Item | Value |
---|---|
geneid | 11138 |
ensemblid | ENSG00000204634.13 |
hgncid | 17791 |
symbol | TBC1D8 |
name | TBC1 domain family member 8 |
refseq_nuc | NM_001330348.2 |
refseq_prot | NP_001317277.1 |
ensembl_nuc | ENST00000409318.2 |
ensembl_prot | ENSP00000386856.1 |
mane_status | MANE Select |
chr | chr2 |
start | 101007228 |
end | 101151382 |
strand | - |
ver | v1.2 |
region | chr2:101007228-101151382 |
region5000 | chr2:101002228-101156382 |
regionname0 | TBC1D8_chr2_101007228_101151382 |
regionname5000 | TBC1D8_chr2_101002228_101156382 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1155 | 152 | 28 | 29 | 74 | 4 | 15 | 60 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0002 | 0/0 | 1155 | 109 | 13 | 24 | 50 | 3 | 19 | 43 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0003 | 0/0 | 1155 | 13 | 0 | 0 | 12 | 0 | 1 | 8 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0004 | 0/0 | 1156 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1151): Show |
chr2 | 101002228 | 101156382 |
a0005 | 0/0 | 1155 | 8 | 0 | 2 | 1 | 3 | 2 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0006 | 0/0 | 1155 | 8 | 6 | 1 | 1 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0007 | 0/0 | 1155 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0008 | 0/0 | 1156 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1151): Show |
chr2 | 101002228 | 101156382 |
a0009 | 0/0 | 1155 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0010 | 0/0 | 1156 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1151): Show |
chr2 | 101002228 | 101156382 |
a0011 | 0/0 | 1155 | 4 | 1 | 0 | 2 | 0 | 1 | 2 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0012 | 0/0 | 1156 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1151): Show |
chr2 | 101002228 | 101156382 |
a0013 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0014 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0015 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0016 | 0/0 | 1156 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1151): Show |
chr2 | 101002228 | 101156382 |
a0017 | 0/0 | 1155 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
a0018 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | MWLKP others(1150): Show |
chr2 | 101002228 | 101156382 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3465 | 146 | 26 | 29 | 70 | 4 | 15 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0001c0009 | 0/0 | 3465 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0001c0021 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0001c0023 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0001c0024 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0002c0002 | 0/0 | 3465 | 59 | 4 | 13 | 27 | 3 | 12 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0002c0003 | 0/0 | 3465 | 45 | 8 | 8 | 22 | 0 | 7 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0002c0016 | 0/0 | 3465 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0002c0018 | 0/0 | 3465 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0002c0032 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0003c0004 | 0/0 | 3465 | 13 | 0 | 0 | 12 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0004c0005 | 0/0 | 3468 | 11 | 10 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0005c0006 | 0/0 | 3465 | 7 | 0 | 2 | 0 | 3 | 2 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0005c0030 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0006c0010 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0006c0012 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0006c0013 | 0/0 | 3465 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0006c0025 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0007c0007 | 0/0 | 3465 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0007c0019 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0008c0011 | 0/0 | 3468 | 3 | 2 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0008c0015 | 0/0 | 3468 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0009c0014 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0009c0020 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0009c0033 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0010c0008 | 0/0 | 3468 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0011c0017 | 0/0 | 3465 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0011c0031 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0011c0036 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0012c0028 | 0/0 | 3468 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0013c0026 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0014c0034 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0015c0029 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0016c0035 | 0/0 | 3468 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3463): Show |
chr2 | 101002228 | 101156382 | ||
a0017c0027 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 | ||
a0018c0022 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | ATGTG others(3460): Show |
chr2 | 101002228 | 101156382 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4190 | 140 | 22 | 28 | 69 | 4 | 15 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0001t0003 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0001t0004 | 0/0 | 4190 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0001t0005 | 0/0 | 4190 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0001t0006 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0009t0001 | 0/0 | 4190 | 3 | 0 | 0 | 3 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0021t0004 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0023t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0001c0024t0003 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0002t0002 | 0/0 | 4190 | 59 | 4 | 13 | 27 | 3 | 12 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0003t0001 | 0/0 | 4190 | 44 | 7 | 8 | 22 | 0 | 7 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0003t0007 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0016t0002 | 0/0 | 4190 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0018t0001 | 0/0 | 4190 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0002c0032t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0003c0004t0001 | 0/0 | 4190 | 13 | 0 | 0 | 12 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0004c0005t0001 | 0/0 | 4193 | 11 | 10 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0005c0006t0001 | 0/0 | 4190 | 7 | 0 | 2 | 0 | 3 | 2 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0005c0030t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0006c0010t0001 | 0/0 | 4190 | 3 | 3 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0006c0012t0002 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0006c0013t0001 | 0/0 | 4190 | 2 | 0 | 1 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0006c0025t0002 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0007c0007t0001 | 0/0 | 4190 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0007c0019t0001 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0008c0011t0001 | 0/0 | 4193 | 3 | 2 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0008c0015t0001 | 0/0 | 4193 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0009c0014t0003 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0009c0020t0003 | 0/0 | 4190 | 2 | 2 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0009c0033t0003 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0010c0008t0001 | 0/0 | 4193 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0011c0017t0001 | 0/0 | 4190 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0011c0031t0001 | 0/0 | 4190 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0011c0036t0001 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0012c0028t0003 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0013c0026t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0014c0034t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0015c0029t0002 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0016c0035t0001 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4188): Show |
chr2 | 101002228 | 101156382 |
a0017c0027t0001 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
a0018c0022t0001 | 0/0 | 4190 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | AGAGC others(4185): Show |
chr2 | 101002228 | 101156382 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0009t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0009t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0009t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0021t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0023t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0001c0024t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0003t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0016t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0016t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0018t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0018t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0002c0032t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0003c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0004c0005t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0006t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0005c0030t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0010t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0010t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0012t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0012t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0013t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0013t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0006c0025t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0007t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0007t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0019t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0007c0019t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0008c0011t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0008c0011t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0008c0011t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0008c0015t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0008c0015t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0009c0014t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0009c0014t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0009c0020t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0009c0020t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0009c0033t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0010c0008t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0010c0008t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0010c0008t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0010c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0011c0017t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0011c0017t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0011c0031t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0011c0036t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0012c0028t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0013c0026t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0014c0034t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0015c0029t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0016c0035t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0017c0027t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
a0018c0022t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0001 | g0053 | EUR | GBR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | GBR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0322 | EUR | GBR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00323 | hp1 | a0005 | c0006 | t0001 | g0051 | EUR | FIN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00639 | hp2 | a0002 | c0018 | t0001 | g0144 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0262 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00735 | hp2 | a0002 | c0018 | t0001 | g0145 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0164 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0199 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0203 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01081 | hp2 | a0005 | c0006 | t0001 | g0054 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0056 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01167 | hp2 | a0008 | c0011 | t0001 | g0208 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0081 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0014 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01256 | hp1 | a0002 | c0003 | t0001 | g0078 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01257 | hp1 | a0005 | c0006 | t0001 | g0211 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01346 | hp1 | a0006 | c0013 | t0001 | g0299 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01346 | hp2 | a0002 | c0016 | t0002 | g0050 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0049 | EUR | IBS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01891 | hp1 | a0008 | c0011 | t0001 | g0036 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01891 | hp2 | a0007 | c0007 | t0001 | g0044 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG01975 | hp2 | a0002 | c0003 | t0001 | g0257 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02015 | hp1 | a0001 | c0023 | t0001 | g0115 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02015 | hp2 | a0005 | c0030 | t0001 | g0169 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02027 | hp1 | a0003 | c0004 | t0001 | g0272 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02074 | hp2 | a0003 | c0004 | t0001 | g0269 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02080 | hp2 | a0003 | c0004 | t0001 | g0271 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02145 | hp1 | a0004 | c0005 | t0001 | g0002 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02145 | hp2 | a0006 | c0012 | t0002 | g0161 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0080 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02280 | hp1 | a0004 | c0005 | t0001 | g0284 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02280 | hp2 | a0011 | c0036 | t0001 | g0037 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02451 | hp1 | a0004 | c0005 | t0001 | g0110 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02451 | hp2 | a0007 | c0007 | t0001 | g0043 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02523 | hp1 | a0003 | c0004 | t0001 | g0266 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02572 | hp1 | a0006 | c0012 | t0002 | g0279 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02572 | hp2 | a0008 | c0015 | t0001 | g0075 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0313 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02630 | hp1 | a0006 | c0010 | t0001 | g0109 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02630 | hp2 | a0007 | c0019 | t0001 | g0061 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02647 | hp1 | a0008 | c0011 | t0001 | g0280 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02647 | hp2 | a0004 | c0005 | t0001 | g0276 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02698 | hp1 | a0005 | c0006 | t0001 | g0099 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02717 | hp1 | a0004 | c0005 | t0001 | g0286 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02723 | hp2 | a0010 | c0008 | t0001 | g0040 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02809 | hp1 | a0002 | c0003 | t0001 | g0218 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02818 | hp2 | a0006 | c0010 | t0001 | g0217 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02886 | hp2 | a0004 | c0005 | t0001 | g0281 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0220 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0219 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02922 | hp1 | a0001 | c0024 | t0003 | g0327 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0287 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02976 | hp1 | a0010 | c0008 | t0001 | g0039 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02976 | hp2 | a0006 | c0010 | t0001 | g0224 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03041 | hp2 | a0008 | c0015 | t0001 | g0100 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03130 | hp2 | a0004 | c0005 | t0001 | g0034 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03139 | hp1 | a0009 | c0020 | t0003 | g0331 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03139 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03195 | hp1 | a0012 | c0028 | t0003 | g0326 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03209 | hp1 | a0007 | c0007 | t0001 | g0045 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03209 | hp2 | a0009 | c0033 | t0003 | g0328 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03225 | hp1 | a0004 | c0005 | t0001 | g0206 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03225 | hp2 | a0007 | c0019 | t0001 | g0060 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0092 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03453 | hp2 | a0010 | c0008 | t0001 | g0159 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03490 | hp1 | a0011 | c0031 | t0001 | g0163 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | ESN | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03540 | hp1 | a0009 | c0014 | t0003 | g0325 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03654 | hp1 | a0002 | c0003 | t0001 | g0171 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0191 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03669 | hp2 | a0002 | c0003 | t0001 | g0079 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0102 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0201 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0105 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03710 | hp2 | a0003 | c0004 | t0001 | g0273 | SAS | PJL | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0095 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0162 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0026 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0188 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0076 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18522 | hp1 | a0009 | c0014 | t0003 | g0330 | AFR | YRI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18522 | hp2 | a0007 | c0007 | t0001 | g0046 | AFR | YRI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | CHB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18943 | hp1 | a0003 | c0004 | t0001 | g0274 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18951 | hp1 | a0003 | c0004 | t0001 | g0227 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18951 | hp2 | a0013 | c0026 | t0001 | g0063 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18952 | hp1 | a0003 | c0004 | t0001 | g0270 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18954 | hp1 | a0011 | c0017 | t0001 | g0087 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18962 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18963 | hp1 | a0003 | c0004 | t0001 | g0267 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0185 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18969 | hp2 | a0014 | c0034 | t0001 | g0158 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18970 | hp1 | a0003 | c0004 | t0001 | g0245 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18974 | hp1 | a0015 | c0029 | t0002 | g0028 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18975 | hp1 | a0011 | c0017 | t0001 | g0088 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18975 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18981 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18986 | hp1 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18992 | hp2 | a0001 | c0009 | t0001 | g0294 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18995 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18999 | hp1 | a0001 | c0009 | t0001 | g0297 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA18999 | hp2 | a0003 | c0004 | t0001 | g0226 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19000 | hp2 | a0006 | c0013 | t0001 | g0165 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19030 | hp1 | a0016 | c0035 | t0001 | g0038 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19030 | hp2 | a0017 | c0027 | t0001 | g0047 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19043 | hp2 | a0001 | c0021 | t0004 | g0282 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19060 | hp1 | a0001 | c0009 | t0001 | g0293 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19074 | hp1 | a0002 | c0032 | t0001 | g0086 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19077 | hp2 | a0003 | c0004 | t0001 | g0181 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19085 | hp2 | a0018 | c0022 | t0001 | g0175 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0197 | EUR | TSI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20805 | hp2 | a0005 | c0006 | t0001 | g0052 | EUR | TSI | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | GIH | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20905 | hp2 | a0005 | c0006 | t0001 | g0098 | SAS | GIH | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02109 | hp1 | a0010 | c0008 | t0001 | g0041 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02109 | hp2 | a0002 | c0016 | t0002 | g0205 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0167 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02559 | hp1 | a0002 | c0003 | t0007 | g0101 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG02559 | hp2 | a0006 | c0025 | t0002 | g0316 | AFR | ACB | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG06807 | hp1 | a0004 | c0005 | t0001 | g0285 | AFR | USA | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
HG06807 | hp2 | a0009 | c0020 | t0003 | g0332 | AFR | USA | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | USA | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0283 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
NA21309 | hp2 | a0004 | c0005 | t0001 | g0215 | AFR | LWK | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0019 | REF | REF | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0027 | REF | REF | TBC1D8_chr2_101002228_101156382 | TBC1D8 | chr2 | 101002228 | 101156382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101007870 | A | AAAG | 5 | a0004 a0008 a0010 others(2): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
conservative_inframe_insertion | MODERATE | c.3416_3418dupCTT | p.Thr1139_Phe1140ins others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 3547/4190 | 3418/3468 | 1140/1155 | chr2 | 101007870 | |||
chr2:101007922 | T | C | 1 | a0003 | 13 | HG02027.hp1 HG02074.hp2 HG02080.hp2 others(10): Show |
missense_variant | MODERATE | c.3367A>G | p.Met1123Val | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 3496/4190 | 3367/3468 | 1123/1155 | chr2 | 101007922 | |||
chr2:101008009 | T | C | 10 | a0002 a0004 a0005 others(7): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
missense_variant | MODERATE | c.3280A>G | p.Arg1094Gly | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 3409/4190 | 3280/3468 | 1094/1155 | chr2 | 101008009 | |||
chr2:101011463 | C | T | 1 | a0005 | 8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
missense_variant | MODERATE | c.2905G>A | p.Gly969Arg | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/20 | 3034/4190 | 2905/3468 | 969/1155 | chr2 | 101011463 | |||
chr2:101027394 | C | T | 1 | a0017 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2509G>A | p.Asp837Asn | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/20 | 2638/4190 | 2509/3468 | 837/1155 | chr2 | 101027394 | |||
chr2:101033570 | G | A | 1 | a0013 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1792C>T | p.Arg598Trp | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/20 | 1921/4190 | 1792/3468 | 598/1155 | chr2 | 101033570 | |||
chr2:101037707 | G | C | 3 | a0009 a0012 a0017 |
7 | HG03139.hp1 HG03195.hp1 HG03209.hp2 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.1277C>G | p.Ala426Gly | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/20 | 1406/4190 | 1277/3468 | 426/1155 | chr2 | 101037707 | |||
chr2:101038624 | C | A | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1112G>T | p.Ser371Ile | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1241/4190 | 1112/3468 | 371/1155 | chr2 | 101038624 | |||
chr2:101038632 | C | A | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1104G>T | p.Glu368Asp | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1233/4190 | 1104/3468 | 368/1155 | chr2 | 101038632 | |||
chr2:101038634 | C | A | 1 | a0018 | 1 | NA19085.hp2 | stop_gained | HIGH | c.1102G>T | p.Glu368* | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1231/4190 | 1102/3468 | 368/1155 | chr2 | 101038634 | |||
chr2:101038635 | C | T | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1101G>A | p.Met367Ile | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1230/4190 | 1101/3468 | 367/1155 | chr2 | 101038635 | |||
chr2:101038638 | C | A | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1098G>T | p.Lys366Asn | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1227/4190 | 1098/3468 | 366/1155 | chr2 | 101038638 | |||
chr2:101038640 | T | G | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1096A>C | p.Lys366Gln | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1225/4190 | 1096/3468 | 366/1155 | chr2 | 101038640 | |||
chr2:101038641 | C | A | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1095G>T | p.Glu365Asp | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1224/4190 | 1095/3468 | 365/1155 | chr2 | 101038641 | |||
chr2:101038643 | C | A | 1 | a0018 | 1 | NA19085.hp2 | stop_gained | HIGH | c.1093G>T | p.Glu365* | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1222/4190 | 1093/3468 | 365/1155 | chr2 | 101038643 | |||
chr2:101038646 | T | A | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1090A>T | p.Ile364Phe | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1219/4190 | 1090/3468 | 364/1155 | chr2 | 101038646 | |||
chr2:101038648 | C | G | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1088G>C | p.Ser363Thr | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1217/4190 | 1088/3468 | 363/1155 | chr2 | 101038648 | |||
chr2:101038649 | T | G | 1 | a0018 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1087A>C | p.Ser363Arg | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1216/4190 | 1087/3468 | 363/1155 | chr2 | 101038649 | |||
chr2:101038651 | A | C | 1 | a0015 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1085T>G | p.Val362Gly | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1214/4190 | 1085/3468 | 362/1155 | chr2 | 101038651 | |||
chr2:101038655 | C | G | 1 | a0018 | 1 | NA19085.hp2 | missense_variant&splice_region_variant | MODERATE | c.1081G>C | p.Val361Leu | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1210/4190 | 1081/3468 | 361/1155 | chr2 | 101038655 | |||
chr2:101040264 | T | C | 7 | a0002 a0004 a0005 others(4): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
missense_variant | MODERATE | c.994A>G | p.Thr332Ala | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/20 | 1123/4190 | 994/3468 | 332/1155 | chr2 | 101040264 | |||
chr2:101050419 | G | A | 1 | a0014 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.854C>T | p.Pro285Leu | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/20 | 983/4190 | 854/3468 | 285/1155 | chr2 | 101050419 | |||
chr2:101054227 | G | A | 3 | a0007 a0010 a0016 |
11 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
missense_variant | MODERATE | c.512C>T | p.Ala171Val | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/20 | 641/4190 | 512/3468 | 171/1155 | chr2 | 101054227 | |||
chr2:101059479 | G | A | 1 | a0016 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.344C>T | p.Thr115Ile | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/20 | 473/4190 | 344/3468 | 115/1155 | chr2 | 101059479 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101007826 | A | G | 1 | a0005c0030 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.3463T>C | p.Leu1155Leu | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 3592/4190 | 3463/3468 | 1155/1155 | chr2 | 101007826 | |||
chr2:101022366 | C | T | 3 | a0005c0006 a0005c0030 a0006c0010 |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
synonymous_variant | LOW | c.2676G>A | p.Thr892Thr | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 16/20 | 2805/4190 | 2676/3468 | 892/1155 | chr2 | 101022366 | |||
chr2:101022426 | A | G | 19 | a0001c0024 a0002c0002 a0002c0003 others(16): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
synonymous_variant | LOW | c.2616T>C | p.Asp872Asp | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 16/20 | 2745/4190 | 2616/3468 | 872/1155 | chr2 | 101022426 | |||
chr2:101028393 | G | A | 3 | a0002c0002 a0006c0012 a0015c0029 |
62 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
synonymous_variant | LOW | c.2262C>T | p.Pro754Pro | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 13/20 | 2391/4190 | 2262/3468 | 754/1155 | chr2 | 101028393 | |||
chr2:101028396 | C | T | 1 | a0001c0023 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2259G>A | p.Gly753Gly | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 13/20 | 2388/4190 | 2259/3468 | 753/1155 | chr2 | 101028396 | |||
chr2:101029670 | C | T | 1 | a0002c0032 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.2043G>A | p.Ser681Ser | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/20 | 2172/4190 | 2043/3468 | 681/1155 | chr2 | 101029670 | |||
chr2:101029682 | G | A | 5 | a0002c0003 a0002c0018 a0002c0032 others(2): Show |
52 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(49): Show |
synonymous_variant | LOW | c.2031C>T | p.Ser677Ser | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/20 | 2160/4190 | 2031/3468 | 677/1155 | chr2 | 101029682 | |||
chr2:101033748 | C | T | 1 | a0001c0009 | 3 | NA18992.hp2 NA18999.hp1 NA19060.hp1 |
synonymous_variant | LOW | c.1614G>A | p.Thr538Thr | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/20 | 1743/4190 | 1614/3468 | 538/1155 | chr2 | 101033748 | |||
chr2:101038485 | G | A | 1 | a0008c0015 | 2 | HG02572.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.1251C>T | p.Tyr417Tyr | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1380/4190 | 1251/3468 | 417/1155 | chr2 | 101038485 | |||
chr2:101038653 | C | A | 1 | a0018c0022 | 1 | NA19085.hp2 | splice_region_variant&synonymous_variant | LOW | c.1083G>T | p.Val361Val | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/20 | 1212/4190 | 1083/3468 | 361/1155 | chr2 | 101038653 | |||
chr2:101040292 | G | C | 1 | a0009c0033 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.966C>G | p.Leu322Leu | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/20 | 1095/4190 | 966/3468 | 322/1155 | chr2 | 101040292 | |||
chr2:101040313 | G | A | 1 | a0001c0021 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.945C>T | p.His315His | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/20 | 1074/4190 | 945/3468 | 315/1155 | chr2 | 101040313 | |||
chr2:101090351 | G | A | 2 | a0009c0020 a0011c0036 |
3 | HG02280.hp2 HG03139.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.141C>T | p.Gly47Gly | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/20 | 270/4190 | 141/3468 | 47/1155 | chr2 | 101090351 | |||
chr2:101090354 | G | T | 2 | a0001c0021 a0007c0007 |
5 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
synonymous_variant | LOW | c.138C>A | p.Val46Val | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/20 | 267/4190 | 138/3468 | 46/1155 | chr2 | 101090354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101007283 | T | A | 5 | a0002c0002t0002 a0002c0016t0002 a0006c0012t0002 others(2): Show |
65 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*538A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 538 | chr2 | 101007283 | ||||||
chr2:101007403 | G | C | 1 | a0001c0001t0006 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 418 | chr2 | 101007403 | ||||||
chr2:101007458 | C | T | 1 | a0001c0001t0005 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 363 | chr2 | 101007458 | ||||||
chr2:101007670 | C | T | 2 | a0001c0001t0004 a0001c0021t0004 |
4 | HG02922.hp2 HG03516.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 151 | chr2 | 101007670 | ||||||
chr2:101007804 | T | G | 1 | a0002c0003t0007 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 20/20 | 17 | chr2 | 101007804 | ||||||
chr2:101151377 | C | A | 6 | a0001c0001t0003 a0001c0024t0003 a0009c0014t0003 others(3): Show |
8 | HG02622.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-124G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/20 | 124 | chr2 | 101151377 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101008282 | G | GAAAT | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3016-13_3016-10dup others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008282 | |||||||
chr2:101008427 | A | G | 8 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.3016-154T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008427 | |||||||
chr2:101008486 | A | G | 1 | a0002c0002t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3016-213T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008486 | |||||||
chr2:101008553 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3016-280C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008553 | |||||||
chr2:101008581 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3016-308C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008581 | |||||||
chr2:101008640 | C | G | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3016-367G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008640 | |||||||
chr2:101008705 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0209 |
3 | HG03453.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3016-432C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008705 | |||||||
chr2:101008746 | A | G | 1 | a0010c0008t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3016-473T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008746 | |||||||
chr2:101008811 | T | TA | 58 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(55): Show |
58 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.3016-539dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008811 | |||||||
chr2:101008845 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3016-572C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101008845 | |||||||
chr2:101009078 | C | G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0001g0305 others(1): Show |
4 | HG02132.hp2 NA18946.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.3016-805G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009078 | |||||||
chr2:101009168 | C | T | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3016-895G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009168 | |||||||
chr2:101009197 | TCCTGGCT others(4): Show |
T | 12 | a0003c0004t0001g0271 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.3016-935_3016-925d others(13): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009197 | |||||||
chr2:101009279 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3016-1006C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009279 | |||||||
chr2:101009311 | C | G | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.3016-1038G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009311 | |||||||
chr2:101009384 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3016-1111G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009384 | |||||||
chr2:101009406 | C | CA | 20 | a0001c0001t0001g0057 a0001c0001t0001g0071 a0001c0001t0001g0120 others(17): Show |
20 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.3016-1134dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009406 | |||||||
chr2:101009406 | CAAAAAAA others(1): Show |
C | 65 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(62): Show |
65 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.3016-1141_3016-113 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009406 | |||||||
chr2:101009418 | A | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3016-1145T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009418 | |||||||
chr2:101009424 | G | A | 1 | a0013c0026t0001g0063 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3016-1151C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009424 | |||||||
chr2:101009487 | G | T | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3016-1214C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009487 | |||||||
chr2:101009821 | C | CA | 58 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0015 others(55): Show |
58 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.3015+1107_3015+110 others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009821 | |||||||
chr2:101009821 | C | CAT | 9 | a0002c0002t0002g0008 a0002c0002t0002g0020 a0002c0002t0002g0024 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.3015+1107_3015+110 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009821 | |||||||
chr2:101009822 | T | A | 79 | a0002c0002t0002g0184 a0002c0002t0002g0191 a0002c0003t0001g0001 others(76): Show |
79 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.3015+1107A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009822 | |||||||
chr2:101009826 | TC | T | 46 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(43): Show |
46 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.3015+1102delG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009826 | |||||||
chr2:101009827 | C | CT | 16 | a0001c0001t0001g0137 a0001c0001t0001g0154 a0001c0001t0001g0230 others(13): Show |
16 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.3015+1101dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009827 | |||||||
chr2:101009827 | C | T | 102 | a0001c0024t0003g0327 a0002c0002t0002g0008 a0002c0002t0002g0012 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3015+1102G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009827 | |||||||
chr2:101009853 | G | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.3015+1076C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009853 | |||||||
chr2:101009891 | G | A | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3015+1038C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009891 | |||||||
chr2:101009922 | T | C | 327 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(324): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.3015+1007A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009922 | |||||||
chr2:101009967 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3015+962C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101009967 | |||||||
chr2:101010044 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | NA18968.hp2 NA19007.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3015+885A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010044 | |||||||
chr2:101010061 | C | T | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015+868G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010061 | |||||||
chr2:101010065 | A | G | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3015+864T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010065 | |||||||
chr2:101010073 | G | A | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015+856C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010073 | |||||||
chr2:101010073 | G | T | 1 | a0002c0002t0002g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3015+856C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010073 | |||||||
chr2:101010132 | T | G | 1 | a0002c0002t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3015+797A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010132 | |||||||
chr2:101010162 | G | T | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015+767C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010162 | |||||||
chr2:101010227 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3015+702A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010227 | |||||||
chr2:101010286 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3015+643G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010286 | |||||||
chr2:101010309 | A | G | 1 | a0002c0002t0002g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3015+620T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010309 | |||||||
chr2:101010445 | C | T | 11 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.3015+484G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010445 | |||||||
chr2:101010606 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3015+323G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010606 | |||||||
chr2:101010612 | C | A | 10 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0110 others(7): Show |
10 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3015+317G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010612 | |||||||
chr2:101010613 | G | A | 4 | a0002c0003t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0011 others(1): Show |
4 | NA18971.hp2 NA18975.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.3015+316C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010613 | |||||||
chr2:101010881 | CA | C | 53 | a0001c0001t0001g0033 a0001c0001t0001g0130 a0001c0001t0001g0221 others(50): Show |
53 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.3015+47delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 19/19 | chr2 | 101010881 | |||||||
chr2:101011041 | AAAC | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0070 a0001c0001t0001g0071 others(3): Show |
6 | NA18946.hp1 NA19066.hp1 NA19067.hp2 others(3): Show |
intron_variant | MODIFIER | c.2918-18_2918-16del others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011041 | |||||||
chr2:101011163 | G | T | 1 | a0011c0036t0001g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2918-137C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011163 | |||||||
