Item | Value |
---|---|
geneid | 96764 |
ensemblid | ENSG00000137574.11 |
hgncid | 17843 |
symbol | TGS1 |
name | trimethylguanosine synthase 1 |
refseq_nuc | NM_024831.8 |
refseq_prot | NP_079107.6 |
ensembl_nuc | ENST00000260129.6 |
ensembl_prot | ENSP00000260129.5 |
mane_status | MANE Select |
chr | chr8 |
start | 55773446 |
end | 55826445 |
strand | + |
ver | v1.2 |
region | chr8:55773446-55826445 |
region5000 | chr8:55768446-55831445 |
regionname0 | TGS1_chr8_55773446_55826445 |
regionname5000 | TGS1_chr8_55768446_55831445 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 853 | 303 | 57 | 48 | 152 | 11 | 34 | 112 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0002 | 0/0 | 853 | 27 | 13 | 7 | 1 | 1 | 5 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0003 | 0/0 | 853 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0004 | 0/0 | 853 | 6 | 2 | 1 | 2 | 0 | 1 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0005 | 0/0 | 853 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0006 | 0/0 | 853 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0007 | 0/0 | 853 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0008 | 0/0 | 853 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0009 | 0/0 | 853 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0010 | 1/0 | 853 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0011 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0012 | 0/0 | 853 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0013 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0014 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0015 | 0/0 | 853 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0016 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0017 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0018 | 0/0 | 853 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0019 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
a0020 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | MCCEK others(848): Show |
chr8 | 55768446 | 55831445 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2559 | 292 | 56 | 45 | 151 | 11 | 28 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0007 | 0/0 | 2559 | 3 | 0 | 0 | 0 | 0 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0008 | 0/0 | 2559 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0009 | 0/0 | 2559 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0014 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0016 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0017 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0001c0020 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0002c0002 | 0/0 | 2559 | 25 | 13 | 5 | 1 | 1 | 5 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0002c0027 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0002c0029 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0003c0003 | 0/0 | 2559 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0004c0004 | 0/0 | 2559 | 6 | 2 | 1 | 2 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0005c0005 | 0/0 | 2559 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0006c0006 | 0/0 | 2559 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0007c0010 | 0/0 | 2559 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0008c0011 | 0/0 | 2559 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0009c0012 | 0/0 | 2559 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0010c0026 | 1/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0011c0025 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0012c0013 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0013c0015 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0014c0023 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0015c0028 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0016c0018 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0017c0019 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0018c0021 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0019c0022 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 | ||
a0020c0024 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ATGTG others(2554): Show |
chr8 | 55768446 | 55831445 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4477 | 190 | 42 | 29 | 95 | 7 | 17 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0002 | 0/1 | 4477 | 65 | 1 | 9 | 45 | 2 | 7 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0004 | 0/0 | 4475 | 13 | 2 | 6 | 0 | 2 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4470): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0006 | 0/0 | 4477 | 6 | 0 | 0 | 6 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0007 | 0/0 | 4472 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4467): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0008 | 0/0 | 4477 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0010 | 0/0 | 4477 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0011 | 0/0 | 4478 | 2 | 1 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0014 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0015 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0017 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0001t0018 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0007t0001 | 0/0 | 4477 | 3 | 0 | 0 | 0 | 0 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0008t0001 | 0/0 | 4477 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0009t0001 | 0/0 | 4477 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0014t0001 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0016t0006 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0017t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0001c0020t0001 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0002c0002t0003 | 0/0 | 4478 | 25 | 13 | 5 | 1 | 1 | 5 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0002c0027t0003 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0002c0029t0013 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0003c0003t0005 | 0/0 | 4477 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0004c0004t0001 | 0/0 | 4477 | 6 | 2 | 1 | 2 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0005c0005t0002 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0005c0005t0009 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0006c0006t0003 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0007c0010t0001 | 0/0 | 4477 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0008c0011t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0008c0011t0016 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0009c0012t0003 | 0/0 | 4478 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0010c0026t0012 | 1/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0011c0025t0002 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0012c0013t0001 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0013c0015t0002 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0014c0023t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0015c0028t0003 | 0/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4473): Show |
chr8 | 55768446 | 55831445 |
a0016c0018t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0017c0019t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0018c0021t0001 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0019c0022t0002 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
a0020c0024t0001 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | ACTTC others(4472): Show |
chr8 | 55768446 | 55831445 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0004 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0011g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0015g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0017g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0018g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0008t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0008t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0009t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0014t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0016t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0017t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0020t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0027t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0029t0013g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0006c0006t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0006c0006t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0007c0010t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0008c0011t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0008c0011t0016g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0009c0012t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0009c0012t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0010c0026t0012g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0011c0025t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0012c0013t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0013c0015t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0014c0023t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0015c0028t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0016c0018t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0017c0019t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0018c0021t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0019c0022t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0020c0024t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0003 | g0278 | EUR | GBR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | FIN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00597 | hp1 | a0011 | c0025 | t0002 | g0089 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00639 | hp2 | a0002 | c0027 | t0003 | g0292 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0171 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00738 | hp1 | a0001 | c0008 | t0001 | g0180 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00741 | hp1 | a0002 | c0002 | t0003 | g0284 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01070 | hp2 | a0007 | c0010 | t0001 | g0033 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01071 | hp2 | a0007 | c0010 | t0001 | g0033 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01109 | hp1 | a0003 | c0003 | t0005 | g0302 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01175 | hp1 | a0001 | c0014 | t0001 | g0149 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0308 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01255 | hp2 | a0002 | c0002 | t0003 | g0312 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0290 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0291 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01433 | hp2 | a0001 | c0008 | t0001 | g0169 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01884 | hp1 | a0005 | c0005 | t0009 | g0300 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0296 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01975 | hp2 | a0012 | c0013 | t0001 | g0173 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02055 | hp1 | a0001 | c0001 | t0014 | g0203 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0280 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02129 | hp2 | a0001 | c0001 | t0018 | g0245 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02145 | hp1 | a0006 | c0006 | t0003 | g0286 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0293 | EAS | CDX | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02257 | hp1 | a0001 | c0017 | t0001 | g0217 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02257 | hp2 | a0003 | c0003 | t0005 | g0032 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02258 | hp2 | a0013 | c0015 | t0002 | g0301 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02451 | hp1 | a0006 | c0006 | t0003 | g0015 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02523 | hp2 | a0001 | c0016 | t0006 | g0035 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0281 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02615 | hp2 | a0014 | c0023 | t0001 | g0310 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02622 | hp1 | a0002 | c0002 | t0003 | g0275 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02622 | hp2 | a0004 | c0004 | t0001 | g0311 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02698 | hp1 | a0001 | c0009 | t0001 | g0018 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02723 | hp2 | a0003 | c0003 | t0005 | g0307 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0287 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0056 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02738 | hp2 | a0015 | c0028 | t0003 | g0298 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02809 | hp1 | a0006 | c0006 | t0003 | g0015 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02809 | hp2 | a0016 | c0018 | t0001 | g0313 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02818 | hp1 | a0003 | c0003 | t0005 | g0303 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02896 | hp2 | a0002 | c0002 | t0003 | g0283 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0288 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02922 | hp2 | a0008 | c0011 | t0001 | g0111 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02965 | hp1 | a0005 | c0005 | t0002 | g0299 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0277 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02976 | hp1 | a0017 | c0019 | t0001 | g0119 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0271 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0276 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03098 | hp1 | a0003 | c0003 | t0005 | g0305 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0282 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03139 | hp1 | a0005 | c0005 | t0009 | g0268 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0309 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03486 | hp2 | a0003 | c0003 | t0005 | g0306 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03516 | hp2 | a0008 | c0011 | t0016 | g0139 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0200 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03579 | hp2 | a0006 | c0006 | t0003 | g0015 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03669 | hp1 | a0001 | c0009 | t0001 | g0018 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03669 | hp2 | a0004 | c0004 | t0001 | g0028 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0295 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03704 | hp1 | a0001 | c0020 | t0001 | g0176 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03704 | hp2 | a0018 | c0021 | t0001 | g0246 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03942 | hp1 | a0002 | c0002 | t0003 | g0289 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03942 | hp2 | a0001 | c0007 | t0001 | g0249 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0259 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04184 | hp1 | a0009 | c0012 | t0003 | g0274 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0297 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0294 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0199 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18906 | hp1 | a0003 | c0003 | t0005 | g0304 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18939 | hp2 | a0001 | c0001 | t0010 | g0202 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0178 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18965 | hp1 | a0001 | c0001 | t0010 | g0257 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19030 | hp1 | a0005 | c0005 | t0009 | g0270 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19059 | hp1 | a0019 | c0022 | t0002 | g0053 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19059 | hp2 | a0004 | c0004 | t0001 | g0179 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19076 | hp1 | a0020 | c0024 | t0001 | g0135 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19085 | hp2 | a0001 | c0001 | t0010 | g0229 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ASW | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ASW | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20905 | hp1 | a0009 | c0012 | t0003 | g0279 | SAS | GIH | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20905 | hp2 | a0001 | c0007 | t0001 | g0248 | SAS | GIH | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01123 | hp2 | a0002 | c0029 | t0013 | g0273 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02109 | hp1 | a0005 | c0005 | t0009 | g0269 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0031 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03471 | hp1 | a0003 | c0003 | t0005 | g0032 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0285 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0262 | REF | REF | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
homoSapiens | grch38p0 | a0010 | c0026 | t0012 | g0272 | REF | REF | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773665 | T | C | 13 | a0001 a0004 a0007 others(10): Show |
321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
missense_variant | MODERATE | c.47T>C | p.Ile16Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | 220/4477 | 47/2562 | 16/853 | chr8 | 55773665 | |||
chr8:55782786 | A | G | 1 | a0011 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.140A>G | p.Tyr47Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/13 | 313/4477 | 140/2562 | 47/853 | chr8 | 55782786 | |||
chr8:55785728 | C | T | 1 | a0020 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.176C>T | p.Ala59Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/13 | 349/4477 | 176/2562 | 59/853 | chr8 | 55785728 | |||
chr8:55785806 | G | A | 1 | a0012 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.254G>A | p.Ser85Asn | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/13 | 427/4477 | 254/2562 | 85/853 | chr8 | 55785806 | |||
chr8:55786265 | A | G | 1 | a0008 | 2 | HG02922.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.367A>G | p.Lys123Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 540/4477 | 367/2562 | 123/853 | chr8 | 55786265 | |||
chr8:55786356 | C | T | 1 | a0015 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.458C>T | p.Ala153Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 631/4477 | 458/2562 | 153/853 | chr8 | 55786356 | |||
chr8:55786376 | A | G | 3 | a0004 a0007 a0014 |
9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
missense_variant | MODERATE | c.478A>G | p.Ile160Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 651/4477 | 478/2562 | 160/853 | chr8 | 55786376 | |||
chr8:55786599 | A | G | 1 | a0009 | 2 | HG04184.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.701A>G | p.Lys234Arg | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 874/4477 | 701/2562 | 234/853 | chr8 | 55786599 | |||
