179863845 | T | G | 10 | a0001 a0004 a0008 others(7): Show |
225 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
missense_variant | MODERATE | c.3305A>C | p.Lys1102Thr | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 3381/5155 | 3305/3702 | 1102/1233 | chr5 | 179863845 | |||
chr5:179863890 | G | A | 2 | a0004 a0008 |
7 | HG02486.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
missense_variant | MODERATE | c.3260C>T | p.Ala1087Val | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 3336/5155 | 3260/3702 | 1087/1233 | chr5 | 179863890 | |||
chr5:179865282 | G | T | 1 | a0011 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.2993C>A | p.Thr998Lys | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/21 | 3069/5155 | 2993/3702 | 998/1233 | chr5 | 179865282 | |||
chr5:179867798 | G | A | 2 | a0004 a0006 |
9 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(6): Show |
missense_variant | MODERATE | c.2843C>T | p.Thr948Ile | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/21 | 2919/5155 | 2843/3702 | 948/1233 | chr5 | 179867798 | |||
chr5:179869831 | C | T | 2 | a0005 a0013 |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.2729G>A | p.Gly910Glu | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/21 | 2805/5155 | 2729/3702 | 910/1233 | chr5 | 179869831 | |||
chr5:179870292 | G | C | 1 | a0006 | 3 | HG02055.hp2 HG02976.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.2688C>G | p.Asp896Glu | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2764/5155 | 2688/3702 | 896/1233 | chr5 | 179870292 | |||
chr5:179870459 | G | A | 1 | a0003 | 9 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
missense_variant | MODERATE | c.2521C>T | p.Arg841Cys | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2597/5155 | 2521/3702 | 841/1233 | chr5 | 179870459 | |||
chr5:179870475 | C | A | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2505G>T | p.Gln835His | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2581/5155 | 2505/3702 | 835/1233 | chr5 | 179870475 | |||
chr5:179871512 | CCACAGGT others(14): Show |
C | 1 | a0015 | 1 | NA18989.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.2416-3_2433delTAGG others(17): Show |
p.Val806_Asp812del | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/21 | 2509/5155 | 2416/3702 | 806/1233 | chr5 | 179871512 | |||
chr5:179879725 | C | T | 1 | a0009 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1319G>A | p.Arg440His | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/21 | 1395/5155 | 1319/3702 | 440/1233 | chr5 | 179879725 | |||
chr5:179888308 | G | C | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1049C>G | p.Thr350Ser | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/21 | 1125/5155 | 1049/3702 | 350/1233 | chr5 | 179888308 | |||
chr5:179893327 | G | A | 1 | a0007 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.718C>T | p.Leu240Phe | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/21 | 794/5155 | 718/3702 | 240/1233 | chr5 | 179893327 | |||
chr5:179893411 | G | A | 1 | a0017 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.634C>T | p.Leu212Phe | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/21 | 710/5155 | 634/3702 | 212/1233 | chr5 | 179893411 | |||
chr5:179894525 | C | A | 1 | a0018 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.438G>T | p.Lys146Asn | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/21 | 514/5155 | 438/3702 | 146/1233 | chr5 | 179894525 | |||
chr5:179894526 | T | C | 1 | a0018 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.437A>G | p.Lys146Arg | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/21 | 513/5155 | 437/3702 | 146/1233 | chr5 | 179894526 | |||
chr5:179904789 | C | T | 1 | a0010 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.142G>A | p.Val48Met | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/21 | 218/5155 | 142/3702 | 48/1233 | chr5 | 179904789 | |||
chr5:179904794 | A | C | 1 | a0016 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.137T>G | p.Leu46Arg | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/21 | 213/5155 | 137/3702 | 46/1233 | chr5 | 179904794 | |||
chr5:179904797 | G | C | 1 | a0016 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.134C>G | p.Thr45Ser | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/21 | 210/5155 | 134/3702 | 45/1233 | chr5 | 179904797 | |||
chr5:179904799 | G | GAGCCACC others(4): Show |
1 | a0016 | 1 | NA19062.hp2 | frameshift_variant | HIGH | c.131_132insGGGGGGTG others(3): Show |
p.Thr45fs | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/21 | 207/5155 | 131/3702 | 44/1233 | chr5 | 179904799 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179863637 | G | A | 1 | a0004c0024 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.3513C>T | p.Ile1171Ile | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 3589/5155 | 3513/3702 | 1171/1233 | chr5 | 179863637 | |||
chr5:179869779 | G | A | 1 | a0001c0022 | 1 | NA19066.hp2 | synonymous_variant | LOW | c.2781C>T | p.His927His | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/21 | 2857/5155 | 2781/3702 | 927/1233 | chr5 | 179869779 | |||
chr5:179870262 | T | C | 8 | a0001c0005 a0001c0011 a0002c0003 others(5): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
synonymous_variant | LOW | c.2718A>G | p.Thr906Thr | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2794/5155 | 2718/3702 | 906/1233 | chr5 | 179870262 | |||
chr5:179870268 | G | A | 1 | a0002c0007 | 6 | HG01243.hp1 HG01261.hp1 HG02083.hp2 others(3): Show |
synonymous_variant | LOW | c.2712C>T | p.Phe904Phe | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2788/5155 | 2712/3702 | 904/1233 | chr5 | 179870268 | |||
chr5:179870352 | A | G | 8 | a0001c0005 a0001c0011 a0002c0003 others(5): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
synonymous_variant | LOW | c.2628T>C | p.Cys876Cys | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/21 | 2704/5155 | 2628/3702 | 876/1233 | chr5 | 179870352 | |||
chr5:179872907 | C | T | 1 | a0001c0017 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.2400G>A | p.Thr800Thr | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/21 | 2476/5155 | 2400/3702 | 800/1233 | chr5 | 179872907 | |||
chr5:179873131 | T | C | 8 | a0001c0005 a0001c0011 a0002c0003 others(5): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
synonymous_variant | LOW | c.2304A>G | p.Lys768Lys | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 13/21 | 2380/5155 | 2304/3702 | 768/1233 | chr5 | 179873131 | |||
chr5:179875921 | C | T | 1 | a0002c0007 | 6 | HG01243.hp1 HG01261.hp1 HG02083.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1899G>A | p.Val633Val | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/21 | 1975/5155 | 1899/3702 | 633/1233 | chr5 | 179875921 | |||
chr5:179878405 | G | A | 2 | a0001c0011 a0002c0006 |
9 | HG02257.hp1 HG02280.hp2 HG02630.hp2 others(6): Show |
synonymous_variant | LOW | c.1686C>T | p.Pro562Pro | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/21 | 1762/5155 | 1686/3702 | 562/1233 | chr5 | 179878405 | |||
chr5:179878462 | G | A | 1 | a0002c0025 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1629C>T | p.Thr543Thr | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/21 | 1705/5155 | 1629/3702 | 543/1233 | chr5 | 179878462 | |||
chr5:179879634 | G | T | 1 | a0001c0016 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1410C>A | p.Ala470Ala | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/21 | 1486/5155 | 1410/3702 | 470/1233 | chr5 | 179879634 | |||
chr5:179879724 | G | A | 1 | a0001c0026 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.1320C>T | p.Arg440Arg | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/21 | 1396/5155 | 1320/3702 | 440/1233 | chr5 | 179879724 | |||
chr5:179888142 | G | A | 1 | a0002c0012 | 2 | HG03834.hp1 NA19010.hp2 |
synonymous_variant | LOW | c.1215C>T | p.Ile405Ile | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/21 | 1291/5155 | 1215/3702 | 405/1233 | chr5 | 179888142 | |||
chr5:179891427 | G | A | 1 | a0001c0028 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.996C>T | p.Phe332Phe | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/21 | 1072/5155 | 996/3702 | 332/1233 | chr5 | 179891427 | |||
chr5:179891514 | G | A | 1 | a0001c0029 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.909C>T | p.Asp303Asp | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/21 | 985/5155 | 909/3702 | 303/1233 | chr5 | 179891514 | |||
chr5:179893325 | G | A | 1 | a0001c0030 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.720C>T | p.Leu240Leu | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/21 | 796/5155 | 720/3702 | 240/1233 | chr5 | 179893325 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179862148 | C | T | 1 | a0001c0001t0011 | 2 | NA18985.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1300G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 1300 | chr5 | 179862148 | ||||||
chr5:179862281 | T | A | 1 | a0002c0007t0017 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1167A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 1167 | chr5 | 179862281 | ||||||
chr5:179862386 | C | T | 1 | a0001c0001t0010 | 2 | HG02165.hp1 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1062G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 1062 | chr5 | 179862386 | ||||||
chr5:179862429 | A | G | 1 | a0001c0001t0018 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 1019 | chr5 | 179862429 | ||||||
chr5:179862659 | G | A | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(9): Show |
65 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*789C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 789 | chr5 | 179862659 | ||||||
chr5:179862895 | G | A | 6 | a0001c0001t0004 a0001c0001t0014 a0001c0016t0004 others(3): Show |
56 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*553C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 553 | chr5 | 179862895 | ||||||
chr5:179862902 | G | A | 1 | a0002c0002t0016 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 546 | chr5 | 179862902 | ||||||
chr5:179863007 | A | G | 9 | a0001c0005t0005 a0002c0002t0005 a0002c0003t0005 others(6): Show |
32 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*441T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 441 | chr5 | 179863007 | ||||||
chr5:179863009 | G | C | 1 | a0001c0001t0019 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 439 | chr5 | 179863009 | ||||||
chr5:179863154 | G | C | 52 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(49): Show |
275 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 294 | chr5 | 179863154 | ||||||
chr5:179863185 | C | T | 1 | a0002c0006t0015 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 263 | chr5 | 179863185 | ||||||
chr5:179863251 | G | A | 1 | a0001c0001t0020 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 197 | chr5 | 179863251 | ||||||
chr5:179863282 | A | G | 1 | a0001c0001t0008 | 5 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*166T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 21/21 | 166 | chr5 | 179863282 | ||||||
chr5:179907857 | A | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
5_prime_UTR_variant | MODIFIER | c.-36T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/21 | 36 | chr5 | 179907857 | ||||||
chr5:179907863 | G | A | 1 | a0002c0006t0021 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/21 | 42 | chr5 | 179907863 | ||||||
chr5:179907884 | C | CCGGAGCG others(7): Show |
3 | a0001c0001t0013 a0001c0001t0014 a0002c0002t0009 |
4 | HG02074.hp1 HG02135.hp2 HG02155.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-64_-63insCACGCTCC others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/21 | 64 | chr5 | 179907884 | ||||||
chr5:179907884 | C | CCGGAGCG others(21): Show |
1 | a0001c0001t0012 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64_-63insCACGCTCC others(20): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/21 | 64 | chr5 | 179907884 | ||||||
chr5:179907884 | CCGGAGCG others(7): Show |
C | 4 | a0001c0001t0006 a0001c0001t0022 a0001c0005t0006 others(1): Show |
14 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-77_-64delCACGCTCC others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/21 | 64 | chr5 | 179907884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179864279 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
223 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.3022-151T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864279 | |||||||
chr5:179864434 | G | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.3022-306C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864434 | |||||||
chr5:179864579 | G | C | 1 | a0002c0002t0002g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3022-451C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864579 | |||||||
chr5:179864585 | C | T | 7 | a0001c0001t0004g0022 a0001c0001t0004g0182 a0001c0001t0004g0185 others(4): Show |
8 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.3022-457G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864585 | |||||||
chr5:179864655 | G | A | 1 | a0002c0002t0002g0052 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3022-527C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864655 | |||||||
chr5:179864674 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3022-546G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864674 | |||||||
chr5:179864721 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3021+533C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864721 | |||||||
chr5:179864885 | G | A | 3 | a0001c0001t0006g0308 a0002c0002t0001g0051 a0002c0002t0001g0103 |
3 | HG02258.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3021+369C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864885 | |||||||
chr5:179864892 | G | C | 1 | a0001c0001t0004g0184 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3021+362C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864892 | |||||||