chr2:101011192 | C | T | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2918-166G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011192 | |||||||
chr2:101011247 | TTGG | T | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2917+201_2917+203d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011247 | |||||||
chr2:101011335 | C | T | 6 | a0002c0002t0002g0126 a0002c0002t0002g0177 a0002c0002t0002g0182 others(3): Show |
6 | NA18941.hp2 NA18967.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.2917+116G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011335 | |||||||
chr2:101011390 | C | T | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2917+61G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 18/19 | chr2 | 101011390 | |||||||
chr2:101011621 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2828-81A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011621 | |||||||
chr2:101011704 | G | A | 1 | a0006c0010t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2828-164C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011704 | |||||||
chr2:101011732 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2828-192G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011732 | |||||||
chr2:101011836 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2828-296C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011836 | |||||||
chr2:101011862 | G | A | 137 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(134): Show |
137 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.2828-322C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011862 | |||||||
chr2:101011997 | C | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2828-457G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101011997 | |||||||
chr2:101012013 | T | G | 10 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2828-473A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012013 | |||||||
chr2:101012027 | TAGTGAAT others(2): Show |
T | 12 | a0001c0001t0001g0057 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2828-496_2828-488d others(11): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012027 | |||||||
chr2:101012111 | G | A | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2828-571C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012111 | |||||||
chr2:101012286 | C | A | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2828-746G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012286 | |||||||
chr2:101012309 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG00438.hp1 HG00544.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.2828-769A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012309 | |||||||
chr2:101012437 | C | A | 2 | a0003c0004t0001g0226 a0003c0004t0001g0227 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2828-897G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012437 | |||||||
chr2:101012438 | G | A | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2828-898C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012438 | |||||||
chr2:101012536 | T | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2828-996A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012536 | |||||||
chr2:101012577 | C | A | 150 | a0001c0001t0001g0057 a0002c0002t0002g0008 a0002c0002t0002g0012 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2828-1037G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012577 | |||||||
chr2:101012625 | C | CA | 9 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0096 others(6): Show |
9 | HG01167.hp2 HG02015.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.2828-1086dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012625 | |||||||
chr2:101012625 | CA | C | 18 | a0001c0001t0001g0160 a0002c0002t0002g0322 a0002c0003t0001g0001 others(15): Show |
18 | HG00140.hp2 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2828-1086delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012625 | |||||||
chr2:101012625 | CAA | C | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.2828-1087_2828-108 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012625 | |||||||
chr2:101012748 | T | C | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2828-1208A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012748 | |||||||
chr2:101012818 | T | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2828-1278A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012818 | |||||||
chr2:101012951 | C | G | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2828-1411G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012951 | |||||||
chr2:101012989 | T | C | 72 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(69): Show |
72 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2828-1449A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101012989 | |||||||
chr2:101013275 | A | G | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2828-1735T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013275 | |||||||
chr2:101013359 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2828-1819T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013359 | |||||||
chr2:101013524 | G | T | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2828-1984C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013524 | |||||||
chr2:101013525 | A | T | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2828-1985T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013525 | |||||||
chr2:101013754 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0003g0329 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2828-2214T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013754 | |||||||
chr2:101013907 | A | G | 1 | a0002c0002t0002g0077 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2828-2367T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013907 | |||||||
chr2:101013959 | T | C | 1 | a0002c0003t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2828-2419A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101013959 | |||||||
chr2:101014048 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2828-2508T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014048 | |||||||
chr2:101014087 | A | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0239 a0001c0001t0001g0263 |
3 | HG00408.hp1 NA18941.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2828-2547T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014087 | |||||||
chr2:101014260 | A | G | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2828-2720T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014260 | |||||||
chr2:101014297 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2828-2757A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014297 | |||||||
chr2:101014336 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2828-2796T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014336 | |||||||
chr2:101014470 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0119 others(1): Show |
4 | NA18982.hp1 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2828-2930T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014470 | |||||||
chr2:101014570 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2828-3030C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014570 | |||||||
chr2:101014723 | C | T | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2828-3183G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014723 | |||||||
chr2:101014926 | C | G | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2828-3386G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014926 | |||||||
chr2:101014928 | T | G | 3 | a0002c0002t0002g0017 a0002c0002t0002g0024 a0002c0002t0002g0104 |
3 | HG00639.hp1 HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2828-3388A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014928 | |||||||
chr2:101014989 | C | CACTT | 72 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(69): Show |
72 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2828-3450_2828-344 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014989 | |||||||
chr2:101014991 | A | G | 2 | a0002c0002t0002g0084 a0017c0027t0001g0047 |
2 | NA19030.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2828-3451T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101014991 | |||||||
chr2:101015034 | G | A | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2828-3494C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015034 | |||||||
chr2:101015049 | TCATA | T | 3 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0001c0001t0004g0278 |
3 | HG02922.hp2 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2828-3513_2828-351 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015049 | |||||||
chr2:101015091 | A | G | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2828-3551T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015091 | |||||||
chr2:101015100 | G | A | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2828-3560C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015100 | |||||||
chr2:101015139 | A | G | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2828-3599T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015139 | |||||||
chr2:101015230 | A | C | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2828-3690T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015230 | |||||||
chr2:101015356 | A | G | 1 | a0011c0031t0001g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2828-3816T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015356 | |||||||
chr2:101015426 | C | G | 84 | a0001c0001t0001g0057 a0002c0003t0001g0001 a0002c0003t0001g0009 others(81): Show |
84 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2828-3886G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015426 | |||||||
chr2:101015653 | C | T | 54 | a0001c0001t0001g0068 a0001c0001t0001g0117 a0001c0001t0001g0118 others(51): Show |
54 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.2828-4113G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015653 | |||||||
chr2:101015656 | T | G | 1 | a0001c0001t0001g0116 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2828-4116A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015656 | |||||||
chr2:101015659 | G | A | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2828-4119C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015659 | |||||||
chr2:101015708 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0295 |
3 | HG01074.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2828-4168G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015708 | |||||||
chr2:101015764 | C | T | 1 | a0002c0002t0002g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2828-4224G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015764 | |||||||
chr2:101015784 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2828-4244T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015784 | |||||||
chr2:101015917 | T | A | 1 | a0002c0003t0001g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2828-4377A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015917 | |||||||
chr2:101015918 | T | C | 3 | a0002c0002t0002g0076 a0002c0002t0002g0184 a0002c0002t0002g0191 |
3 | HG02735.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2828-4378A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015918 | |||||||
chr2:101015932 | T | C | 2 | a0004c0005t0001g0034 a0012c0028t0003g0326 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2828-4392A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015932 | |||||||
chr2:101015945 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2828-4405G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101015945 | |||||||
chr2:101016134 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2828-4594C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016134 | |||||||
chr2:101016178 | A | G | 3 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0033t0003g0328 |
3 | HG03209.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2828-4638T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016178 | |||||||
chr2:101016451 | A | C | 9 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(6): Show |
9 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2828-4911T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016451 | |||||||
chr2:101016517 | G | T | 3 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0220 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2828-4977C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016517 | |||||||
chr2:101016540 | G | C | 5 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0020t0003g0331 others(2): Show |
5 | HG03139.hp1 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2828-5000C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016540 | |||||||
chr2:101016579 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2828-5039G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016579 | |||||||
chr2:101016634 | T | C | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2827+5047A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016634 | |||||||
chr2:101016928 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2827+4753C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016928 | |||||||
chr2:101016932 | G | C | 1 | a0001c0001t0004g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2827+4749C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101016932 | |||||||
chr2:101017074 | TA | T | 13 | a0001c0001t0001g0138 a0001c0001t0001g0179 a0001c0001t0001g0260 others(10): Show |
13 | HG00642.hp1 HG01074.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.2827+4606delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017074 | |||||||
chr2:101017074 | TAAAA | T | 8 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2827+4603_2827+460 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017074 | |||||||
chr2:101017075 | A | T | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2827+4606T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017075 | |||||||
chr2:101017083 | AAAAAAAA others(1): Show |
A | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2827+4590_2827+459 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017083 | |||||||
chr2:101017134 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2827+4547C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017134 | |||||||
chr2:101017192 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2827+4489T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017192 | |||||||
chr2:101017247 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2827+4434G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017247 | |||||||
chr2:101017488 | T | C | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2827+4193A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017488 | |||||||
chr2:101017574 | A | T | 1 | a0006c0010t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2827+4107T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017574 | |||||||
chr2:101017765 | G | C | 1 | a0002c0002t0002g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2827+3916C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017765 | |||||||
chr2:101017920 | A | G | 3 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0131 |
3 | HG01099.hp1 HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2827+3761T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017920 | |||||||
chr2:101017971 | A | G | 1 | a0012c0028t0003g0326 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2827+3710T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101017971 | |||||||
chr2:101018103 | C | G | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2827+3578G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018103 | |||||||
chr2:101018245 | T | C | 12 | a0001c0001t0001g0057 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2827+3436A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018245 | |||||||
chr2:101018331 | GTTCA | G | 63 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(60): Show |
63 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2827+3346_2827+334 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018331 | |||||||
chr2:101018338 | C | A | 1 | a0005c0006t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2827+3343G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018338 | |||||||
chr2:101018350 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2827+3331C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018350 | |||||||
chr2:101018368 | T | A | 11 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2827+3313A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018368 | |||||||
chr2:101018825 | C | T | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2827+2856G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018825 | |||||||
chr2:101018886 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2827+2795C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018886 | |||||||
chr2:101018907 | G | A | 11 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2827+2774C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018907 | |||||||
chr2:101018934 | G | C | 3 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0002c0002t0002g0131 |
3 | HG01099.hp1 HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2827+2747C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018934 | |||||||
chr2:101018944 | C | T | 2 | a0002c0003t0001g0283 a0002c0003t0007g0101 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2827+2737G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101018944 | |||||||
chr2:101019076 | C | T | 64 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(61): Show |
64 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2827+2605G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019076 | |||||||
chr2:101019527 | T | A | 10 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2827+2154A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019527 | |||||||
chr2:101019533 | C | T | 1 | a0002c0002t0002g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2827+2148G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019533 | |||||||
chr2:101019904 | T | TA | 50 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(47): Show |
50 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2827+1776dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019904 | |||||||
chr2:101019913 | A | G | 1 | a0002c0002t0002g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2827+1768T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019913 | |||||||
chr2:101019914 | T | A | 1 | a0002c0003t0001g0257 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2827+1767A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019914 | |||||||
chr2:101019948 | T | G | 11 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2827+1733A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019948 | |||||||
chr2:101019997 | C | T | 1 | a0006c0010t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2827+1684G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101019997 | |||||||
chr2:101020052 | C | G | 2 | a0002c0002t0002g0287 a0006c0012t0002g0161 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2827+1629G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020052 | |||||||
chr2:101020068 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2827+1613C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020068 | |||||||
chr2:101020072 | C | CA | 73 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0136 others(70): Show |
73 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2827+1608dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020072 | |||||||
chr2:101020157 | TATACC | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(100): Show |
103 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2827+1519_2827+152 others(9): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020157 | |||||||
chr2:101020180 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2827+1501C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020180 | |||||||
chr2:101020257 | T | C | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2827+1424A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020257 | |||||||
chr2:101020324 | AGAT | A | 47 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(44): Show |
47 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.2827+1354_2827+135 others(7): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020324 | |||||||
chr2:101020430 | G | A | 147 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2827+1251C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020430 | |||||||
chr2:101020547 | T | C | 12 | a0001c0001t0001g0057 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2827+1134A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020547 | |||||||
chr2:101020589 | G | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2827+1092C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020589 | |||||||
chr2:101020771 | T | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2827+910A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020771 | |||||||
chr2:101020775 | G | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2827+906C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101020775 | |||||||
chr2:101021053 | T | G | 147 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(144): Show |
147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.2827+628A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101021053 | |||||||
chr2:101021400 | A | G | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2827+281T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 17/19 | chr2 | 101021400 | |||||||
chr2:101021942 | G | A | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2762-196C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 16/19 | chr2 | 101021942 | |||||||
chr2:101022202 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2761+79C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 16/19 | chr2 | 101022202 | |||||||
chr2:101022600 | AAATT | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(28): Show |
31 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(28): Show |
intron_variant | MODIFIER | c.2521-83_2521-80del others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101022600 | |||||||
chr2:101022692 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2521-171G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101022692 | |||||||
chr2:101022695 | TGGTTTTT others(7): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2521-188_2521-175d others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101022695 | |||||||
chr2:101022923 | G | A | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2521-402C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101022923 | |||||||
chr2:101022999 | G | A | 2 | a0002c0003t0001g0001 a0002c0003t0001g0035 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2521-478C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101022999 | |||||||
chr2:101023010 | C | T | 1 | a0002c0003t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2521-489G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023010 | |||||||
chr2:101023100 | G | A | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2521-579C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023100 | |||||||
chr2:101023132 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2521-611C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023132 | |||||||
chr2:101023132 | G | GT | 13 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0134 others(10): Show |
13 | HG01192.hp2 HG01255.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.2521-612dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023132 | |||||||
chr2:101023137 | T | G | 1 | a0006c0010t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2521-616A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023137 | |||||||
chr2:101023269 | C | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2521-748G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023269 | |||||||
chr2:101023553 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2521-1032C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023553 | |||||||
chr2:101023605 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2521-1084G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023605 | |||||||
chr2:101023679 | C | T | 2 | a0002c0002t0002g0287 a0006c0012t0002g0161 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2521-1158G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101023679 | |||||||
chr2:101024057 | T | C | 3 | a0002c0002t0002g0076 a0002c0002t0002g0184 a0002c0002t0002g0191 |
3 | HG02735.hp2 HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2521-1536A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024057 | |||||||
chr2:101024175 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(100): Show |
103 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2521-1654A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024175 | |||||||
chr2:101024236 | C | T | 11 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2521-1715G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024236 | |||||||
chr2:101024347 | G | C | 1 | a0001c0001t0001g0003 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2521-1826C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024347 | |||||||
chr2:101024402 | A | AT | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.2521-1882dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024402 | |||||||
chr2:101024402 | A | ATT | 58 | a0001c0001t0001g0059 a0001c0001t0001g0229 a0001c0001t0001g0242 others(55): Show |
58 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.2521-1883_2521-188 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024402 | |||||||
chr2:101024573 | A | G | 12 | a0001c0001t0001g0057 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2521-2052T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024573 | |||||||
chr2:101024596 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2521-2075C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024596 | |||||||
chr2:101024703 | G | A | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2521-2182C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024703 | |||||||
chr2:101024711 | C | G | 22 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.2521-2190G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024711 | |||||||
chr2:101024729 | A | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2521-2208T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024729 | |||||||
chr2:101024956 | A | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2520+2427T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101024956 | |||||||
chr2:101025018 | GAAAC | G | 4 | a0002c0003t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0011 others(1): Show |
4 | NA18971.hp2 NA18975.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.2520+2361_2520+236 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025018 | |||||||
chr2:101025086 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
5 | NA18951.hp2 NA18966.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2520+2297C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025086 | |||||||
chr2:101025197 | C | T | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2520+2186G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025197 | |||||||
chr2:101025198 | G | A | 1 | a0016c0035t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2520+2185C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025198 | |||||||
chr2:101025204 | A | G | 148 | a0001c0001t0001g0057 a0002c0002t0002g0008 a0002c0002t0002g0012 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.2520+2179T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025204 | |||||||
chr2:101025212 | C | CT | 10 | a0001c0001t0001g0302 a0005c0006t0001g0051 a0005c0006t0001g0052 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2520+2170dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025212 | |||||||
chr2:101025212 | CT | C | 49 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(46): Show |
49 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.2520+2170delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025212 | |||||||
chr2:101025302 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2520+2081A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025302 | |||||||
chr2:101025426 | G | A | 3 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0015c0029t0002g0028 |
3 | HG02074.hp1 NA18974.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2520+1957C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025426 | |||||||
chr2:101025475 | C | T | 1 | a0002c0002t0002g0021 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2520+1908G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025475 | |||||||
chr2:101025477 | C | T | 65 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(62): Show |
65 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2520+1906G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025477 | |||||||
chr2:101025573 | A | C | 1 | a0016c0035t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2520+1810T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025573 | |||||||
chr2:101025688 | A | T | 1 | a0012c0028t0003g0326 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2520+1695T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025688 | |||||||
chr2:101025785 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2520+1598G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025785 | |||||||
chr2:101025798 | A | G | 82 | a0001c0001t0001g0057 a0002c0003t0001g0001 a0002c0003t0001g0009 others(79): Show |
82 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.2520+1585T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025798 | |||||||
chr2:101025820 | G | A | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2520+1563C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101025820 | |||||||
chr2:101026027 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0240 |
2 | NA18962.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2520+1356T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026027 | |||||||
chr2:101026154 | G | A | 9 | a0008c0011t0001g0208 a0008c0011t0001g0280 a0008c0015t0001g0075 others(6): Show |
9 | HG01167.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2520+1229C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026154 | |||||||
chr2:101026201 | CAA | C | 24 | a0002c0003t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0011 others(21): Show |
24 | HG01975.hp2 NA18612.hp1 NA18939.hp1 others(21): Show |
intron_variant | MODIFIER | c.2520+1180_2520+118 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026201 | |||||||
chr2:101026381 | G | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(108): Show |
111 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2520+1002C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026381 | |||||||
chr2:101026481 | C | T | 12 | a0001c0001t0001g0057 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2520+902G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026481 | |||||||
chr2:101026529 | G | A | 1 | a0006c0013t0001g0299 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2520+854C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026529 | |||||||
chr2:101026889 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2520+494G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101026889 | |||||||
chr2:101027044 | G | A | 10 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0053 others(7): Show |
10 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2520+339C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101027044 | |||||||
chr2:101027059 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2520+324G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101027059 | |||||||
chr2:101027073 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2520+310C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101027073 | |||||||
chr2:101027153 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2520+230C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 15/19 | chr2 | 101027153 | |||||||
chr2:101027523 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2452-72G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 14/19 | chr2 | 101027523 | |||||||
chr2:101027743 | G | A | 10 | a0002c0003t0001g0055 a0002c0003t0001g0056 a0002c0003t0001g0078 others(7): Show |
10 | HG01071.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.2452-292C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 14/19 | chr2 | 101027743 | |||||||
chr2:101027837 | G | A | 55 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(52): Show |
55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.2451+211C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 14/19 | chr2 | 101027837 | |||||||
chr2:101027854 | A | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0015c0029t0002g0028 |
3 | HG02074.hp1 NA18974.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2451+194T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 14/19 | chr2 | 101027854 | |||||||
chr2:101027878 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | NA18961.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2451+170C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 14/19 | chr2 | 101027878 | |||||||
chr2:101028186 | C | T | 11 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2353-40G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 13/19 | chr2 | 101028186 | |||||||
chr2:101028284 | G | C | 1 | a0002c0003t0007g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2352+19C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 13/19 | chr2 | 101028284 | |||||||
chr2:101028296 | C | A | 1 | a0002c0003t0007g0101 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.2352+7G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 13/19 | chr2 | 101028296 | |||||||
chr2:101028448 | C | T | 19 | a0004c0005t0001g0034 a0004c0005t0001g0110 a0004c0005t0001g0206 others(16): Show |
19 | HG01167.hp2 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2223-16G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028448 | |||||||
chr2:101028526 | C | T | 2 | a0002c0003t0001g0171 a0002c0003t0001g0262 |
2 | HG00735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2223-94G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028526 | |||||||
chr2:101028569 | G | A | 19 | a0002c0002t0002g0008 a0002c0002t0002g0076 a0002c0002t0002g0084 others(16): Show |
19 | HG00423.hp2 HG00438.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.2223-137C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028569 | |||||||
chr2:101028657 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2223-225C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028657 | |||||||
chr2:101028689 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0042 others(12): Show |
15 | HG01261.hp2 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2223-257G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028689 | |||||||
chr2:101028741 | T | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2223-309A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028741 | |||||||
chr2:101028780 | G | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2223-348C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028780 | |||||||
chr2:101028842 | A | T | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2223-410T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028842 | |||||||
chr2:101028954 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2223-522A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028954 | |||||||
chr2:101028991 | A | C | 1 | a0002c0003t0001g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2222+500T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101028991 | |||||||
chr2:101029010 | G | A | 21 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(18): Show |
21 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2222+481C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029010 | |||||||
chr2:101029011 | C | A | 21 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(18): Show |
21 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.2222+480G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029011 | |||||||
chr2:101029165 | G | A | 56 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(53): Show |
56 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.2222+326C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029165 | |||||||
chr2:101029251 | T | C | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2222+240A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029251 | |||||||
chr2:101029255 | G | C | 1 | a0002c0002t0002g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2222+236C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029255 | |||||||
chr2:101029394 | T | TA | 44 | a0001c0001t0001g0180 a0001c0001t0001g0229 a0002c0002t0002g0298 others(41): Show |
44 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.2222+96dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 12/19 | chr2 | 101029394 | |||||||
chr2:101029785 | G | C | 1 | a0010c0008t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-9C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101029785 | |||||||
chr2:101029897 | G | C | 66 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(63): Show |
66 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1937-121C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101029897 | |||||||
chr2:101029966 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1937-190T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101029966 | |||||||
chr2:101030287 | G | A | 47 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(44): Show |
47 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1937-511C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030287 | |||||||
chr2:101030392 | C | T | 1 | a0018c0022t0001g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1937-616G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030392 | |||||||
chr2:101030455 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1937-679T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030455 | |||||||
chr2:101030729 | A | G | 21 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(18): Show |
21 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1937-953T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030729 | |||||||
chr2:101030890 | C | T | 12 | a0001c0001t0001g0160 a0005c0006t0001g0051 a0005c0006t0001g0052 others(9): Show |
12 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1937-1114G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030890 | |||||||
chr2:101030900 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1937-1124T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030900 | |||||||
chr2:101030930 | G | A | 1 | a0002c0002t0002g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1937-1154C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030930 | |||||||
chr2:101030987 | G | C | 1 | a0001c0001t0004g0278 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1937-1211C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030987 | |||||||
chr2:101030987 | G | T | 1 | a0001c0001t0003g0329 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1937-1211C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101030987 | |||||||
chr2:101031031 | T | TC | 13 | a0001c0001t0001g0057 a0001c0001t0001g0160 a0005c0006t0001g0051 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1936+1236dupG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031031 | |||||||
chr2:101031222 | A | G | 1 | a0002c0032t0001g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1936+1046T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031222 | |||||||
chr2:101031301 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1936+967C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031301 | |||||||
chr2:101031392 | T | A | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1936+876A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031392 | |||||||
chr2:101031404 | A | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(99): Show |
102 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1936+864T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031404 | |||||||
chr2:101031432 | G | A | 13 | a0001c0001t0001g0057 a0001c0001t0001g0160 a0005c0006t0001g0051 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1936+836C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031432 | |||||||
chr2:101031681 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1936+587G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031681 | |||||||
chr2:101031762 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1936+506G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101031762 | |||||||
chr2:101032081 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1936+187A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101032081 | |||||||
chr2:101032112 | G | C | 1 | a0002c0002t0002g0197 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1936+156C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 11/19 | chr2 | 101032112 | |||||||
chr2:101032417 | C | T | 1 | a0002c0002t0002g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1819-32G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032417 | |||||||
chr2:101032421 | C | T | 1 | a0005c0006t0001g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1819-36G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032421 | |||||||
chr2:101032464 | C | A | 11 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1819-79G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032464 | |||||||
chr2:101032784 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1819-399T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032784 | |||||||
chr2:101032807 | C | T | 48 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(45): Show |
48 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1819-422G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032807 | |||||||
chr2:101032965 | C | T | 69 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(66): Show |
69 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1818+579G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101032965 | |||||||