chr8:55786698 | G | C | 1 | a0014 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.800G>C | p.Ser267Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 973/4477 | 800/2562 | 267/853 | chr8 | 55786698 | |||
chr8:55786793 | C | T | 1 | a0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.895C>T | p.Pro299Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1068/4477 | 895/2562 | 299/853 | chr8 | 55786793 | |||
chr8:55787001 | G | C | 1 | a0013 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1103G>C | p.Gly368Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1276/4477 | 1103/2562 | 368/853 | chr8 | 55787001 | |||
chr8:55787028 | C | T | 1 | a0007 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.1130C>T | p.Ser377Leu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1303/4477 | 1130/2562 | 377/853 | chr8 | 55787028 | |||
chr8:55790199 | G | A | 1 | a0016 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1180G>A | p.Gly394Arg | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/13 | 1353/4477 | 1180/2562 | 394/853 | chr8 | 55790199 | |||
chr8:55790239 | C | G | 1 | a0016 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1220C>G | p.Thr407Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/13 | 1393/4477 | 1220/2562 | 407/853 | chr8 | 55790239 | |||
chr8:55792721 | A | C | 1 | a0016 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1304A>C | p.Asn435Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/13 | 1477/4477 | 1304/2562 | 435/853 | chr8 | 55792721 | |||
chr8:55796142 | T | C | 7 | a0002 a0003 a0005 others(4): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
missense_variant | MODERATE | c.1532T>C | p.Ile511Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1705/4477 | 1532/2562 | 511/853 | chr8 | 55796142 | |||
chr8:55799097 | G | A | 1 | a0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.1726G>A | p.Val576Ile | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1899/4477 | 1726/2562 | 576/853 | chr8 | 55799097 | |||
chr8:55799112 | G | A | 1 | a0017 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1741G>A | p.Glu581Lys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1914/4477 | 1741/2562 | 581/853 | chr8 | 55799112 | |||
chr8:55799154 | A | G | 4 | a0002 a0006 a0009 others(1): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
missense_variant | MODERATE | c.1783A>G | p.Thr595Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1956/4477 | 1783/2562 | 595/853 | chr8 | 55799154 | |||
chr8:55802576 | C | T | 1 | a0019 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.1969C>T | p.Arg657Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/13 | 2142/4477 | 1969/2562 | 657/853 | chr8 | 55802576 | |||
chr8:55804956 | C | T | 1 | a0018 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.2063C>T | p.Ser688Phe | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/13 | 2236/4477 | 2063/2562 | 688/853 | chr8 | 55804956 | |||
chr8:55810998 | T | G | 7 | a0002 a0003 a0005 others(4): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
missense_variant | MODERATE | c.2261T>G | p.Phe754Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/13 | 2434/4477 | 2261/2562 | 754/853 | chr8 | 55810998 | |||
chr8:55813044 | G | A | 1 | a0006 | 4 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.2365G>A | p.Glu789Lys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/13 | 2538/4477 | 2365/2562 | 789/853 | chr8 | 55813044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55786345 | C | T | 1 | a0002c0029 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.447C>T | p.Asp149Asp | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 620/4477 | 447/2562 | 149/853 | chr8 | 55786345 | |||
chr8:55786555 | G | A | 1 | a0001c0014 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.657G>A | p.Pro219Pro | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 830/4477 | 657/2562 | 219/853 | chr8 | 55786555 | |||
chr8:55786564 | A | C | 1 | a0001c0009 | 2 | HG02698.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.666A>C | p.Ala222Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 839/4477 | 666/2562 | 222/853 | chr8 | 55786564 | |||
chr8:55786978 | C | T | 1 | a0002c0027 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1080C>T | p.Ser360Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1253/4477 | 1080/2562 | 360/853 | chr8 | 55786978 | |||
chr8:55786990 | A | G | 1 | a0001c0007 | 3 | HG03942.hp2 HG04115.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.1092A>G | p.Glu364Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1265/4477 | 1092/2562 | 364/853 | chr8 | 55786990 | |||
chr8:55787014 | G | A | 1 | a0001c0016 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1116G>A | p.Glu372Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1289/4477 | 1116/2562 | 372/853 | chr8 | 55787014 | |||
chr8:55787029 | G | A | 1 | a0001c0017 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1131G>A | p.Ser377Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1304/4477 | 1131/2562 | 377/853 | chr8 | 55787029 | |||
chr8:55796011 | G | A | 1 | a0003c0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
synonymous_variant | LOW | c.1401G>A | p.Gln467Gln | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1574/4477 | 1401/2562 | 467/853 | chr8 | 55796011 | |||
chr8:55796023 | A | G | 1 | a0001c0008 | 2 | HG00738.hp1 HG01433.hp2 |
synonymous_variant | LOW | c.1413A>G | p.Leu471Leu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1586/4477 | 1413/2562 | 471/853 | chr8 | 55796023 | |||
chr8:55813079 | T | C | 1 | a0001c0020 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2400T>C | p.Asn800Asn | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/13 | 2573/4477 | 2400/2562 | 800/853 | chr8 | 55813079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773476 | C | T | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(32): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-143C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | chr8 | 55773476 | |||||||
chr8:55773495 | C | A | 1 | a0001c0001t0014 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | 124 | chr8 | 55773495 | ||||||
chr8:55824817 | G | T | 1 | a0001c0001t0010 | 3 | NA18939.hp2 NA18965.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 114 | chr8 | 55824817 | ||||||
chr8:55824865 | G | A | 2 | a0001c0001t0008 a0001c0001t0014 |
5 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*162G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 162 | chr8 | 55824865 | ||||||
chr8:55825003 | G | A | 1 | a0001c0001t0015 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 300 | chr8 | 55825003 | ||||||
chr8:55825042 | C | T | 1 | a0003c0003t0005 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 339 | chr8 | 55825042 | ||||||
chr8:55825081 | C | T | 1 | a0001c0001t0018 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 378 | chr8 | 55825081 | ||||||
chr8:55825425 | A | C | 2 | a0001c0001t0006 a0001c0016t0006 |
7 | HG02523.hp2 NA18946.hp2 NA18950.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*722A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 722 | chr8 | 55825425 | ||||||
chr8:55825680 | A | G | 1 | a0001c0001t0017 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 977 | chr8 | 55825680 | ||||||
chr8:55825697 | A | G | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(24): Show |
253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*994A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 994 | chr8 | 55825697 | ||||||
chr8:55825775 | GCAA | G | 1 | a0001c0001t0007 | 5 | HG02559.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074_*1076delAAC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1074 | INFO_REALIGN_3_PRIME | chr8 | 55825775 | |||||
chr8:55825874 | C | CT | 8 | a0001c0001t0011 a0002c0002t0003 a0002c0027t0003 others(5): Show |
40 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1185dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1186 | INFO_REALIGN_3_PRIME | chr8 | 55825874 | |||||
chr8:55825892 | CAG | C | 2 | a0001c0001t0004 a0001c0001t0007 |
18 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1192_*1193delAG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1192 | INFO_REALIGN_3_PRIME | chr8 | 55825892 | |||||
chr8:55826127 | G | A | 1 | a0002c0029t0013 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1424 | chr8 | 55826127 | ||||||
chr8:55826198 | G | T | 1 | a0008c0011t0016 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1495G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1495 | chr8 | 55826198 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773749 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+30C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773749 | |||||||
chr8:55773764 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+45C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773764 | |||||||
chr8:55773971 | A | G | 1 | a0002c0002t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101+252A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773971 | |||||||
chr8:55774005 | G | T | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+286G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774005 | |||||||
chr8:55774080 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.101+361C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774080 | |||||||
chr8:55774115 | A | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+396A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774115 | |||||||
chr8:55774253 | G | A | 1 | a0001c0016t0006g0035 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101+534G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774253 | |||||||
chr8:55774319 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.101+600G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774319 | |||||||
chr8:55774320 | C | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+601C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774320 | |||||||
chr8:55774356 | A | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+637A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774356 | |||||||
chr8:55774579 | G | A | 1 | a0002c0002t0003g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.101+860G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774579 | |||||||
chr8:55774586 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+867G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774586 | |||||||
chr8:55774615 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
320 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.101+896G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774615 | |||||||
chr8:55774708 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
319 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.101+989A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774708 | |||||||
chr8:55774790 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+1071A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774790 | |||||||
chr8:55774801 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+1082T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774801 | |||||||
chr8:55774977 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
5 | HG00408.hp1 HG02165.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1258C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774977 | |||||||
chr8:55775016 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+1297G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775016 | |||||||
chr8:55775038 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
320 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.101+1319C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775038 | |||||||
chr8:55775039 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.101+1320C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775039 | |||||||
chr8:55775091 | A | T | 1 | a0001c0001t0002g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.101+1372A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775091 | |||||||
chr8:55775101 | A | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
320 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.101+1382A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775101 | |||||||
chr8:55775152 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.101+1433G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775152 | |||||||
chr8:55775155 | T | G | 17 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0050 others(14): Show |
23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.101+1436T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775155 | |||||||
chr8:55775240 | GA | G | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(120): Show |
149 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.101+1532delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775240 | ||||||
chr8:55775246 | AAAAAAG | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
170 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.101+1532_101+1537d others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775246 | ||||||
chr8:55775328 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
329 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.101+1609C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775328 | |||||||
chr8:55775510 | GAGAA | G | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1803_101+1806d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775510 | ||||||
chr8:55775667 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
169 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.101+1948G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775667 | |||||||
chr8:55775900 | C | T | 1 | a0005c0005t0009g0300 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.101+2181C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775900 | |||||||
chr8:55775962 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2243G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775962 | |||||||
chr8:55776026 | G | T | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.101+2307G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776026 | |||||||
chr8:55776030 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.101+2311A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776030 | |||||||
chr8:55776102 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0260 |
3 | HG01081.hp1 HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.101+2383C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776102 | |||||||
chr8:55776173 | A | G | 11 | a0002c0002t0003g0289 a0002c0002t0003g0290 a0002c0002t0003g0291 others(8): Show |
11 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+2454A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776173 | |||||||
chr8:55776250 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+2531C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776250 | |||||||
chr8:55776277 | C | CT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0028 others(36): Show |
43 | HG00423.hp2 HG02056.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.101+2579dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | ||||||
chr8:55776277 | C | CTT | 6 | a0003c0003t0005g0032 a0003c0003t0005g0303 a0003c0003t0005g0304 others(3): Show |
7 | HG02257.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2578_101+2579d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | ||||||
chr8:55776277 | CT | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0140 others(9): Show |
12 | HG01516.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2579delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | ||||||
chr8:55776358 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | NA18950.hp2 NA18957.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+2639G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776358 | |||||||
chr8:55776362 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.101+2643G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776362 | |||||||
chr8:55776371 | C | G | 45 | a0001c0001t0001g0124 a0002c0002t0003g0031 a0002c0002t0003g0037 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.101+2652C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776371 | |||||||
chr8:55776381 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.101+2662C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776381 | |||||||
chr8:55776382 | G | A | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+2663G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776382 | |||||||
chr8:55776400 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+2681C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776400 | |||||||
chr8:55776463 | A | G | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.101+2744A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776463 | |||||||
chr8:55776610 | G | C | 1 | a0002c0002t0003g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.101+2891G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776610 | |||||||
chr8:55776675 | A | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.101+2956A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776675 | |||||||
chr8:55776675 | A | G | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.101+2956A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776675 | |||||||
chr8:55776735 | T | C | 1 | a0001c0001t0017g0056 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.101+3016T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776735 | |||||||
chr8:55776768 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.101+3049A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776768 | |||||||
chr8:55776794 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
79 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.101+3075T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776794 | |||||||
chr8:55776799 | A | C | 1 | a0001c0001t0002g0102 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+3080A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776799 | |||||||
chr8:55776873 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+3154T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776873 | |||||||
chr8:55776967 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.101+3248C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776967 | |||||||
chr8:55776980 | G | C | 1 | a0002c0029t0013g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.101+3261G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776980 | |||||||
chr8:55777135 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(17): Show |
21 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+3416A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777135 | |||||||
chr8:55777289 | GT | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.101+3585delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777289 | ||||||
