Item | Value |
---|---|
geneid | 219931 |
ensemblid | ENSG00000162341.18 |
hgncid | 20820 |
symbol | TPCN2 |
name | two pore segment channel 2 |
refseq_nuc | NM_139075.4 |
refseq_prot | NP_620714.2 |
ensembl_nuc | ENST00000294309.8 |
ensembl_prot | ENSP00000294309.3 |
mane_status | MANE Select |
chr | chr11 |
start | 69048932 |
end | 69090597 |
strand | + |
ver | v1.2 |
region | chr11:69048932-69090597 |
region5000 | chr11:69043932-69095597 |
regionname0 | TPCN2_chr11_69048932_69090597 |
regionname5000 | TPCN2_chr11_69043932_69095597 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 752 | 119 | 20 | 23 | 74 | 0 | 1 | 54 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0002 | 0/1 | 752 | 85 | 19 | 16 | 28 | 4 | 17 | 20 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0003 | 0/0 | 752 | 64 | 4 | 13 | 34 | 8 | 5 | 27 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0004 | 0/0 | 752 | 49 | 42 | 2 | 4 | 0 | 1 | 4 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0005 | 0/0 | 752 | 30 | 1 | 10 | 13 | 3 | 3 | 8 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0006 | 0/0 | 752 | 18 | 1 | 9 | 1 | 1 | 6 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0007 | 0/0 | 752 | 8 | 0 | 2 | 6 | 0 | 0 | 4 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0008 | 0/0 | 752 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0009 | 0/0 | 752 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0010 | 0/0 | 752 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0011 | 0/0 | 752 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0012 | 0/0 | 752 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0013 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(397): Show |
chr11 | 69043932 | 69095597 |
a0014 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0015 | 0/0 | 47 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(42): Show |
chr11 | 69043932 | 69095597 |
a0016 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0017 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0018 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0019 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0020 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0021 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0022 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0023 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0024 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
a0025 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | MAEPQ others(747): Show |
chr11 | 69043932 | 69095597 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2256 | 94 | 14 | 16 | 63 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0001c0005 | 0/0 | 2256 | 25 | 6 | 7 | 11 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0002 | 0/0 | 2256 | 77 | 13 | 16 | 28 | 3 | 17 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0018 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0019 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0022 | 0/1 | 2256 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0028 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0030 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0002c0034 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0003c0003 | 0/0 | 2256 | 60 | 4 | 12 | 31 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0003c0020 | 0/0 | 2256 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0003c0026 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0003c0042 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0006 | 0/0 | 2256 | 21 | 15 | 2 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0008 | 0/0 | 2256 | 10 | 9 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0011 | 0/0 | 2256 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0013 | 0/0 | 2256 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0015 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0016 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0024 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0004c0032 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0005c0004 | 0/0 | 2256 | 30 | 1 | 10 | 13 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0006c0007 | 0/0 | 2256 | 17 | 1 | 9 | 1 | 1 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0006c0031 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0007c0009 | 0/0 | 2256 | 8 | 0 | 2 | 6 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0008c0010 | 0/0 | 2256 | 6 | 0 | 2 | 0 | 2 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0009c0012 | 0/0 | 2256 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0010c0014 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0011c0017 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0012c0021 | 0/0 | 2256 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0013c0025 | 0/0 | 2289 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2284): Show |
chr11 | 69043932 | 69095597 | ||
a0014c0040 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0015c0038 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0016c0041 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0017c0036 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0018c0039 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0019c0037 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0020c0029 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0021c0023 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0022c0035 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0023c0027 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0024c0033 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 | ||
a0025c0043 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | ATGGC others(2251): Show |
chr11 | 69043932 | 69095597 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 4969 | 43 | 0 | 9 | 34 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0004 | 1/0 | 4969 | 5 | 1 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0005 | 0/0 | 4969 | 26 | 3 | 6 | 17 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0010 | 0/0 | 4969 | 9 | 0 | 0 | 9 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0011 | 0/0 | 4969 | 7 | 7 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0016 | 0/0 | 4969 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0001t0022 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0005t0004 | 0/0 | 4969 | 24 | 6 | 6 | 11 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0001c0005t0041 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0001 | 0/0 | 4969 | 70 | 12 | 16 | 24 | 3 | 15 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0023 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0026 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0027 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0028 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0029 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0030 