chr2:101033031 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1818+513C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033031 | |||||||
chr2:101033122 | A | ATTT | 135 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(132): Show |
135 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1818+419_1818+421d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033122 | |||||||
chr2:101033122 | A | ATTTT | 13 | a0001c0001t0001g0057 a0001c0001t0001g0160 a0002c0003t0001g0268 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1818+418_1818+421d others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033122 | |||||||
chr2:101033146 | C | G | 1 | a0003c0004t0001g0273 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1818+398G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033146 | |||||||
chr2:101033266 | G | A | 1 | a0002c0003t0001g0094 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1818+278C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033266 | |||||||
chr2:101033277 | C | A | 1 | a0015c0029t0002g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1818+267G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033277 | |||||||
chr2:101033278 | A | G | 1 | a0015c0029t0002g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1818+266T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033278 | |||||||
chr2:101033279 | G | C | 1 | a0015c0029t0002g0028 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1818+265C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033279 | |||||||
chr2:101033407 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1818+137G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 10/19 | chr2 | 101033407 | |||||||
chr2:101033767 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0137 |
2 | NA18953.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1604-9A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101033767 | |||||||
chr2:101033934 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1604-176G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101033934 | |||||||
chr2:101034061 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0190 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1604-303C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034061 | |||||||
chr2:101034160 | A | G | 1 | a0010c0008t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-402T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034160 | |||||||
chr2:101034197 | A | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1604-439T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034197 | |||||||
chr2:101034217 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1604-459G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034217 | |||||||
chr2:101034254 | A | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1604-496T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034254 | |||||||
chr2:101034423 | G | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1604-665C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034423 | |||||||
chr2:101034559 | G | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0187 others(2): Show |
5 | HG02132.hp1 HG02132.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-801C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034559 | |||||||
chr2:101034585 | G | A | 2 | a0001c0001t0001g0254 a0002c0032t0001g0086 |
2 | NA18950.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1604-827C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034585 | |||||||
chr2:101034618 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0315 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1604-860G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034618 | |||||||
chr2:101034702 | G | C | 13 | a0004c0005t0001g0002 a0004c0005t0001g0014 a0004c0005t0001g0034 others(10): Show |
13 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1604-944C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034702 | |||||||
chr2:101034706 | C | T | 1 | a0002c0002t0002g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1604-948G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034706 | |||||||
chr2:101034941 | T | C | 1 | a0002c0003t0001g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1603+1077A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034941 | |||||||
chr2:101034957 | A | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1603+1061T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034957 | |||||||
chr2:101034980 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1603+1038T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101034980 | |||||||
chr2:101035010 | T | G | 6 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0020t0003g0331 others(3): Show |
6 | HG03139.hp1 HG03209.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603+1008A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035010 | |||||||
chr2:101035025 | G | A | 6 | a0010c0008t0001g0039 a0010c0008t0001g0040 a0010c0008t0001g0041 others(3): Show |
6 | HG02109.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+993C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035025 | |||||||
chr2:101035043 | G | A | 56 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0136 others(53): Show |
56 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1603+975C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035043 | |||||||
chr2:101035072 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1603+946C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035072 | |||||||
chr2:101035079 | A | G | 2 | a0002c0002t0002g0022 a0002c0002t0002g0026 |
2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1603+939T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035079 | |||||||
chr2:101035189 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1603+829C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035189 | |||||||
chr2:101035278 | C | G | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1603+740G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035278 | |||||||
chr2:101035411 | T | C | 2 | a0002c0003t0001g0283 a0002c0003t0007g0101 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1603+607A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035411 | |||||||
chr2:101035460 | T | G | 151 | a0001c0001t0001g0160 a0001c0001t0001g0247 a0002c0002t0002g0008 others(148): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1603+558A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035460 | |||||||
chr2:101035811 | C | T | 2 | a0002c0003t0001g0001 a0002c0003t0001g0035 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1603+207G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035811 | |||||||
chr2:101035869 | A | T | 1 | a0002c0003t0001g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1603+149T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 9/19 | chr2 | 101035869 | |||||||
chr2:101036270 | C | T | 60 | a0002c0002t0002g0012 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
60 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1453-102G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036270 | |||||||
chr2:101036271 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(110): Show |
113 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1453-103C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036271 | |||||||
chr2:101036335 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1453-167A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036335 | |||||||
chr2:101036350 | T | G | 8 | a0006c0010t0001g0109 a0009c0014t0003g0325 a0009c0014t0003g0330 others(5): Show |
8 | HG02630.hp1 HG03139.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453-182A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036350 | |||||||
chr2:101036352 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1453-184G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036352 | |||||||
chr2:101036454 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1453-286C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036454 | |||||||
chr2:101036517 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1453-349G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036517 | |||||||
chr2:101036670 | T | C | 1 | a0009c0033t0003g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1453-502A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036670 | |||||||
chr2:101036677 | A | G | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1453-509T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036677 | |||||||
chr2:101036823 | A | T | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1453-655T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036823 | |||||||
chr2:101036871 | C | T | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1452+661G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036871 | |||||||
chr2:101036904 | G | A | 1 | a0002c0002t0002g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1452+628C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036904 | |||||||
chr2:101036976 | C | A | 2 | a0008c0015t0001g0075 a0008c0015t0001g0100 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1452+556G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101036976 | |||||||
chr2:101037066 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1452+466G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101037066 | |||||||
chr2:101037322 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1452+210G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101037322 | |||||||
chr2:101037393 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1452+139G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101037393 | |||||||
chr2:101037440 | G | A | 1 | a0005c0030t0001g0169 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1452+92C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101037440 | |||||||
chr2:101037474 | C | T | 1 | a0002c0002t0002g0016 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1452+58G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 8/19 | chr2 | 101037474 | |||||||
chr2:101037760 | T | C | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1276-52A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/19 | chr2 | 101037760 | |||||||
chr2:101037928 | G | A | 1 | a0005c0006t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1276-220C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/19 | chr2 | 101037928 | |||||||
chr2:101037959 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1276-251A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/19 | chr2 | 101037959 | |||||||
chr2:101037999 | C | T | 52 | a0002c0003t0001g0001 a0002c0003t0001g0009 a0002c0003t0001g0010 others(49): Show |
52 | HG00735.hp1 HG01099.hp2 HG01192.hp1 others(49): Show |
intron_variant | MODIFIER | c.1276-291G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/19 | chr2 | 101037999 | |||||||
chr2:101038164 | C | T | 2 | a0001c0021t0004g0282 a0006c0012t0002g0279 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1275+297G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 7/19 | chr2 | 101038164 | |||||||
chr2:101038656 | C | A | 1 | a0018c0022t0001g0175 | 1 | NA19085.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1081-1G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038656 | |||||||
chr2:101038657 | T | TATGCGTA others(6): Show |
1 | a0018c0022t0001g0175 | 1 | NA19085.hp2 | splice_region_variant&intron_variant | LOW | c.1081-3_1081-2insGT others(11): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038657 | |||||||
chr2:101038658 | G | C | 1 | a0018c0022t0001g0175 | 1 | NA19085.hp2 | splice_region_variant&intron_variant | LOW | c.1081-3C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038658 | |||||||
chr2:101038782 | C | T | 3 | a0002c0002t0002g0164 a0002c0002t0002g0167 a0002c0002t0002g0173 |
3 | HG00738.hp2 HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1081-127G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038782 | |||||||
chr2:101038881 | CG | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1081-227delC | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038881 | |||||||
chr2:101038943 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1081-288C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101038943 | |||||||
chr2:101039191 | C | T | 1 | a0003c0004t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1081-536G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101039191 | |||||||
chr2:101039546 | T | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1080+632A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101039546 | |||||||
chr2:101039852 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1080+326C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101039852 | |||||||
chr2:101039909 | T | C | 8 | a0006c0010t0001g0217 a0006c0010t0001g0224 a0009c0014t0003g0325 others(5): Show |
8 | HG02818.hp2 HG02976.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080+269A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 6/19 | chr2 | 101039909 | |||||||
chr2:101040478 | T | C | 8 | a0006c0010t0001g0217 a0006c0010t0001g0224 a0009c0014t0003g0325 others(5): Show |
8 | HG02818.hp2 HG02976.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-93A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040478 | |||||||
chr2:101040503 | T | C | 1 | a0002c0016t0002g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.873-118A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040503 | |||||||
chr2:101040555 | C | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.873-170G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040555 | |||||||
chr2:101040619 | G | A | 1 | a0002c0002t0002g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.873-234C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040619 | |||||||
chr2:101040625 | G | A | 3 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0001c0001t0004g0278 |
3 | HG02922.hp2 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.873-240C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040625 | |||||||
chr2:101040760 | G | A | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.873-375C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040760 | |||||||
chr2:101040761 | C | T | 1 | a0002c0003t0001g0192 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.873-376G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040761 | |||||||
chr2:101040876 | C | T | 1 | a0002c0003t0001g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.873-491G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040876 | |||||||
chr2:101040912 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.873-527C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101040912 | |||||||
chr2:101041020 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0216 |
3 | HG02809.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.873-635G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041020 | |||||||
chr2:101041068 | T | C | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.873-683A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041068 | |||||||
chr2:101041181 | C | T | 135 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(132): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.873-796G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041181 | |||||||
chr2:101041265 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.873-880T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041265 | |||||||
chr2:101041298 | A | G | 2 | a0002c0002t0002g0089 a0002c0002t0002g0291 |
2 | HG00423.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.873-913T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041298 | |||||||
chr2:101041352 | T | TA | 16 | a0001c0001t0001g0029 a0001c0001t0001g0064 a0001c0001t0001g0065 others(13): Show |
16 | HG03834.hp2 NA18942.hp2 NA18946.hp1 others(13): Show |
intron_variant | MODIFIER | c.873-968dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041352 | |||||||
chr2:101041441 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.873-1056G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041441 | |||||||
chr2:101041715 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0157 |
3 | HG00408.hp2 NA18950.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.873-1330A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041715 | |||||||
chr2:101041981 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG03453.hp1 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-1596G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041981 | |||||||
chr2:101041981 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.873-1596G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101041981 | |||||||
chr2:101042024 | C | CA | 6 | a0002c0002t0002g0111 a0007c0007t0001g0045 a0009c0020t0003g0331 others(3): Show |
6 | HG02040.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-1640dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101042024 | |||||||
chr2:101042130 | G | A | 1 | a0002c0002t0002g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.873-1745C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101042130 | |||||||
chr2:101042176 | T | C | 4 | a0002c0002t0002g0168 a0002c0002t0002g0259 a0006c0010t0001g0217 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-1791A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101042176 | |||||||
chr2:101042614 | T | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.873-2229A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101042614 | |||||||
chr2:101042748 | T | TA | 11 | a0002c0002t0002g0183 a0002c0002t0002g0195 a0002c0002t0002g0197 others(8): Show |
11 | HG01071.hp1 HG01071.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.873-2364dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101042748 | |||||||
chr2:101043026 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.873-2641G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101043026 | |||||||
chr2:101043227 | G | A | 2 | a0001c0021t0004g0282 a0006c0012t0002g0279 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.873-2842C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101043227 | |||||||
chr2:101043400 | T | C | 138 | a0002c0002t0002g0008 a0002c0002t0002g0012 a0002c0002t0002g0013 others(135): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.873-3015A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101043400 | |||||||
chr2:101043847 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.873-3462T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101043847 | |||||||
chr2:101043865 | G | A | 1 | a0002c0002t0002g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.873-3480C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101043865 | |||||||
chr2:101044087 | T | A | 1 | a0002c0002t0002g0121 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.873-3702A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101044087 | |||||||
chr2:101044366 | C | T | 2 | a0002c0003t0001g0055 a0002c0003t0001g0080 |
2 | HG01255.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.873-3981G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101044366 | |||||||
chr2:101044489 | C | T | 2 | a0003c0004t0001g0226 a0003c0004t0001g0227 |
2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.873-4104G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101044489 | |||||||
chr2:101044566 | T | C | 6 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0020t0003g0331 others(3): Show |
6 | HG03139.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-4181A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101044566 | |||||||
chr2:101044873 | T | C | 1 | a0005c0006t0001g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.873-4488A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101044873 | |||||||
chr2:101045025 | C | T | 53 | a0001c0001t0001g0096 a0002c0003t0001g0001 a0002c0003t0001g0009 others(50): Show |
53 | HG00735.hp1 HG01099.hp2 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.873-4640G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045025 | |||||||
chr2:101045078 | A | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(122): Show |
125 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.873-4693T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045078 | |||||||
chr2:101045102 | C | T | 1 | a0005c0006t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.873-4717G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045102 | |||||||
chr2:101045210 | T | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.873-4825A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045210 | |||||||
chr2:101045230 | A | C | 5 | a0003c0004t0001g0245 a0003c0004t0001g0267 a0003c0004t0001g0270 others(2): Show |
5 | HG02027.hp1 HG02080.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.873-4845T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045230 | |||||||
chr2:101045415 | T | C | 1 | a0002c0003t0001g0011 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.872+4986A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045415 | |||||||
chr2:101045434 | C | T | 19 | a0002c0002t0002g0008 a0002c0002t0002g0102 a0004c0005t0001g0002 others(16): Show |
19 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+4967G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045434 | |||||||
chr2:101045489 | G | A | 2 | a0008c0015t0001g0075 a0008c0015t0001g0100 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.872+4912C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045489 | |||||||
chr2:101045639 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.872+4762G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045639 | |||||||
chr2:101045760 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0042 others(16): Show |
19 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+4641C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045760 | |||||||
chr2:101045876 | C | G | 9 | a0002c0002t0002g0008 a0002c0002t0002g0102 a0005c0006t0001g0051 others(6): Show |
9 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+4525G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045876 | |||||||
chr2:101045898 | C | G | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872+4503G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045898 | |||||||
chr2:101045955 | C | T | 19 | a0002c0002t0002g0008 a0002c0002t0002g0102 a0004c0005t0001g0002 others(16): Show |
19 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.872+4446G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045955 | |||||||
chr2:101045964 | G | A | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.872+4437C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101045964 | |||||||
chr2:101046231 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.872+4170G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046231 | |||||||
chr2:101046232 | G | T | 129 | a0001c0001t0001g0096 a0002c0002t0002g0008 a0002c0002t0002g0012 others(126): Show |
129 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.872+4169C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046232 | |||||||
chr2:101046260 | G | A | 130 | a0001c0001t0001g0096 a0002c0002t0002g0008 a0002c0002t0002g0012 others(127): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.872+4141C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046260 | |||||||
chr2:101046275 | C | G | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.872+4126G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046275 | |||||||
chr2:101046458 | C | T | 3 | a0001c0009t0001g0293 a0001c0009t0001g0294 a0001c0009t0001g0297 |
3 | NA18992.hp2 NA18999.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.872+3943G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046458 | |||||||
chr2:101046459 | G | A | 1 | a0002c0002t0002g0021 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.872+3942C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046459 | |||||||
chr2:101046537 | G | T | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.872+3864C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046537 | |||||||
chr2:101046607 | G | A | 1 | a0006c0012t0002g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.872+3794C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046607 | |||||||
chr2:101046638 | G | A | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872+3763C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046638 | |||||||
chr2:101046987 | C | T | 1 | a0002c0002t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.872+3414G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101046987 | |||||||
chr2:101047014 | C | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.872+3387G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047014 | |||||||
chr2:101047033 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(102): Show |
105 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.872+3368A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047033 | |||||||
chr2:101047122 | T | C | 125 | a0001c0001t0001g0096 a0002c0002t0002g0008 a0002c0002t0002g0016 others(122): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.872+3279A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047122 | |||||||
chr2:101047246 | G | A | 138 | a0001c0001t0001g0096 a0002c0002t0002g0008 a0002c0002t0002g0012 others(135): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.872+3155C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047246 | |||||||
chr2:101047260 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.872+3141G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047260 | |||||||
chr2:101047271 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.872+3130C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047271 | |||||||
chr2:101047284 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.872+3117G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047284 | |||||||
chr2:101047369 | C | T | 1 | a0008c0011t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.872+3032G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047369 | |||||||
chr2:101047448 | C | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0116 others(36): Show |
39 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.872+2953G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047448 | |||||||
chr2:101047475 | T | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.872+2926A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047475 | |||||||
chr2:101047563 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0216 |
3 | HG02809.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.872+2838C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047563 | |||||||
chr2:101047712 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0058 others(5): Show |
8 | HG01261.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+2689A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101047712 | |||||||
chr2:101048124 | G | A | 1 | a0005c0030t0001g0169 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.872+2277C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048124 | |||||||
chr2:101048365 | T | C | 1 | a0002c0003t0001g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.872+2036A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048365 | |||||||
chr2:101048422 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.872+1979C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048422 | |||||||
chr2:101048491 | C | G | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872+1910G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048491 | |||||||
chr2:101048612 | G | C | 1 | a0016c0035t0001g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.872+1789C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048612 | |||||||
chr2:101048667 | T | G | 2 | a0006c0012t0002g0279 a0006c0025t0002g0316 |
2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.872+1734A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048667 | |||||||
chr2:101048667 | T | TGAAG | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(231): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.872+1733_872+1734i others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048667 | |||||||
chr2:101048689 | T | C | 16 | a0002c0002t0002g0008 a0002c0002t0002g0102 a0002c0002t0002g0198 others(13): Show |
16 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.872+1712A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048689 | |||||||
chr2:101048735 | C | CT | 59 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0236 others(56): Show |
59 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.872+1665dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048735 | |||||||
chr2:101048735 | CT | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(56): Show |
59 | HG01167.hp2 HG01243.hp1 HG01261.hp2 others(56): Show |
intron_variant | MODIFIER | c.872+1665delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048735 | |||||||
chr2:101048740 | TA | T | 7 | a0001c0001t0001g0289 a0002c0002t0002g0200 a0002c0003t0001g0170 others(4): Show |
7 | HG01168.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+1660delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048740 | |||||||
chr2:101048741 | A | T | 121 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.872+1660T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048741 | |||||||
chr2:101048742 | A | T | 2 | a0002c0002t0002g0200 a0002c0003t0001g0170 |
2 | HG01168.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.872+1659T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101048742 | |||||||
chr2:101049085 | G | A | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872+1316C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049085 | |||||||
chr2:101049110 | G | A | 110 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(107): Show |
110 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.872+1291C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049110 | |||||||
chr2:101049367 | G | A | 124 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.872+1034C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049367 | |||||||
chr2:101049368 | A | G | 1 | a0008c0011t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.872+1033T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049368 | |||||||
chr2:101049453 | G | A | 54 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.872+948C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049453 | |||||||
chr2:101049457 | G | A | 1 | a0006c0010t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.872+944C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049457 | |||||||
chr2:101049588 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.872+813G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049588 | |||||||
chr2:101049676 | C | CGAGATAG others(161): Show |
1 | a0002c0002t0002g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.872+557_872+724dup others(168): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049676 | |||||||
chr2:101049740 | A | G | 13 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.872+661T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049740 | |||||||
chr2:101049758 | C | T | 7 | a0001c0001t0001g0277 a0001c0001t0004g0106 a0001c0001t0004g0210 others(4): Show |
7 | HG01167.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+643G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049758 | |||||||
chr2:101049972 | G | A | 7 | a0002c0003t0001g0283 a0002c0003t0007g0101 a0004c0005t0001g0276 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+429C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101049972 | |||||||
chr2:101050021 | T | G | 125 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.872+380A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101050021 | |||||||
chr2:101050107 | G | A | 1 | a0001c0001t0005g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.872+294C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101050107 | |||||||
chr2:101050122 | C | T | 13 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(10): Show |
13 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.872+279G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101050122 | |||||||
chr2:101050275 | T | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0190 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.872+126A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101050275 | |||||||
chr2:101050382 | C | T | 5 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0220 others(2): Show |
5 | HG02809.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+19G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 5/19 | chr2 | 101050382 | |||||||
chr2:101050777 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.632-136C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101050777 | |||||||
chr2:101051363 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.632-722G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101051363 | |||||||
chr2:101051686 | C | T | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.632-1045G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101051686 | |||||||
chr2:101051701 | A | G | 2 | a0001c0001t0001g0057 a0004c0005t0001g0110 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.632-1060T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101051701 | |||||||
chr2:101051933 | T | C | 1 | a0002c0002t0002g0077 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.632-1292A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101051933 | |||||||
chr2:101052395 | G | A | 46 | a0001c0001t0001g0029 a0002c0002t0002g0008 a0002c0002t0002g0012 others(43): Show |
46 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.631+1713C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052395 | |||||||
chr2:101052442 | G | A | 2 | a0001c0001t0001g0160 a0006c0012t0002g0161 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.631+1666C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052442 | |||||||
chr2:101052479 | C | CT | 19 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0070 others(16): Show |
19 | HG02273.hp2 HG02698.hp1 HG03834.hp2 others(16): Show |
intron_variant | MODIFIER | c.631+1628dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052479 | |||||||
chr2:101052479 | C | CTT | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.631+1627_631+1628d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052479 | |||||||
chr2:101052508 | G | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.631+1600C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052508 | |||||||
chr2:101052519 | C | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.631+1589G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052519 | |||||||
chr2:101052532 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(40): Show |
43 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.631+1576C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052532 | |||||||
chr2:101052665 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.631+1443G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052665 | |||||||
chr2:101052750 | A | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.631+1358T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052750 | |||||||
chr2:101052899 | C | T | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1209G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052899 | |||||||
chr2:101052990 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.631+1118G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052990 | |||||||
chr2:101052995 | T | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.631+1113A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101052995 | |||||||
chr2:101053286 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.631+822C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053286 | |||||||
chr2:101053289 | G | A | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+819C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053289 | |||||||
chr2:101053368 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.631+740G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053368 | |||||||
chr2:101053592 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.631+516G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053592 | |||||||
chr2:101053737 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.631+371C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053737 | |||||||
chr2:101053813 | T | C | 4 | a0010c0008t0001g0039 a0010c0008t0001g0040 a0010c0008t0001g0041 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+295A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101053813 | |||||||
chr2:101054008 | T | G | 1 | a0002c0002t0002g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.631+100A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101054008 | |||||||
chr2:101054071 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.631+37T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 4/19 | chr2 | 101054071 | |||||||
chr2:101054426 | G | A | 2 | a0004c0005t0001g0002 a0004c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.403-90C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054426 | |||||||
chr2:101054466 | C | A | 113 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(110): Show |
113 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.403-130G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054466 | |||||||
chr2:101054475 | C | T | 54 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.403-139G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054475 | |||||||
chr2:101054493 | C | T | 54 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.403-157G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054493 | |||||||
chr2:101054587 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.403-251C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054587 | |||||||
chr2:101054606 | G | A | 1 | a0002c0003t0001g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.403-270C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054606 | |||||||
chr2:101054609 | T | C | 1 | a0002c0003t0001g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.403-273A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054609 | |||||||
chr2:101054611 | T | G | 1 | a0002c0003t0001g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.403-275A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054611 | |||||||
chr2:101054612 | GGGCAAAT others(55): Show |
G | 1 | a0002c0003t0001g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.403-338_403-277del others(62): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054612 | |||||||
chr2:101054639 | GTTCTCAA others(27): Show |
G | 18 | a0001c0001t0001g0193 a0001c0001t0001g0230 a0001c0001t0001g0236 others(15): Show |
18 | HG00423.hp1 HG00642.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.403-337_403-304del others(34): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054639 | |||||||
chr2:101054639 | GTTCTCAA others(28): Show |
G | 86 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(83): Show |
86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.403-338_403-304del others(35): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054639 | |||||||
chr2:101054639 | GTTCTCAA others(29): Show |
G | 9 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-339_403-304del others(36): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054639 | |||||||
chr2:101054648 | CAAACA | C | 4 | a0002c0003t0001g0219 a0002c0003t0001g0220 a0006c0010t0001g0217 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-317_403-313del others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054648 | |||||||
chr2:101054667 | C | CT | 8 | a0002c0002t0002g0020 a0002c0002t0002g0023 a0002c0002t0002g0026 others(5): Show |
8 | HG00741.hp2 HG02040.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-332dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054667 | |||||||
chr2:101054667 | C | CTTT | 4 | a0002c0002t0002g0024 a0002c0002t0002g0166 a0002c0002t0002g0298 others(1): Show |
4 | HG00642.hp1 HG02056.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-334_403-332dup others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054667 | |||||||
chr2:101054667 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0301 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.403-332_403-331ins others(23): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054667 | |||||||
chr2:101054667 | CTTTTCTT others(3): Show |
C | 4 | a0001c0024t0003g0327 a0004c0005t0001g0206 a0004c0005t0001g0215 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-341_403-332del others(10): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054667 | |||||||
chr2:101054667 | CTTTTCTT others(9): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403-347_403-332del others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054667 | |||||||
chr2:101054668 | TTTTC | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(46): Show |
49 | HG01167.hp2 HG01261.hp2 HG01516.hp1 others(46): Show |
intron_variant | MODIFIER | c.403-336_403-333del others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054668 | |||||||
chr2:101054669 | TTTC | T | 19 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0071 others(16): Show |
19 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.403-336_403-334del others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054669 | |||||||
chr2:101054670 | TTC | T | 6 | a0001c0021t0004g0282 a0002c0002t0002g0126 a0002c0003t0001g0055 others(3): Show |
6 | HG01255.hp2 HG01346.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-336_403-335del others(2): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054670 | |||||||
chr2:101054671 | TC | T | 10 | a0002c0002t0002g0162 a0002c0002t0002g0168 a0002c0002t0002g0176 others(7): Show |
10 | HG02735.hp2 HG03669.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-336delG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054671 | |||||||
chr2:101054672 | C | CTTTTCTT others(8): Show |
1 | a0014c0034t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.403-337_403-336ins others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTCTT others(9): Show |
1 | a0006c0013t0001g0299 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.403-337_403-336ins others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTCTT others(17): Show |