chr8:55777361 | G | A | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.101+3642G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777361 | |||||||
chr8:55777368 | C | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+3649C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777368 | |||||||
chr8:55777609 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+3890G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777609 | |||||||
chr8:55777662 | C | T | 1 | a0001c0001t0004g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.101+3943C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777662 | |||||||
chr8:55777700 | C | T | 1 | a0002c0002t0003g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.101+3981C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777700 | |||||||
chr8:55777902 | AT | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.101+4197delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777902 | ||||||
chr8:55777902 | ATT | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
54 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.101+4196_101+4197d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777902 | ||||||
chr8:55777904 | T | A | 47 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0002c0002t0003g0031 others(44): Show |
51 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.101+4185T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777904 | |||||||
chr8:55777905 | T | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
96 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.101+4186T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777905 | |||||||
chr8:55777906 | T | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
54 | HG00438.hp2 HG00673.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.101+4187T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777906 | |||||||
chr8:55778101 | A | T | 1 | a0001c0001t0007g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101+4382A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778101 | |||||||
chr8:55778230 | G | A | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+4511G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778230 | |||||||
chr8:55778273 | TA | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-4467delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55778273 | ||||||
chr8:55778351 | A | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-4397A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778351 | |||||||
chr8:55778471 | C | T | 1 | a0017c0019t0001g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.102-4277C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778471 | |||||||
chr8:55778557 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG01978.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.102-4191T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778557 | |||||||
chr8:55778567 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.102-4181T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778567 | |||||||
chr8:55778593 | A | G | 1 | a0001c0001t0002g0101 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.102-4155A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778593 | |||||||
chr8:55778843 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.102-3905T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778843 | |||||||
chr8:55778874 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.102-3874C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778874 | |||||||
chr8:55778904 | A | G | 6 | a0001c0001t0001g0188 a0001c0001t0006g0024 a0001c0001t0006g0186 others(3): Show |
7 | HG02523.hp2 NA18946.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-3844A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778904 | |||||||
chr8:55779018 | C | T | 2 | a0001c0007t0001g0248 a0001c0007t0001g0249 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.102-3730C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779018 | |||||||
chr8:55779197 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102-3551A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779197 | |||||||
chr8:55779578 | G | C | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-3170G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779578 | |||||||
chr8:55779605 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.102-3143C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779605 | |||||||
chr8:55779875 | CT | C | 48 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(45): Show |
52 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-2860delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55779875 | ||||||
chr8:55780045 | C | T | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-2703C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780045 | |||||||
chr8:55780160 | C | CT | 35 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(32): Show |
38 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.102-2573dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780160 | ||||||
chr8:55780160 | CT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.102-2573delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780160 | ||||||
chr8:55780175 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.102-2573T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780175 | |||||||
chr8:55780175 | T | TTC | 15 | a0002c0002t0003g0282 a0002c0002t0003g0283 a0002c0002t0003g0284 others(12): Show |
15 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.102-2573_102-2572i others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780175 | |||||||
chr8:55780176 | C | CT | 21 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0055 others(18): Show |
25 | HG00673.hp2 HG01109.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-2561dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780176 | ||||||
chr8:55780176 | C | T | 17 | a0001c0001t0001g0183 a0002c0002t0003g0282 a0002c0002t0003g0283 others(14): Show |
17 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-2572C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780176 | |||||||
chr8:55780379 | C | A | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-2369C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780379 | |||||||
chr8:55780492 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00621.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.102-2256C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780492 | |||||||
chr8:55780499 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.102-2249C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780499 | |||||||
chr8:55780657 | C | A | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.102-2091C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780657 | |||||||
chr8:55780663 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-2085A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780663 | |||||||
chr8:55780769 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.102-1979T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780769 | |||||||
chr8:55780906 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102-1842G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780906 | |||||||
chr8:55780973 | GT | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0147 |
3 | HG00639.hp1 HG01070.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.102-1772delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780973 | ||||||
chr8:55781090 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102-1658C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781090 | |||||||
chr8:55781148 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.102-1600C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781148 | |||||||
chr8:55781164 | T | A | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-1584T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781164 | |||||||
chr8:55781370 | C | A | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-1378C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781370 | |||||||
chr8:55781423 | ATAAG | A | 2 | a0002c0002t0003g0031 a0002c0002t0003g0275 |
3 | HG02486.hp1 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.102-1321_102-1318d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55781423 | ||||||
chr8:55781518 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.102-1230G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781518 | |||||||
chr8:55781521 | C | T | 1 | a0017c0019t0001g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.102-1227C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781521 | |||||||
chr8:55781609 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-1139C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781609 | |||||||
chr8:55781847 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-901G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781847 | |||||||
chr8:55781856 | G | A | 3 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0300 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.102-892G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781856 | |||||||
chr8:55782079 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.102-669C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782079 | |||||||
chr8:55782146 | CTTTA | C | 56 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-554_102-551del others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782146 | CTTTATTT others(1): Show |
C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
197 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.102-558_102-551del others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782146 | CTTTATTT others(5): Show |
C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG02109.hp2 HG02965.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-562_102-551del others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782146 | CTTTATTT others(9): Show |
C | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-566_102-551del others(16): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782146 | CTTTATTT others(13): Show |
C | 1 | a0001c0001t0001g0254 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.102-570_102-551del others(20): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782146 | CTTTATTT others(17): Show |
C | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-574_102-551del others(24): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | ||||||
chr8:55782149 | T | A | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG02976.hp1 NA18944.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.102-599T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782149 | |||||||
chr8:55782151 | T | A | 1 | a0001c0001t0002g0069 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.102-597T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782151 | |||||||
chr8:55782153 | T | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
47 | HG00438.hp2 HG00673.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.102-595T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782153 | |||||||
chr8:55782157 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
191 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.102-591T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782157 | |||||||
chr8:55782161 | T | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0050 others(2): Show |
6 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-587T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782161 | |||||||
chr8:55782165 | T | A | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-583T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782165 | |||||||
chr8:55782169 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.102-579T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782169 | |||||||
chr8:55782173 | T | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-575T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782173 | |||||||
chr8:55782221 | G | A | 1 | a0001c0014t0001g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.102-527G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782221 | |||||||
chr8:55782222 | C | T | 1 | a0002c0002t0003g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.102-526C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782222 | |||||||
chr8:55782295 | C | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-453C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782295 | |||||||
chr8:55782298 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-450C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782298 | |||||||
chr8:55782312 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02027.hp1 NA18966.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-436G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782312 | |||||||
chr8:55782338 | C | T | 1 | a0001c0007t0001g0259 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102-410C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782338 | |||||||
chr8:55782610 | G | A | 3 | a0002c0002t0003g0290 a0002c0002t0003g0291 a0002c0027t0003g0292 |
3 | HG00639.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.102-138G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782610 | |||||||
chr8:55782707 | C | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-41C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782707 | |||||||
chr8:55782743 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0185 |
2 | HG04115.hp1 HG04228.hp1 |
splice_region_variant&intron_variant | LOW | c.102-5C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782743 | |||||||
chr8:55783215 | A | T | 1 | a0001c0001t0010g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166+403A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783215 | |||||||
chr8:55783216 | C | G | 1 | a0001c0001t0010g0229 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166+404C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783216 | |||||||
chr8:55783454 | T | G | 1 | a0001c0001t0001g0025 | 2 | NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.166+642T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783454 | |||||||
chr8:55783572 | A | G | 1 | a0001c0008t0001g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.166+760A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783572 | |||||||
chr8:55783825 | T | G | 1 | a0001c0001t0008g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.166+1013T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783825 | |||||||
chr8:55784036 | C | T | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
97 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.166+1224C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784036 | |||||||
chr8:55784096 | C | A | 3 | a0002c0002t0003g0276 a0006c0006t0003g0015 a0006c0006t0003g0286 |
5 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+1284C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784096 | |||||||
chr8:55784137 | A | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.166+1325A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784137 | |||||||
chr8:55784167 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.166+1355G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784167 | |||||||
chr8:55784343 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.167-1376T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784343 | |||||||
chr8:55784630 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.167-1089A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784630 | |||||||
chr8:55784997 | C | T | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.167-722C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784997 | |||||||
chr8:55785058 | G | GT | 4 | a0002c0002t0003g0289 a0002c0002t0003g0297 a0006c0006t0003g0286 others(1): Show |
4 | HG02145.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-655dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785058 | ||||||
chr8:55785065 | G | T | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-654G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785065 | |||||||
chr8:55785071 | TG | T | 8 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(5): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.167-647delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785071 | |||||||
chr8:55785072 | G | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.167-647G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785072 | |||||||
chr8:55785138 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.167-581C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785138 | |||||||
chr8:55785244 | CG | C | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.167-472delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785244 | ||||||
chr8:55785365 | T | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.167-354T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785365 | |||||||
chr8:55785371 | TTTTG | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0190 others(3): Show |
7 | HG03669.hp2 NA18944.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-336_167-333del others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785371 | ||||||
chr8:55785379 | G | T | 1 | a0005c0005t0009g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.167-340G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785379 | |||||||
chr8:55785416 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.167-303C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785416 | |||||||
chr8:55785452 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02129.hp1 NA18986.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-267C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785452 | |||||||
chr8:55785480 | G | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.167-239G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785480 | |||||||
chr8:55785490 | G | A | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.167-229G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785490 | |||||||
chr8:55785515 | T | C | 1 | a0002c0002t0003g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.167-204T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785515 | |||||||
chr8:55785929 | G | A | 2 | a0001c0007t0001g0248 a0001c0007t0001g0259 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.339+38G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/12 | chr8 | 55785929 | |||||||
chr8:55787087 | C | A | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+27C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787087 | |||||||
chr8:55787222 | C | A | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1162+162C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787222 | |||||||
chr8:55787231 | TTAA | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+175_1162+177d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55787231 | ||||||