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0002t0040 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0018t0001 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0019t0001 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0022t0001 | 0/1 | 4969 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0028t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0030t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0002c0034t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0003c0003t0002 | 0/0 | 4928 | 59 | 4 | 12 | 30 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0003c0003t0038 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0003c0020t0002 | 0/0 | 4928 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0003c0026t0002 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0003c0042t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0009 | 0/0 | 4962 | 10 | 9 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0018 | 0/0 | 4928 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0019 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0020 | 0/0 | 4962 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0033 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0035 | 0/0 | 4962 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0006t0036 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0004 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0013 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0017 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0031 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0008t0034 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0011t0012 | 0/0 | 4962 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0013t0015 | 0/0 | 4963 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4958): Show |
chr11 | 69043932 | 69095597 |
a0004c0015t0014 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0016t0014 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0004c0024t0019 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0004c0032t0012 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0005c0004t0007 | 0/0 | 4928 | 16 | 0 | 7 | 3 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0005c0004t0008 | 0/0 | 4928 | 12 | 0 | 2 | 10 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0005c0004t0032 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0005c0004t0037 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0006c0007t0006 | 0/0 | 4969 | 15 | 1 | 7 | 1 | 1 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0006c0007t0021 | 0/0 | 4969 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0006c0031t0006 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0007c0009t0004 | 0/0 | 4969 | 8 | 0 | 2 | 6 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0008c0010t0006 | 0/0 | 4969 | 5 | 0 | 2 | 0 | 2 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0008c0010t0024 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0009c0012t0002 | 0/0 | 4928 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0010c0014t0013 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0011c0017t0016 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0012c0021t0001 | 0/0 | 4969 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0013c0025t0007 | 0/0 | 4961 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4956): Show |
chr11 | 69043932 | 69095597 |
a0014c0040t0014 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0015c0038t0009 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4957): Show |
chr11 | 69043932 | 69095597 |
a0016c0041t0004 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0017c0036t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0018c0039t0006 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0019c0037t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0020c0029t0039 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0021c0023t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0022c0035t0003 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0023c0027t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4923): Show |
chr11 | 69043932 | 69095597 |
a0024c0033t0003 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
a0025c0043t0025 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | GCAGT others(4964): Show |
chr11 | 69043932 | 69095597 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0004g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0011g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0016g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0022g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0001t0022g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0001c0005t0041g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0003 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0023g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0026g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0027g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0028g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0029g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0030g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0002t0040g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0018t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0019t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0022t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0028t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0030t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0002c0034t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0003t0038g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0020t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0020t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0026t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0003c0042t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0018g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0019g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0020g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0033g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0035g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0006t0036g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0031g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0008t0034g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0011t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0013t0015g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0013t0015g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0013t0015g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0013t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0015t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0015t0014g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0015t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0016t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0016t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