1 | a0001c0001t0001g0314 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.403-337_403-336ins others(24): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0295 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.403-346_403-337dup others(10): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0289 a0002c0002t0002g0121 a0002c0003t0001g0122 |
3 | HG02896.hp2 NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.403-350_403-337dup others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0149 others(8): Show |
11 | HG00544.hp2 HG02040.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-351_403-337dup others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(9): Show |
12 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0119 others(9): Show |
12 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.403-352_403-337dup others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(10): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0137 others(3): Show |
6 | HG01975.hp1 NA18965.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-353_403-337dup others(17): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0305 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.403-354_403-337dup others(18): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(12): Show |
1 | a0002c0002t0002g0156 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.403-355_403-337dup others(19): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.403-356_403-337dup others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(14): Show |
1 | a0002c0002t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.403-357_403-337dup others(21): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.403-358_403-337dup others(22): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.403-359_403-337dup others(23): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(18): Show |
2 | a0002c0002t0002g0084 a0005c0006t0001g0211 |
2 | HG01257.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.403-361_403-337dup others(25): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(19): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0153 |
3 | HG00438.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.403-362_403-337dup others(26): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(20): Show |
1 | a0002c0002t0002g0303 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.403-337_403-336ins others(27): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.403-337_403-336ins others(31): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0117 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.403-337_403-336ins others(32): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.403-337_403-336ins others(33): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(29): Show |
1 | a0001c0001t0001g0323 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.403-337_403-336ins others(36): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | CTTTTTTT others(33): Show |
1 | a0002c0002t0002g0304 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.403-337_403-336ins others(40): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | C | T | 47 | a0001c0001t0001g0048 a0001c0001t0001g0301 a0002c0002t0002g0008 others(44): Show |
47 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.403-336G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054672 | CTTTTT | C | 7 | a0001c0001t0001g0029 a0002c0002t0002g0012 a0002c0002t0002g0013 others(4): Show |
7 | HG02074.hp1 NA18971.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-341_403-337del others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054672 | |||||||
chr2:101054683 | T | C | 14 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-347A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054683 | |||||||
chr2:101054713 | G | C | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-377C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054713 | |||||||
chr2:101054754 | C | G | 1 | a0002c0003t0001g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.403-418G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054754 | |||||||
chr2:101054833 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.403-497G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054833 | |||||||
chr2:101054840 | G | A | 53 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(50): Show |
53 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.403-504C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054840 | |||||||
chr2:101054855 | T | G | 188 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(185): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.403-519A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054855 | |||||||
chr2:101054883 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.403-547A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054883 | |||||||
chr2:101054974 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.403-638C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101054974 | |||||||
chr2:101055051 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.403-715G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055051 | |||||||
chr2:101055147 | T | C | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403-811A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055147 | |||||||
chr2:101055154 | C | T | 14 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-818G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055154 | |||||||
chr2:101055315 | G | A | 1 | a0002c0002t0002g0291 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.403-979C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055315 | |||||||
chr2:101055597 | A | G | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403-1261T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055597 | |||||||
chr2:101055606 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-1270G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055606 | |||||||
chr2:101055608 | A | C | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-1272T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101055608 | |||||||
chr2:101056041 | C | CT | 14 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-1706dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056041 | |||||||
chr2:101056041 | CT | C | 25 | a0001c0001t0001g0119 a0001c0021t0004g0282 a0001c0024t0003g0327 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.403-1706delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056041 | |||||||
chr2:101056154 | C | T | 191 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(188): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.403-1818G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056154 | |||||||
chr2:101056161 | G | A | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.403-1825C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056161 | |||||||
chr2:101056186 | T | C | 1 | a0006c0012t0002g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.403-1850A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056186 | |||||||
chr2:101056207 | A | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.403-1871T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056207 | |||||||
chr2:101056207 | ATT | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(45): Show |
48 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.403-1873_403-1872d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056207 | |||||||
chr2:101056209 | T | G | 1 | a0001c0001t0001g0018 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.403-1873A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056209 | |||||||
chr2:101056209 | T | TA | 3 | a0001c0001t0001g0231 a0001c0001t0005g0097 a0002c0003t0001g0080 |
3 | HG00099.hp2 HG01358.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.403-1874_403-1873i others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056209 | |||||||
chr2:101056210 | T | A | 202 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(199): Show |
202 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.403-1874A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056210 | |||||||
chr2:101056211 | T | A | 2 | a0004c0005t0001g0110 a0017c0027t0001g0047 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.403-1875A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056211 | |||||||
chr2:101056212 | T | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01167.hp2 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-1876A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056212 | |||||||
chr2:101056213 | T | A | 57 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(54): Show |
57 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.403-1877A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056213 | |||||||
chr2:101056214 | T | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403-1878A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056214 | |||||||
chr2:101056216 | T | A | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-1880A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056216 | |||||||
chr2:101056219 | T | A | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-1883A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056219 | |||||||
chr2:101056228 | C | CAG | 212 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.403-1894_403-1893d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056228 | |||||||
chr2:101056234 | C | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(45): Show |
48 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.403-1898G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056234 | |||||||
chr2:101056273 | G | A | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403-1937C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056273 | |||||||
chr2:101056323 | T | C | 195 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(192): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.403-1987A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056323 | |||||||
chr2:101056355 | CA | C | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.403-2020delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056355 | |||||||
chr2:101056392 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.403-2056G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056392 | |||||||
chr2:101056403 | C | T | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403-2067G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056403 | |||||||
chr2:101056406 | G | A | 192 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(189): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.403-2070C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056406 | |||||||
chr2:101056491 | C | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(3): Show |
6 | NA18946.hp1 NA18964.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-2155G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056491 | |||||||
chr2:101056589 | T | A | 2 | a0004c0005t0001g0002 a0004c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.403-2253A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056589 | |||||||
chr2:101056799 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.403-2463C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056799 | |||||||
chr2:101056810 | C | A | 188 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(185): Show |
188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.403-2474G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056810 | |||||||
chr2:101056960 | T | A | 1 | a0014c0034t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.402+2461A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101056960 | |||||||
chr2:101057057 | G | A | 24 | a0001c0001t0001g0029 a0002c0002t0002g0008 a0002c0002t0002g0012 others(21): Show |
24 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.402+2364C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057057 | |||||||
chr2:101057137 | A | C | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.402+2284T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057137 | |||||||
chr2:101057280 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.402+2141G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057280 | |||||||
chr2:101057604 | T | C | 1 | a0006c0010t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.402+1817A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057604 | |||||||
chr2:101057623 | C | T | 2 | a0001c0001t0001g0160 a0006c0012t0002g0161 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.402+1798G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057623 | |||||||
chr2:101057671 | A | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.402+1750T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057671 | |||||||
chr2:101057680 | C | T | 1 | a0002c0002t0002g0194 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.402+1741G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101057680 | |||||||
chr2:101058002 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.402+1419G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058002 | |||||||
chr2:101058301 | A | C | 11 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.402+1120T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058301 | |||||||
chr2:101058435 | G | C | 14 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.402+986C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058435 | |||||||
chr2:101058734 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.402+687C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058734 | |||||||
chr2:101058752 | C | CA | 8 | a0001c0001t0001g0295 a0002c0002t0002g0104 a0002c0018t0001g0144 others(5): Show |
8 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+668dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058752 | |||||||
chr2:101058848 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.402+573C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058848 | |||||||
chr2:101058911 | AT | A | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.402+509delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101058911 | |||||||
chr2:101059111 | G | A | 53 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(50): Show |
53 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.402+310C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059111 | |||||||
chr2:101059129 | G | A | 1 | a0002c0002t0002g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.402+292C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059129 | |||||||
chr2:101059142 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0239 a0001c0001t0001g0263 |
3 | HG00408.hp1 NA18941.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.402+279G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059142 | |||||||
chr2:101059211 | CT | C | 122 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.402+209delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059211 | |||||||
chr2:101059211 | CTTT | C | 73 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0107 others(70): Show |
73 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.402+207_402+209del others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059211 | |||||||
chr2:101059346 | A | G | 74 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0107 others(71): Show |
74 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.402+75T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 3/19 | chr2 | 101059346 | |||||||
chr2:101059716 | G | A | 1 | a0004c0005t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.284-177C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101059716 | |||||||
chr2:101059870 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.284-331G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101059870 | |||||||
chr2:101060052 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-513C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060052 | |||||||
chr2:101060201 | C | T | 53 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0125 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.284-662G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060201 | |||||||
chr2:101060202 | G | A | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.284-663C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060202 | |||||||
chr2:101060304 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.284-765G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060304 | |||||||
chr2:101060348 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-809G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060348 | |||||||
chr2:101060507 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-968C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101060507 | |||||||
chr2:101061149 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-1610A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061149 | |||||||
chr2:101061164 | G | A | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-1625C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061164 | |||||||
chr2:101061183 | G | A | 11 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-1644C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061183 | |||||||
chr2:101061187 | C | CA | 141 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0066 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.284-1649dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061187 | |||||||
chr2:101061187 | C | CAA | 8 | a0001c0001t0001g0125 a0001c0001t0001g0236 a0001c0001t0001g0238 others(5): Show |
8 | HG00438.hp2 HG01192.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-1650_284-1649d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061187 | |||||||
chr2:101061187 | CA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0160 a0001c0001t0001g0179 others(5): Show |
8 | HG01074.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-1649delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061187 | |||||||
chr2:101061187 | CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0272 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.284-1658_284-1649d others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061187 | |||||||
chr2:101061680 | G | A | 4 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0033t0003g0328 others(1): Show |
4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-2141C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061680 | |||||||
chr2:101061704 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(45): Show |
48 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.284-2165C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061704 | |||||||
chr2:101061708 | T | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.284-2169A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061708 | |||||||
chr2:101061795 | G | A | 6 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-2256C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061795 | |||||||
chr2:101061808 | G | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.284-2269C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101061808 | |||||||
chr2:101062086 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-2547C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101062086 | |||||||
chr2:101062230 | G | A | 1 | a0002c0002t0002g0020 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.284-2691C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101062230 | |||||||
chr2:101062887 | G | A | 3 | a0001c0021t0004g0282 a0001c0024t0003g0327 a0006c0012t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.284-3348C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101062887 | |||||||
chr2:101062982 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp1 HG00544.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-3443C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101062982 | |||||||
chr2:101063237 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.284-3698A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101063237 | |||||||
chr2:101063713 | G | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-4174C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101063713 | |||||||
chr2:101064015 | C | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-4476G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064015 | |||||||
chr2:101064032 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(39): Show |
42 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.284-4493G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064032 | |||||||
chr2:101064194 | C | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284-4655G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064194 | |||||||
chr2:101064213 | G | A | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-4674C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064213 | |||||||
chr2:101064235 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-4696C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064235 | |||||||
chr2:101064241 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.284-4702C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064241 | |||||||
chr2:101064248 | T | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0143 |
2 | NA18970.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.284-4709A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064248 | |||||||
chr2:101064427 | G | T | 14 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG02145.hp2 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-4888C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101064427 | |||||||
chr2:101065003 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-5464C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101065003 | |||||||
chr2:101065227 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.284-5688A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101065227 | |||||||
chr2:101065659 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0263 |
2 | NA18941.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.284-6120A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101065659 | |||||||
chr2:101065801 | A | G | 1 | a0003c0004t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.284-6262T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101065801 | |||||||
chr2:101066323 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284-6784G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066323 | |||||||
chr2:101066420 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284-6881A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066420 | |||||||
chr2:101066577 | T | G | 1 | a0002c0002t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.284-7038A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066577 | |||||||
chr2:101066578 | A | G | 1 | a0003c0004t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.284-7039T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066578 | |||||||
chr2:101066717 | C | T | 106 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0125 others(103): Show |
106 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.284-7178G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066717 | |||||||
chr2:101066851 | A | G | 1 | a0001c0001t0005g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.284-7312T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066851 | |||||||
chr2:101066933 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.284-7394G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066933 | |||||||
chr2:101066944 | C | CA | 9 | a0001c0001t0001g0114 a0001c0001t0001g0120 a0001c0001t0001g0124 others(6): Show |
9 | HG01928.hp1 HG02027.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-7406dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101066944 | CA | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0140 a0002c0003t0001g0001 others(6): Show |
9 | HG01975.hp1 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-7406delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101066944 | CAA | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(52): Show |
55 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.284-7407_284-7406d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101066944 | CAAA | C | 55 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0096 others(52): Show |
55 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.284-7408_284-7406d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101066944 | CAAAAAA | C | 115 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0107 others(112): Show |
115 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.284-7411_284-7406d others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101066944 | CAAAAAAA | C | 6 | a0001c0001t0001g0277 a0001c0001t0004g0106 a0001c0001t0004g0210 others(3): Show |
6 | HG02572.hp2 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-7412_284-7406d others(9): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101066944 | |||||||
chr2:101067014 | T | C | 2 | a0004c0005t0001g0110 a0017c0027t0001g0047 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284-7475A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067014 | |||||||
chr2:101067025 | C | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0107 others(124): Show |
127 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.284-7486G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067025 | |||||||
chr2:101067255 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.284-7716C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067255 | |||||||
chr2:101067402 | A | G | 71 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.284-7863T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067402 | |||||||
chr2:101067486 | G | A | 198 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0096 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.284-7947C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067486 | |||||||
chr2:101067547 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.284-8008A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067547 | |||||||
chr2:101067671 | A | G | 198 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0096 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.284-8132T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067671 | |||||||
chr2:101067674 | T | A | 14 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-8135A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067674 | |||||||
chr2:101067744 | T | G | 1 | a0010c0008t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.284-8205A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067744 | |||||||
chr2:101067923 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.284-8384G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101067923 | |||||||
chr2:101068029 | C | T | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-8490G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068029 | |||||||
chr2:101068276 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.284-8737G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068276 | |||||||
chr2:101068409 | G | A | 131 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0107 others(128): Show |
131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.284-8870C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068409 | |||||||
chr2:101068451 | C | G | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.284-8912G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068451 | |||||||
chr2:101068497 | G | A | 110 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0125 others(107): Show |
110 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.284-8958C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068497 | |||||||
chr2:101068588 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284-9049G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068588 | |||||||
chr2:101068666 | C | T | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-9127G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068666 | |||||||
chr2:101068773 | G | C | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.284-9234C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068773 | |||||||
chr2:101068797 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0212 |
2 | HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.284-9258C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068797 | |||||||
chr2:101068844 | C | T | 1 | a0005c0006t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.284-9305G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068844 | |||||||
chr2:101068915 | G | A | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-9376C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101068915 | |||||||
chr2:101069003 | G | GA | 33 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0059 others(30): Show |
33 | HG01081.hp1 HG01243.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.284-9465dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069003 | |||||||
chr2:101069014 | A | G | 1 | a0008c0015t0001g0075 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9475T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069014 | |||||||
chr2:101069081 | T | C | 1 | a0002c0002t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.284-9542A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069081 | |||||||
chr2:101069096 | G | A | 2 | a0002c0003t0001g0146 a0002c0003t0001g0147 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.284-9557C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069096 | |||||||
chr2:101069114 | A | G | 1 | a0005c0006t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.284-9575T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069114 | |||||||
chr2:101069115 | T | A | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.284-9576A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069115 | |||||||
chr2:101069158 | C | T | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-9619G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069158 | |||||||
chr2:101069254 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284-9715G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069254 | |||||||
chr2:101069324 | C | T | 14 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-9785G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069324 | |||||||
chr2:101069467 | T | G | 11 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-9928A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069467 | |||||||
chr2:101069510 | T | C | 14 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-9971A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069510 | |||||||
chr2:101069573 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-10034G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069573 | |||||||
chr2:101069611 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284-10072G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069611 | |||||||
chr2:101069777 | T | A | 1 | a0002c0003t0001g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.284-10238A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069777 | |||||||
chr2:101069785 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284-10246C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069785 | |||||||
chr2:101069804 | T | C | 1 | a0002c0002t0002g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.284-10265A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069804 | |||||||
chr2:101069917 | CT | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.284-10379delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069917 | |||||||
chr2:101069956 | C | T | 4 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0009c0033t0003g0328 others(1): Show |
4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-10417G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101069956 | |||||||
chr2:101070066 | C | T | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-10527G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070066 | |||||||
chr2:101070212 | C | T | 4 | a0001c0001t0001g0029 a0002c0003t0001g0009 a0002c0003t0001g0010 others(1): Show |
4 | NA18971.hp2 NA18975.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-10673G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070212 | |||||||
chr2:101070213 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-10674C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070213 | |||||||
chr2:101070352 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.284-10813T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070352 | |||||||
chr2:101070416 | A | AT | 213 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0048 others(210): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.284-10878dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070416 | |||||||
chr2:101070416 | A | ATT | 40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(37): Show |
40 | HG01243.hp1 HG01261.hp2 HG02280.hp2 others(37): Show |
intron_variant | MODIFIER | c.284-10879_284-1087 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070416 | |||||||
chr2:101070608 | T | G | 2 | a0007c0019t0001g0060 a0007c0019t0001g0061 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.284-11069A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101070608 | |||||||
chr2:101071122 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284-11583C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071122 | |||||||
chr2:101071136 | G | C | 1 | a0002c0003t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-11597C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071136 | |||||||
chr2:101071156 | G | A | 1 | a0002c0016t0002g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284-11617C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071156 | |||||||
chr2:101071164 | T | C | 206 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0096 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.284-11625A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071164 | |||||||
chr2:101071232 | C | G | 1 | a0002c0003t0001g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.284-11693G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071232 | |||||||
chr2:101071238 | G | A | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.284-11699C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071238 | |||||||
chr2:101071270 | G | A | 1 | a0001c0024t0003g0327 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.284-11731C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071270 | |||||||
chr2:101071346 | A | AAAAC | 7 | a0001c0001t0001g0057 a0001c0001t0001g0107 a0002c0002t0002g0008 others(4): Show |
7 | HG00642.hp1 HG01074.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-11811_284-1180 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071346 | |||||||
chr2:101071366 | C | CAAAT | 89 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0066 others(86): Show |
89 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-11831_284-1182 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071366 | |||||||
chr2:101071366 | C | T | 2 | a0002c0002t0002g0112 a0002c0003t0001g0185 |
2 | NA18953.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.284-11827G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071366 | |||||||
chr2:101071366 | CAAAT | C | 44 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(41): Show |
44 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.284-11831_284-1182 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071366 | |||||||
chr2:101071370 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0253 a0001c0001t0001g0264 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-11831A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071370 | |||||||
chr2:101071373 | AT | A | 3 | a0002c0002t0002g0076 a0002c0002t0002g0077 a0002c0002t0002g0188 |
3 | HG04199.hp1 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.284-11835delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071373 | |||||||
chr2:101071455 | A | G | 1 | a0003c0004t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.284-11916T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071455 | |||||||
chr2:101071593 | C | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.284-12054G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071593 | |||||||
chr2:101071616 | C | T | 3 | a0002c0002t0002g0195 a0002c0002t0002g0202 a0002c0003t0001g0199 |
3 | HG01071.hp1 HG01071.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.284-12077G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071616 | |||||||
chr2:101071680 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-12141A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071680 | |||||||
chr2:101071718 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.284-12179C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071718 | |||||||
chr2:101071884 | G | A | 2 | a0002c0003t0001g0146 a0002c0003t0001g0147 |
2 | NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.284-12345C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101071884 | |||||||
chr2:101072123 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0143 |
2 | NA18970.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.284-12584C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072123 | |||||||
chr2:101072219 | G | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284-12680C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072219 | |||||||
chr2:101072349 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.284-12810C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072349 | |||||||
chr2:101072665 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284-13126T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072665 | |||||||
chr2:101072754 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(39): Show |
42 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.284-13215G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072754 | |||||||
chr2:101072874 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-13335G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072874 | |||||||
chr2:101072877 | C | T | 1 | a0002c0032t0001g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.284-13338G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072877 | |||||||
chr2:101072940 | C | T | 2 | a0002c0002t0002g0173 a0006c0012t0002g0279 |
2 | HG00741.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.284-13401G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072940 | |||||||
chr2:101072952 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0004g0106 a0001c0001t0004g0210 others(3): Show |
6 | HG02572.hp2 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-13413T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101072952 | |||||||
chr2:101073148 | CTA | C | 198 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0096 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.284-13611_284-1361 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073148 | |||||||
chr2:101073260 | A | AT | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(47): Show |
50 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.284-13722dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073260 | |||||||
chr2:101073264 | T | G | 54 | a0001c0001t0001g0048 a0002c0002t0002g0008 a0002c0002t0002g0015 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-13725A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073264 | |||||||
chr2:101073291 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0329 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.284-13752T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073291 | |||||||
chr2:101073296 | A | AT | 8 | a0001c0001t0001g0207 a0001c0001t0001g0248 a0002c0002t0002g0022 others(5): Show |
8 | HG01071.hp1 HG01071.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-13758dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073296 | |||||||
chr2:101073296 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0329 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.284-13757T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073296 | |||||||
chr2:101073300 | A | AT | 72 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.284-13762dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073300 | |||||||
chr2:101073300 | A | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(164): Show |
167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.284-13761T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073300 | |||||||
chr2:101073301 | T | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0057 others(121): Show |
124 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.284-13762A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073301 | |||||||
chr2:101073302 | T | A | 1 | a0003c0004t0001g0270 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.284-13763A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073302 | |||||||
chr2:101073306 | T | A | 1 | a0002c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284-13767A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073306 | |||||||
chr2:101073346 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.284-13807C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073346 | |||||||
chr2:101073380 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.284-13841G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073380 | |||||||
chr2:101073444 | G | A | 1 | a0002c0002t0002g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.284-13905C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073444 | |||||||
chr2:101073451 | C | T | 1 | a0002c0002t0002g0287 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.284-13912G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073451 | |||||||
chr2:101073497 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.284-13958A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073497 | |||||||
chr2:101073594 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.284-14055G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073594 | |||||||
chr2:101073643 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.284-14104G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073643 | |||||||
chr2:101073701 | G | A | 2 | a0004c0005t0001g0002 a0004c0005t0001g0014 |