chr8:55787302 | A | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+242A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787302 | |||||||
chr8:55787423 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1162+363G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787423 | |||||||
chr8:55787434 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162+374A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787434 | |||||||
chr8:55787605 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+545G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787605 | |||||||
chr8:55787626 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1162+566C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787626 | |||||||
chr8:55787769 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162+709C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787769 | |||||||
chr8:55787891 | G | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+831G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787891 | |||||||
chr8:55787894 | C | A | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+834C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787894 | |||||||
chr8:55787895 | A | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+835A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787895 | |||||||
chr8:55787896 | A | C | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+836A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787896 | |||||||
chr8:55787897 | G | A | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+837G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787897 | |||||||
chr8:55787909 | A | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+849A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787909 | |||||||
chr8:55787981 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1162+921G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787981 | |||||||
chr8:55788114 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1162+1054G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788114 | |||||||
chr8:55788151 | A | T | 3 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0300 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1162+1091A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788151 | |||||||
chr8:55788235 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1162+1175C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788235 | |||||||
chr8:55788278 | TAAC | T | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1162+1221_1162+122 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788278 | ||||||
chr8:55788353 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1162+1293G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788353 | |||||||
chr8:55788376 | A | C | 16 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
22 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1162+1316A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788376 | |||||||
chr8:55788399 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1162+1339G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788399 | |||||||
chr8:55788454 | C | CTTT | 27 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(24): Show |
28 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1162+1411_1162+141 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788454 | ||||||
chr8:55788454 | CT | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
207 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1162+1413delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788454 | ||||||
chr8:55788548 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1162+1488G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788548 | |||||||
chr8:55788607 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162+1547C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788607 | |||||||
chr8:55788664 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1163-1518G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788664 | |||||||
chr8:55788710 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1163-1472C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788710 | |||||||
chr8:55788790 | T | C | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163-1392T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788790 | |||||||
chr8:55788889 | A | T | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1163-1293A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788889 | |||||||
chr8:55788943 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-1239G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788943 | |||||||
chr8:55789061 | T | G | 1 | a0001c0001t0001g0039 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1163-1121T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789061 | |||||||
chr8:55789263 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0020t0001g0176 |
3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1163-919A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789263 | |||||||
chr8:55789332 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1163-850T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789332 | |||||||
chr8:55789423 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1163-759C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789423 | |||||||
chr8:55789424 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-758G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789424 | |||||||
chr8:55789500 | A | G | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1163-682A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789500 | |||||||
chr8:55789592 | C | G | 1 | a0012c0013t0001g0173 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1163-590C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789592 | |||||||
chr8:55789666 | G | A | 3 | a0001c0001t0010g0202 a0001c0001t0010g0229 a0001c0001t0010g0257 |
3 | NA18939.hp2 NA18965.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1163-516G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789666 | |||||||
chr8:55789993 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1163-189A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789993 | |||||||
chr8:55790000 | A | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-182A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55790000 | |||||||
chr8:55790007 | T | A | 1 | a0020c0024t0001g0135 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1163-175T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55790007 | |||||||
chr8:55790470 | C | T | 1 | a0014c0023t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1280+171C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790470 | |||||||
chr8:55790504 | CT | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.1280+220delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790504 | ||||||
chr8:55790588 | A | C | 1 | a0020c0024t0001g0135 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280+289A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790588 | |||||||
chr8:55790597 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1280+298C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790597 | |||||||
chr8:55790682 | A | C | 1 | a0020c0024t0001g0135 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280+383A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790682 | |||||||
chr8:55790706 | A | G | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+407A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790706 | |||||||
chr8:55790708 | A | G | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280+409A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790708 | |||||||
chr8:55790716 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1280+417G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790716 | |||||||
chr8:55790733 | G | A | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+434G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790733 | |||||||
chr8:55790750 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(43): Show |
57 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1280+451C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790750 | |||||||
chr8:55790760 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1280+461C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790760 | |||||||
chr8:55790803 | G | A | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1280+504G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790803 | |||||||
chr8:55790966 | T | TTC | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1280+688_1280+689d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | ||||||
chr8:55790966 | T | TTCTC | 26 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0057 others(23): Show |
33 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1280+686_1280+689d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | ||||||
chr8:55790966 | T | TTCTCTC | 21 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(18): Show |
22 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1280+684_1280+689d others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | ||||||
chr8:55790966 | TTCTC | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.1280+686_1280+689d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | ||||||
chr8:55790966 | TTCTCTCT others(1): Show |
T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280+682_1280+689d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | ||||||
chr8:55791055 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1280+756C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791055 | |||||||
chr8:55791319 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280+1020G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791319 | |||||||
chr8:55791525 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1281-1173T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791525 | |||||||
chr8:55791618 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1281-1080C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791618 | |||||||
chr8:55791766 | T | C | 35 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(32): Show |
38 | HG00140.hp1 HG00639.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1281-932T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791766 | |||||||
chr8:55791790 | A | C | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-908A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791790 | |||||||
chr8:55791792 | A | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-906A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791792 | |||||||
chr8:55791848 | T | C | 14 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0004g0004 others(11): Show |
20 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1281-850T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791848 | |||||||
chr8:55791861 | G | A | 3 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0300 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1281-837G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791861 | |||||||
chr8:55791930 | A | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1281-768A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791930 | |||||||
chr8:55791953 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1281-745A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791953 | |||||||
chr8:55791980 | A | T | 3 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 |
3 | HG01192.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1281-718A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791980 | |||||||
chr8:55791996 | G | A | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1281-702G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791996 | |||||||
chr8:55792000 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1281-698A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792000 | |||||||
chr8:55792027 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1281-671T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792027 | |||||||
chr8:55792089 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1281-609A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792089 | |||||||
chr8:55792102 | G | A | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1281-596G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792102 | |||||||
chr8:55792105 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1281-593C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792105 | |||||||
chr8:55792106 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281-592G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792106 | |||||||
chr8:55792244 | G | C | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-454G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792244 | |||||||
chr8:55792364 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0206 a0001c0001t0001g0207 others(4): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281-334G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792364 | |||||||
chr8:55792439 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1281-259C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792439 | |||||||
chr8:55792593 | G | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-105G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792593 | |||||||
chr8:55792632 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1281-66A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792632 | |||||||
chr8:55792879 | G | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1367+95G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55792879 | |||||||
chr8:55792893 | T | A | 6 | a0001c0001t0002g0017 a0001c0001t0002g0077 a0001c0001t0002g0078 others(3): Show |
7 | HG01081.hp2 HG01358.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+109T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55792893 | |||||||
chr8:55793017 | C | G | 5 | a0005c0005t0002g0299 a0005c0005t0009g0268 a0005c0005t0009g0269 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+233C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793017 | |||||||
chr8:55793103 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1367+319C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793103 | |||||||
chr8:55793169 | A | G | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+385A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793169 | |||||||
chr8:55793259 | A | G | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367+475A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793259 | |||||||
chr8:55793416 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+632C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793416 | |||||||
chr8:55793458 | C | T | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+674C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793458 | |||||||
chr8:55793495 | A | G | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+711A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793495 | |||||||
chr8:55793535 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1367+751T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793535 | |||||||
chr8:55793556 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1367+772A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793556 | |||||||
chr8:55793579 | GT | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+801delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793579 | ||||||
chr8:55793653 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1367+869C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793653 | |||||||
chr8:55793694 | A | G | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+910A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793694 | |||||||
chr8:55793722 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367+938C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793722 | |||||||
chr8:55793733 | A | AATTT | 26 | a0001c0001t0001g0034 a0001c0001t0001g0105 a0001c0001t0001g0106 others(23): Show |
27 | HG01243.hp2 HG02071.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1367+990_1367+993d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | ||||||
chr8:55793733 | AATTT | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0113 others(41): Show |
50 | HG00639.hp2 HG00741.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1367+990_1367+993d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | ||||||
chr8:55793733 | AATTTATT others(1): Show |
A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0057 others(5): Show |
8 | HG00642.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+986_1367+993d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | ||||||
chr8:55793733 | AATTTATT others(5): Show |
A | 23 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0060 others(20): Show |
30 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1367+982_1367+993d others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | ||||||
chr8:55793733 | AATTTATT others(9): Show |
A | 8 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(5): Show |
9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+978_1367+993d others(18): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | ||||||
chr8:55793762 | A | T | 1 | a0005c0005t0009g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1367+978A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793762 | |||||||
chr8:55793766 | A | T | 3 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0300 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1367+982A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793766 | |||||||
chr8:55793770 | A | T | 5 | a0005c0005t0002g0299 a0005c0005t0009g0268 a0005c0005t0009g0269 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+986A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793770 | |||||||
chr8:55793774 | A | T | 5 | a0005c0005t0002g0299 a0005c0005t0009g0268 a0005c0005t0009g0269 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+990A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793774 | |||||||
chr8:55793810 | G | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+1026G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793810 | |||||||
chr8:55793864 | C | T | 2 | a0001c0001t0008g0200 a0001c0001t0014g0203 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1367+1080C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793864 | |||||||
chr8:55793866 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+1082C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793866 | |||||||
chr8:55793919 | C | T | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367+1135C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793919 | |||||||
chr8:55793925 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1367+1141C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793925 | |||||||
chr8:55793928 | A | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1367+1144A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793928 | |||||||