0024t0019g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0004c0032t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0032g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0005c0004t0037g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0006g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0007t0021g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0006c0031t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0007c0009t0004g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0007c0009t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0007c0009t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0007c0009t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0007c0009t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0008c0010t0024g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0009c0012t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0009c0012t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0009c0012t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0009c0012t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0010c0014t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0010c0014t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0010c0014t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0011c0017t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0011c0017t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0012c0021t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0012c0021t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0013c0025t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0014c0040t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0015c0038t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0016c0041t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0017c0036t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0018c0039t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0019c0037t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0020c0029t0039g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0021c0023t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0022c0035t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0023c0027t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0024c0033t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
a0025c0043t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0008 | c0010 | t0006 | g0101 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00099 | hp2 | a0005 | c0004 | t0007 | g0142 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00140 | hp2 | a0003 | c0003 | t0002 | g0013 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00280 | hp2 | a0003 | c0003 | t0002 | g0013 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00323 | hp1 | a0008 | c0010 | t0006 | g0102 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00323 | hp2 | a0003 | c0003 | t0002 | g0135 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00408 | hp2 | a0002 | c0002 | t0027 | g0237 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00423 | hp1 | a0001 | c0005 | t0004 | g0001 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00423 | hp2 | a0003 | c0003 | t0002 | g0149 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00544 | hp1 | a0009 | c0012 | t0002 | g0031 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00558 | hp1 | a0003 | c0003 | t0002 | g0113 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00558 | hp2 | a0001 | c0001 | t0010 | g0299 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00597 | hp1 | a0001 | c0001 | t0010 | g0275 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00597 | hp2 | a0003 | c0003 | t0002 | g0148 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00609 | hp1 | a0009 | c0012 | t0002 | g0035 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00621 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00639 | hp1 | a0001 | c0005 | t0041 | g0091 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0248 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00642 | hp2 | a0005 | c0004 | t0032 | g0161 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00733 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00735 | hp2 | a0006 | c0007 | t0006 | g0016 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00738 | hp1 | a0003 | c0003 | t0002 | g0130 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00741 | hp1 | a0005 | c0004 | t0007 | g0259 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01069 | hp1 | a0007 | c0009 | t0004 | g0001 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01070 | hp2 | a0005 | c0004 | t0007 | g0042 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01071 | hp2 | a0005 | c0004 | t0007 | g0042 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01074 | hp2 | a0003 | c0003 | t0002 | g0124 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01081 | hp2 | a0005 | c0004 | t0007 | g0144 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01099 | hp1 | a0003 | c0003 | t0002 | g0134 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01106 | hp1 | a0005 | c0004 | t0007 | g0153 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01106 | hp2 | a0006 | c0007 | t0006 | g0166 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01167 | hp1 | a0006 | c0007 | t0006 | g0005 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01168 | hp1 | a0006 | c0007 | t0021 | g0040 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01168 | hp2 | a0005 | c0004 | t0007 | g0141 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01169 | hp1 | a0006 | c0007 | t0021 | g0040 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01169 | hp2 | a0006 | c0007 | t0006 | g0005 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01175 | hp1 | a0003 | c0003 | t0002 | g0030 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01192 | hp2 | a0007 | c0009 | t0004 | g0001 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01243 | hp1 | a0003 | c0003 | t0002 | g0014 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01243 | hp2 | a0004 | c0006 | t0035 | g0209 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01255 | hp2 | a0013 | c0025 | t0007 | g0172 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01257 | hp1 | a0006 | c0007 | t0006 | g0005 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01257 | hp2 | a0003 | c0003 | t0002 | g0112 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01258 | hp1 | a0006 | c0007 | t0006 | g0005 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01261 | hp1 | a0006 | c0007 | t0006 | g0005 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01261 | hp2 | a0003 | c0003 | t0002 | g0117 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01346 | hp1 | a0003 | c0003 | t0002 | g0033 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01346 | hp2 | a0004 | c0006 | t0009 | g0183 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01433 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0264 