chr5:179864941 | G | C | 2 | a0001c0001t0001g0151 a0002c0002t0001g0152 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3021+313C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864941 | |||||||
chr5:179864951 | G | T | 2 | a0001c0001t0003g0150 a0001c0001t0003g0234 |
2 | HG02486.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3021+303C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179864951 | |||||||
chr5:179865010 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(228): Show |
274 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.3021+244A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179865010 | |||||||
chr5:179865109 | G | C | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3021+145C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179865109 | |||||||
chr5:179865183 | C | T | 4 | a0002c0003t0005g0119 a0002c0003t0005g0120 a0002c0003t0005g0121 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3021+71G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179865183 | |||||||
chr5:179865184 | G | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3021+70C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 20/20 | chr5 | 179865184 | |||||||
chr5:179865409 | C | T | 2 | a0001c0001t0003g0209 a0001c0001t0003g0211 |
2 | HG03490.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2915-49G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 19/20 | chr5 | 179865409 | |||||||
chr5:179865429 | G | A | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915-69C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 19/20 | chr5 | 179865429 | |||||||
chr5:179865694 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0194 others(6): Show |
12 | HG00609.hp1 HG02015.hp2 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.2914+144G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 19/20 | chr5 | 179865694 | |||||||
chr5:179865901 | A | C | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2864-13T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179865901 | |||||||
chr5:179865951 | T | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2864-63A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179865951 | |||||||
chr5:179866120 | C | T | 1 | a0002c0002t0002g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2864-232G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866120 | |||||||
chr5:179866229 | AGTTCCTG others(17): Show |
A | 51 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0168 others(48): Show |
62 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.2864-365_2864-342d others(26): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866229 | |||||||
chr5:179866290 | T | C | 1 | a0001c0001t0019g0285 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2864-402A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866290 | |||||||
chr5:179866298 | G | A | 1 | a0001c0001t0003g0244 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2864-410C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866298 | |||||||
chr5:179866309 | G | C | 9 | a0004c0009t0005g0123 a0004c0009t0005g0124 a0004c0009t0005g0125 others(6): Show |
9 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.2864-421C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866309 | |||||||
chr5:179866348 | T | C | 7 | a0003c0004t0005g0008 a0003c0004t0005g0109 a0003c0004t0005g0110 others(4): Show |
9 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2864-460A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866348 | |||||||
chr5:179866580 | T | C | 1 | a0002c0002t0002g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2864-692A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866580 | |||||||
chr5:179866653 | G | A | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2864-765C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866653 | |||||||
chr5:179866733 | T | C | 3 | a0002c0003t0006g0030 a0002c0003t0006g0306 a0002c0003t0006g0307 |
4 | HG03041.hp2 HG03195.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2864-845A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866733 | |||||||
chr5:179866748 | A | C | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2864-860T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866748 | |||||||
chr5:179866989 | T | A | 1 | a0015c0018t0003g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2863+789A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179866989 | |||||||
chr5:179867081 | A | G | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2863+697T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867081 | |||||||
chr5:179867111 | C | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2863+667G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867111 | |||||||
chr5:179867112 | A | C | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2863+666T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867112 | |||||||
chr5:179867113 | C | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2863+665G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867113 | |||||||
chr5:179867172 | T | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2863+606A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867172 | |||||||
chr5:179867396 | G | A | 1 | a0001c0005t0005g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2863+382C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867396 | |||||||
chr5:179867601 | C | G | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2863+177G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867601 | |||||||
chr5:179867751 | A | G | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2863+27T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867751 | |||||||
chr5:179867758 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2863+20C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 18/20 | chr5 | 179867758 | |||||||
chr5:179868056 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG00323.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2792-207A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868056 | |||||||
chr5:179868060 | T | C | 51 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0168 others(48): Show |
62 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.2792-211A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868060 | |||||||
chr5:179868062 | G | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0103 a0002c0002t0005g0050 |
3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2792-213C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868062 | |||||||
chr5:179868090 | T | G | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2792-241A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868090 | |||||||
chr5:179868137 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2792-288G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868137 | |||||||
chr5:179868150 | A | G | 49 | a0001c0005t0001g0036 a0001c0005t0001g0113 a0001c0005t0005g0111 others(46): Show |
52 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(49): Show |
intron_variant | MODIFIER | c.2792-301T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868150 | |||||||
chr5:179868166 | G | C | 6 | a0001c0001t0001g0208 a0001c0001t0003g0025 a0001c0001t0003g0146 others(3): Show |
7 | HG00408.hp2 HG02074.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.2792-317C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868166 | |||||||
chr5:179868368 | G | A | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2792-519C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868368 | |||||||
chr5:179868551 | G | A | 48 | a0001c0005t0001g0036 a0001c0005t0001g0113 a0001c0005t0005g0111 others(45): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
intron_variant | MODIFIER | c.2792-702C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868551 | |||||||
chr5:179868612 | G | A | 1 | a0002c0006t0001g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2792-763C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868612 | |||||||
chr5:179868626 | C | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2792-777G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868626 | |||||||
chr5:179868627 | A | C | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2792-778T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868627 | |||||||
chr5:179868628 | C | T | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2792-779G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868628 | |||||||
chr5:179868676 | C | T | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2792-827G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868676 | |||||||
chr5:179868683 | T | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2792-834A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868683 | |||||||
chr5:179868689 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2792-840G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868689 | |||||||
chr5:179868777 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2792-928C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868777 | |||||||
chr5:179868948 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2791+821T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179868948 | |||||||
chr5:179869124 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0255 a0001c0001t0001g0258 others(3): Show |
7 | HG00544.hp2 HG00621.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.2791+645T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869124 | |||||||
chr5:179869198 | C | T | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2791+571G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869198 | |||||||
chr5:179869270 | A | T | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2791+499T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869270 | |||||||
chr5:179869279 | G | A | 3 | a0001c0011t0001g0134 a0002c0006t0005g0132 a0002c0006t0005g0133 |
3 | HG02257.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2791+490C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869279 | |||||||
chr5:179869286 | G | C | 48 | a0001c0005t0001g0036 a0001c0005t0001g0113 a0001c0005t0005g0111 others(45): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
intron_variant | MODIFIER | c.2791+483C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869286 | |||||||
chr5:179869299 | A | C | 1 | a0002c0002t0007g0293 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2791+470T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869299 | |||||||
chr5:179869441 | C | T | 28 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(25): Show |
30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2791+328G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869441 | |||||||
chr5:179869646 | C | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2791+123G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869646 | |||||||
chr5:179869734 | A | AGACCCTG others(6): Show |
1 | a0015c0018t0003g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2791+22_2791+34dup others(13): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869734 | |||||||
chr5:179869752 | G | A | 31 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(28): Show |
33 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.2791+17C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 17/20 | chr5 | 179869752 | |||||||
chr5:179870152 | C | G | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2725+103G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 16/20 | chr5 | 179870152 | |||||||
chr5:179870515 | G | C | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2485-20C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870515 | |||||||
chr5:179870571 | T | A | 1 | a0001c0001t0002g0082 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2485-76A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870571 | |||||||
chr5:179870598 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2485-103G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870598 | |||||||
chr5:179870599 | G | A | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2485-104C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870599 | |||||||
chr5:179870733 | A | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
214 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.2485-238T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870733 | |||||||
chr5:179870871 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2485-376C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870871 | |||||||
chr5:179870978 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2485-483A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179870978 | |||||||
chr5:179871294 | AGGAGGTT others(23): Show |
A | 1 | a0003c0004t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2484+138_2484+167d others(32): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179871294 | |||||||
chr5:179871327 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2484+135G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179871327 | |||||||
chr5:179871335 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2484+127A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179871335 | |||||||
chr5:179871342 | G | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2484+120C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 15/20 | chr5 | 179871342 | |||||||
chr5:179871682 | G | C | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-152C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871682 | |||||||
chr5:179871690 | C | T | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2416-160G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871690 | |||||||
chr5:179871746 | TCCAGGAT others(134): Show |
T | 1 | a0001c0001t0003g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2416-357_2416-217d others(2): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871746 | |||||||
chr5:179871767 | TCTCTCTC others(40): Show |
T | 1 | a0002c0002t0002g0088 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2416-284_2416-238d others(49): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871767 | |||||||