2 | HG01243.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.284-14162C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073701 | |||||||
chr2:101073874 | T | C | 192 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(189): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.284-14335A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101073874 | |||||||
chr2:101074073 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.284-14534G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074073 | |||||||
chr2:101074126 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | NA18961.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.284-14587G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074126 | |||||||
chr2:101074229 | G | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.284-14690C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074229 | |||||||
chr2:101074234 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.284-14695G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074234 | |||||||
chr2:101074247 | C | A | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.284-14708G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074247 | |||||||
chr2:101074288 | C | T | 58 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(55): Show |
58 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.284-14749G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074288 | |||||||
chr2:101074497 | C | A | 117 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0123 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.284-14958G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074497 | |||||||
chr2:101074539 | C | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.284-15000G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074539 | |||||||
chr2:101074668 | G | A | 11 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0129 others(8): Show |
11 | HG00438.hp2 NA18906.hp1 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-15129C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074668 | |||||||
chr2:101074674 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.284-15135C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074674 | |||||||
chr2:101074702 | T | C | 209 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.284-15163A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074702 | |||||||
chr2:101074705 | G | A | 1 | a0002c0003t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.284-15166C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074705 | |||||||
chr2:101074791 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.284-15252T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074791 | |||||||
chr2:101074949 | G | A | 5 | a0010c0008t0001g0039 a0010c0008t0001g0040 a0010c0008t0001g0041 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+15260C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101074949 | |||||||
chr2:101075009 | A | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0029 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.283+15200T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075009 | |||||||
chr2:101075115 | C | T | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.283+15094G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075115 | |||||||
chr2:101075116 | G | A | 3 | a0002c0003t0001g0001 a0002c0003t0001g0035 a0004c0005t0001g0034 |
3 | HG02258.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.283+15093C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075116 | |||||||
chr2:101075131 | C | T | 196 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(193): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.283+15078G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075131 | |||||||
chr2:101075166 | G | C | 1 | a0010c0008t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.283+15043C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075166 | |||||||
chr2:101075227 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.283+14982A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075227 | |||||||
chr2:101075289 | T | C | 12 | a0001c0023t0001g0115 a0002c0003t0001g0275 a0003c0004t0001g0226 others(9): Show |
12 | HG02015.hp1 HG02027.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+14920A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075289 | |||||||
chr2:101075369 | C | T | 193 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0057 others(190): Show |
193 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.283+14840G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075369 | |||||||
chr2:101075390 | C | CA | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(55): Show |
58 | HG00438.hp2 HG01167.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+14818dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075390 | |||||||
chr2:101075390 | C | CAA | 178 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0066 others(175): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.283+14817_283+1481 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075390 | |||||||
chr2:101075390 | C | CAAA | 9 | a0001c0001t0001g0048 a0001c0001t0001g0237 a0002c0002t0002g0076 others(6): Show |
9 | HG01261.hp1 HG02027.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+14816_283+1481 others(7): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075390 | |||||||
chr2:101075390 | CA | C | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+14818delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075390 | |||||||
chr2:101075412 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0239 a0001c0001t0001g0263 |
3 | HG00408.hp1 NA18941.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.283+14797A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075412 | |||||||
chr2:101075720 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.283+14489C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101075720 | |||||||
chr2:101076152 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(44): Show |
47 | HG01167.hp2 HG01261.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.283+14057A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076152 | |||||||
chr2:101076300 | A | T | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+13909T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076300 | |||||||
chr2:101076307 | C | T | 15 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+13902G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076307 | |||||||
chr2:101076516 | A | G | 1 | a0002c0018t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.283+13693T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076516 | |||||||
chr2:101076560 | A | T | 1 | a0014c0034t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.283+13649T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076560 | |||||||
chr2:101076593 | G | C | 5 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0220 others(2): Show |
5 | HG02809.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+13616C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076593 | |||||||
chr2:101076756 | C | T | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283+13453G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076756 | |||||||
chr2:101076786 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.283+13423G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076786 | |||||||
chr2:101076870 | G | A | 107 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0125 others(104): Show |
107 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.283+13339C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076870 | |||||||
chr2:101076887 | C | T | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+13322G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101076887 | |||||||
chr2:101077069 | ACTGGAGT others(217): Show |
A | 1 | a0006c0012t0002g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+12916_283+1313 others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077069 | |||||||
chr2:101077092 | T | C | 212 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0048 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.283+13117A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077092 | |||||||
chr2:101077167 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.283+13042C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077167 | |||||||
chr2:101077259 | G | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.283+12950C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077259 | |||||||
chr2:101077276 | G | T | 1 | a0002c0002t0002g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.283+12933C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077276 | |||||||
chr2:101077349 | G | A | 2 | a0002c0002t0002g0198 a0002c0002t0002g0322 |
2 | HG00140.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.283+12860C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077349 | |||||||
chr2:101077405 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(42): Show |
45 | HG01167.hp2 HG01261.hp2 HG02486.hp2 others(42): Show |
intron_variant | MODIFIER | c.283+12804C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077405 | |||||||
chr2:101077546 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0003g0329 |
2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.283+12663G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077546 | |||||||
chr2:101077547 | G | A | 58 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(55): Show |
58 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.283+12662C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077547 | |||||||
chr2:101077570 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0004g0106 a0001c0001t0004g0210 others(1): Show |
4 | HG02922.hp2 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+12639C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077570 | |||||||
chr2:101077578 | G | C | 58 | a0001c0001t0001g0096 a0001c0001t0001g0180 a0001c0001t0001g0190 others(55): Show |
58 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.283+12631C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077578 | |||||||
chr2:101077759 | T | A | 2 | a0001c0001t0001g0160 a0006c0012t0002g0161 |
2 | HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.283+12450A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077759 | |||||||
chr2:101077874 | C | T | 9 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0136 others(6): Show |
9 | HG00438.hp2 NA18953.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+12335G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101077874 | |||||||
chr2:101078098 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0160 a0001c0001t0001g0277 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+12111G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078098 | |||||||
chr2:101078461 | C | T | 15 | a0001c0001t0001g0042 a0001c0001t0001g0315 a0002c0002t0002g0049 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+11748G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078461 | |||||||
chr2:101078673 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0206 |
3 | HG03225.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.283+11536G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078673 | |||||||
chr2:101078685 | T | C | 325 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.283+11524A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078685 | |||||||
chr2:101078696 | C | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0032 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.283+11513G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078696 | |||||||
chr2:101078714 | C | CA | 106 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0108 others(103): Show |
106 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.283+11494dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078714 | |||||||
chr2:101078714 | C | CAA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0212 others(6): Show |
9 | HG02615.hp1 HG02723.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+11493_283+1149 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078714 | |||||||
chr2:101078753 | C | CA | 9 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0321 others(6): Show |
9 | HG01433.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+11455dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CA | C | 71 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0193 others(68): Show |
71 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.283+11455delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CAA | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0212 others(9): Show |
12 | HG02559.hp2 HG02615.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+11454_283+1145 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CAAA | C | 15 | a0001c0001t0001g0042 a0001c0001t0001g0315 a0002c0002t0002g0049 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+11453_283+1145 others(7): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CAAAAAAA others(1): Show |
C | 47 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(44): Show |
47 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.283+11448_283+1145 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0002g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.283+11446_283+1145 others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101078753 | CAAAAAAA others(4): Show |
C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(90): Show |
93 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.283+11445_283+1145 others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101078753 | |||||||
chr2:101079029 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.283+11180G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079029 | |||||||
chr2:101079115 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.283+11094T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079115 | |||||||
chr2:101079168 | A | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0004g0106 others(7): Show |
10 | HG01167.hp2 HG01261.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+11041T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079168 | |||||||
chr2:101079241 | C | T | 4 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0002c0003t0001g0283 others(1): Show |
4 | HG01167.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10968G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079241 | |||||||
chr2:101079364 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.283+10845C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079364 | |||||||
chr2:101079431 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.283+10778C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079431 | |||||||
chr2:101079532 | G | A | 1 | a0002c0003t0001g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.283+10677C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079532 | |||||||
chr2:101079536 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.283+10673C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079536 | |||||||
chr2:101079584 | C | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.283+10625G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079584 | |||||||
chr2:101079597 | A | G | 8 | a0001c0001t0001g0096 a0002c0003t0001g0082 a0002c0003t0001g0083 others(5): Show |
8 | NA18612.hp1 NA18939.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+10612T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079597 | |||||||
chr2:101079660 | G | C | 14 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(11): Show |
14 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+10549C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079660 | |||||||
chr2:101079680 | G | GT | 167 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0032 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.283+10528dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079680 | |||||||
chr2:101079680 | G | GTT | 24 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0213 others(21): Show |
24 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.283+10527_283+1052 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079680 | |||||||
chr2:101079680 | GT | G | 17 | a0001c0001t0001g0062 a0001c0001t0001g0136 a0001c0001t0001g0221 others(14): Show |
17 | HG01169.hp1 HG02559.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+10528delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079680 | |||||||
chr2:101079686 | T | G | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.283+10523A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079686 | |||||||
chr2:101079745 | G | A | 5 | a0001c0021t0004g0282 a0007c0007t0001g0043 a0007c0007t0001g0044 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+10464C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079745 | |||||||
chr2:101079830 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+10379G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079830 | |||||||
chr2:101079901 | C | T | 4 | a0010c0008t0001g0039 a0010c0008t0001g0040 a0010c0008t0001g0041 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+10308G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079901 | |||||||
chr2:101079902 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.283+10307C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079902 | |||||||
chr2:101079929 | G | A | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+10280C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101079929 | |||||||
chr2:101080187 | G | A | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.283+10022C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080187 | |||||||
chr2:101080228 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01257.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.283+9981C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080228 | |||||||
chr2:101080375 | G | A | 1 | a0002c0002t0002g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.283+9834C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080375 | |||||||
chr2:101080391 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+9818C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080391 | |||||||
chr2:101080534 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+9675T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080534 | |||||||
chr2:101080655 | T | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+9554A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080655 | |||||||
chr2:101080786 | A | AT | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.283+9422dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080786 | |||||||
chr2:101080972 | C | T | 5 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+9237G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101080972 | |||||||
chr2:101081426 | T | C | 5 | a0001c0021t0004g0282 a0007c0007t0001g0043 a0007c0007t0001g0044 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+8783A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081426 | |||||||
chr2:101081459 | G | A | 1 | a0014c0034t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.283+8750C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081459 | |||||||
chr2:101081573 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(33): Show |
36 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.283+8636C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081573 | |||||||
chr2:101081602 | C | A | 6 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+8607G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081602 | |||||||
chr2:101081682 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(275): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.283+8527C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081682 | |||||||
chr2:101081829 | C | A | 9 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+8380G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081829 | |||||||
chr2:101081954 | C | A | 1 | a0002c0002t0002g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283+8255G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101081954 | |||||||
chr2:101082012 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.283+8197T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082012 | |||||||
chr2:101082071 | G | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0033 others(81): Show |
84 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.283+8138C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082071 | |||||||
chr2:101082145 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0190 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.283+8064G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082145 | |||||||
chr2:101082320 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.283+7889C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082320 | |||||||
chr2:101082385 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+7824A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082385 | |||||||
chr2:101082481 | A | T | 1 | a0002c0002t0002g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+7728T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082481 | |||||||
chr2:101082578 | A | G | 5 | a0001c0021t0004g0282 a0007c0007t0001g0043 a0007c0007t0001g0044 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+7631T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082578 | |||||||
chr2:101082601 | C | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.283+7608G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082601 | |||||||
chr2:101082643 | A | G | 2 | a0002c0003t0001g0082 a0002c0003t0001g0083 |
2 | NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.283+7566T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082643 | |||||||
chr2:101082665 | T | C | 5 | a0001c0021t0004g0282 a0007c0007t0001g0043 a0007c0007t0001g0044 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+7544A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082665 | |||||||
chr2:101082691 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02602.hp1 HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.283+7518C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082691 | |||||||
chr2:101082722 | A | G | 91 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0062 others(88): Show |
91 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.283+7487T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082722 | |||||||
chr2:101082831 | A | G | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.283+7378T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082831 | |||||||
chr2:101082853 | GTGATGGT | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0033 others(82): Show |
85 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.283+7349_283+7355d others(9): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101082853 | |||||||
chr2:101083132 | A | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.283+7077T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083132 | |||||||
chr2:101083262 | C | CT | 3 | a0002c0003t0001g0001 a0002c0003t0001g0035 a0004c0005t0001g0034 |
3 | HG02258.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.283+6946dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083262 | |||||||
chr2:101083323 | T | G | 1 | a0010c0008t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.283+6886A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083323 | |||||||
chr2:101083354 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0323 a0001c0001t0001g0324 |
3 | HG02602.hp1 HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.283+6855C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083354 | |||||||
chr2:101083420 | C | T | 2 | a0001c0001t0004g0106 a0001c0001t0004g0210 |
2 | HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.283+6789G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083420 | |||||||
chr2:101083860 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(31): Show |
34 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.283+6349G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101083860 | |||||||
chr2:101084028 | G | C | 93 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0062 others(90): Show |
93 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+6181C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084028 | |||||||
chr2:101084045 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.283+6164T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084045 | |||||||
chr2:101084056 | T | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0032 others(89): Show |
92 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.283+6153A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084056 | |||||||
chr2:101084227 | A | G | 1 | a0002c0003t0001g0288 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.283+5982T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084227 | |||||||
chr2:101084274 | T | C | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.283+5935A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084274 | |||||||
chr2:101084345 | T | C | 1 | a0002c0003t0001g0091 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.283+5864A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084345 | |||||||
chr2:101084419 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+5790G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084419 | |||||||
chr2:101084560 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(88): Show |
91 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.283+5649T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084560 | |||||||
chr2:101084670 | A | C | 1 | a0002c0032t0001g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.283+5539T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084670 | |||||||
chr2:101084742 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.283+5467G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084742 | |||||||
chr2:101084796 | G | T | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.283+5413C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084796 | |||||||
chr2:101084849 | A | AT | 103 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(100): Show |
103 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.283+5359dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084849 | |||||||
chr2:101084849 | A | ATT | 91 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.283+5358_283+5359d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084849 | |||||||
chr2:101084849 | A | ATTT | 6 | a0001c0001t0001g0066 a0001c0001t0001g0193 a0001c0001t0001g0229 others(3): Show |
6 | HG01243.hp2 HG02027.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+5357_283+5359d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084849 | |||||||
chr2:101084850 | T | TA | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+5358_283+5359i others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084850 | |||||||
chr2:101084912 | G | A | 1 | a0002c0002t0002g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.283+5297C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101084912 | |||||||
chr2:101085044 | G | C | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+5165C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085044 | |||||||
chr2:101085087 | G | A | 1 | a0002c0002t0002g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.283+5122C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085087 | |||||||
chr2:101085143 | G | A | 1 | a0002c0003t0001g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283+5066C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085143 | |||||||
chr2:101085176 | A | C | 1 | a0002c0002t0002g0020 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.283+5033T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085176 | |||||||
chr2:101085620 | C | T | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+4589G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085620 | |||||||
chr2:101085722 | G | A | 1 | a0006c0012t0002g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+4487C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085722 | |||||||
chr2:101085813 | T | C | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.283+4396A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085813 | |||||||
chr2:101085831 | G | A | 37 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0002c0002t0002g0008 others(34): Show |
37 | HG00642.hp1 HG01071.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.283+4378C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085831 | |||||||
chr2:101085863 | C | T | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.283+4346G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085863 | |||||||
chr2:101085864 | G | A | 7 | a0001c0001t0001g0042 a0008c0011t0001g0036 a0010c0008t0001g0039 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+4345C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085864 | |||||||
chr2:101085895 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.283+4314T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085895 | |||||||
chr2:101085945 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+4264A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085945 | |||||||
chr2:101085977 | T | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(90): Show |
93 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.283+4232A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101085977 | |||||||
chr2:101086141 | C | CA | 89 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(86): Show |
89 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+4067dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086141 | |||||||
chr2:101086146 | A | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+4063T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086146 | |||||||
chr2:101086316 | CATA | C | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+3890_283+3892d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086316 | |||||||
chr2:101086412 | T | C | 30 | a0001c0001t0001g0048 a0001c0001t0001g0160 a0001c0001t0001g0180 others(27): Show |
30 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.283+3797A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086412 | |||||||
chr2:101086424 | C | T | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.283+3785G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086424 | |||||||
chr2:101086441 | A | G | 1 | a0002c0002t0002g0031 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.283+3768T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086441 | |||||||
chr2:101086515 | T | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+3694A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086515 | |||||||
chr2:101086568 | C | CA | 6 | a0002c0002t0002g0177 a0002c0002t0002g0182 a0002c0002t0002g0183 others(3): Show |
6 | HG02976.hp2 NA18941.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+3640dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086568 | |||||||
chr2:101086765 | A | T | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+3444T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086765 | |||||||
chr2:101086876 | T | C | 2 | a0001c0001t0001g0174 a0018c0022t0001g0175 |
2 | NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.283+3333A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086876 | |||||||
chr2:101086947 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.283+3262G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101086947 | |||||||
chr2:101087088 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+3121A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087088 | |||||||
chr2:101087125 | G | A | 1 | a0001c0001t0003g0329 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+3084C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087125 | |||||||
chr2:101087150 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0004g0278 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+3059G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087150 | |||||||
chr2:101087160 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+3049G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087160 | |||||||
chr2:101087230 | T | C | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+2979A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087230 | |||||||
chr2:101087234 | G | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0032 others(82): Show |
85 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.283+2975C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087234 | |||||||
chr2:101087302 | G | C | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283+2907C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087302 | |||||||
chr2:101087309 | A | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.283+2900T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087309 | |||||||
chr2:101087351 | T | C | 2 | a0009c0014t0003g0325 a0012c0028t0003g0326 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283+2858A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087351 | |||||||
chr2:101087379 | G | A | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+2830C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087379 | |||||||
chr2:101087637 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+2572G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087637 | |||||||
chr2:101087639 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+2570C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087639 | |||||||
chr2:101087642 | T | A | 1 | a0001c0001t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+2567A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087642 | |||||||
chr2:101087643 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+2566G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087643 | |||||||
chr2:101087643 | C | CA | 93 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(90): Show |
93 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(90): Show |
intron_variant | MODIFIER | c.283+2565dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087643 | |||||||
chr2:101087643 | C | CAA | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0004g0106 others(5): Show |
8 | HG01167.hp2 HG02145.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+2564_283+2565d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087643 | |||||||
chr2:101087643 | CA | C | 8 | a0001c0001t0001g0264 a0001c0001t0006g0148 a0001c0021t0004g0282 others(5): Show |
8 | HG01167.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+2565delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087643 | |||||||
chr2:101087822 | A | C | 1 | a0002c0002t0002g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.283+2387T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087822 | |||||||
chr2:101087825 | A | G | 2 | a0008c0015t0001g0075 a0008c0015t0001g0100 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.283+2384T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087825 | |||||||
chr2:101087975 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.283+2234A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101087975 | |||||||
chr2:101088334 | G | A | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+1875C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101088334 | |||||||
chr2:101088363 | C | T | 1 | a0002c0003t0001g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.283+1846G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101088363 | |||||||
chr2:101088477 | G | A | 2 | a0001c0001t0001g0057 a0004c0005t0001g0206 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.283+1732C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101088477 | |||||||
chr2:101088958 | G | GA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+1250dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101088958 | |||||||
chr2:101089142 | G | C | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.283+1067C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089142 | |||||||
chr2:101089189 | T | A | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.283+1020A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089189 | |||||||
chr2:101089212 | T | A | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.283+997A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089212 | |||||||
chr2:101089223 | T | C | 3 | a0001c0009t0001g0293 a0001c0009t0001g0294 a0001c0009t0001g0297 |
3 | NA18992.hp2 NA18999.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.283+986A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089223 | |||||||
chr2:101089287 | T | C | 9 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(6): Show |
9 | HG02622.hp2 HG02723.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+922A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089287 | |||||||
chr2:101089422 | T | TA | 76 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(73): Show |
76 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.283+786dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089422 | |||||||
chr2:101089422 | TA | T | 11 | a0001c0021t0004g0282 a0002c0002t0002g0195 a0002c0002t0002g0313 others(8): Show |
11 | HG01167.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+786delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089422 | |||||||
chr2:101089475 | G | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+734C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089475 | |||||||
chr2:101089527 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.283+682C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089527 | |||||||
chr2:101089778 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+431T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089778 | |||||||
chr2:101089855 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01261.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.283+354G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089855 | |||||||
chr2:101089920 | GT | G | 107 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0065 others(104): Show |
107 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.283+288delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089920 | |||||||
chr2:101089920 | GTT | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0132 others(2): Show |
5 | HG01256.hp1 HG03041.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+287_283+288del others(2): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089920 | |||||||
chr2:101089924 | T | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0265 a0001c0021t0004g0282 others(5): Show |
8 | HG01516.hp1 HG01891.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+285A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089924 | |||||||
chr2:101089924 | T | TA | 3 | a0001c0001t0001g0307 a0002c0002t0002g0030 a0002c0002t0002g0031 |
3 | HG01099.hp1 HG02293.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.283+284_283+285ins others(1): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089924 | |||||||
chr2:101089925 | T | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.283+284A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 2/19 | chr2 | 101089925 | |||||||
chr2:101090547 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.128-183G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090547 | |||||||
chr2:101090553 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.128-189T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090553 | |||||||
chr2:101090629 | C | T | 1 | a0011c0036t0001g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.128-265G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090629 | |||||||
chr2:101090630 | G | A | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.128-266C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090630 | |||||||
chr2:101090657 | C | G | 1 | a0002c0002t0002g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.128-293G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090657 | |||||||
chr2:101090980 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-616A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101090980 | |||||||
chr2:101091080 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-716G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091080 | |||||||
chr2:101091146 | G | A | 3 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0008c0011t0001g0208 |
3 | HG01167.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.128-782C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091146 | |||||||
chr2:101091473 | C | A | 2 | a0002c0002t0002g0017 a0002c0002t0002g0024 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.128-1109G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091473 | |||||||
chr2:101091631 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.128-1267C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091631 | |||||||
chr2:101091837 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.128-1473C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091837 | |||||||
chr2:101091928 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.128-1564C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101091928 | |||||||
chr2:101092027 | A | C | 1 | a0011c0031t0001g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.128-1663T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092027 | |||||||
chr2:101092027 | A | G | 3 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0008c0011t0001g0208 |
3 | HG01167.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.128-1663T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092027 | |||||||
chr2:101092465 | G | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0263 |
2 | HG00408.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.128-2101C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092465 | |||||||
chr2:101092573 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.128-2209C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092573 | |||||||
chr2:101092609 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-2245C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092609 | |||||||
chr2:101092676 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-2312T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092676 | |||||||
chr2:101092817 | G | T | 2 | a0001c0001t0001g0057 a0004c0005t0001g0206 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-2453C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092817 | |||||||