chr8:55794006 | A | G | 16 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
22 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1367+1222A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794006 | |||||||
chr8:55794070 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+1286G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794070 | |||||||
chr8:55794175 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1367+1391T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794175 | |||||||
chr8:55794213 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367+1429T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794213 | |||||||
chr8:55794390 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1368-1588A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794390 | |||||||
chr8:55794426 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1368-1552C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794426 | |||||||
chr8:55794435 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
204 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1368-1543G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794435 | |||||||
chr8:55794542 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1368-1436T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794542 | |||||||
chr8:55794644 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1368-1334T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794644 | |||||||
chr8:55794796 | C | T | 1 | a0002c0002t0003g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1368-1182C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794796 | |||||||
chr8:55794864 | T | C | 1 | a0002c0002t0003g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1368-1114T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794864 | |||||||
chr8:55794872 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1368-1106A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794872 | |||||||
chr8:55794915 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1368-1063A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794915 | |||||||
chr8:55795102 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1368-876G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795102 | |||||||
chr8:55795209 | C | A | 1 | a0014c0023t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-769C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795209 | |||||||
chr8:55795245 | T | C | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1368-733T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795245 | |||||||
chr8:55795530 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0002g0263 a0011c0025t0002g0089 |
3 | HG00597.hp1 HG02027.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1368-448T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795530 | |||||||
chr8:55795612 | A | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1368-366A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795612 | |||||||
chr8:55795672 | CGTTT | C | 4 | a0001c0001t0010g0202 a0001c0001t0010g0229 a0001c0001t0010g0257 others(1): Show |
4 | HG01123.hp2 NA18939.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-289_1368-286d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55795672 | ||||||
chr8:55795824 | G | C | 1 | a0002c0002t0003g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1368-154G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795824 | |||||||
chr8:55795970 | T | TG | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1368-7dupG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55795970 | ||||||
chr8:55796345 | G | A | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+193G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796345 | |||||||
chr8:55796374 | G | A | 3 | a0001c0001t0004g0004 a0001c0001t0004g0040 a0001c0001t0004g0047 |
6 | HG00323.hp1 HG01255.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542+222G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796374 | |||||||
chr8:55796476 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1542+324G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796476 | |||||||
chr8:55796523 | T | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(36): Show |
47 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1542+371T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796523 | |||||||
chr8:55796526 | T | C | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+374T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796526 | |||||||
chr8:55796577 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1542+425A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796577 | |||||||
chr8:55796603 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0256 |
2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1542+451G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796603 | |||||||
chr8:55796642 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+490C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796642 | |||||||
chr8:55796656 | T | C | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1542+504T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796656 | |||||||
chr8:55796712 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+560C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796712 | |||||||
chr8:55796731 | C | G | 1 | a0002c0002t0003g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1542+579C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796731 | |||||||
chr8:55796884 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1542+732G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796884 | |||||||
chr8:55796943 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1542+791A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796943 | |||||||
chr8:55797012 | A | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1542+860A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797012 | |||||||
chr8:55797058 | G | C | 11 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(8): Show |
14 | HG01123.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1542+906G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797058 | |||||||
chr8:55797339 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1542+1187C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797339 | |||||||
chr8:55797571 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-1343G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797571 | |||||||
chr8:55797616 | G | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1543-1298G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797616 | |||||||
chr8:55797789 | A | T | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-1125A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797789 | |||||||
chr8:55797977 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1543-937C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797977 | |||||||
chr8:55798069 | A | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1543-845A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798069 | |||||||
chr8:55798122 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-792A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798122 | |||||||
chr8:55798219 | C | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1543-695C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798219 | |||||||
chr8:55798426 | C | T | 3 | a0003c0003t0005g0032 a0003c0003t0005g0306 a0003c0003t0005g0307 |
4 | HG02257.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-488C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798426 | |||||||
chr8:55798468 | G | A | 1 | a0007c0010t0001g0033 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1543-446G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798468 | |||||||
chr8:55798502 | A | G | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1543-412A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798502 | |||||||
chr8:55798708 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
180 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1543-206A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798708 | |||||||
chr8:55798777 | CT | C | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-135delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 55798777 | ||||||
chr8:55798822 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1543-92G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798822 | |||||||
chr8:55798890 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0054 others(24): Show |
31 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1543-24C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798890 | |||||||
chr8:55799454 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0001g0158 others(1): Show |
5 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849+234G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799454 | |||||||
chr8:55799457 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1849+237G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799457 | |||||||
chr8:55799662 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1849+442T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799662 | |||||||
chr8:55799672 | G | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1849+452G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799672 | |||||||
chr8:55799813 | G | A | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1849+593G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799813 | |||||||
chr8:55799842 | G | A | 1 | a0003c0003t0005g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1849+622G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799842 | |||||||
chr8:55799885 | T | A | 1 | a0001c0001t0002g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1849+665T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799885 | |||||||
chr8:55799954 | T | C | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1849+734T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799954 | |||||||
chr8:55799955 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849+735A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799955 | |||||||
chr8:55800174 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1849+954T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800174 | |||||||
chr8:55800235 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1849+1015A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800235 | |||||||
chr8:55800275 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0001g0158 |
4 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849+1055G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800275 | |||||||
chr8:55800282 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1849+1062A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800282 | |||||||
chr8:55800510 | A | G | 2 | a0001c0001t0002g0096 a0013c0015t0002g0301 |
2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1849+1290A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800510 | |||||||
chr8:55800617 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849+1397C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800617 | |||||||
chr8:55800686 | A | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849+1466A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800686 | |||||||
chr8:55801057 | A | G | 6 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0304 others(3): Show |
7 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1850-1400A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801057 | |||||||
chr8:55801134 | T | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1850-1323T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801134 | |||||||
chr8:55801241 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1850-1216A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801241 | |||||||
chr8:55801433 | G | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1850-1024G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801433 | |||||||
chr8:55801445 | AT | A | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1850-1003delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801445 | ||||||
chr8:55801449 | TTTTTTAG others(307): Show |
T | 1 | a0001c0001t0001g0019 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1850-990_1850-677d others(2): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801449 | ||||||
chr8:55801565 | C | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1850-892C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801565 | |||||||
chr8:55801581 | T | TC | 22 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(19): Show |
23 | HG00140.hp1 HG00741.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1850-875dupC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801581 | ||||||
chr8:55801582 | C | CCT | 7 | a0002c0002t0003g0276 a0002c0002t0003g0290 a0002c0002t0003g0291 others(4): Show |
9 | HG00639.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1850-875_1850-874i others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTT | 5 | a0002c0029t0013g0273 a0005c0005t0002g0299 a0005c0005t0009g0268 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850-875_1850-874i others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(15): Show |
1 | a0003c0003t0005g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1850-875_1850-874i others(24): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(18): Show |
1 | a0003c0003t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1850-875_1850-874i others(27): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(20): Show |
1 | a0003c0003t0005g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850-875_1850-874i others(29): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(21): Show |
2 | a0003c0003t0005g0032 a0003c0003t0005g0304 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1850-875_1850-874i others(30): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(23): Show |
2 | a0003c0003t0005g0302 a0003c0003t0005g0305 |
2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1850-875_1850-874i others(32): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CCTTTTTT others(25): Show |
1 | a0003c0003t0005g0306 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1850-875_1850-874i others(34): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | |||||||
chr8:55801582 | C | CT | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1850-851dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | ||||||
chr8:55801582 | C | CTT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1850-852_1850-851d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | ||||||
chr8:55801582 | C | CTTT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0115 others(21): Show |
24 | HG01175.hp1 HG01358.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1850-853_1850-851d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | ||||||
chr8:55801582 | CTTTTTTT others(3): Show |
C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1850-860_1850-851d others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | ||||||
chr8:55801583 | T | C | 1 | a0002c0002t0003g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1850-874T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801583 | |||||||
chr8:55801644 | A | G | 1 | a0002c0002t0003g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1850-813A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801644 | |||||||
chr8:55801674 | C | T | 19 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 others(16): Show |
20 | HG01109.hp1 HG01243.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1850-783C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801674 | |||||||
chr8:55801689 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0148 others(3): Show |
6 | HG01175.hp1 HG01358.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850-768C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801689 | |||||||
chr8:55801741 | A | G | 1 | a0001c0007t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1850-716A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801741 | |||||||
chr8:55801885 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1850-572T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801885 | |||||||
chr8:55802022 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1850-435G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802022 | |||||||
chr8:55802051 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1850-406G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802051 | |||||||
chr8:55802055 | G | A | 10 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(7): Show |
13 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1850-402G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802055 | |||||||
chr8:55802062 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1850-395C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802062 | |||||||
chr8:55802066 | C | T | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1850-391C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802066 | |||||||
chr8:55802125 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1850-332C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802125 | |||||||
chr8:55802233 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850-224G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802233 | |||||||
chr8:55802302 | T | C | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1850-155T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802302 | |||||||
chr8:55802412 | A | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0045 |
4 | HG01192.hp2 HG01261.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-45A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802412 | |||||||
chr8:55802624 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0147 a0001c0001t0001g0158 others(1): Show |
5 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999+18T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802624 | |||||||
chr8:55802666 | G | A | 1 | a0003c0003t0005g0303 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1999+60G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802666 | |||||||
chr8:55802737 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1999+131G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802737 | |||||||
chr8:55802913 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1999+307A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802913 | |||||||
chr8:55802918 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1999+312A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802918 | |||||||
chr8:55802941 | C | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1999+335C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802941 | |||||||
chr8:55802952 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1999+346C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802952 | |||||||