chr5:179871767 | TCTCTCTC others(228): Show |
T | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2416-472_2416-238d others(2): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871767 | |||||||
chr5:179871807 | G | A | 1 | a0001c0001t0006g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2416-277C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871807 | |||||||
chr5:179871852 | T | G | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2416-322A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871852 | |||||||
chr5:179871852 | TTGGGGGA others(134): Show |
T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
209 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.2416-463_2416-323d others(2): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871852 | |||||||
chr5:179871853 | T | C | 1 | a0001c0005t0006g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2416-323A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871853 | |||||||
chr5:179871857 | G | A | 7 | a0003c0004t0005g0008 a0003c0004t0005g0109 a0003c0004t0005g0110 others(4): Show |
9 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2416-327C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871857 | |||||||
chr5:179871861 | CCTCTCTC others(40): Show |
C | 40 | a0001c0005t0001g0036 a0001c0005t0001g0113 a0001c0005t0005g0111 others(37): Show |
42 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.2416-378_2416-332d others(49): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871861 | |||||||
chr5:179871881 | CCCCTTCC others(133): Show |
C | 1 | a0015c0018t0003g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2416-491_2416-352d others(2): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871881 | |||||||
chr5:179871908 | T | C | 20 | a0001c0001t0001g0035 a0001c0001t0003g0245 a0001c0005t0006g0300 others(17): Show |
21 | HG00738.hp1 HG02071.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.2416-378A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871908 | |||||||
chr5:179871908 | TCTCTCTC others(40): Show |
C | 2 | a0005c0008t0001g0037 a0005c0008t0001g0041 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2416-424_2416-378d others(49): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871908 | |||||||
chr5:179871946 | G | T | 37 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(34): Show |
39 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.2416-416C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871946 | |||||||
chr5:179871963 | T | G | 1 | a0002c0003t0005g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2416-433A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871963 | |||||||
chr5:179871975 | C | T | 1 | a0002c0002t0002g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2416-445G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871975 | |||||||
chr5:179871993 | G | T | 1 | a0001c0001t0003g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2416-463C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179871993 | |||||||
chr5:179872065 | C | T | 43 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(40): Show |
46 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.2416-535G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872065 | |||||||
chr5:179872066 | G | A | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-536C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872066 | |||||||
chr5:179872089 | G | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2416-559C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872089 | |||||||
chr5:179872124 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2416-594G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872124 | |||||||
chr5:179872126 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2416-596C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872126 | |||||||
chr5:179872159 | C | T | 1 | a0001c0001t0018g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2416-629G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872159 | |||||||
chr5:179872242 | C | T | 1 | a0001c0005t0006g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2415+650G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872242 | |||||||
chr5:179872247 | G | A | 1 | a0001c0001t0004g0172 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2415+645C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872247 | |||||||
chr5:179872363 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2415+529G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872363 | |||||||
chr5:179872595 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2415+297T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872595 | |||||||
chr5:179872734 | C | T | 2 | a0002c0002t0002g0073 a0002c0002t0002g0074 |
2 | HG02132.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2415+158G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872734 | |||||||
chr5:179872792 | G | T | 12 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2415+100C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872792 | |||||||
chr5:179872804 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2415+88C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872804 | |||||||
chr5:179872867 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(224): Show |
270 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.2415+25A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872867 | |||||||
chr5:179872867 | T | G | 3 | a0002c0003t0001g0117 a0002c0003t0005g0116 a0002c0003t0005g0118 |
3 | HG02055.hp1 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2415+25A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 14/20 | chr5 | 179872867 | |||||||
chr5:179873349 | C | T | 10 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(7): Show |
11 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2187-101G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873349 | |||||||
chr5:179873411 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2187-163G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873411 | |||||||
chr5:179873412 | G | A | 1 | a0002c0002t0007g0297 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2187-164C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873412 | |||||||
chr5:179873592 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
137 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2187-344G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873592 | |||||||
chr5:179873594 | G | T | 1 | a0001c0001t0019g0285 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2187-346C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873594 | |||||||
chr5:179873651 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2187-403C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873651 | |||||||
chr5:179873732 | C | T | 48 | a0001c0005t0001g0036 a0001c0005t0001g0113 a0001c0005t0005g0111 others(45): Show |
51 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(48): Show |
intron_variant | MODIFIER | c.2187-484G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873732 | |||||||
chr5:179873895 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.2187-647T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179873895 | |||||||
chr5:179874097 | G | A | 1 | a0014c0021t0001g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2186+805C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874097 | |||||||
chr5:179874205 | A | G | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2186+697T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874205 | |||||||
chr5:179874219 | G | C | 2 | a0001c0001t0003g0201 a0001c0001t0022g0309 |
2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2186+683C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874219 | |||||||
chr5:179874260 | A | G | 303 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(300): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.2186+642T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874260 | |||||||
chr5:179874427 | A | G | 2 | a0002c0007t0001g0173 a0002c0007t0001g0238 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2186+475T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874427 | |||||||
chr5:179874596 | T | C | 1 | a0002c0002t0002g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2186+306A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874596 | |||||||
chr5:179874659 | G | A | 1 | a0002c0002t0002g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2186+243C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 12/20 | chr5 | 179874659 | |||||||
chr5:179875307 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0248 |
2 | HG01975.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1901-120C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875307 | |||||||
chr5:179875356 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1901-169A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875356 | |||||||
chr5:179875530 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1901-343C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875530 | |||||||
chr5:179875555 | G | A | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900+365C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875555 | |||||||
chr5:179875636 | C | T | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1900+284G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875636 | |||||||
chr5:179875682 | A | G | 2 | a0004c0009t0005g0123 a0004c0009t0005g0125 |
2 | HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1900+238T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 11/20 | chr5 | 179875682 | |||||||
chr5:179876083 | G | A | 7 | a0003c0004t0005g0008 a0003c0004t0005g0109 a0003c0004t0005g0110 others(4): Show |
9 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1783-46C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876083 | |||||||
chr5:179876112 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1783-75G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876112 | |||||||
chr5:179876250 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1783-213C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876250 | |||||||
chr5:179876429 | G | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0026 others(6): Show |
15 | HG00609.hp1 HG02015.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1783-392C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876429 | |||||||
chr5:179876719 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1783-682G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876719 | |||||||
chr5:179876724 | G | C | 29 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(26): Show |
30 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1783-687C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876724 | |||||||
chr5:179876786 | A | T | 1 | a0015c0018t0003g0213 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1783-749T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876786 | |||||||
chr5:179876809 | C | T | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1783-772G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876809 | |||||||
chr5:179876900 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1783-863T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179876900 | |||||||
chr5:179877070 | C | CA | 30 | a0001c0001t0001g0151 a0001c0001t0003g0229 a0001c0001t0003g0230 others(27): Show |
32 | HG00597.hp2 HG01255.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1783-1034dupT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877070 | |||||||
chr5:179877070 | C | CAA | 14 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1783-1035_1783-103 others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877070 | |||||||
chr5:179877070 | CA | C | 36 | a0001c0001t0001g0262 a0001c0001t0002g0069 a0001c0001t0003g0174 others(33): Show |
37 | HG00323.hp1 HG01070.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.1783-1034delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877070 | |||||||
chr5:179877156 | G | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1783-1119C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877156 | |||||||
chr5:179877270 | A | G | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1782+1039T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877270 | |||||||
chr5:179877273 | G | A | 3 | a0001c0001t0012g0031 a0001c0001t0013g0032 a0002c0025t0001g0127 |
3 | HG00423.hp1 HG02135.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1782+1036C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877273 | |||||||
chr5:179877293 | G | A | 1 | a0002c0002t0002g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1782+1016C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877293 | |||||||
chr5:179877329 | T | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(297): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.1782+980A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877329 | |||||||
chr5:179877338 | A | T | 29 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(26): Show |
30 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1782+971T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877338 | |||||||
chr5:179877499 | C | G | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1782+810G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877499 | |||||||
chr5:179877664 | C | CA | 20 | a0001c0001t0001g0014 a0001c0001t0001g0265 a0001c0001t0008g0003 others(17): Show |
24 | HG00323.hp2 HG01243.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1782+644dupT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877664 | |||||||
chr5:179877664 | C | CAA | 10 | a0002c0025t0001g0127 a0004c0009t0005g0123 a0004c0009t0005g0124 others(7): Show |
10 | HG02055.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1782+643_1782+644d others(4): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877664 | |||||||