chr2:101092980 | T | C | 1 | a0004c0005t0001g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-2616A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101092980 | |||||||
chr2:101093199 | T | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-2835A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093199 | |||||||
chr2:101093211 | G | C | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.128-2847C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093211 | |||||||
chr2:101093305 | G | C | 1 | a0004c0005t0001g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-2941C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093305 | |||||||
chr2:101093624 | A | G | 9 | a0002c0002t0002g0104 a0002c0003t0001g0056 a0002c0003t0001g0078 others(6): Show |
9 | HG00639.hp1 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3260T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093624 | |||||||
chr2:101093759 | G | T | 1 | a0006c0013t0001g0299 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.128-3395C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093759 | |||||||
chr2:101093907 | C | T | 2 | a0002c0002t0002g0030 a0002c0002t0002g0031 |
2 | HG01099.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.128-3543G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093907 | |||||||
chr2:101093908 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-3544C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101093908 | |||||||
chr2:101094034 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.128-3670A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094034 | |||||||
chr2:101094319 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.128-3955C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094319 | |||||||
chr2:101094334 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-3970C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094334 | |||||||
chr2:101094562 | C | T | 2 | a0001c0001t0001g0096 a0002c0003t0001g0103 |
2 | NA18959.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.128-4198G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094562 | |||||||
chr2:101094897 | C | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0190 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.128-4533G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094897 | |||||||
chr2:101094974 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.128-4610T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101094974 | |||||||
chr2:101095006 | T | C | 3 | a0001c0001t0001g0302 a0002c0002t0002g0303 a0002c0002t0002g0304 |
3 | NA18939.hp2 NA18942.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.128-4642A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095006 | |||||||
chr2:101095073 | A | G | 3 | a0001c0001t0001g0160 a0006c0012t0002g0161 a0010c0008t0001g0159 |
3 | HG02145.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.128-4709T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095073 | |||||||
chr2:101095077 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0157 |
3 | HG00408.hp2 NA18950.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.128-4713A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095077 | |||||||
chr2:101095096 | GTT | G | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-4734_128-4733d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095096 | |||||||
chr2:101095116 | G | T | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.128-4752C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095116 | |||||||
chr2:101095249 | T | TTATTATT others(10): Show |
1 | a0011c0017t0001g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.128-4886_128-4885i others(19): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(2): Show |
94 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-4894_128-4886d others(11): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(5): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0066 others(25): Show |
28 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.128-4897_128-4886d others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(8): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0228 |
2 | HG02056.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.128-4900_128-4886d others(17): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(11): Show |
3 | a0001c0001t0001g0136 a0002c0003t0001g0079 a0002c0003t0001g0283 |
3 | HG03669.hp2 NA18954.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.128-4903_128-4886d others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(14): Show |
53 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(50): Show |
53 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.128-4886_128-4885i others(23): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(17): Show |
10 | a0001c0001t0001g0096 a0001c0001t0001g0127 a0001c0001t0001g0149 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-4886_128-4885i others(26): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095249 | T | TTTATTAT others(20): Show |
2 | a0001c0001t0001g0133 a0004c0005t0001g0284 |
2 | HG02280.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.128-4886_128-4885i others(29): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095249 | |||||||
chr2:101095305 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.128-4941C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095305 | |||||||
chr2:101095323 | C | CA | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-4960dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095323 | |||||||
chr2:101095334 | T | C | 15 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0221 others(12): Show |
15 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-4970A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095334 | |||||||
chr2:101095393 | T | TC | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0032 others(76): Show |
79 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.128-5030dupG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095393 | |||||||
chr2:101095396 | C | T | 6 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-5032G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095396 | |||||||
chr2:101095399 | C | A | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-5035G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095399 | |||||||
chr2:101095473 | A | G | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.128-5109T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095473 | |||||||
chr2:101095706 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.128-5342T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095706 | |||||||
chr2:101095840 | T | C | 1 | a0004c0005t0001g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.128-5476A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095840 | |||||||
chr2:101095971 | T | C | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-5607A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101095971 | |||||||
chr2:101096282 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-5918C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096282 | |||||||
chr2:101096283 | A | T | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-5919T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096283 | |||||||
chr2:101096419 | C | CA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0042 others(37): Show |
40 | HG00423.hp2 HG00544.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-6056dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | C | CAA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.128-6057_128-6056d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | C | CAAA | 39 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0070 others(36): Show |
39 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.128-6058_128-6056d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | C | CAAAA | 6 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0128 others(3): Show |
6 | HG01928.hp1 HG02486.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-6059_128-6056d others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | CA | C | 18 | a0001c0001t0001g0032 a0001c0001t0001g0209 a0001c0001t0001g0225 others(15): Show |
18 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.128-6056delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | CAAA | C | 11 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(8): Show |
11 | HG02559.hp2 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-6058_128-6056d others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-6065_128-6056d others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096419 | CAAAAAAA others(9): Show |
C | 1 | a0002c0002t0002g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.128-6071_128-6056d others(18): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096419 | |||||||
chr2:101096438 | A | C | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128-6074T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096438 | |||||||
chr2:101096443 | A | AAC | 11 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0236 others(8): Show |
11 | HG01192.hp2 HG01261.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.128-6080_128-6079i others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096443 | |||||||
chr2:101096443 | A | AC | 40 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(37): Show |
40 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.128-6080_128-6079i others(3): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096443 | |||||||
chr2:101096443 | A | C | 2 | a0001c0001t0001g0256 a0003c0004t0001g0245 |
2 | NA18612.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.128-6079T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096443 | |||||||
chr2:101096796 | G | GGA | 84 | a0001c0001t0001g0057 a0001c0001t0001g0096 a0001c0001t0001g0116 others(81): Show |
84 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.128-6434_128-6433d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096796 | |||||||
chr2:101096796 | G | GGAGA | 68 | a0001c0001t0001g0062 a0001c0001t0001g0107 a0001c0001t0001g0108 others(65): Show |
68 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.128-6436_128-6433d others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096796 | |||||||
chr2:101096796 | G | GGAGAGA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(32): Show |
35 | HG00099.hp1 HG01081.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.128-6438_128-6433d others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096796 | |||||||
chr2:101096821 | C | G | 76 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(73): Show |
76 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.128-6457G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096821 | |||||||
chr2:101096891 | T | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-6527A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096891 | |||||||
chr2:101096922 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.128-6558G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101096922 | |||||||
chr2:101097088 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-6724T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097088 | |||||||
chr2:101097093 | C | G | 5 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-6729G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097093 | |||||||
chr2:101097188 | G | GA | 6 | a0001c0001t0001g0068 a0001c0001t0001g0124 a0001c0001t0001g0306 others(3): Show |
6 | HG02145.hp1 HG02922.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-6825dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097188 | |||||||
chr2:101097248 | G | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0007c0019t0001g0060 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-6884C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097248 | |||||||
chr2:101097265 | A | G | 1 | a0002c0003t0001g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.128-6901T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097265 | |||||||
chr2:101097268 | G | A | 1 | a0006c0012t0002g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.128-6904C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097268 | |||||||
chr2:101097442 | C | T | 15 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0221 others(12): Show |
15 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-7078G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097442 | |||||||
chr2:101097443 | G | A | 6 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-7079C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097443 | |||||||
chr2:101097451 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.128-7087A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097451 | |||||||
chr2:101097557 | T | TA | 116 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.128-7194dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097557 | |||||||
chr2:101097557 | T | TAA | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-7195_128-7194d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097557 | |||||||
chr2:101097631 | T | C | 8 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | NA18961.hp1 NA18966.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-7267A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097631 | |||||||
chr2:101097790 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.128-7426G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097790 | |||||||
chr2:101097833 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.128-7469G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097833 | |||||||
chr2:101097926 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-7562C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101097926 | |||||||
chr2:101098125 | G | C | 1 | a0009c0014t0003g0325 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.128-7761C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098125 | |||||||
chr2:101098213 | T | C | 1 | a0002c0002t0002g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-7849A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098213 | |||||||
chr2:101098246 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.128-7882C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098246 | |||||||
chr2:101098261 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(193): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.128-7897T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098261 | |||||||
chr2:101098374 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.128-8010G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098374 | |||||||
chr2:101098379 | C | CA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.128-8016dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098379 | |||||||
chr2:101098379 | CA | C | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-8016delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098379 | |||||||
chr2:101098734 | T | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-8370A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098734 | |||||||
chr2:101098739 | A | T | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.128-8375T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098739 | |||||||
chr2:101098939 | C | G | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-8575G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101098939 | |||||||
chr2:101099025 | G | A | 1 | a0001c0001t0006g0148 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-8661C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099025 | |||||||
chr2:101099034 | G | A | 9 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(6): Show |
9 | HG02622.hp2 HG02723.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-8670C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099034 | |||||||
chr2:101099039 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.128-8675T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099039 | |||||||
chr2:101099052 | CA | C | 82 | a0001c0001t0001g0068 a0001c0001t0001g0096 a0001c0001t0001g0116 others(79): Show |
82 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.128-8689delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099052 | |||||||
chr2:101099053 | A | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0240 a0001c0001t0001g0246 others(2): Show |
5 | HG03834.hp2 NA18950.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-8689T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099053 | |||||||
chr2:101099068 | C | A | 2 | a0001c0001t0001g0042 a0008c0011t0001g0036 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.128-8704G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099068 | |||||||
chr2:101099086 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.128-8722C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099086 | |||||||
chr2:101099100 | T | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-8736A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099100 | |||||||
chr2:101099530 | T | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.128-9166A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099530 | |||||||
chr2:101099552 | A | G | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.128-9188T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099552 | |||||||
chr2:101099575 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.128-9211G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099575 | |||||||
chr2:101099601 | A | G | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-9237T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099601 | |||||||
chr2:101099661 | C | T | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-9297G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099661 | |||||||
chr2:101099808 | A | G | 1 | a0002c0003t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-9444T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099808 | |||||||
chr2:101099938 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-9574A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099938 | |||||||
chr2:101099980 | C | T | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-9616G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101099980 | |||||||
chr2:101100130 | A | C | 1 | a0006c0013t0001g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.128-9766T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100130 | |||||||
chr2:101100259 | A | G | 5 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0001c0024t0003g0327 others(2): Show |
5 | HG01167.hp2 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-9895T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100259 | |||||||
chr2:101100387 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-10023A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100387 | |||||||
chr2:101100393 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128-10029G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100393 | |||||||
chr2:101100877 | G | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.128-10513C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100877 | |||||||
chr2:101100903 | G | A | 1 | a0002c0002t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.128-10539C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100903 | |||||||
chr2:101100917 | A | G | 1 | a0002c0002t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.128-10553T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101100917 | |||||||
chr2:101101021 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.128-10657C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101021 | |||||||
chr2:101101231 | G | A | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.128-10867C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101231 | |||||||
chr2:101101408 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.128-11044G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101408 | |||||||
chr2:101101486 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-11122A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101486 | |||||||
chr2:101101596 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.128-11232T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101596 | |||||||
chr2:101101608 | T | G | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-11244A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101608 | |||||||
chr2:101101637 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-11273C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101637 | |||||||
chr2:101101701 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.128-11337T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101701 | |||||||
chr2:101101713 | A | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(39): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-11349T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101713 | |||||||
chr2:101101841 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-11477C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101841 | |||||||
chr2:101101865 | G | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-11501C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101101865 | |||||||
chr2:101102017 | T | G | 11 | a0002c0002t0002g0049 a0002c0002t0002g0102 a0002c0003t0001g0055 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.128-11653A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102017 | |||||||
chr2:101102063 | A | AAGGGGAG others(3): Show |
1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.128-11709_128-1170 others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102063 | |||||||
chr2:101102180 | G | A | 15 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0221 others(12): Show |
15 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-11816C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102180 | |||||||
chr2:101102391 | T | G | 2 | a0002c0002t0002g0164 a0002c0002t0002g0173 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.128-12027A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102391 | |||||||
chr2:101102458 | TA | T | 17 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0107 others(14): Show |
17 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.128-12095delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102458 | |||||||
chr2:101102496 | A | G | 1 | a0002c0003t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.128-12132T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102496 | |||||||
chr2:101102511 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.128-12147A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102511 | |||||||
chr2:101102537 | C | CA | 79 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(76): Show |
79 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.128-12174dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102537 | |||||||
chr2:101102548 | C | A | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-12184G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102548 | |||||||
chr2:101102713 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.128-12349A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102713 | |||||||
chr2:101102768 | C | T | 49 | a0001c0001t0001g0193 a0001c0001t0001g0207 a0001c0001t0001g0228 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.128-12404G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102768 | |||||||
chr2:101102991 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-12627G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101102991 | |||||||
chr2:101103024 | C | T | 9 | a0001c0009t0001g0293 a0001c0009t0001g0294 a0001c0009t0001g0297 others(6): Show |
9 | HG00423.hp2 HG02080.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-12660G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103024 | |||||||
chr2:101103155 | C | T | 1 | a0009c0033t0003g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.128-12791G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103155 | |||||||
chr2:101103318 | T | TA | 80 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(77): Show |
80 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.128-12955_128-1295 others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103318 | |||||||
chr2:101103319 | T | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.128-12955A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103319 | |||||||
chr2:101103333 | C | G | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-12969G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103333 | |||||||
chr2:101103341 | G | A | 1 | a0004c0005t0001g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-12977C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103341 | |||||||
chr2:101103355 | C | CA | 6 | a0001c0009t0001g0297 a0006c0010t0001g0224 a0008c0011t0001g0036 others(3): Show |
6 | HG01891.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-12992dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103355 | |||||||
chr2:101103355 | CA | C | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-12992delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103355 | |||||||
chr2:101103386 | C | CT | 18 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(15): Show |
18 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.128-13023dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103386 | |||||||
chr2:101103527 | G | GA | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-13164dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103527 | |||||||
chr2:101103613 | C | T | 2 | a0002c0002t0002g0030 a0002c0002t0002g0031 |
2 | HG01099.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.128-13249G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103613 | |||||||
chr2:101103614 | G | A | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-13250C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103614 | |||||||
chr2:101103628 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-13264T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103628 | |||||||
chr2:101103635 | G | A | 1 | a0002c0002t0002g0016 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.128-13271C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103635 | |||||||
chr2:101103638 | C | T | 1 | a0002c0003t0001g0078 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.128-13274G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103638 | |||||||
chr2:101103674 | G | A | 6 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-13310C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103674 | |||||||
chr2:101103681 | C | T | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-13317G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103681 | |||||||
chr2:101103746 | T | G | 1 | a0009c0020t0003g0332 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-13382A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103746 | |||||||
chr2:101103771 | C | T | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-13407G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103771 | |||||||
chr2:101103859 | G | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.128-13495C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103859 | |||||||
chr2:101103877 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
5 | NA18946.hp1 NA19011.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-13513A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103877 | |||||||
chr2:101103881 | T | G | 3 | a0001c0024t0003g0327 a0002c0002t0002g0298 a0004c0005t0001g0002 |
3 | HG02080.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.128-13517A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103881 | |||||||
chr2:101103883 | G | T | 7 | a0001c0001t0001g0004 a0002c0002t0002g0313 a0002c0003t0001g0218 others(4): Show |
7 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-13519C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101103883 | |||||||
chr2:101104226 | AATAG | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.128-13866_128-1386 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104226 | |||||||
chr2:101104228 | T | C | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(39): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-13864A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104228 | |||||||
chr2:101104238 | T | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-13874A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104238 | |||||||
chr2:101104546 | G | A | 3 | a0002c0003t0001g0001 a0002c0003t0001g0035 a0004c0005t0001g0034 |
3 | HG02258.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.128-14182C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104546 | |||||||
chr2:101104586 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.128-14222A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104586 | |||||||
chr2:101104657 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0143 |
2 | NA18970.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.128-14293T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104657 | |||||||
chr2:101104742 | G | A | 5 | a0004c0005t0001g0276 a0004c0005t0001g0281 a0004c0005t0001g0284 others(2): Show |
5 | HG02280.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-14378C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104742 | |||||||
chr2:101104795 | A | G | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-14431T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104795 | |||||||
chr2:101104907 | T | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.128-14543A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104907 | |||||||
chr2:101104979 | C | G | 29 | a0001c0001t0001g0048 a0001c0001t0001g0160 a0001c0001t0001g0180 others(26): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.128-14615G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104979 | |||||||
chr2:101104980 | A | G | 29 | a0001c0001t0001g0048 a0001c0001t0001g0160 a0001c0001t0001g0180 others(26): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.128-14616T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104980 | |||||||
chr2:101104981 | C | T | 29 | a0001c0001t0001g0048 a0001c0001t0001g0160 a0001c0001t0001g0180 others(26): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.128-14617G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104981 | |||||||
chr2:101104982 | A | G | 29 | a0001c0001t0001g0048 a0001c0001t0001g0160 a0001c0001t0001g0180 others(26): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.128-14618T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101104982 | |||||||
chr2:101105022 | T | C | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.128-14658A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105022 | |||||||
chr2:101105025 | C | CA | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(45): Show |
48 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.128-14662dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105025 | |||||||
chr2:101105025 | CA | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.128-14662delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105025 | |||||||
chr2:101105025 | CAA | C | 78 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(75): Show |
78 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.128-14663_128-1466 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105025 | |||||||
chr2:101105061 | C | T | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-14697G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105061 | |||||||
chr2:101105178 | G | C | 3 | a0002c0003t0001g0288 a0002c0003t0001g0300 a0002c0003t0001g0310 |
3 | NA18981.hp2 NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.128-14814C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105178 | |||||||
chr2:101105356 | T | C | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-14992A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105356 | |||||||
chr2:101105432 | T | C | 1 | a0002c0002t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.128-15068A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105432 | |||||||
chr2:101105514 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.128-15150C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105514 | |||||||
chr2:101105607 | A | AAAAAC | 81 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.128-15244_128-1524 others(9): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105607 | |||||||
chr2:101105607 | A | AAAAC | 7 | a0001c0001t0001g0066 a0001c0001t0001g0249 a0002c0003t0001g0257 others(4): Show |
7 | HG01975.hp2 HG02074.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-15244_128-1524 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105607 | |||||||
chr2:101105609 | C | CAT | 23 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0221 others(20): Show |
23 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-15247_128-1524 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105609 | |||||||
chr2:101105609 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.128-15245G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105609 | |||||||
chr2:101105917 | A | C | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-15553T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101105917 | |||||||
chr2:101106038 | T | TA | 7 | a0001c0001t0001g0057 a0001c0001t0001g0277 a0001c0001t0001g0315 others(4): Show |
7 | HG03130.hp1 HG03139.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-15675dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106038 | |||||||
chr2:101106253 | G | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0187 |
2 | HG02132.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.128-15889C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106253 | |||||||
chr2:101106610 | C | T | 5 | a0002c0002t0002g0177 a0002c0002t0002g0182 a0002c0002t0002g0183 others(2): Show |
5 | NA18941.hp2 NA18967.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-16246G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106610 | |||||||
chr2:101106693 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-16329A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106693 | |||||||
chr2:101106817 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-16453G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106817 | |||||||
chr2:101106818 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128-16454C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106818 | |||||||
chr2:101106881 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.128-16517C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106881 | |||||||
chr2:101106982 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.128-16618G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101106982 | |||||||
chr2:101107137 | G | A | 2 | a0001c0001t0001g0174 a0018c0022t0001g0175 |
2 | NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.128-16773C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107137 | |||||||
chr2:101107194 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.128-16830C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107194 | |||||||
chr2:101107287 | G | A | 1 | a0002c0003t0001g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.128-16923C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107287 | |||||||
chr2:101107359 | A | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(39): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-16995T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107359 | |||||||
chr2:101107425 | T | C | 7 | a0001c0001t0001g0004 a0001c0023t0001g0115 a0002c0003t0001g0218 others(4): Show |
7 | HG02015.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-17061A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107425 | |||||||
chr2:101107945 | G | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.128-17581C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101107945 | |||||||
chr2:101108025 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-17661C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108025 | |||||||
chr2:101108144 | G | T | 1 | a0002c0002t0002g0252 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.128-17780C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108144 | |||||||
chr2:101108160 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 |
3 | HG03130.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.128-17796C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108160 | |||||||
chr2:101108205 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.128-17841C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108205 | |||||||
chr2:101108709 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.128-18345A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108709 | |||||||
chr2:101108727 | C | T | 3 | a0009c0014t0003g0325 a0009c0014t0003g0330 a0012c0028t0003g0326 |
3 | HG03195.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.128-18363G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108727 | |||||||
chr2:101108816 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-18452G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101108816 | |||||||
chr2:101109031 | T | G | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.128-18667A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109031 | |||||||
chr2:101109119 | T | A | 78 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(75): Show |
78 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.128-18755A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109119 | |||||||
chr2:101109137 | A | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0058 others(169): Show |
172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.128-18773T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109137 | |||||||
chr2:101109604 | G | A | 1 | a0003c0004t0001g0273 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.128-19240C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109604 | |||||||
chr2:101109642 | G | A | 3 | a0004c0005t0001g0276 a0009c0020t0003g0331 a0009c0020t0003g0332 |
3 | HG02647.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.128-19278C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109642 | |||||||
chr2:101109846 | T | A | 6 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-19482A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109846 | |||||||
chr2:101109885 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0315 a0001c0001t0004g0278 others(1): Show |
4 | HG02572.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-19521C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109885 | |||||||
chr2:101109965 | T | C | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.128-19601A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101109965 | |||||||
chr2:101110014 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(39): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-19650G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110014 | |||||||
chr2:101110042 | A | G | 1 | a0004c0005t0001g0014 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.128-19678T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110042 | |||||||
chr2:101110308 | A | G | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-19944T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110308 | |||||||
chr2:101110357 | A | G | 3 | a0001c0001t0001g0318 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG00140.hp1 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.128-19993T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110357 | |||||||
chr2:101110399 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(39): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.128-20035G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110399 | |||||||
chr2:101110568 | G | A | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-20204C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110568 | |||||||
chr2:101110830 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.128-20466G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110830 | |||||||
chr2:101110865 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.128-20501A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110865 | |||||||
chr2:101110960 | A | G | 3 | a0001c0001t0001g0057 a0004c0005t0001g0206 a0006c0025t0002g0316 |
3 | HG02559.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-20596T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110960 | |||||||
chr2:101110980 | CA | C | 155 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0058 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.128-20617delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101110980 | |||||||
chr2:101111030 | C | T | 74 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(71): Show |
74 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.128-20666G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111030 | |||||||
chr2:101111049 | G | A | 2 | a0002c0003t0001g0093 a0002c0003t0001g0095 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.128-20685C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111049 | |||||||
chr2:101111139 | C | T | 77 | a0001c0001t0001g0096 a0001c0001t0001g0116 a0001c0001t0001g0117 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-20775G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111139 | |||||||
chr2:101111231 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0057 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.128-20867C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111231 | |||||||
chr2:101111304 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0134 a0004c0005t0001g0206 others(1): Show |
4 | HG02027.hp2 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-20940G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111304 | |||||||
chr2:101111322 | G | A | 1 | a0003c0004t0001g0273 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.128-20958C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111322 | |||||||
chr2:101111345 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128-20981C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111345 | |||||||
chr2:101111358 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.128-20994A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111358 | |||||||
chr2:101111397 | C | T | 2 | a0001c0001t0001g0096 a0002c0003t0001g0103 |