chr8:55802961 | GT | G | 32 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(29): Show |
35 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1999+365delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55802961 | ||||||
chr8:55803000 | C | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1999+394C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803000 | |||||||
chr8:55803001 | G | A | 1 | a0004c0004t0001g0178 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1999+395G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803001 | |||||||
chr8:55803068 | G | A | 1 | a0014c0023t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1999+462G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803068 | |||||||
chr8:55803124 | TGG | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1999+524_1999+525d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803124 | ||||||
chr8:55803130 | G | GGT | 46 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
53 | HG00673.hp2 HG01109.hp1 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.1999+543_1999+544d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803130 | ||||||
chr8:55803130 | G | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1999+524G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803130 | |||||||
chr8:55803132 | T | G | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1999+526T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803132 | |||||||
chr8:55803235 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1999+629A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803235 | |||||||
chr8:55803356 | C | G | 1 | a0001c0008t0001g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1999+750C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803356 | |||||||
chr8:55803414 | T | C | 3 | a0003c0003t0005g0032 a0003c0003t0005g0306 a0003c0003t0005g0307 |
4 | HG02257.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999+808T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803414 | |||||||
chr8:55803439 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1999+833A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803439 | |||||||
chr8:55803520 | G | C | 3 | a0002c0002t0003g0282 a0002c0002t0003g0283 a0002c0002t0003g0288 |
3 | HG02896.hp2 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1999+914G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803520 | |||||||
chr8:55803538 | G | A | 13 | a0001c0001t0001g0048 a0001c0001t0004g0004 a0001c0001t0004g0007 others(10): Show |
19 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1999+932G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803538 | |||||||
chr8:55803543 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1999+937A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803543 | |||||||
chr8:55803629 | A | T | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1999+1023A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803629 | |||||||
chr8:55803692 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0128 others(8): Show |
14 | HG02129.hp1 NA18945.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.1999+1097dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803692 | ||||||
chr8:55803692 | CT | C | 45 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1999+1097delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803692 | ||||||
chr8:55803809 | C | T | 1 | a0001c0001t0001g0014 | 3 | NA18971.hp2 NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2000-1084C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803809 | |||||||
chr8:55803872 | C | T | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2000-1021C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803872 | |||||||
chr8:55803931 | C | T | 1 | a0001c0001t0018g0245 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2000-962C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803931 | |||||||
chr8:55803932 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000-961G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803932 | |||||||
chr8:55803940 | C | G | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0074 |
3 | HG02071.hp1 HG02523.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2000-953C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803940 | |||||||
chr8:55804041 | A | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2000-852A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804041 | |||||||
chr8:55804372 | C | T | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000-521C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804372 | |||||||
chr8:55804401 | G | A | 2 | a0001c0001t0001g0188 a0001c0007t0001g0248 |
2 | NA19056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2000-492G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804401 | |||||||
chr8:55804529 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-364C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804529 | |||||||
chr8:55804654 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000-239A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804654 | |||||||
chr8:55804726 | A | G | 1 | a0003c0003t0005g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2000-167A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804726 | |||||||
chr8:55804776 | TA | T | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2000-112delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55804776 | ||||||
chr8:55804837 | G | T | 8 | a0002c0002t0003g0037 a0002c0002t0003g0271 a0002c0002t0003g0276 others(5): Show |
10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2000-56G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804837 | |||||||
chr8:55804876 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2000-17A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804876 | |||||||
chr8:55805088 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2143+52A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805088 | |||||||
chr8:55805171 | C | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+135C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805171 | |||||||
chr8:55805396 | C | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | NA18939.hp1 NA19072.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2143+360C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805396 | |||||||
chr8:55805462 | A | C | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143+426A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805462 | |||||||
chr8:55805683 | C | G | 3 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 |
3 | HG01192.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2143+647C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805683 | |||||||
chr8:55805775 | A | G | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+739A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805775 | |||||||
chr8:55805831 | G | A | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2143+795G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805831 | |||||||
chr8:55805881 | TA | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
181 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2143+868delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | ||||||
chr8:55805881 | TAA | T | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(19): Show |
22 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2143+867_2143+868d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | ||||||
chr8:55805881 | TAAAA | T | 8 | a0001c0001t0001g0057 a0003c0003t0005g0032 a0003c0003t0005g0302 others(5): Show |
9 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2143+865_2143+868d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | ||||||
chr8:55805881 | TAAAAA | T | 33 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(30): Show |
36 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2143+864_2143+868d others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | ||||||
chr8:55805903 | A | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2143+867A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805903 | |||||||
chr8:55805906 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+870T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805906 | |||||||
chr8:55805923 | G | A | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+887G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805923 | |||||||
chr8:55805961 | AGATGAGA others(1): Show |
A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0141 others(22): Show |
30 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2143+931_2143+938d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805961 | ||||||
chr8:55805962 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+926G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805962 | |||||||
chr8:55805997 | T | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+961T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805997 | |||||||
chr8:55806042 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1006G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806042 | |||||||
chr8:55806077 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2143+1041C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806077 | |||||||
chr8:55806114 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2143+1078A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806114 | |||||||
chr8:55806225 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2143+1189G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806225 | |||||||
chr8:55806356 | C | CA | 59 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0105 others(56): Show |
63 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2143+1341dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | ||||||
chr8:55806356 | C | CAA | 12 | a0001c0008t0001g0169 a0002c0002t0003g0280 a0002c0002t0003g0297 others(9): Show |
13 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.2143+1340_2143+134 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | ||||||
chr8:55806356 | CA | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
10 | HG01192.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.2143+1341delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | ||||||
chr8:55806385 | GA | G | 45 | a0001c0001t0002g0083 a0002c0002t0003g0031 a0002c0002t0003g0037 others(42): Show |
49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.2143+1360delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806385 | ||||||
chr8:55806640 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2143+1604A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806640 | |||||||
chr8:55806851 | T | C | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1815T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806851 | |||||||
chr8:55806871 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
169 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.2143+1835C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806871 | |||||||
chr8:55806899 | T | C | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143+1863T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806899 | |||||||
chr8:55806924 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2143+1888A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806924 | |||||||
chr8:55806936 | C | CT | 17 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0050 others(14): Show |
23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.2143+1909dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806936 | ||||||
chr8:55806937 | T | C | 1 | a0002c0002t0003g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2143+1901T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806937 | |||||||
chr8:55806951 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1915G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806951 | |||||||
chr8:55806959 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2143+1923A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806959 | |||||||
chr8:55807506 | G | GT | 40 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(37): Show |
48 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.2143+2483dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55807506 | ||||||
chr8:55807506 | G | GTT | 9 | a0001c0001t0001g0030 a0001c0001t0001g0184 a0001c0001t0001g0212 others(6): Show |
10 | HG00408.hp1 HG01978.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2143+2482_2143+248 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55807506 | ||||||
chr8:55807506 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2143+2470G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807506 | |||||||
chr8:55807770 | A | G | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+2734A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807770 | |||||||
chr8:55807874 | T | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0079 others(3): Show |
12 | HG01123.hp1 HG01975.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2143+2838T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807874 | |||||||
chr8:55808033 | C | G | 1 | a0002c0002t0003g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2144-2848C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808033 | |||||||
chr8:55808070 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2144-2811C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808070 | |||||||
chr8:55808143 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2144-2738A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808143 | |||||||
chr8:55808356 | A | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0234 a0001c0001t0001g0235 others(17): Show |
21 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2144-2525A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808356 | |||||||
chr8:55808394 | G | A | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-2487G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808394 | |||||||
chr8:55808470 | C | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-2411C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808470 | |||||||
chr8:55808511 | CT | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.2144-2355delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55808511 | ||||||
chr8:55808757 | A | G | 1 | a0002c0029t0013g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2144-2124A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808757 | |||||||
chr8:55808762 | G | A | 6 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0304 others(3): Show |
7 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2144-2119G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808762 | |||||||
chr8:55808921 | A | G | 2 | a0001c0001t0001g0247 a0001c0007t0001g0249 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2144-1960A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808921 | |||||||
chr8:55809038 | A | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2144-1843A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809038 | |||||||
chr8:55809056 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
204 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.2144-1825G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809056 | |||||||
chr8:55809128 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0020t0001g0176 |
3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2144-1753C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809128 | |||||||
chr8:55809194 | T | A | 1 | a0004c0004t0001g0179 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2144-1687T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809194 | |||||||
chr8:55809312 | C | G | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2144-1569C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809312 | |||||||
chr8:55809384 | C | T | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2144-1497C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809384 | |||||||
chr8:55809453 | A | AT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
181 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2144-1414dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55809453 | ||||||
chr8:55809491 | C | A | 1 | a0017c0019t0001g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2144-1390C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809491 | |||||||
chr8:55809497 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2144-1384G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809497 | |||||||
chr8:55809619 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2144-1262G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809619 | |||||||
chr8:55809666 | C | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0172 |
3 | HG00408.hp2 NA18987.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2144-1215C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809666 | |||||||
chr8:55809682 | G | A | 1 | a0002c0002t0003g0278 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2144-1199G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809682 | |||||||
chr8:55809725 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2144-1156G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809725 | |||||||
chr8:55809797 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-1084G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809797 | |||||||
chr8:55809879 | TATC | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2144-997_2144-995d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55809879 | ||||||
chr8:55809957 | AC | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0020t0001g0176 |
3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2144-923delC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809957 | |||||||
chr8:55810016 | A | G | 32 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(29): Show |
35 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2144-865A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810016 | |||||||
chr8:55810116 | A | G | 2 | a0001c0001t0006g0186 a0001c0001t0006g0187 |
2 | NA18950.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2144-765A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810116 | |||||||
chr8:55810132 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-749C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810132 | |||||||
chr8:55810166 | A | G | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2144-715A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810166 | |||||||
chr8:55810168 | A | G | 1 | a0001c0001t0004g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2144-713A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810168 | |||||||
chr8:55810301 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2144-580C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810301 | |||||||
chr8:55810316 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2144-565A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810316 | |||||||