chr5:179877664 | CA | C | 11 | a0001c0001t0001g0203 a0001c0001t0001g0257 a0001c0001t0001g0271 others(8): Show |
11 | HG01070.hp2 HG01167.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1782+644delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877664 | |||||||
chr5:179877679 | A | AG | 18 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(15): Show |
20 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1782+629_1782+630i others(3): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877679 | |||||||
chr5:179877679 | A | G | 1 | a0003c0004t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1782+630T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877679 | |||||||
chr5:179877680 | A | G | 1 | a0002c0003t0006g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1782+629T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877680 | |||||||
chr5:179877689 | G | A | 1 | a0003c0004t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1782+620C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877689 | |||||||
chr5:179877690 | A | G | 1 | a0003c0004t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1782+619T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877690 | |||||||
chr5:179877727 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1782+582C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877727 | |||||||
chr5:179877815 | C | G | 2 | a0002c0002t0002g0083 a0002c0002t0002g0095 |
2 | HG01255.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1782+494G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877815 | |||||||
chr5:179877933 | T | G | 2 | a0002c0006t0001g0141 a0002c0006t0001g0144 |
2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1782+376A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179877933 | |||||||
chr5:179878015 | C | T | 3 | a0001c0011t0001g0134 a0002c0006t0005g0132 a0002c0006t0005g0133 |
3 | HG02257.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1782+294G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179878015 | |||||||
chr5:179878249 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0029 others(79): Show |
100 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1782+60G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179878249 | |||||||
chr5:179878301 | C | T | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1782+8G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 10/20 | chr5 | 179878301 | |||||||
chr5:179878575 | G | T | 9 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568-52C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878575 | |||||||
chr5:179878655 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1568-132G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878655 | |||||||
chr5:179878733 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0082 a0009c0015t0001g0034 |
3 | HG02572.hp1 HG02922.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1568-210C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878733 | |||||||
chr5:179878749 | A | G | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1568-226T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878749 | |||||||
chr5:179878884 | G | C | 1 | a0003c0004t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1567+163C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878884 | |||||||
chr5:179878886 | G | GCCAGAGC | 35 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(32): Show |
37 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1567+154_1567+160d others(9): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878886 | |||||||
chr5:179878886 | G | GCCAGAGC others(7): Show |
1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1567+147_1567+160d others(16): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878886 | |||||||
chr5:179878898 | A | C | 1 | a0002c0003t0006g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1567+149T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878898 | |||||||
chr5:179878903 | A | AGAGCCCA others(7): Show |
1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1567+143_1567+144i others(16): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 9/20 | chr5 | 179878903 | |||||||
chr5:179879211 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1417-14C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879211 | |||||||
chr5:179879237 | G | A | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1417-40C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879237 | |||||||
chr5:179879267 | G | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1417-70C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879267 | |||||||
chr5:179879333 | A | G | 11 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(8): Show |
11 | HG01243.hp1 HG01261.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1417-136T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879333 | |||||||
chr5:179879344 | G | A | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1417-147C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879344 | |||||||
chr5:179879477 | G | A | 1 | a0002c0002t0002g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1416+151C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879477 | |||||||
chr5:179879490 | A | G | 44 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(41): Show |
46 | HG01243.hp1 HG01243.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.1416+138T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879490 | |||||||
chr5:179879517 | A | G | 47 | a0001c0001t0001g0168 a0001c0001t0004g0001 a0001c0001t0004g0020 others(44): Show |
57 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1416+111T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 8/20 | chr5 | 179879517 | |||||||
chr5:179879909 | G | A | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1255-120C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179879909 | |||||||
chr5:179879911 | T | A | 1 | a0001c0001t0004g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1255-122A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179879911 | |||||||
chr5:179879992 | C | T | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-203G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179879992 | |||||||
chr5:179880042 | G | A | 2 | a0001c0001t0003g0217 a0015c0018t0003g0213 |
2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1255-253C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880042 | |||||||
chr5:179880144 | C | T | 1 | a0001c0001t0014g0033 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1255-355G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880144 | |||||||
chr5:179880159 | T | C | 1 | a0002c0002t0004g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1255-370A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880159 | |||||||
chr5:179880331 | C | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
265 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1255-542G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880331 | |||||||
chr5:179880349 | G | C | 1 | a0001c0001t0003g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1255-560C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880349 | |||||||
chr5:179880654 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1255-865C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880654 | |||||||
chr5:179880669 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1255-880G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880669 | |||||||
chr5:179880798 | CCT | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
224 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1255-1011_1255-101 others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880798 | |||||||
chr5:179880882 | G | A | 1 | a0002c0007t0017g0266 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1255-1093C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880882 | |||||||
chr5:179880930 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1255-1141G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880930 | |||||||
chr5:179880939 | C | T | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-1150G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179880939 | |||||||
chr5:179881012 | G | A | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1255-1223C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881012 | |||||||
chr5:179881076 | G | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255-1287C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881076 | |||||||
chr5:179881157 | C | T | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1255-1368G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881157 | |||||||
chr5:179881242 | T | C | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255-1453A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881242 | |||||||
chr5:179881311 | C | T | 1 | a0001c0001t0006g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-1522G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881311 | |||||||
chr5:179881444 | C | T | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255-1655G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881444 | |||||||
chr5:179881708 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1255-1919G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881708 | |||||||
chr5:179881800 | C | T | 1 | a0001c0001t0006g0308 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1255-2011G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881800 | |||||||
chr5:179881946 | G | GT | 38 | a0001c0001t0001g0270 a0001c0001t0001g0277 a0001c0001t0003g0230 others(35): Show |
40 | HG00597.hp1 HG00642.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.1255-2158dupA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(8): Show |
2 | a0001c0011t0001g0134 a0002c0006t0005g0133 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1255-2172_1255-215 others(19): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(9): Show |
1 | a0002c0006t0005g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1255-2173_1255-215 others(20): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(11): Show |
2 | a0002c0006t0021g0298 a0004c0009t0005g0125 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1255-2158_1255-215 others(22): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(12): Show |
4 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0004c0009t0005g0123 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-2158_1255-215 others(23): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(13): Show |
6 | a0004c0009t0005g0124 a0004c0009t0005g0126 a0004c0009t0005g0131 others(3): Show |
6 | HG02055.hp2 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-2158_1255-215 others(24): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(14): Show |
2 | a0002c0006t0001g0144 a0002c0006t0015g0143 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1255-2158_1255-215 others(25): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179881946 | G | GTTTTTTT others(18): Show |
1 | a0002c0006t0001g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1255-2158_1255-215 others(29): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179881946 | |||||||
chr5:179882046 | GC | G | 6 | a0002c0002t0002g0053 a0002c0002t0002g0054 a0002c0002t0002g0055 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-2258delG | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882046 | |||||||
chr5:179882065 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1255-2276A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882065 | |||||||
chr5:179882134 | G | A | 1 | a0001c0001t0020g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1255-2345C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882134 | |||||||
chr5:179882199 | C | T | 10 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(7): Show |
11 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-2410G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882199 | |||||||
chr5:179882376 | C | A | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1255-2587G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882376 | |||||||
chr5:179882464 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1255-2675G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882464 | |||||||
chr5:179882513 | C | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1255-2724G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882513 | |||||||
chr5:179882633 | C | T | 2 | a0002c0012t0002g0093 a0002c0012t0002g0094 |
2 | HG03834.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1255-2844G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882633 | |||||||
chr5:179882677 | C | A | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1255-2888G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882677 | |||||||
chr5:179882742 | C | T | 2 | a0001c0001t0001g0151 a0002c0002t0001g0152 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1255-2953G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882742 | |||||||
chr5:179882752 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1255-2963T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882752 | |||||||
chr5:179882797 | C | T | 1 | a0009c0015t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1255-3008G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882797 | |||||||
chr5:179882843 | A | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1255-3054T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179882843 | |||||||
chr5:179883211 | A | C | 2 | a0002c0002t0002g0067 a0002c0002t0002g0068 |
2 | NA18955.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1255-3422T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883211 | |||||||
chr5:179883235 | T | C | 17 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(14): Show |
17 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1255-3446A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883235 | |||||||
chr5:179883285 | A | G | 4 | a0002c0002t0002g0016 a0002c0002t0002g0048 a0002c0002t0002g0077 others(1): Show |