2 | NA18959.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.128-21033G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111397 | |||||||
chr2:101111449 | G | A | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-21085C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111449 | |||||||
chr2:101111469 | G | A | 9 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0141 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-21105C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111469 | |||||||
chr2:101111511 | G | A | 2 | a0009c0014t0003g0325 a0012c0028t0003g0326 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.128-21147C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111511 | |||||||
chr2:101111693 | T | A | 5 | a0004c0005t0001g0276 a0004c0005t0001g0281 a0004c0005t0001g0284 others(2): Show |
5 | HG02280.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-21329A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111693 | |||||||
chr2:101111883 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.128-21519T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111883 | |||||||
chr2:101111916 | TA | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(207): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.128-21553delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111916 | |||||||
chr2:101111916 | TAA | T | 58 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0001g0107 others(55): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.128-21554_128-2155 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111916 | |||||||
chr2:101111917 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.128-21553T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111917 | |||||||
chr2:101111970 | A | G | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.128-21606T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101111970 | |||||||
chr2:101112608 | A | G | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-22244T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112608 | |||||||
chr2:101112695 | G | A | 5 | a0010c0008t0001g0039 a0010c0008t0001g0040 a0010c0008t0001g0041 others(2): Show |
5 | HG02109.hp1 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-22331C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112695 | |||||||
chr2:101112727 | C | G | 1 | a0002c0002t0002g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.128-22363G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112727 | |||||||
chr2:101112874 | T | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(40): Show |
43 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.128-22510A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112874 | |||||||
chr2:101112902 | C | G | 42 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.128-22538G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112902 | |||||||
chr2:101112981 | C | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
200 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.128-22617G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112981 | |||||||
chr2:101112995 | C | A | 2 | a0001c0024t0003g0327 a0004c0005t0001g0002 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.128-22631G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101112995 | |||||||
chr2:101113042 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.128-22678A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113042 | |||||||
chr2:101113220 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.128-22856C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113220 | |||||||
chr2:101113224 | T | C | 1 | a0002c0002t0002g0104 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.128-22860A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113224 | |||||||
chr2:101113389 | TA | T | 52 | a0001c0001t0001g0179 a0001c0001t0001g0193 a0001c0001t0001g0207 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.128-23026delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113389 | |||||||
chr2:101113631 | T | G | 38 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.128-23267A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113631 | |||||||
chr2:101113826 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.128-23462G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113826 | |||||||
chr2:101113834 | G | A | 1 | a0001c0001t0005g0097 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.128-23470C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101113834 | |||||||
chr2:101114109 | C | G | 82 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(79): Show |
82 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.128-23745G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114109 | |||||||
chr2:101114294 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | NA18948.hp1 NA18951.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-23930A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114294 | |||||||
chr2:101114355 | TC | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(38): Show |
41 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.128-23992delG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114355 | |||||||
chr2:101114609 | T | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(38): Show |
41 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.128-24245A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114609 | |||||||
chr2:101114673 | G | A | 53 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0193 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.128-24309C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114673 | |||||||
chr2:101114695 | G | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(79): Show |
82 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.128-24331C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114695 | |||||||
chr2:101114789 | T | C | 3 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0220 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.128-24425A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114789 | |||||||
chr2:101114892 | T | TG | 38 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.128-24529dupC | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114892 | |||||||
chr2:101114935 | C | T | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
60 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.128-24571G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114935 | |||||||
chr2:101114979 | T | G | 1 | a0001c0001t0001g0317 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.128-24615A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101114979 | |||||||
chr2:101115145 | G | GCTAT | 5 | a0002c0002t0002g0177 a0002c0002t0002g0182 a0002c0002t0002g0183 others(2): Show |
5 | NA18941.hp2 NA18967.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-24785_128-2478 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115145 | |||||||
chr2:101115224 | G | A | 3 | a0001c0001t0004g0106 a0001c0001t0004g0210 a0008c0011t0001g0208 |
3 | HG01167.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.128-24860C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115224 | |||||||
chr2:101115243 | C | T | 92 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.128-24879G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115243 | |||||||
chr2:101115278 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.128-24914A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115278 | |||||||
chr2:101115293 | T | C | 1 | a0004c0005t0001g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.128-24929A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115293 | |||||||
chr2:101115638 | C | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(78): Show |
81 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.128-25274G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115638 | |||||||
chr2:101115644 | G | C | 1 | a0004c0005t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.128-25280C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115644 | |||||||
chr2:101115750 | C | CA | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(6): Show |
9 | HG02622.hp2 HG02723.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-25387dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101115750 | |||||||
chr2:101116194 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(81): Show |
84 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.128-25830A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116194 | |||||||
chr2:101116213 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.128-25849T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116213 | |||||||
chr2:101116215 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(81): Show |
84 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.128-25851C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116215 | |||||||
chr2:101116266 | G | A | 2 | a0001c0001t0001g0057 a0004c0005t0001g0206 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-25902C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116266 | |||||||
chr2:101116436 | G | A | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(291): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.128-26072C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116436 | |||||||
chr2:101116602 | A | G | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-26238T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116602 | |||||||
chr2:101116616 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.128-26252C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116616 | |||||||
chr2:101116644 | A | AT | 9 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
9 | HG01192.hp2 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-26281dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116644 | |||||||
chr2:101116872 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.128-26508A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101116872 | |||||||
chr2:101117214 | G | A | 5 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-26850C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117214 | |||||||
chr2:101117495 | T | A | 5 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.128-27131A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117495 | |||||||
chr2:101117568 | C | CT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0212 a0001c0001t0001g0236 others(11): Show |
14 | HG00642.hp2 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.128-27205dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117568 | |||||||
chr2:101117568 | CT | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0042 others(118): Show |
121 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.128-27205delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117568 | |||||||
chr2:101117568 | CTT | C | 6 | a0001c0021t0004g0282 a0002c0002t0002g0313 a0007c0007t0001g0043 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-27206_128-2720 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117568 | |||||||
chr2:101117577 | T | A | 3 | a0001c0001t0001g0117 a0002c0003t0001g0146 a0002c0003t0001g0147 |
3 | NA18974.hp2 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.128-27213A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117577 | |||||||
chr2:101117578 | T | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0116 others(74): Show |
77 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-27214A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117578 | |||||||
chr2:101117643 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-27279C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117643 | |||||||
chr2:101117645 | T | C | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.128-27281A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117645 | |||||||
chr2:101117723 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.128-27359C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117723 | |||||||
chr2:101117737 | C | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG00323.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.128-27373G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117737 | |||||||
chr2:101117822 | G | A | 3 | a0002c0002t0002g0102 a0005c0006t0001g0098 a0005c0006t0001g0099 |
3 | HG02698.hp1 HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-27458C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117822 | |||||||
chr2:101117874 | C | CT | 173 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.128-27511dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117874 | |||||||
chr2:101117874 | CT | C | 8 | a0001c0001t0001g0223 a0002c0002t0002g0164 a0002c0002t0002g0200 others(5): Show |
8 | HG00738.hp2 HG01168.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-27511delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117874 | |||||||
chr2:101117941 | G | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0209 others(3): Show |
6 | HG01261.hp2 HG02258.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-27577C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101117941 | |||||||
chr2:101118090 | G | A | 2 | a0001c0001t0001g0057 a0004c0005t0001g0206 |
2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.128-27726C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118090 | |||||||
chr2:101118207 | G | GGGGCCTG others(4): Show |
1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.128-27854_128-2784 others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118207 | |||||||
chr2:101118377 | G | A | 1 | a0002c0016t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.128-28013C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118377 | |||||||
chr2:101118423 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.128-28059T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118423 | |||||||
chr2:101118425 | A | G | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0151 others(4): Show |
7 | HG00438.hp1 HG00544.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-28061T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118425 | |||||||
chr2:101118432 | C | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp1 HG00544.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-28068G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118432 | |||||||
chr2:101118433 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp1 HG00544.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-28069T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118433 | |||||||
chr2:101118434 | T | C | 47 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0058 others(44): Show |
47 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.128-28070A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118434 | |||||||
chr2:101118437 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.128-28073G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118437 | |||||||
chr2:101118463 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.128-28099T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118463 | |||||||
chr2:101118467 | C | T | 39 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.128-28103G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118467 | |||||||
chr2:101118471 | T | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0263 |
2 | HG00408.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.128-28107A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118471 | |||||||
chr2:101118471 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.128-28107A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118471 | |||||||
chr2:101118499 | A | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG04184.hp2 NA18960.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-28135T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118499 | |||||||
chr2:101118503 | T | C | 64 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0001t0001g0116 others(61): Show |
64 | HG00408.hp2 HG00639.hp1 HG01192.hp1 others(61): Show |
intron_variant | MODIFIER | c.128-28139A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118503 | |||||||
chr2:101118523 | T | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0058 others(40): Show |
43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.128-28159A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118523 | |||||||
chr2:101118558 | T | G | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-28194A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118558 | |||||||
chr2:101118566 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.128-28202T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118566 | |||||||
chr2:101118569 | C | T | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-28205G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118569 | |||||||
chr2:101118570 | A | G | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-28206T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118570 | |||||||
chr2:101118583 | A | G | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-28219T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118583 | |||||||
chr2:101118596 | T | C | 2 | a0005c0006t0001g0098 a0005c0006t0001g0099 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.128-28232A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118596 | |||||||
chr2:101118622 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128-28258C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118622 | |||||||
chr2:101118696 | C | CA | 66 | a0001c0001t0001g0003 a0001c0001t0001g0096 a0001c0001t0001g0118 others(63): Show |
66 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.128-28333dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118696 | |||||||
chr2:101118752 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.128-28388G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118752 | |||||||
chr2:101118814 | A | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.128-28450T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118814 | |||||||
chr2:101118873 | G | A | 49 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.128-28509C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101118873 | |||||||
chr2:101119211 | C | A | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.128-28847G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119211 | |||||||
chr2:101119309 | A | C | 1 | a0002c0002t0002g0015 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.128-28945T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119309 | |||||||
chr2:101119371 | C | CT | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.128-29008_128-2900 others(5): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119371 | |||||||
chr2:101119376 | T | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.128-29012A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119376 | |||||||
chr2:101119527 | G | C | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.128-29163C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119527 | |||||||
chr2:101119692 | T | G | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG01257.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-29328A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101119692 | |||||||
chr2:101120241 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.128-29877C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120241 | |||||||
chr2:101120408 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.128-30044G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120408 | |||||||
chr2:101120425 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.128-30061C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120425 | |||||||
chr2:101120555 | G | A | 1 | a0002c0003t0001g0268 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.128-30191C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120555 | |||||||
chr2:101120631 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.128-30267A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120631 | |||||||
chr2:101120788 | G | C | 1 | a0002c0002t0002g0031 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.127+30339C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120788 | |||||||
chr2:101120917 | G | A | 54 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(51): Show |
54 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.127+30210C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101120917 | |||||||
chr2:101121010 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+30117A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121010 | |||||||
chr2:101121252 | G | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+29875C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121252 | |||||||
chr2:101121317 | A | T | 1 | a0002c0002t0002g0196 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.127+29810T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121317 | |||||||
chr2:101121473 | A | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(38): Show |
41 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.127+29654T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121473 | |||||||
chr2:101121594 | C | G | 1 | a0002c0002t0002g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127+29533G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121594 | |||||||
chr2:101121728 | A | G | 4 | a0001c0024t0003g0327 a0009c0014t0003g0325 a0009c0014t0003g0330 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+29399T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121728 | |||||||
chr2:101121776 | C | A | 1 | a0002c0002t0002g0259 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127+29351G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121776 | |||||||
chr2:101121776 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(78): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.127+29351G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121776 | |||||||
chr2:101121923 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127+29204T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101121923 | |||||||
chr2:101122022 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0113 others(38): Show |
41 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.127+29105G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122022 | |||||||
chr2:101122071 | C | CT | 7 | a0001c0001t0001g0120 a0001c0001t0001g0150 a0002c0003t0001g0103 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+29055dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122071 | |||||||
chr2:101122071 | CT | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
74 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.127+29055delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122071 | |||||||
chr2:101122078 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127+29049A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122078 | |||||||
chr2:101122350 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.127+28777G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122350 | |||||||
chr2:101122383 | C | CA | 28 | a0001c0001t0001g0193 a0001c0001t0001g0209 a0001c0001t0001g0221 others(25): Show |
28 | HG00741.hp2 HG01099.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.127+28743dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAA | 20 | a0001c0001t0001g0029 a0001c0001t0001g0222 a0001c0001t0001g0223 others(17): Show |
20 | HG00140.hp2 HG01243.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.127+28742_127+2874 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0231 a0001c0001t0001g0243 a0001c0001t0001g0244 others(8): Show |
11 | HG00099.hp2 HG01167.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+28735_127+2874 others(13): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(3): Show |
23 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0232 others(20): Show |
23 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.127+28734_127+2874 others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0233 others(9): Show |
12 | HG00323.hp2 HG00423.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+28733_127+2874 others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG01192.hp2 HG01261.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.127+28732_127+2874 others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(8): Show |
1 | a0003c0004t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.127+28729_127+2874 others(19): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | C | CAAAAAAA others(11): Show |
1 | a0002c0003t0001g0218 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127+28726_127+2874 others(22): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CA | C | 11 | a0001c0001t0001g0153 a0001c0001t0001g0289 a0001c0001t0001g0290 others(8): Show |
11 | HG00438.hp1 HG01256.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+28743delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CAA | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0107 others(37): Show |
40 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+28742_127+2874 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CAAAAAAA | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0116 others(69): Show |
72 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.127+28737_127+2874 others(11): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0001g0130 a0001c0001t0005g0097 a0002c0002t0002g0084 others(4): Show |
7 | HG01358.hp1 HG02559.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+28736_127+2874 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CAAAAAAA others(6): Show |
C | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+28731_127+2874 others(17): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122383 | CAAAAAAA others(9): Show |
C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01167.hp2 HG01257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+28728_127+2874 others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122383 | |||||||
chr2:101122492 | T | C | 1 | a0011c0031t0001g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.127+28635A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122492 | |||||||
chr2:101122749 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0048 others(113): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.127+28378G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122749 | |||||||
chr2:101122838 | C | T | 1 | a0002c0002t0002g0291 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.127+28289G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122838 | |||||||
chr2:101122931 | AAACATC | A | 54 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(51): Show |
54 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.127+28190_127+2819 others(10): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101122931 | |||||||
chr2:101123247 | G | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.127+27880C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123247 | |||||||
chr2:101123344 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(78): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.127+27783A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123344 | |||||||
chr2:101123368 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0263 |
2 | HG00408.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.127+27759C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123368 | |||||||
chr2:101123382 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.127+27745A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123382 | |||||||
chr2:101123534 | G | A | 1 | a0009c0014t0003g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.127+27593C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123534 | |||||||
chr2:101123534 | G | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.127+27593C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123534 | |||||||
chr2:101123643 | C | T | 28 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+27484G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123643 | |||||||
chr2:101123700 | T | C | 2 | a0001c0001t0006g0148 a0002c0003t0001g0147 |
2 | NA18983.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.127+27427A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123700 | |||||||
chr2:101123704 | A | G | 2 | a0009c0020t0003g0331 a0009c0020t0003g0332 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127+27423T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123704 | |||||||
chr2:101123769 | T | G | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+27358A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123769 | |||||||
chr2:101123809 | C | T | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | NA18942.hp2 NA18946.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.127+27318G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101123809 | |||||||
chr2:101124047 | C | T | 2 | a0002c0002t0002g0313 a0002c0003t0001g0083 |
2 | HG02615.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.127+27080G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124047 | |||||||
chr2:101124219 | T | C | 1 | a0003c0004t0001g0271 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.127+26908A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124219 | |||||||
chr2:101124279 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02486.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.127+26848T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124279 | |||||||
chr2:101124288 | T | C | 3 | a0002c0003t0001g0288 a0002c0003t0001g0300 a0002c0003t0001g0310 |
3 | NA18981.hp2 NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.127+26839A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124288 | |||||||
chr2:101124354 | C | A | 1 | a0003c0004t0001g0272 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127+26773G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124354 | |||||||
chr2:101124420 | G | A | 1 | a0005c0006t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.127+26707C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124420 | |||||||
chr2:101124601 | G | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.127+26526C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124601 | |||||||
chr2:101124729 | G | C | 1 | a0002c0002t0002g0008 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.127+26398C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124729 | |||||||
chr2:101124779 | T | C | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+26348A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124779 | |||||||
chr2:101124855 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+26272A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124855 | |||||||
chr2:101124983 | TA | T | 6 | a0001c0001t0003g0329 a0001c0024t0003g0327 a0009c0014t0003g0325 others(3): Show |
6 | HG02622.hp2 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+26143delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101124983 | |||||||
chr2:101125101 | T | A | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+26026A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125101 | |||||||
chr2:101125137 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.127+25990G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125137 | |||||||
chr2:101125196 | AG | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
71 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.127+25930delC | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125196 | |||||||
chr2:101125640 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.127+25487G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125640 | |||||||
chr2:101125849 | T | C | 8 | a0002c0002t0002g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+25278A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125849 | |||||||
chr2:101125986 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.127+25141A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101125986 | |||||||
chr2:101126057 | G | C | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127+25070C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126057 | |||||||
chr2:101126063 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.127+25064C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126063 | |||||||
chr2:101126137 | G | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+24990C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126137 | |||||||
chr2:101126375 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.127+24752T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126375 | |||||||
chr2:101126796 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127+24331T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126796 | |||||||
chr2:101126805 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127+24322T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126805 | |||||||
chr2:101126817 | GA | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+24309delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101126817 | |||||||
chr2:101127059 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
186 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.127+24068T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127059 | |||||||
chr2:101127132 | C | T | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+23995G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127132 | |||||||
chr2:101127197 | G | A | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+23930C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127197 | |||||||
chr2:101127337 | GA | G | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0002c0002t0002g0016 others(6): Show |
9 | HG02735.hp2 NA18951.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+23789delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127337 | |||||||
chr2:101127381 | GC | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+23745delG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127381 | |||||||
chr2:101127472 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
152 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.127+23655G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127472 | |||||||
chr2:101127521 | A | C | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(6): Show |
9 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+23606T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127521 | |||||||
chr2:101127671 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+23456C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127671 | |||||||
chr2:101127681 | A | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
65 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.127+23446T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127681 | |||||||
chr2:101127682 | C | T | 3 | a0002c0002t0002g0177 a0002c0002t0002g0182 a0002c0002t0002g0183 |
3 | NA18941.hp2 NA18967.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.127+23445G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127682 | |||||||
chr2:101127797 | G | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+23330C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127797 | |||||||
chr2:101127825 | G | A | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+23302C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127825 | |||||||
chr2:101127828 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+23299G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127828 | |||||||
chr2:101127969 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.127+23158A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101127969 | |||||||
chr2:101128020 | A | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+23107T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128020 | |||||||
chr2:101128022 | T | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0213 others(27): Show |
30 | HG01167.hp2 HG01257.hp1 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.127+23105A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128022 | |||||||
chr2:101128119 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+23008A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128119 | |||||||
chr2:101128445 | C | G | 1 | a0002c0003t0001g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127+22682G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128445 | |||||||
chr2:101128523 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127+22604T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128523 | |||||||
chr2:101128545 | A | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0263 |
2 | HG00408.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.127+22582T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128545 | |||||||
chr2:101128582 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+22545G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128582 | |||||||
chr2:101128627 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02723.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127+22500T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128627 | |||||||
chr2:101128648 | C | A | 3 | a0001c0001t0001g0160 a0006c0012t0002g0161 a0010c0008t0001g0159 |
3 | HG02145.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.127+22479G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101128648 | |||||||
chr2:101129120 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+22007A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129120 | |||||||
chr2:101129134 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+21993T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129134 | |||||||
chr2:101129297 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
65 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.127+21830G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129297 | |||||||
chr2:101129324 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02723.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127+21803C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129324 | |||||||
chr2:101129373 | A | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+21754T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129373 | |||||||
chr2:101129377 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(85): Show |
88 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.127+21750C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129377 | |||||||
chr2:101129457 | T | C | 1 | a0002c0003t0001g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127+21670A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129457 | |||||||
chr2:101129604 | A | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+21523T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129604 | |||||||
chr2:101129732 | C | A | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+21395G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129732 | |||||||
chr2:101129737 | C | G | 30 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0213 others(27): Show |
30 | HG01167.hp2 HG01257.hp1 HG02572.hp1 others(27): Show |
intron_variant | MODIFIER | c.127+21390G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129737 | |||||||
chr2:101129904 | C | CA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(90): Show |
93 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.127+21222dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129904 | |||||||
chr2:101129904 | C | CAA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
7 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+21221_127+2122 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129904 | |||||||
chr2:101129912 | AAAAAAGA others(4): Show |
A | 1 | a0002c0003t0001g0275 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.127+21204_127+2121 others(15): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101129912 | |||||||
chr2:101130025 | G | A | 1 | a0002c0002t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.127+21102C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130025 | |||||||
chr2:101130125 | C | G | 8 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
8 | NA18961.hp1 NA18966.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+21002G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130125 | |||||||
chr2:101130130 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+20997G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130130 | |||||||
chr2:101130211 | C | T | 3 | a0002c0002t0002g0177 a0002c0002t0002g0182 a0002c0002t0002g0183 |
3 | NA18941.hp2 NA18967.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.127+20916G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130211 | |||||||
chr2:101130260 | C | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
65 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.127+20867G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130260 | |||||||
chr2:101130379 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.127+20748C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130379 | |||||||
chr2:101130398 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+20729G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130398 | |||||||
chr2:101130439 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02723.hp1 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127+20688C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130439 | |||||||
chr2:101130477 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.127+20650C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130477 | |||||||
chr2:101130481 | G | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG01192.hp2 HG01261.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.127+20646C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130481 | |||||||
chr2:101130554 | T | C | 1 | a0003c0004t0001g0273 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127+20573A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130554 | |||||||
chr2:101130861 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.127+20266T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130861 | |||||||
chr2:101130877 | C | T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+20250G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130877 | |||||||
chr2:101130920 | T | A | 6 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0305 others(3): Show |