chr8:55810332 | C | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-549C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810332 | |||||||
chr8:55810438 | A | G | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-443A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810438 | |||||||
chr8:55810448 | G | A | 17 | a0002c0002t0003g0282 a0002c0002t0003g0283 a0002c0002t0003g0284 others(14): Show |
17 | HG00639.hp2 HG00741.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2144-433G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810448 | |||||||
chr8:55810467 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2144-414G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810467 | |||||||
chr8:55810496 | T | A | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2144-385T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810496 | |||||||
chr8:55810547 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2144-334A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810547 | |||||||
chr8:55810719 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2144-162A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810719 | |||||||
chr8:55810818 | A | G | 5 | a0001c0001t0007g0041 a0001c0001t0007g0042 a0001c0001t0007g0043 others(2): Show |
5 | HG02559.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2144-63A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810818 | |||||||
chr8:55810825 | C | T | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-56C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810825 | |||||||
chr8:55811260 | C | T | 13 | a0001c0001t0001g0048 a0001c0001t0004g0004 a0001c0001t0004g0007 others(10): Show |
19 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.2360+163C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811260 | |||||||
chr8:55811261 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2360+164G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811261 | |||||||
chr8:55811561 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360+464A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811561 | |||||||
chr8:55811571 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2360+474C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811571 | |||||||
chr8:55811596 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2360+499C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811596 | |||||||
chr8:55811618 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360+521G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811618 | |||||||
chr8:55811775 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG01978.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2360+678G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811775 | |||||||
chr8:55811851 | G | A | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+754G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811851 | |||||||
chr8:55811905 | C | A | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2360+808C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811905 | |||||||
chr8:55812012 | C | T | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360+915C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812012 | |||||||
chr8:55812055 | T | C | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+958T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812055 | |||||||
chr8:55812066 | A | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+969A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812066 | |||||||
chr8:55812330 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2361-710C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812330 | |||||||
chr8:55812392 | G | A | 1 | a0001c0001t0017g0056 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2361-648G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812392 | |||||||
chr8:55812441 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2361-599T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812441 | |||||||
chr8:55812495 | C | CA | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(62): Show |
77 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2361-525dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | ||||||
chr8:55812495 | C | CAA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(78): Show |
94 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2361-526_2361-525d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | ||||||
chr8:55812495 | C | CAAA | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG00597.hp2 HG04184.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.2361-527_2361-525d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | ||||||
chr8:55812495 | CA | C | 19 | a0001c0001t0001g0059 a0001c0001t0001g0264 a0001c0001t0002g0084 others(16): Show |
19 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.2361-525delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | ||||||
chr8:55812640 | C | T | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2361-400C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812640 | |||||||
chr8:55812765 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2361-275C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812765 | |||||||
chr8:55812827 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0206 a0001c0001t0001g0207 others(4): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2361-213C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812827 | |||||||
chr8:55812876 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0117 |
2 | HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2361-164A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812876 | |||||||
chr8:55813011 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2361-29T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55813011 | |||||||
chr8:55813146 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2439+28A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813146 | |||||||
chr8:55813159 | A | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+41A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813159 | |||||||
chr8:55813160 | C | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+42C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813160 | |||||||
chr8:55813192 | A | T | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+74A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813192 | |||||||
chr8:55813245 | A | C | 1 | a0001c0020t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2439+127A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813245 | |||||||
chr8:55813302 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2439+184A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813302 | |||||||
chr8:55813354 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2439+236C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813354 | |||||||
chr8:55813424 | T | G | 6 | a0001c0001t0001g0192 a0001c0001t0008g0195 a0001c0001t0008g0198 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2439+306T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813424 | |||||||
chr8:55813543 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+425A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813543 | |||||||
chr8:55813708 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2439+590C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813708 | |||||||
chr8:55813718 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2439+600A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813718 | |||||||
chr8:55814115 | T | G | 3 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0300 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2439+997T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814115 | |||||||
chr8:55814176 | A | G | 1 | a0002c0002t0003g0296 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2439+1058A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814176 | |||||||
chr8:55814208 | T | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2439+1090T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814208 | |||||||
chr8:55814240 | G | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1122G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814240 | |||||||
chr8:55814316 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2439+1198G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814316 | |||||||
chr8:55814436 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2439+1318T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814436 | |||||||
chr8:55814506 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2439+1388T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814506 | |||||||
chr8:55814525 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2439+1407C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814525 | |||||||
chr8:55814531 | T | C | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1413T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814531 | |||||||
chr8:55814581 | TG | T | 6 | a0001c0001t0001g0027 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
7 | HG00597.hp2 NA18943.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.2439+1466delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814581 | ||||||
chr8:55814601 | A | G | 1 | a0017c0019t0001g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2439+1483A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814601 | |||||||
chr8:55814650 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2439+1532G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814650 | |||||||
chr8:55814659 | T | TA | 5 | a0001c0001t0001g0014 a0001c0001t0001g0264 a0001c0001t0002g0126 others(2): Show |
7 | HG02717.hp2 NA18950.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.2439+1557dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814659 | ||||||
chr8:55814660 | A | T | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02280.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+1542A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814660 | |||||||
chr8:55814672 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2439+1555_2439+155 others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814672 | ||||||
chr8:55814672 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2439+1555_2439+155 others(16): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814672 | ||||||
chr8:55814672 | A | ATATATAT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2439+1554_2439+155 others(11): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814672 | |||||||
chr8:55814672 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2439+1554_2439+155 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814672 | |||||||
chr8:55814673 | AAATATAT others(4): Show |
A | 1 | a0003c0003t0005g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2439+1557_2439+156 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814673 | ||||||
chr8:55814674 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2439+1557_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | ||||||
chr8:55814674 | A | AAATATAT others(4): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18989.hp1 NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2439+1557_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | ||||||
chr8:55814674 | A | AAT | 8 | a0001c0001t0001g0212 a0001c0001t0006g0187 a0001c0001t0007g0043 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1579_2439+158 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | ||||||
chr8:55814674 | A | AATAT | 9 | a0001c0001t0001g0247 a0001c0001t0002g0064 a0001c0001t0002g0065 others(6): Show |
9 | HG02071.hp1 HG02523.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1577_2439+158 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | ||||||
chr8:55814674 | A | ATAT | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0112 others(16): Show |
21 | HG00438.hp2 HG01123.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | ATATAT | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0129 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(9): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | ATATATAT others(2): Show |
3 | a0003c0003t0005g0032 a0008c0011t0001g0111 a0008c0011t0016g0139 |
4 | HG02257.hp2 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(13): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0108 |
4 | HG00673.hp2 HG02135.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0117 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2439+1556_2439+155 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0010 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2439+1556_2439+155 others(19): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814674 | A | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0036 others(17): Show |
21 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.2439+1556A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | |||||||
chr8:55814675 | AT | A | 31 | a0001c0001t0001g0147 a0001c0001t0001g0165 a0001c0001t0001g0196 others(28): Show |
34 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+1558delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814675 | |||||||
chr8:55814676 | T | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(87): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2439+1558T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814676 | |||||||
chr8:55814678 | T | A | 2 | a0001c0001t0001g0251 a0002c0002t0003g0293 |
2 | HG02165.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2439+1560T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814678 | |||||||
chr8:55814730 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+1612A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814730 | |||||||
chr8:55814733 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+1615G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814733 | |||||||
chr8:55814740 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0128 others(8): Show |
14 | HG02129.hp1 NA18945.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.2439+1622C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814740 | |||||||
chr8:55814833 | C | CT | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+1716dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814833 | ||||||
chr8:55814834 | T | TA | 35 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(32): Show |
38 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.2439+1727dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814834 | ||||||
chr8:55814843 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2439+1725A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814843 | |||||||
chr8:55814919 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+1801T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814919 | |||||||
chr8:55814924 | T | C | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1806T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814924 | |||||||
chr8:55814960 | A | G | 1 | a0002c0029t0013g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2439+1842A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814960 | |||||||
chr8:55815015 | G | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+1897G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815015 | |||||||
chr8:55815218 | CT | C | 4 | a0002c0002t0003g0278 a0002c0002t0003g0287 a0009c0012t0003g0274 others(1): Show |
4 | HG00140.hp1 HG02735.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+2103delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815218 | ||||||
chr8:55815420 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2439+2302G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815420 | |||||||
chr8:55815551 | C | T | 1 | a0001c0001t0018g0245 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2439+2433C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815551 | |||||||
chr8:55815640 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2439+2522A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815640 | |||||||
chr8:55815843 | C | A | 1 | a0001c0017t0001g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2439+2725C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815843 | |||||||
chr8:55815918 | T | TTTTA | 5 | a0001c0001t0001g0014 a0001c0001t0002g0017 a0001c0001t0002g0066 others(2): Show |
8 | HG02809.hp2 NA18943.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+2828_2439+283 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815918 | ||||||
chr8:55815918 | TTTTATTT others(1): Show |
T | 35 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(32): Show |
38 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.2439+2824_2439+283 others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815918 | ||||||
chr8:55815926 | A | ATTTATTT others(1981): Show |
1 | a0002c0002t0003g0280 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2439+2823_2439+282 others(1992): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815926 | ||||||
chr8:55815930 | ATTTATTT others(10): Show |
A | 7 | a0001c0001t0002g0103 a0003c0003t0005g0032 a0003c0003t0005g0302 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+2830_2439+284 others(21): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815930 | ||||||
chr8:55815938 | A | T | 1 | a0001c0001t0006g0024 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2439+2820A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815938 | |||||||
chr8:55815984 | G | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+2866G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815984 | |||||||
chr8:55816126 | A | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2439+3008A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816126 | |||||||
chr8:55816187 | C | T | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3069C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816187 | |||||||
chr8:55816188 | A | G | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3070A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816188 | |||||||
chr8:55816448 | C | T | 5 | a0004c0004t0001g0308 a0004c0004t0001g0309 a0004c0004t0001g0311 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2439+3330C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816448 | |||||||
chr8:55816449 | T | C | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3331T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816449 | |||||||
chr8:55816656 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2439+3538T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816656 | |||||||
chr8:55816735 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2439+3617G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816735 | |||||||
chr8:55816796 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2439+3678T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816796 | |||||||