5 | HG00423.hp2 NA18957.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-3496T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883285 | |||||||
chr5:179883330 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1255-3541G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883330 | |||||||
chr5:179883501 | T | C | 1 | a0001c0001t0003g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1255-3712A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883501 | |||||||
chr5:179883533 | G | T | 2 | a0001c0001t0001g0256 a0001c0001t0018g0281 |
2 | HG03492.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1255-3744C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883533 | |||||||
chr5:179883534 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0262 a0001c0001t0001g0274 |
4 | HG01081.hp1 HG01257.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-3745A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883534 | |||||||
chr5:179883627 | T | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
15 | HG00621.hp1 NA18941.hp2 NA18950.hp2 others(12): Show |
intron_variant | MODIFIER | c.1255-3838A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883627 | |||||||
chr5:179883636 | C | A | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1255-3847G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883636 | |||||||
chr5:179883658 | G | A | 1 | a0002c0002t0002g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1255-3869C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883658 | |||||||
chr5:179883772 | T | G | 25 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(22): Show |
27 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1255-3983A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883772 | |||||||
chr5:179883807 | G | A | 1 | a0001c0001t0004g0260 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1255-4018C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883807 | |||||||
chr5:179883811 | CT | C | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1255-4023delA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883811 | |||||||
chr5:179883922 | A | T | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1255-4133T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883922 | |||||||
chr5:179883984 | T | C | 9 | a0004c0009t0005g0123 a0004c0009t0005g0124 a0004c0009t0005g0125 others(6): Show |
9 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+4119A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179883984 | |||||||
chr5:179884112 | G | A | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+3991C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884112 | |||||||
chr5:179884121 | G | A | 5 | a0001c0001t0003g0010 a0001c0001t0003g0231 a0001c0001t0003g0233 others(2): Show |
7 | HG01074.hp2 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+3982C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884121 | |||||||
chr5:179884354 | G | A | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+3749C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884354 | |||||||
chr5:179884450 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1254+3653C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884450 | |||||||
chr5:179884632 | A | G | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1254+3471T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884632 | |||||||
chr5:179884638 | C | T | 26 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0076 others(23): Show |
28 | HG00323.hp1 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1254+3465G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884638 | |||||||
chr5:179884691 | C | A | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+3412G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884691 | |||||||
chr5:179884711 | G | A | 3 | a0001c0001t0001g0035 a0008c0027t0001g0108 a0009c0015t0001g0034 |
3 | HG02486.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+3392C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884711 | |||||||
chr5:179884942 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1254+3161A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179884942 | |||||||
chr5:179885194 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1254+2909T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885194 | |||||||
chr5:179885271 | C | G | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1254+2832G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885271 | |||||||
chr5:179885272 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1254+2831C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885272 | |||||||
chr5:179885461 | C | T | 16 | a0001c0001t0001g0236 a0001c0001t0003g0251 a0001c0001t0004g0001 others(13): Show |
23 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1254+2642G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885461 | |||||||
chr5:179885482 | G | A | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1254+2621C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885482 | |||||||
chr5:179885484 | G | A | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+2619C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885484 | |||||||
chr5:179885508 | G | C | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1254+2595C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885508 | |||||||
chr5:179885567 | T | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0074 |
2 | HG02132.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1254+2536A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885567 | |||||||
chr5:179885585 | TC | T | 20 | a0001c0001t0001g0035 a0001c0005t0001g0036 a0001c0005t0006g0300 others(17): Show |
21 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.1254+2517delG | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885585 | |||||||
chr5:179885588 | C | A | 1 | a0002c0002t0004g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1254+2515G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885588 | |||||||
chr5:179885592 | C | A | 1 | a0002c0012t0002g0094 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1254+2511G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885592 | |||||||
chr5:179885592 | C | T | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+2511G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885592 | |||||||
chr5:179885594 | CA | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1254+2508delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885594 | |||||||
chr5:179885595 | A | C | 7 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(4): Show |
7 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+2508T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885595 | |||||||
chr5:179885728 | G | A | 1 | a0002c0007t0003g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1254+2375C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885728 | |||||||
chr5:179885811 | G | A | 19 | a0001c0001t0001g0225 a0001c0011t0001g0134 a0001c0011t0001g0145 others(16): Show |
19 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1254+2292C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179885811 | |||||||
chr5:179886091 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1254+2012A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886091 | |||||||
chr5:179886233 | G | C | 1 | a0001c0001t0004g0260 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1254+1870C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886233 | |||||||
chr5:179886283 | T | C | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+1820A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886283 | |||||||
chr5:179886500 | C | T | 1 | a0001c0017t0003g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1254+1603G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886500 | |||||||
chr5:179886522 | C | T | 1 | a0016c0033t0002g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1254+1581G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886522 | |||||||
chr5:179886523 | C | T | 1 | a0002c0002t0002g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1254+1580G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886523 | |||||||
chr5:179886552 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1254+1551A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886552 | |||||||
chr5:179886578 | G | A | 1 | a0002c0002t0002g0067 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1254+1525C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886578 | |||||||
chr5:179886656 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1254+1447G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886656 | |||||||
chr5:179886679 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1254+1424C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886679 | |||||||
chr5:179886714 | G | C | 1 | a0002c0003t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1254+1389C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886714 | |||||||
chr5:179886776 | T | A | 1 | a0002c0002t0002g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1254+1327A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886776 | |||||||
chr5:179886880 | G | A | 1 | a0002c0002t0002g0092 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1254+1223C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886880 | |||||||
chr5:179886883 | G | A | 4 | a0002c0002t0002g0071 a0002c0002t0002g0072 a0002c0002t0002g0100 others(1): Show |
4 | HG00323.hp1 HG01952.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+1220C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886883 | |||||||
chr5:179886887 | C | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1254+1216G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179886887 | |||||||
chr5:179887081 | GGTGA | G | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+1018_1254+102 others(8): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887081 | |||||||
chr5:179887180 | G | A | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1254+923C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887180 | |||||||
chr5:179887185 | G | A | 1 | a0002c0002t0007g0292 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1254+918C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887185 | |||||||
chr5:179887217 | G | C | 1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1254+886C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887217 | |||||||
chr5:179887326 | G | A | 13 | a0001c0011t0001g0134 a0002c0006t0005g0132 a0002c0006t0005g0133 others(10): Show |
13 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1254+777C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887326 | |||||||
chr5:179887630 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1254+473T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887630 | |||||||
chr5:179887834 | A | G | 1 | a0001c0005t0001g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1254+269T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887834 | |||||||
chr5:179887954 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1254+149A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179887954 | |||||||
chr5:179888008 | G | A | 1 | a0001c0017t0003g0218 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1254+95C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 7/20 | chr5 | 179888008 | |||||||
chr5:179888365 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1045-53C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888365 | |||||||
chr5:179888476 | CCCGAGCA others(10): Show |
C | 1 | a0002c0002t0002g0049 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1045-181_1045-165d others(19): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888476 | |||||||
chr5:179888525 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1045-213G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888525 | |||||||
chr5:179888794 | C | T | 47 | a0001c0001t0001g0168 a0001c0001t0004g0001 a0001c0001t0004g0020 others(44): Show |
57 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1045-482G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888794 | |||||||
chr5:179888839 | G | C | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1045-527C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888839 | |||||||
chr5:179888942 | C | T | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1045-630G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179888942 | |||||||
chr5:179889036 | C | A | 36 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(33): Show |
38 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.1045-724G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889036 | |||||||
chr5:179889036 | C | CT | 9 | a0001c0001t0011g0219 a0001c0001t0020g0147 a0002c0002t0002g0054 others(6): Show |
9 | HG01169.hp2 HG02922.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045-725dupA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889036 | |||||||
chr5:179889036 | C | T | 1 | a0006c0010t0005g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1045-724G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889036 | |||||||
chr5:179889037 | T | C | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1045-725A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889037 | |||||||
chr5:179889154 | C | T | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045-842G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889154 | |||||||
chr5:179889191 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0011g0219 a0001c0001t0011g0220 |
3 | NA18985.hp2 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1045-879C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889191 | |||||||
chr5:179889239 | AG | A | 2 | a0001c0001t0008g0003 a0001c0001t0008g0200 |
5 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1045-928delC | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889239 | |||||||
chr5:179889348 | C | G | 2 | a0002c0007t0001g0190 a0002c0007t0001g0191 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1045-1036G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889348 | |||||||