6 | NA18939.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+20207A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101130920 | |||||||
chr2:101131058 | TTTTA | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+20065_127+2006 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131058 | |||||||
chr2:101131092 | G | A | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+20035C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131092 | |||||||
chr2:101131103 | A | G | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+20024T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131103 | |||||||
chr2:101131234 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+19893G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131234 | |||||||
chr2:101131235 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.127+19892C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131235 | |||||||
chr2:101131338 | A | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+19789T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131338 | |||||||
chr2:101131500 | C | T | 1 | a0001c0001t0004g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.127+19627G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131500 | |||||||
chr2:101131508 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127+19619G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131508 | |||||||
chr2:101131658 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+19469G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131658 | |||||||
chr2:101131708 | G | A | 3 | a0002c0002t0002g0030 a0002c0002t0002g0031 a0003c0004t0001g0274 |
3 | HG01099.hp1 HG02293.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.127+19419C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131708 | |||||||
chr2:101131709 | G | A | 1 | a0009c0020t0003g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+19418C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131709 | |||||||
chr2:101131728 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.127+19399A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131728 | |||||||
chr2:101131802 | G | A | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+19325C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131802 | |||||||
chr2:101131948 | A | C | 1 | a0002c0002t0002g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.127+19179T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101131948 | |||||||
chr2:101132238 | T | C | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+18889A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101132238 | |||||||
chr2:101132401 | C | T | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+18726G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101132401 | |||||||
chr2:101132620 | A | C | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+18507T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101132620 | |||||||
chr2:101132835 | A | C | 1 | a0005c0006t0001g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.127+18292T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101132835 | |||||||
chr2:101133058 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.127+18069C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133058 | |||||||
chr2:101133059 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.127+18068G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133059 | |||||||
chr2:101133123 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127+18004C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133123 | |||||||
chr2:101133124 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127+18003G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133124 | |||||||
chr2:101133147 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.127+17980C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133147 | |||||||
chr2:101133159 | CA | C | 69 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0207 others(66): Show |
69 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.127+17967delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133159 | |||||||
chr2:101133304 | A | T | 68 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0207 others(65): Show |
68 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.127+17823T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133304 | |||||||
chr2:101133461 | A | G | 4 | a0002c0003t0001g0078 a0002c0003t0001g0079 a0002c0003t0001g0080 others(1): Show |
4 | HG01192.hp1 HG01256.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+17666T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133461 | |||||||
chr2:101133470 | A | G | 1 | a0002c0003t0001g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127+17657T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133470 | |||||||
chr2:101133778 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.127+17349G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133778 | |||||||
chr2:101133886 | C | T | 3 | a0001c0001t0001g0160 a0006c0012t0002g0161 a0010c0008t0001g0159 |
3 | HG02145.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.127+17241G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133886 | |||||||
chr2:101133888 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+17239G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101133888 | |||||||
chr2:101134170 | TTC | T | 41 | a0001c0001t0001g0018 a0001c0001t0001g0160 a0001c0001t0001g0209 others(38): Show |
41 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.127+16955_127+1695 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134170 | |||||||
chr2:101134191 | TCTCTCTC others(7): Show |
T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG02723.hp1 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+16922_127+1693 others(18): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134191 | |||||||
chr2:101134191 | TCTCTCTC others(9): Show |
T | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+16920_127+1693 others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134191 | |||||||
chr2:101134193 | TCTCTCAC others(1): Show |
T | 16 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0001g0193 others(13): Show |
16 | HG02132.hp2 HG02735.hp2 HG03669.hp1 others(13): Show |
intron_variant | MODIFIER | c.127+16926_127+1693 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134193 | |||||||
chr2:101134193 | TCTCTCAC others(3): Show |
T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0128 others(1): Show |
4 | NA18969.hp2 NA18974.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+16924_127+1693 others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134193 | |||||||
chr2:101134193 | TCTCTCAC others(5): Show |
T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(78): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.127+16922_127+1693 others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134193 | |||||||
chr2:101134193 | TCTCTCAC others(7): Show |
T | 57 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(54): Show |
57 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.127+16920_127+1693 others(18): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134193 | |||||||
chr2:101134193 | TCTCTCAC others(9): Show |
T | 6 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0315 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+16918_127+1693 others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134193 | |||||||
chr2:101134195 | T | A | 1 | a0002c0002t0002g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.127+16932A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134195 | TCTCA | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0002c0002t0002g0200 others(4): Show |
7 | HG01168.hp1 HG01261.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+16928_127+1693 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134195 | TCTCACAC others(1): Show |
T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0277 a0001c0001t0004g0278 others(1): Show |
4 | HG01516.hp2 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+16924_127+1693 others(12): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134195 | TCTCACAC others(3): Show |
T | 1 | a0001c0023t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.127+16922_127+1693 others(14): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134195 | TCTCACAC others(5): Show |
T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0152 others(16): Show |
19 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+16920_127+1693 others(16): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134195 | TCTCACAC others(7): Show |
T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG01257.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+16918_127+1693 others(18): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134195 | |||||||
chr2:101134197 | T | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0225 a0002c0002t0002g0030 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+16930A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134197 | |||||||
chr2:101134197 | TCA | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(11): Show |
14 | HG00323.hp1 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.127+16928_127+1692 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134197 | |||||||
chr2:101134197 | TCACA | T | 30 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0066 others(27): Show |
30 | HG00099.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.127+16926_127+1692 others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134197 | |||||||
chr2:101134197 | TCACACA | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(21): Show |
24 | HG00140.hp1 HG00544.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.127+16924_127+1692 others(10): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134197 | |||||||
chr2:101134197 | TCACACAC others(9): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+16914_127+1692 others(20): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134197 | |||||||
chr2:101134199 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127+16928T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134199 | |||||||
chr2:101134201 | A | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(9): Show |
12 | HG00323.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+16926T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134201 | |||||||
chr2:101134203 | A | T | 26 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0058 others(23): Show |
26 | HG00099.hp1 HG01081.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.127+16924T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134203 | |||||||
chr2:101134205 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.127+16922T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134205 | |||||||
chr2:101134215 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127+16912T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134215 | |||||||
chr2:101134226 | C | G | 1 | a0017c0027t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127+16901G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134226 | |||||||
chr2:101134228 | C | T | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+16899G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134228 | |||||||
chr2:101134247 | G | C | 12 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 others(9): Show |
12 | HG00140.hp2 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+16880C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134247 | |||||||
chr2:101134323 | C | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+16804G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134323 | |||||||
chr2:101134337 | T | C | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127+16790A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134337 | |||||||
chr2:101134410 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+16717A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134410 | |||||||
chr2:101134799 | A | G | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+16328T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134799 | |||||||
chr2:101134884 | C | T | 7 | a0001c0001t0001g0042 a0008c0011t0001g0036 a0010c0008t0001g0039 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+16243G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101134884 | |||||||
chr2:101135028 | C | A | 1 | a0008c0011t0001g0208 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127+16099G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135028 | |||||||
chr2:101135044 | C | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+16083G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135044 | |||||||
chr2:101135104 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127+16023T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135104 | |||||||
chr2:101135129 | G | A | 1 | a0004c0005t0001g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127+15998C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135129 | |||||||
chr2:101135145 | C | A | 1 | a0009c0020t0003g0332 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127+15982G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135145 | |||||||
chr2:101135167 | G | C | 1 | a0001c0001t0001g0308 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.127+15960C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135167 | |||||||
chr2:101135223 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.127+15904T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135223 | |||||||
chr2:101135386 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+15741T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135386 | |||||||
chr2:101135417 | TA | T | 6 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0117 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+15709delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135417 | |||||||
chr2:101135867 | G | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+15260C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135867 | |||||||
chr2:101135895 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+15232C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101135895 | |||||||
chr2:101136123 | A | G | 305 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.127+15004T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101136123 | |||||||
chr2:101136124 | G | C | 1 | a0014c0034t0001g0158 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.127+15003C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101136124 | |||||||
chr2:101136286 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+14841T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101136286 | |||||||
chr2:101136772 | G | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+14355C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101136772 | |||||||
chr2:101136986 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+14141T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101136986 | |||||||
chr2:101137031 | C | CT | 67 | a0001c0001t0001g0029 a0001c0001t0001g0207 a0001c0001t0001g0228 others(64): Show |
67 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.127+14095dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137031 | |||||||
chr2:101137031 | CT | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0042 others(94): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.127+14095delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137031 | |||||||
chr2:101137031 | CTT | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0062 others(83): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.127+14094_127+1409 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137031 | |||||||
chr2:101137102 | G | A | 1 | a0002c0003t0007g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127+14025C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137102 | |||||||
chr2:101137253 | G | A | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+13874C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137253 | |||||||
chr2:101137333 | G | A | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+13794C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137333 | |||||||
chr2:101137436 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.127+13691A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137436 | |||||||
chr2:101137472 | C | T | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+13655G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137472 | |||||||
chr2:101137474 | G | A | 2 | a0002c0003t0001g0055 a0002c0003t0001g0056 |
2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.127+13653C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137474 | |||||||
chr2:101137679 | G | C | 6 | a0002c0002t0002g0164 a0002c0002t0002g0166 a0002c0002t0002g0167 others(3): Show |
6 | HG00738.hp2 HG00741.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+13448C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137679 | |||||||
chr2:101137726 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(21): Show |
24 | HG00423.hp2 HG00639.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.127+13401G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137726 | |||||||
chr2:101137836 | T | C | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+13291A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137836 | |||||||
chr2:101137926 | C | T | 2 | a0002c0003t0001g0288 a0002c0003t0001g0310 |
2 | NA18981.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.127+13201G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101137926 | |||||||
chr2:101138229 | T | G | 35 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(32): Show |
35 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+12898A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138229 | |||||||
chr2:101138261 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+12866G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138261 | |||||||
chr2:101138283 | T | C | 8 | a0002c0002t0002g0049 a0002c0003t0001g0055 a0002c0003t0001g0056 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+12844A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138283 | |||||||
chr2:101138304 | G | GA | 18 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
18 | HG02486.hp2 HG02630.hp2 HG02897.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+12822dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138304 | |||||||
chr2:101138495 | G | A | 3 | a0002c0002t0002g0202 a0002c0003t0001g0201 a0002c0003t0001g0203 |
3 | HG01071.hp2 HG01081.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.127+12632C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138495 | |||||||
chr2:101138716 | G | GTGCCCTC others(11): Show |
1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+12393_127+1241 others(22): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138716 | |||||||
chr2:101138744 | T | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp1 HG00544.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+12383A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138744 | |||||||
chr2:101138773 | C | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+12354G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138773 | |||||||
chr2:101138810 | C | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.127+12317G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138810 | |||||||
chr2:101138821 | C | G | 2 | a0002c0002t0002g0076 a0002c0002t0002g0077 |
2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.127+12306G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138821 | |||||||
chr2:101138842 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+12285T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138842 | |||||||
chr2:101138894 | A | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0212 a0001c0001t0001g0213 others(26): Show |
29 | HG01167.hp2 HG01257.hp1 HG02572.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+12233T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101138894 | |||||||
chr2:101139140 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.127+11987G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139140 | |||||||
chr2:101139325 | AC | A | 13 | a0001c0021t0004g0282 a0002c0003t0001g0268 a0002c0003t0001g0275 others(10): Show |
13 | HG02027.hp1 HG02074.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+11801delG | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139325 | |||||||
chr2:101139326 | CA | C | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.127+11800delT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139326 | |||||||
chr2:101139329 | A | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+11798T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139329 | |||||||
chr2:101139361 | G | A | 36 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0129 others(33): Show |
36 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.127+11766C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139361 | |||||||
chr2:101139673 | T | A | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
12 | NA18942.hp2 NA18946.hp1 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.127+11454A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139673 | |||||||
chr2:101139874 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0311 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.127+11253C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101139874 | |||||||
chr2:101140127 | G | A | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+11000C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140127 | |||||||
chr2:101140467 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(84): Show |
87 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.127+10660C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140467 | |||||||
chr2:101140492 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127+10635C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140492 | |||||||
chr2:101140651 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01257.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.127+10476A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140651 | |||||||
chr2:101140666 | A | T | 28 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+10461T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140666 | |||||||
chr2:101140693 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+10434A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140693 | |||||||
chr2:101140760 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.127+10367G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140760 | |||||||
chr2:101140760 | CT | C | 13 | a0001c0001t0001g0029 a0001c0023t0001g0115 a0002c0002t0002g0030 others(10): Show |
13 | HG00438.hp2 HG01099.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.127+10366delA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140760 | |||||||
chr2:101140760 | CTT | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0048 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.127+10365_127+1036 others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140760 | |||||||
chr2:101140772 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.127+10355A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140772 | |||||||
chr2:101140801 | C | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+10326G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140801 | |||||||
chr2:101140854 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.127+10273G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140854 | |||||||
chr2:101140897 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0209 others(4): Show |
7 | HG01261.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+10230C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140897 | |||||||
chr2:101140915 | C | T | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+10212G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140915 | |||||||
chr2:101140953 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.127+10174C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101140953 | |||||||
chr2:101141003 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.127+10124G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141003 | |||||||
chr2:101141162 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0289 others(32): Show |
35 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.127+9965G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141162 | |||||||
chr2:101141678 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.127+9449T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141678 | |||||||
chr2:101141691 | T | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+9436A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141691 | |||||||
chr2:101141803 | G | A | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(3): Show |
6 | HG00438.hp2 NA18946.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+9324C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141803 | |||||||
chr2:101141803 | G | GCA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0157 a0001c0001t0001g0212 others(12): Show |
15 | HG00408.hp2 HG01257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.127+9322_127+9323d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141803 | |||||||
chr2:101141803 | GCA | G | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+9322_127+9323d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141803 | |||||||
chr2:101141805 | A | G | 53 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(50): Show |
53 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.127+9322T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141805 | |||||||
chr2:101141849 | T | TA | 52 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.127+9277dupT | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101141849 | |||||||
chr2:101142239 | A | G | 9 | a0001c0001t0001g0315 a0001c0001t0004g0106 a0001c0021t0004g0282 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+8888T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142239 | |||||||
chr2:101142412 | G | C | 4 | a0001c0001t0001g0277 a0001c0001t0004g0278 a0006c0012t0002g0279 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+8715C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142412 | |||||||
chr2:101142594 | G | A | 28 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+8533C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142594 | |||||||
chr2:101142661 | A | G | 52 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0229 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.127+8466T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142661 | |||||||
chr2:101142720 | G | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.127+8407C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142720 | |||||||
chr2:101142738 | G | A | 1 | a0002c0002t0002g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.127+8389C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142738 | |||||||
chr2:101142888 | T | C | 36 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(33): Show |
36 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.127+8239A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101142888 | |||||||
chr2:101143000 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127+8127G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143000 | |||||||
chr2:101143050 | T | A | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+8077A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143050 | |||||||
chr2:101143063 | C | CT | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.127+8063dupA | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143063 | |||||||
chr2:101143165 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+7962G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143165 | |||||||
chr2:101143417 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+7710T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143417 | |||||||
chr2:101143476 | C | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.127+7651G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143476 | |||||||
chr2:101143551 | T | C | 28 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+7576A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143551 | |||||||
chr2:101143566 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127+7561G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143566 | |||||||
chr2:101143828 | T | C | 52 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.127+7299A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143828 | |||||||
chr2:101143847 | C | A | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+7280G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101143847 | |||||||
chr2:101144079 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.127+7048A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144079 | |||||||
chr2:101144134 | T | C | 1 | a0002c0002t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+6993A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144134 | |||||||
chr2:101144217 | G | A | 2 | a0002c0002t0002g0104 a0002c0003t0001g0105 |
2 | HG00639.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.127+6910C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144217 | |||||||
chr2:101144354 | A | C | 1 | a0004c0005t0001g0002 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127+6773T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144354 | |||||||
chr2:101144517 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0004g0278 a0006c0012t0002g0279 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+6610C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144517 | |||||||
chr2:101144658 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.127+6469G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144658 | |||||||
chr2:101144674 | C | A | 7 | a0001c0021t0004g0282 a0002c0003t0001g0283 a0004c0005t0001g0276 others(4): Show |
7 | HG02280.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+6453G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144674 | |||||||
chr2:101144707 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0096 others(30): Show |
33 | HG00423.hp2 HG00639.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.127+6420G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144707 | |||||||
chr2:101144795 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.127+6332C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144795 | |||||||
chr2:101144974 | A | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0209 a0001c0001t0001g0212 others(23): Show |
26 | HG01257.hp1 HG02145.hp1 HG02615.hp1 others(23): Show |
intron_variant | MODIFIER | c.127+6153T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101144974 | |||||||
chr2:101145056 | C | T | 1 | a0008c0011t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.127+6071G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145056 | |||||||
chr2:101145173 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.127+5954G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145173 | |||||||
chr2:101145223 | T | C | 1 | a0006c0010t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+5904A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145223 | |||||||
chr2:101145282 | C | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.127+5845G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145282 | |||||||
chr2:101145373 | T | C | 1 | a0002c0003t0001g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127+5754A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145373 | |||||||
chr2:101145374 | G | A | 4 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+5753C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145374 | |||||||
chr2:101145589 | C | T | 1 | a0004c0005t0001g0002 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127+5538G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145589 | |||||||
chr2:101145728 | A | T | 1 | a0002c0002t0002g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127+5399T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145728 | |||||||
chr2:101145766 | C | G | 5 | a0001c0001t0001g0004 a0002c0003t0001g0218 a0002c0003t0001g0219 others(2): Show |
5 | HG02615.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+5361G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145766 | |||||||
chr2:101145817 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.127+5310G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145817 | |||||||
chr2:101145997 | C | T | 1 | a0002c0002t0002g0287 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127+5130G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101145997 | |||||||
chr2:101146058 | A | ATT | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.127+5067_127+5068d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146058 | |||||||
chr2:101146332 | CCTAA | C | 9 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG01257.hp1 HG02145.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+4791_127+4794d others(6): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146332 | |||||||
chr2:101146375 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.127+4752A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146375 | |||||||
chr2:101146416 | A | G | 5 | a0007c0007t0001g0043 a0007c0007t0001g0044 a0007c0007t0001g0045 others(2): Show |
5 | HG01167.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+4711T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146416 | |||||||
chr2:101146493 | C | T | 4 | a0001c0001t0001g0277 a0001c0001t0004g0278 a0006c0012t0002g0279 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+4634G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146493 | |||||||
chr2:101146733 | A | G | 1 | a0001c0021t0004g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+4394T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146733 | |||||||
chr2:101146765 | C | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.127+4362G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146765 | |||||||
chr2:101146937 | A | T | 7 | a0001c0001t0001g0042 a0008c0011t0001g0036 a0010c0008t0001g0039 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+4190T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146937 | |||||||
chr2:101146992 | C | T | 40 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.127+4135G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101146992 | |||||||
chr2:101147072 | AGAGGCC | A | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.127+4049_127+4054d others(8): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147072 | |||||||
chr2:101147084 | C | A | 1 | a0001c0001t0001g0315 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.127+4043G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147084 | |||||||
chr2:101147107 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.127+4020A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147107 | |||||||
chr2:101147215 | CTT | C | 50 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.127+3910_127+3911d others(4): Show |
TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147215 | |||||||
chr2:101147225 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.127+3902T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147225 | |||||||
chr2:101147278 | G | A | 1 | a0006c0025t0002g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+3849C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147278 | |||||||
chr2:101147343 | G | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.127+3784C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147343 | |||||||
chr2:101147496 | T | C | 1 | a0001c0001t0004g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.127+3631A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147496 | |||||||
chr2:101147551 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127+3576C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147551 | |||||||
chr2:101147795 | C | T | 1 | a0004c0005t0001g0281 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+3332G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147795 | |||||||
chr2:101147835 | G | C | 1 | a0002c0002t0002g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+3292C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101147835 | |||||||
chr2:101148050 | G | T | 4 | a0001c0001t0001g0277 a0001c0001t0004g0278 a0006c0012t0002g0279 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3077C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148050 | |||||||
chr2:101148051 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.127+3076G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148051 | |||||||
chr2:101148160 | A | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.127+2967T>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148160 | |||||||
chr2:101148190 | T | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0004c0005t0001g0110 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+2937A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148190 | |||||||
chr2:101148199 | T | A | 1 | a0002c0002t0002g0111 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.127+2928A>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148199 | |||||||
chr2:101148201 | G | A | 1 | a0002c0002t0002g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.127+2926C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148201 | |||||||
chr2:101148207 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.127+2920G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148207 | |||||||
chr2:101148269 | G | A | 48 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(45): Show |
48 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.127+2858C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148269 | |||||||
chr2:101148897 | A | T | 1 | a0002c0002t0002g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.127+2230T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148897 | |||||||
chr2:101148908 | A | C | 1 | a0002c0002t0002g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.127+2219T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148908 | |||||||
chr2:101148909 | C | A | 1 | a0002c0002t0002g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.127+2218G>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148909 | |||||||
chr2:101148995 | G | C | 2 | a0001c0001t0001g0174 a0018c0022t0001g0175 |
2 | NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.127+2132C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101148995 | |||||||
chr2:101149099 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.127+2028T>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149099 | |||||||
chr2:101149274 | G | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+1853C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149274 | |||||||
chr2:101149460 | T | G | 82 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.127+1667A>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149460 | |||||||
chr2:101149656 | A | T | 3 | a0001c0024t0003g0327 a0009c0014t0003g0325 a0012c0028t0003g0326 |
3 | HG02922.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.127+1471T>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149656 | |||||||
chr2:101149712 | G | A | 19 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01255.hp1 HG01516.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.127+1415C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149712 | |||||||
chr2:101149921 | G | A | 1 | a0002c0016t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127+1206C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101149921 | |||||||
chr2:101150001 | C | T | 1 | a0004c0005t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+1126G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150001 | |||||||
chr2:101150164 | C | T | 1 | a0004c0005t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127+963G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150164 | |||||||
chr2:101150427 | G | A | 5 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
5 | HG00140.hp1 HG01433.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+700C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150427 | |||||||
chr2:101150604 | C | T | 11 | a0001c0001t0001g0277 a0001c0001t0004g0278 a0001c0021t0004g0282 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+523G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150604 | |||||||
chr2:101150608 | T | C | 48 | a0001c0001t0001g0277 a0001c0001t0001g0289 a0001c0001t0001g0290 others(45): Show |
48 | HG00140.hp1 HG00544.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.127+519A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150608 | |||||||
chr2:101150646 | G | C | 12 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 others(9): Show |
12 | HG00140.hp2 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+481C>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150646 | |||||||
chr2:101150699 | C | G | 1 | a0001c0001t0001g0003 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.127+428G>C | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150699 | |||||||
chr2:101150827 | C | T | 1 | a0002c0002t0002g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.127+300G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150827 | |||||||
chr2:101150852 | T | C | 127 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0212 others(124): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.127+275A>G | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150852 | |||||||
chr2:101150885 | G | A | 1 | a0002c0002t0002g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.127+242C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101150885 | |||||||
chr2:101151011 | C | T | 1 | a0004c0005t0001g0002 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.127+116G>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101151011 | |||||||
chr2:101151056 | G | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0324 |
2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.127+71C>T | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101151056 | |||||||
chr2:101151089 | G | T | 1 | a0002c0003t0001g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+38C>A | TBC1D8 | ENSG00000204634.13 | transcript | ENST00000409318.2 | protein_coding | 1/19 | chr2 | 101151089 |