chr8:55816860 | A | AT | 4 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0163 others(1): Show |
4 | HG02080.hp1 HG02109.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439+3745dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55816860 | ||||||
chr8:55816864 | A | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
298 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2439+3746A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816864 | |||||||
chr8:55816865 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2439+3747T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816865 | |||||||
chr8:55816866 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0062 a0001c0001t0001g0142 |
3 | HG02970.hp1 NA18957.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2439+3748T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816866 | |||||||
chr8:55816867 | T | A | 1 | a0014c0023t0001g0310 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2439+3749T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816867 | |||||||
chr8:55816870 | T | A | 46 | a0001c0001t0001g0260 a0002c0002t0003g0031 a0002c0002t0003g0037 others(43): Show |
50 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.2439+3752T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816870 | |||||||
chr8:55817009 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2439+3891C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817009 | |||||||
chr8:55817049 | G | T | 10 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(7): Show |
13 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2439+3931G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817049 | |||||||
chr8:55817067 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2439+3949G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817067 | |||||||
chr8:55817109 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3991C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817109 | |||||||
chr8:55817151 | C | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+4033C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817151 | |||||||
chr8:55817201 | A | G | 12 | a0001c0001t0004g0004 a0001c0001t0004g0007 a0001c0001t0004g0016 others(9): Show |
18 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2439+4083A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817201 | |||||||
chr8:55817226 | G | A | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+4108G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817226 | |||||||
chr8:55817314 | C | T | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2439+4196C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817314 | |||||||
chr8:55817368 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2439+4250A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817368 | |||||||
chr8:55817518 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2439+4400A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817518 | |||||||
chr8:55817635 | A | G | 1 | a0001c0001t0001g0014 | 3 | NA18971.hp2 NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2439+4517A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817635 | |||||||
chr8:55817688 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+4570C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817688 | |||||||
chr8:55818066 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2439+4948T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818066 | |||||||
chr8:55818093 | A | G | 31 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(28): Show |
34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+4975A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818093 | |||||||
chr8:55818199 | A | AT | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+5091dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55818199 | ||||||
chr8:55818243 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2439+5125T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818243 | |||||||
chr8:55818289 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2439+5171G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818289 | |||||||
chr8:55818455 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2439+5337G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818455 | |||||||
chr8:55818531 | G | C | 1 | a0002c0029t0013g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2439+5413G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818531 | |||||||
chr8:55818535 | C | T | 1 | a0003c0003t0005g0306 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2439+5417C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818535 | |||||||
chr8:55818576 | C | A | 1 | a0016c0018t0001g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+5458C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818576 | |||||||
chr8:55818589 | G | C | 1 | a0001c0001t0002g0125 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2439+5471G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818589 | |||||||
chr8:55818705 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+5587A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818705 | |||||||
chr8:55818852 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-5729G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818852 | |||||||
chr8:55819033 | C | T | 1 | a0005c0005t0009g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2440-5548C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819033 | |||||||
chr8:55819171 | A | G | 8 | a0002c0002t0003g0037 a0002c0002t0003g0271 a0002c0002t0003g0276 others(5): Show |
10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-5410A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819171 | |||||||
chr8:55819288 | A | AT | 7 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2440-5268dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819288 | AT | A | 44 | a0001c0001t0001g0039 a0001c0001t0001g0048 a0001c0001t0001g0051 others(41): Show |
50 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2440-5268delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819288 | ATT | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
173 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.2440-5269_2440-526 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819288 | ATTT | A | 6 | a0001c0001t0001g0177 a0001c0001t0006g0182 a0002c0002t0003g0289 others(3): Show |
6 | HG02145.hp1 HG02965.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-5270_2440-526 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819288 | ATTTT | A | 26 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(23): Show |
29 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2440-5271_2440-526 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819288 | ATTTTTTT others(6): Show |
A | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
39 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-5280_2440-526 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | ||||||
chr8:55819401 | A | G | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-5180A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819401 | |||||||
chr8:55819526 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0077 a0001c0001t0002g0093 |
4 | NA18943.hp2 NA18973.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-5055G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819526 | |||||||
chr8:55819553 | C | A | 1 | a0005c0005t0009g0300 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2440-5028C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819553 | |||||||
chr8:55819618 | CCTGCCAC others(3): Show |
C | 1 | a0019c0022t0002g0053 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2440-4962_2440-495 others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819618 | |||||||
chr8:55819656 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2440-4925A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819656 | |||||||
chr8:55820057 | G | C | 1 | a0001c0001t0002g0067 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2440-4524G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820057 | |||||||
chr8:55820069 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-4512T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820069 | |||||||
chr8:55820104 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2440-4477C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820104 | |||||||
chr8:55820162 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2440-4419A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820162 | |||||||
chr8:55820190 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-4391G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820190 | |||||||
chr8:55820312 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2440-4269C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820312 | |||||||
chr8:55820531 | C | T | 1 | a0001c0020t0001g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2440-4050C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820531 | |||||||
chr8:55820898 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2440-3683G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820898 | |||||||
chr8:55820976 | A | G | 30 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(27): Show |
33 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.2440-3605A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820976 | |||||||
chr8:55821150 | A | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0091 |
3 | HG02071.hp2 HG02132.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2440-3431A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821150 | |||||||
chr8:55821268 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2440-3313G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821268 | |||||||
chr8:55821296 | T | TGGAGGTG others(660): Show |
1 | a0001c0001t0002g0069 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2440-3268_2440-326 others(671): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821296 | ||||||
chr8:55821399 | G | C | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-3182G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821399 | |||||||
chr8:55821399 | G | T | 1 | a0002c0002t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2440-3182G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821399 | |||||||
chr8:55821502 | G | T | 1 | a0019c0022t0002g0053 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2440-3079G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821502 | |||||||
chr8:55821544 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2440-3037G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821544 | |||||||
chr8:55821623 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2440-2958C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821623 | |||||||
chr8:55821642 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2440-2939G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821642 | |||||||
chr8:55821679 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2902C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821679 | |||||||
chr8:55821698 | C | T | 44 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-2883C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821698 | |||||||
chr8:55821700 | T | C | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2440-2881T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821700 | |||||||
chr8:55821861 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2440-2720C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821861 | |||||||
chr8:55821911 | CTTTA | C | 6 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
7 | HG00438.hp2 HG02698.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2666_2440-266 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821911 | ||||||
chr8:55821950 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2440-2631T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821950 | |||||||
chr8:55821976 | GAGAT | G | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2601_2440-259 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821976 | ||||||
chr8:55822076 | C | A | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2505C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822076 | |||||||
chr8:55822076 | C | CT | 8 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(5): Show |
9 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-2494dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822076 | ||||||
chr8:55822076 | CT | C | 6 | a0001c0001t0001g0147 a0004c0004t0001g0308 a0004c0004t0001g0309 others(3): Show |
7 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-2494delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822076 | ||||||
chr8:55822080 | T | C | 3 | a0001c0001t0001g0034 a0013c0015t0002g0301 a0016c0018t0001g0313 |
3 | HG02258.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2440-2501T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822080 | |||||||
chr8:55822091 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2440-2490G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822091 | |||||||
chr8:55822132 | C | T | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-2449C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822132 | |||||||
chr8:55822156 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2425G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822156 | |||||||
chr8:55822260 | C | T | 1 | a0005c0005t0002g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2440-2321C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822260 | |||||||
chr8:55822284 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2440-2297A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822284 | |||||||
chr8:55822366 | G | A | 27 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(24): Show |
31 | HG00140.hp1 HG01109.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.2440-2215G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822366 | |||||||
chr8:55822454 | T | C | 1 | a0001c0014t0001g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2440-2127T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822454 | |||||||
chr8:55822476 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2440-2105A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822476 | |||||||
chr8:55822530 | T | C | 1 | a0013c0015t0002g0301 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-2051T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822530 | |||||||
chr8:55822549 | C | CT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0206 a0001c0001t0001g0207 others(4): Show |
10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-2020dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822549 | ||||||
chr8:55822549 | CT | C | 14 | a0001c0001t0001g0112 a0002c0002t0003g0278 a0002c0002t0003g0287 others(11): Show |
15 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-2020delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822549 | ||||||
chr8:55822559 | T | C | 1 | a0002c0002t0003g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2440-2022T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822559 | |||||||
chr8:55822559 | T | TC | 9 | a0002c0002t0003g0031 a0002c0002t0003g0271 a0002c0002t0003g0275 others(6): Show |
12 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2440-2022_2440-202 others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822559 | |||||||
chr8:55822560 | T | C | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2021T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822560 | |||||||
chr8:55822561 | T | C | 71 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
81 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2440-2020T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822561 | |||||||
chr8:55822653 | T | C | 1 | a0002c0002t0003g0284 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2440-1928T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822653 | |||||||
chr8:55822717 | G | A | 7 | a0003c0003t0005g0032 a0003c0003t0005g0302 a0003c0003t0005g0303 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-1864G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822717 | |||||||
chr8:55822807 | T | A | 1 | a0001c0001t0001g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2440-1774T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822807 | |||||||
chr8:55822908 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2440-1673C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822908 | |||||||
chr8:55822961 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-1620A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822961 | |||||||
chr8:55822975 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0130 |
4 | NA18957.hp1 NA18994.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1606T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822975 | |||||||
chr8:55823121 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2440-1460C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823121 | |||||||
chr8:55823178 | A | G | 36 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(33): Show |
39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-1403A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823178 | |||||||
chr8:55823267 | A | G | 43 | a0002c0002t0003g0031 a0002c0002t0003g0037 a0002c0002t0003g0271 others(40): Show |
47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2440-1314A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823267 | |||||||
chr8:55823292 | C | T | 1 | a0001c0001t0004g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2440-1289C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823292 | |||||||
chr8:55823950 | TA | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.2440-623delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55823950 | ||||||
chr8:55824071 | G | A | 1 | a0002c0029t0013g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2440-510G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824071 | |||||||
chr8:55824095 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.2440-486G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824095 | |||||||
chr8:55824210 | CAGTG | C | 4 | a0005c0005t0009g0268 a0005c0005t0009g0269 a0005c0005t0009g0270 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-368_2440-365d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55824210 | ||||||
chr8:55824417 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0030 others(6): Show |
15 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-164A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824417 | |||||||
chr8:55824422 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-159A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824422 | |||||||
chr8:55824487 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02129.hp1 NA18986.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-94G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824487 |