chr5:179889384 | C | G | 1 | a0004c0009t0005g0125 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1045-1072G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889384 | |||||||
chr5:179889396 | GGGGAGAG others(36): Show |
G | 9 | a0001c0005t0001g0036 a0001c0005t0006g0305 a0002c0003t0006g0030 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045-1127_1045-108 others(47): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889396 | |||||||
chr5:179889616 | T | G | 1 | a0002c0002t0002g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1045-1304A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889616 | |||||||
chr5:179889717 | T | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(218): Show |
264 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1045-1405A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889717 | |||||||
chr5:179889871 | C | CA | 30 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(27): Show |
32 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1044+1507dupT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889871 | |||||||
chr5:179889871 | C | CAA | 14 | a0001c0011t0001g0134 a0002c0003t0005g0118 a0002c0006t0005g0132 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1044+1506_1044+150 others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889871 | |||||||
chr5:179889871 | CA | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
214 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1044+1507delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889871 | |||||||
chr5:179889895 | A | G | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1044+1484T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889895 | |||||||
chr5:179889897 | G | A | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1044+1482C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889897 | |||||||
chr5:179889988 | C | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0103 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1044+1391G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889988 | |||||||
chr5:179889988 | C | T | 1 | a0002c0002t0002g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1044+1391G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179889988 | |||||||
chr5:179890080 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1044+1299C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890080 | |||||||
chr5:179890283 | G | A | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044+1096C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890283 | |||||||
chr5:179890397 | C | T | 4 | a0002c0002t0002g0016 a0002c0002t0002g0048 a0002c0002t0002g0077 others(1): Show |
5 | HG00423.hp2 NA18957.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044+982G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890397 | |||||||
chr5:179890787 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1044+592G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890787 | |||||||
chr5:179890901 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0262 |
3 | HG01081.hp1 HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1044+478C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890901 | |||||||
chr5:179890942 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1044+437G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 6/20 | chr5 | 179890942 | |||||||
chr5:179891801 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.837-215G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179891801 | |||||||
chr5:179892056 | C | T | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.837-470G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892056 | |||||||
chr5:179892057 | G | T | 37 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(34): Show |
39 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.837-471C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892057 | |||||||
chr5:179892174 | C | T | 1 | a0004c0009t0005g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.837-588G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892174 | |||||||
chr5:179892208 | G | A | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.837-622C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892208 | |||||||
chr5:179892231 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.837-645C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892231 | |||||||
chr5:179892262 | C | T | 1 | a0002c0002t0002g0047 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.837-676G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892262 | |||||||
chr5:179892279 | G | A | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.837-693C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892279 | |||||||
chr5:179892345 | A | G | 3 | a0002c0002t0001g0051 a0002c0002t0001g0103 a0002c0002t0005g0050 |
3 | HG01884.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.837-759T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892345 | |||||||
chr5:179892375 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(218): Show |
264 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.837-789G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892375 | |||||||
chr5:179892473 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.836+736C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892473 | |||||||
chr5:179892499 | TCTGGAGT others(17): Show |
T | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.836+686_836+709del others(24): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892499 | |||||||
chr5:179892586 | G | A | 4 | a0001c0001t0003g0155 a0001c0001t0003g0226 a0001c0001t0003g0227 others(1): Show |
4 | HG02683.hp2 HG04115.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.836+623C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892586 | |||||||
chr5:179892600 | G | A | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.836+609C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892600 | |||||||
chr5:179892697 | C | A | 1 | a0001c0001t0004g0177 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.836+512G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892697 | |||||||
chr5:179892766 | C | T | 49 | a0001c0001t0001g0168 a0001c0001t0001g0255 a0001c0001t0002g0076 others(46): Show |
59 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.836+443G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892766 | |||||||
chr5:179892943 | C | T | 4 | a0002c0002t0002g0047 a0002c0002t0002g0073 a0002c0002t0002g0074 others(1): Show |
4 | HG02129.hp2 HG02132.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.836+266G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892943 | |||||||
chr5:179892988 | C | CCCCATTA others(7): Show |
1 | a0002c0002t0002g0049 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.836+220_836+221ins others(14): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179892988 | |||||||
chr5:179893073 | C | T | 1 | a0002c0003t0006g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.836+136G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 5/20 | chr5 | 179893073 | |||||||
chr5:179893511 | G | C | 1 | a0002c0002t0016g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.578-44C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893511 | |||||||
chr5:179893584 | G | T | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.578-117C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893584 | |||||||
chr5:179893601 | T | A | 2 | a0001c0001t0003g0154 a0001c0001t0003g0232 |
2 | HG02135.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.578-134A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893601 | |||||||
chr5:179893645 | G | A | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.578-178C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893645 | |||||||
chr5:179893675 | C | T | 6 | a0004c0009t0005g0123 a0004c0009t0005g0124 a0004c0009t0005g0125 others(3): Show |
6 | HG02896.hp1 HG02970.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.578-208G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893675 | |||||||
chr5:179893720 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(224): Show |
270 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.578-253G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893720 | |||||||
chr5:179893775 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.578-308G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893775 | |||||||
chr5:179893874 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.578-407C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893874 | |||||||
chr5:179893967 | G | A | 1 | a0016c0033t0002g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.577+419C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179893967 | |||||||
chr5:179894009 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.577+377C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894009 | |||||||
chr5:179894098 | T | C | 38 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(35): Show |
40 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.577+288A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894098 | |||||||
chr5:179894107 | C | T | 6 | a0005c0008t0001g0037 a0005c0008t0001g0038 a0005c0008t0001g0039 others(3): Show |
6 | HG02922.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.577+279G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894107 | |||||||
chr5:179894121 | C | T | 44 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(41): Show |
46 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.577+265G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894121 | |||||||
chr5:179894140 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.577+246C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894140 | |||||||
chr5:179894155 | C | G | 1 | a0002c0025t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.577+231G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894155 | |||||||
chr5:179894185 | G | A | 1 | a0002c0002t0002g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.577+201C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894185 | |||||||
chr5:179894310 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.577+76C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894310 | |||||||
chr5:179894377 | C | T | 1 | a0002c0002t0007g0293 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.577+9G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 4/20 | chr5 | 179894377 | |||||||
chr5:179894657 | C | T | 23 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0002t0002g0046 others(20): Show |
23 | HG00323.hp1 HG01361.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.349-43G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179894657 | |||||||
chr5:179894728 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(23): Show |
37 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.349-114T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179894728 | |||||||
chr5:179894819 | T | G | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-205A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179894819 | |||||||
chr5:179894865 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
243 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.349-251C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179894865 | |||||||
chr5:179894887 | G | A | 1 | a0002c0003t0005g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-273C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179894887 | |||||||
chr5:179895004 | G | A | 2 | a0001c0001t0003g0201 a0001c0001t0022g0309 |
2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.349-390C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895004 | |||||||
chr5:179895007 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.349-393C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895007 | |||||||
chr5:179895063 | G | A | 1 | a0002c0002t0002g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.349-449C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895063 | |||||||
chr5:179895072 | G | C | 1 | a0018c0032t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.349-458C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895072 | |||||||
chr5:179895081 | A | C | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.349-467T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895081 | |||||||
chr5:179895101 | T | G | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-487A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895101 | |||||||
chr5:179895103 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.349-489G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895103 | |||||||
chr5:179895156 | T | A | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-542A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895156 | |||||||
chr5:179895217 | T | A | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-603A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895217 | |||||||
chr5:179895229 | G | A | 1 | a0002c0002t0002g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.349-615C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895229 | |||||||
chr5:179895342 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349-728C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895342 | |||||||
chr5:179895403 | G | A | 1 | a0001c0001t0004g0183 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.349-789C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895403 | |||||||
chr5:179895514 | T | C | 40 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(37): Show |
42 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.349-900A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895514 | |||||||
chr5:179895616 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-1002G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895616 | |||||||
chr5:179895617 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-1003A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895617 | |||||||
chr5:179895626 | A | T | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-1012T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895626 | |||||||
chr5:179895670 | G | T | 1 | a0001c0001t0020g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.349-1056C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895670 | |||||||
chr5:179895713 | G | A | 17 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(14): Show |
17 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.349-1099C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895713 | |||||||
chr5:179895853 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.349-1239A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179895853 | |||||||
chr5:179896088 | TCA | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
212 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.349-1476_349-1475d others(4): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896088 | |||||||
chr5:179896119 | G | A | 4 | a0002c0003t0005g0119 a0002c0003t0005g0120 a0002c0003t0005g0121 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-1505C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896119 | |||||||
chr5:179896365 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.349-1751G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896365 | |||||||
chr5:179896384 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.349-1770G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896384 | |||||||
chr5:179896513 | G | A | 1 | a0008c0027t0001g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349-1899C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896513 | |||||||
chr5:179896550 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-1936A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896550 | |||||||
chr5:179896551 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-1937G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896551 | |||||||
chr5:179896578 | T | A | 37 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(34): Show |
39 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.349-1964A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896578 | |||||||
chr5:179896616 | G | A | 1 | a0002c0002t0002g0068 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.349-2002C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896616 | |||||||
chr5:179896762 | G | GATCCACC others(16): Show |
1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.349-2171_349-2149d others(25): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896762 | |||||||
chr5:179896909 | C | A | 2 | a0001c0001t0004g0021 a0001c0001t0004g0172 |
3 | NA18969.hp2 NA18983.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.348+2280G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896909 | |||||||
chr5:179896912 | C | T | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2277G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896912 | |||||||
chr5:179896930 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.348+2259C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896930 | |||||||
chr5:179896992 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.348+2197G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896992 | |||||||
chr5:179896998 | C | G | 31 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(28): Show |
33 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.348+2191G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896998 | |||||||
chr5:179896999 | C | A | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.348+2190G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179896999 | |||||||
chr5:179897000 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.348+2189T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897000 | |||||||
chr5:179897002 | G | C | 1 | a0001c0001t0002g0069 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.348+2187C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897002 | |||||||
chr5:179897071 | TA | T | 3 | a0006c0010t0005g0128 a0006c0010t0005g0129 a0006c0010t0005g0130 |
3 | HG02055.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.348+2117delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897071 | |||||||
chr5:179897122 | T | C | 1 | a0002c0003t0006g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+2067A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897122 | |||||||
chr5:179897153 | C | T | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+2036G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897153 | |||||||
chr5:179897198 | C | T | 2 | a0001c0001t0004g0160 a0002c0002t0002g0052 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.348+1991G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897198 | |||||||
chr5:179897316 | C | CT | 43 | a0001c0001t0001g0156 a0001c0001t0001g0168 a0001c0001t0004g0001 others(40): Show |
53 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.348+1872dupA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897316 | |||||||
chr5:179897408 | G | A | 1 | a0002c0006t0021g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+1781C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897408 | |||||||
chr5:179897446 | T | C | 1 | a0002c0003t0006g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+1743A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897446 | |||||||
chr5:179897469 | C | T | 1 | a0002c0003t0006g0307 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.348+1720G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179897469 | |||||||
chr5:179898064 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0202 |
3 | HG01358.hp1 HG01433.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.348+1125G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898064 | |||||||
chr5:179898141 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.348+1048G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898141 | |||||||
chr5:179898142 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.348+1047G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898142 | |||||||
chr5:179898152 | C | CT | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(197): Show |
241 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.348+1036dupA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898152 | |||||||
chr5:179898152 | C | CTT | 27 | a0001c0001t0001g0035 a0001c0001t0003g0230 a0001c0001t0003g0231 others(24): Show |
29 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.348+1035_348+1036d others(4): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898152 | |||||||
chr5:179898225 | C | T | 1 | a0001c0001t0003g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.348+964G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898225 | |||||||
chr5:179898435 | G | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0103 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.348+754C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898435 | |||||||
chr5:179898435 | G | C | 1 | a0001c0001t0001g0019 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.348+754C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898435 | |||||||
chr5:179898471 | T | C | 1 | a0017c0031t0001g0250 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.348+718A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898471 | |||||||
chr5:179898519 | G | A | 1 | a0001c0001t0004g0287 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.348+670C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898519 | |||||||
chr5:179898574 | G | A | 2 | a0002c0002t0002g0049 a0002c0002t0002g0101 |
2 | HG03927.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.348+615C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898574 | |||||||
chr5:179898710 | T | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.348+479A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898710 | |||||||
chr5:179898737 | C | T | 1 | a0002c0003t0006g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+452G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898737 | |||||||
chr5:179898988 | C | T | 3 | a0003c0004t0005g0008 a0003c0004t0005g0109 a0003c0004t0005g0110 |
5 | HG02109.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+201G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898988 | |||||||
chr5:179898997 | G | A | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.348+192C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179898997 | |||||||
chr5:179899023 | G | A | 1 | a0001c0001t0004g0177 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.348+166C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179899023 | |||||||
chr5:179899134 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.348+55C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 3/20 | chr5 | 179899134 | |||||||
chr5:179899362 | C | T | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.230-55G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899362 | |||||||
chr5:179899512 | G | A | 1 | a0009c0015t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.230-205C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899512 | |||||||
chr5:179899616 | T | C | 18 | a0001c0011t0001g0134 a0001c0011t0001g0145 a0002c0006t0001g0141 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.230-309A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899616 | |||||||
chr5:179899707 | A | T | 5 | a0001c0001t0001g0208 a0001c0001t0003g0025 a0001c0001t0003g0146 others(2): Show |
6 | HG00408.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-400T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899707 | |||||||
chr5:179899958 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.230-651G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899958 | |||||||
chr5:179899969 | C | T | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-662G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899969 | |||||||
chr5:179899977 | C | A | 2 | a0002c0006t0005g0132 a0002c0006t0005g0133 |
2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.230-670G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179899977 | |||||||
chr5:179900304 | C | T | 1 | a0001c0001t0004g0022 | 2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.230-997G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900304 | |||||||
chr5:179900513 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(138): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.230-1206C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900513 | |||||||
chr5:179900582 | T | C | 8 | a0001c0001t0004g0022 a0001c0001t0004g0185 a0001c0001t0004g0186 others(5): Show |
9 | HG00733.hp1 HG01074.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-1275A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900582 | |||||||
chr5:179900590 | C | T | 1 | a0002c0002t0002g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.230-1283G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900590 | |||||||
chr5:179900631 | G | A | 1 | a0001c0005t0006g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.230-1324C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900631 | |||||||
chr5:179900689 | G | A | 1 | a0001c0011t0001g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.230-1382C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900689 | |||||||
chr5:179900751 | A | C | 55 | a0001c0001t0001g0168 a0001c0001t0001g0224 a0001c0001t0001g0225 others(52): Show |
65 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.230-1444T>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900751 | |||||||
chr5:179900758 | C | T | 1 | a0002c0002t0002g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.230-1451G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900758 | |||||||
chr5:179900759 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0194 a0018c0032t0001g0222 |
5 | NA18956.hp1 NA18979.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-1452C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900759 | |||||||
chr5:179900826 | C | T | 14 | a0001c0001t0001g0221 a0001c0001t0001g0284 a0001c0001t0003g0024 others(11): Show |
15 | HG00408.hp1 HG00639.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.230-1519G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900826 | |||||||
chr5:179900827 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
293 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.230-1520T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900827 | |||||||
chr5:179900985 | C | T | 1 | a0001c0001t0003g0209 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.230-1678G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900985 | |||||||
chr5:179900986 | G | A | 9 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.230-1679C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179900986 | |||||||
chr5:179901109 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0006g0308 others(5): Show |
9 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-1802C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901109 | |||||||
chr5:179901111 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 |
3 | HG00597.hp2 NA18943.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.230-1804A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901111 | |||||||
chr5:179901191 | G | C | 6 | a0001c0005t0006g0300 a0002c0003t0006g0299 a0002c0003t0006g0301 others(3): Show |
6 | HG02451.hp2 HG03195.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-1884C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901191 | |||||||
chr5:179901228 | C | T | 114 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0151 others(111): Show |
127 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(124): Show |
intron_variant | MODIFIER | c.230-1921G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901228 | |||||||
chr5:179901421 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.230-2114T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901421 | |||||||
chr5:179901506 | C | T | 1 | a0001c0001t0004g0158 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.230-2199G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901506 | |||||||
chr5:179901512 | CAGTGGCT others(3): Show |
C | 2 | a0001c0001t0004g0205 a0001c0001t0004g0280 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.230-2215_230-2206d others(12): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901512 | |||||||
chr5:179901565 | G | A | 1 | a0001c0001t0020g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.230-2258C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901565 | |||||||
chr5:179901729 | C | T | 2 | a0002c0003t0006g0301 a0002c0003t0006g0302 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.230-2422G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901729 | |||||||
chr5:179901803 | A | G | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-2496T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901803 | |||||||
chr5:179901916 | T | C | 1 | a0002c0002t0002g0102 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.230-2609A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901916 | |||||||
chr5:179901977 | G | A | 1 | a0001c0001t0018g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.230-2670C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179901977 | |||||||
chr5:179902125 | G | A | 38 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(35): Show |
40 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.229+2577C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902125 | |||||||
chr5:179902151 | G | A | 12 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(9): Show |
13 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.229+2551C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902151 | |||||||
chr5:179902568 | T | C | 1 | a0001c0001t0014g0033 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.229+2134A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902568 | |||||||
chr5:179902581 | G | A | 1 | a0001c0001t0004g0206 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.229+2121C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902581 | |||||||
chr5:179902650 | G | C | 1 | a0014c0021t0001g0282 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.229+2052C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902650 | |||||||
chr5:179902905 | TCTTA | T | 41 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(38): Show |
43 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.229+1793_229+1796d others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902905 | |||||||
chr5:179902931 | A | G | 41 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(38): Show |
43 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.229+1771T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902931 | |||||||
chr5:179902970 | G | A | 1 | a0002c0002t0002g0104 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.229+1732C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179902970 | |||||||
chr5:179903185 | G | A | 2 | a0002c0003t0006g0030 a0002c0003t0006g0307 |
3 | HG03041.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.229+1517C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903185 | |||||||
chr5:179903287 | T | A | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+1415A>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903287 | |||||||
chr5:179903290 | TTCAGGCA others(4): Show |
T | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+1401_229+1411d others(13): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903290 | |||||||
chr5:179903302 | C | A | 5 | a0001c0011t0001g0145 a0002c0006t0001g0141 a0002c0006t0001g0142 others(2): Show |
5 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+1400G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903302 | |||||||
chr5:179903327 | A | G | 1 | a0005c0008t0001g0037 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.229+1375T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903327 | |||||||
chr5:179903636 | C | T | 41 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(38): Show |
43 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.229+1066G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903636 | |||||||
chr5:179903696 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
272 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.229+1006A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903696 | |||||||
chr5:179903701 | C | A | 3 | a0001c0001t0001g0035 a0008c0027t0001g0108 a0009c0015t0001g0034 |
3 | HG02486.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.229+1001G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903701 | |||||||
chr5:179903764 | A | G | 41 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(38): Show |
43 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.229+938T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903764 | |||||||
chr5:179903926 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.229+776G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179903926 | |||||||
chr5:179904150 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.229+552C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904150 | |||||||
chr5:179904219 | C | CCTTT | 7 | a0001c0001t0004g0157 a0005c0008t0001g0037 a0005c0008t0001g0038 others(4): Show |
7 | HG02056.hp1 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.229+479_229+482dup others(4): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904219 | |||||||
chr5:179904220 | C | CT | 9 | a0001c0001t0002g0044 a0002c0002t0002g0043 a0002c0002t0002g0045 others(6): Show |
9 | HG01361.hp2 HG02071.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+481dupA | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904220 | |||||||
chr5:179904220 | C | CTTTCT | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.229+481_229+482ins others(5): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904220 | |||||||
chr5:179904220 | C | CTTTCTT | 40 | a0001c0001t0001g0035 a0001c0005t0001g0113 a0001c0005t0005g0111 others(37): Show |
42 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.229+481_229+482ins others(6): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904220 | |||||||
chr5:179904221 | T | TTTC | 67 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0001g0156 others(64): Show |
81 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.229+480_229+481ins others(3): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904221 | |||||||
chr5:179904222 | T | TTC | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
126 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.229+479_229+480ins others(2): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904222 | |||||||
chr5:179904223 | T | TC | 3 | a0001c0001t0001g0284 a0001c0001t0001g0286 a0001c0001t0019g0285 |
3 | HG00639.hp1 NA18957.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.229+478_229+479ins others(1): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904223 | |||||||
chr5:179904255 | C | G | 1 | a0002c0006t0001g0141 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.229+447G>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904255 | |||||||
chr5:179904296 | C | T | 11 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(8): Show |
12 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.229+406G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904296 | |||||||
chr5:179904368 | G | A | 3 | a0003c0004t0005g0137 a0003c0004t0005g0138 a0003c0004t0005g0139 |
3 | HG02717.hp1 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.229+334C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904368 | |||||||
chr5:179904410 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.229+292T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904410 | |||||||
chr5:179904417 | T | G | 1 | a0002c0002t0002g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.229+285A>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904417 | |||||||
chr5:179904446 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.229+256G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904446 | |||||||
chr5:179904503 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0151 a0001c0001t0003g0154 others(2): Show |
6 | HG02135.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.229+199T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904503 | |||||||
chr5:179904519 | C | T | 2 | a0001c0001t0003g0150 a0002c0006t0021g0298 |
2 | HG03471.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.229+183G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 2/20 | chr5 | 179904519 | |||||||
chr5:179904940 | G | A | 2 | a0001c0001t0004g0287 a0001c0001t0014g0033 |
2 | HG02683.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.119-128C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179904940 | |||||||
chr5:179904983 | G | C | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.119-171C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179904983 | |||||||
chr5:179905430 | C | A | 17 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(14): Show |
18 | HG02145.hp1 HG02451.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.119-618G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905430 | |||||||
chr5:179905440 | CA | C | 3 | a0001c0001t0001g0035 a0008c0027t0001g0108 a0009c0015t0001g0034 |
3 | HG02486.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.119-629delT | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905440 | |||||||
chr5:179905598 | G | T | 1 | a0002c0002t0004g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.119-786C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905598 | |||||||
chr5:179905602 | C | T | 1 | a0001c0001t0003g0148 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.119-790G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905602 | |||||||
chr5:179905672 | G | A | 1 | a0001c0001t0003g0288 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.119-860C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905672 | |||||||
chr5:179905924 | A | G | 10 | a0001c0005t0006g0300 a0001c0005t0006g0305 a0002c0003t0006g0030 others(7): Show |
11 | HG02145.hp1 HG02451.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-1112T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905924 | |||||||
chr5:179905982 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
213 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.119-1170G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179905982 | |||||||
chr5:179906018 | A | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
272 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.119-1206T>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906018 | |||||||
chr5:179906213 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.119-1401G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906213 | |||||||
chr5:179906233 | G | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
210 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.119-1421C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906233 | |||||||
chr5:179906487 | TATGACAC others(12): Show |
T | 2 | a0001c0005t0006g0300 a0002c0003t0006g0299 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.118+1198_118+1216d others(21): Show |
TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906487 | |||||||
chr5:179906518 | G | C | 1 | a0001c0001t0004g0289 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.118+1186C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906518 | |||||||
chr5:179906702 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(170): Show |
213 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.118+1002A>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906702 | |||||||
chr5:179906740 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
209 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.118+964C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906740 | |||||||
chr5:179906820 | G | A | 32 | a0001c0005t0001g0113 a0001c0005t0005g0111 a0001c0005t0005g0112 others(29): Show |
34 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.118+884C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906820 | |||||||
chr5:179906826 | C | A | 1 | a0001c0011t0001g0145 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118+878G>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906826 | |||||||
chr5:179906889 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.118+815T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906889 | |||||||
chr5:179906903 | C | T | 23 | a0001c0005t0001g0036 a0001c0005t0006g0300 a0001c0005t0006g0305 others(20): Show |
24 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+801G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179906903 | |||||||
chr5:179907029 | G | A | 1 | a0013c0019t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.118+675C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907029 | |||||||
chr5:179907052 | G | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
217 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.118+652C>G | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907052 | |||||||
chr5:179907053 | A | G | 1 | a0002c0002t0007g0291 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.118+651T>C | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907053 | |||||||
chr5:179907167 | G | T | 1 | a0009c0015t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.118+537C>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907167 | |||||||
chr5:179907337 | G | A | 1 | a0002c0002t0002g0290 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118+367C>T | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907337 | |||||||
chr5:179907563 | C | T | 2 | a0001c0001t0001g0035 a0009c0015t0001g0034 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.118+141G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907563 | |||||||
chr5:179907631 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG00323.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.118+73G>A | TBC1D9B | ENSG00000197226.13 | transcript | ENST00000355235.8 | protein_coding | 1/20 | chr5 | 179907631 |