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01496 | hp2 | a0003 | c0003 | t0002 | g0129 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01515 | hp1 | a0003 | c0003 | t0002 | g0038 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01515 | hp2 | a0005 | c0004 | t0007 | g0029 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01516 | hp1 | a0002 | c0034 | t0001 | g0046 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01516 | hp2 | a0003 | c0003 | t0002 | g0014 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01517 | hp1 | a0005 | c0004 | t0007 | g0029 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01517 | hp2 | a0003 | c0003 | t0002 | g0014 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0286 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01884 | hp2 | a0010 | c0014 | t0013 | g0191 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01891 | hp1 | a0002 | c0002 | t0029 | g0216 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01891 | hp2 | a0004 | c0006 | t0009 | g0017 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01928 | hp1 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01934 | hp1 | a0001 | c0001 | t0016 | g0019 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01934 | hp2 | a0003 | c0026 | t0002 | g0136 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01943 | hp1 | a0005 | c0004 | t0008 | g0173 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01952 | hp1 | a0001 | c0005 | t0004 | g0098 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01952 | hp2 | a0001 | c0005 | t0004 | g0093 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01975 | hp2 | a0001 | c0005 | t0004 | g0089 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01978 | hp1 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01981 | hp2 | a0001 | c0001 | t0005 | g0272 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02015 | hp2 | a0001 | c0001 | t0010 | g0297 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02040 | hp2 | a0003 | c0003 | t0038 | g0126 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0283 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02071 | hp1 | a0002 | c0002 | t0023 | g0004 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02074 | hp2 | a0009 | c0012 | t0002 | g0114 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02080 | hp2 | a0005 | c0004 | t0007 | g0111 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02083 | hp2 | a0007 | c0009 | t0004 | g0088 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02129 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02129 | hp2 | a0005 | c0004 | t0008 | g0083 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02132 | hp2 | a0003 | c0003 | t0002 | g0035 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02145 | hp1 | a0004 | c0006 | t0019 | g0260 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0273 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02148 | hp2 | a0008 | c0010 | t0006 | g0028 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02155 | hp1 | a0006 | c0007 | t0006 | g0171 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02155 | hp2 | a0001 | c0001 | t0010 | g0296 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02165 | hp2 | a0003 | c0003 | t0002 | g0116 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02257 | hp2 | a0006 | c0007 | t0006 | g0167 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02258 | hp1 | a0002 | c0018 | t0001 | g0006 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02258 | hp2 | a0004 | c0008 | t0017 | g0176 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02280 | hp1 | a0011 | c0017 | t0016 | g0019 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0288 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02293 | hp1 | a0005 | c0004 | t0008 | g0131 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02300 | hp2 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02451 | hp1 | a0004 | c0016 | t0014 | g0055 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02451 | hp2 | a0002 | c0030 | t0001 | g0263 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02523 | hp1 | a0005 | c0004 | t0007 | g0147 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02523 | hp2 | a0007 | c0009 | t0004 | g0001 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02572 | hp2 | a0004 | c0006 | t0009 | g0206 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02615 | hp1 | a0014 | c0040 | t0014 | g0059 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02615 | hp2 | a0001 | c0001 | t0022 | g0291 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02622 | hp1 | a0015 | c0038 | t0009 | g0205 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0123 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02630 | hp1 | a0004 | c0008 | t0017 | g0106 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02683 | hp1 | a0001 | c0005 | t0004 | g0061 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02683 | hp2 | a0003 | c0003 | t0002 | g0013 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02698 | hp2 | a0006 | c0007 | t0006 | g0170 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02717 | hp1 | a0004 | c0006 | t0009 | g0185 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02717 | hp2 | a0016 | c0041 | t0004 | g0090 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02723 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02735 | hp1 | a0005 | c0004 | t0007 | g0146 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02735 | hp2 | a0008 | c0010 | t0024 | g0028 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02738 | hp1 | a0006 | c0007 | t0006 | g0041 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0249 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02809 | hp1 | a0004 | c0011 | t0012 | g0197 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02809 | hp2 | a0004 | c0006 | t0033 | g0200 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02818 | hp1 | a0004 | c0006 | t0009 | g0044 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02886 | hp1 | a0004 | c0008 | t0013 | g0187 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02886 | hp2 | a0004 | c0013 | t0015 | g0201 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02895 | hp1 | a0004 | c0011 | t0012 | g0199 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02895 | hp2 | a0004 | c0006 | t0020 | g0051 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02896 | hp2 | a0004 | c0013 | t0015 | g0043 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02897 | hp1 | a0004 | c0006 | t0020 | g0051 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02897 | hp2 | a0004 | c0013 | t0015 | g0043 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02922 | hp1 | a0005 | c0004 | t0037 | g0139 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02965 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02965 | hp2 | a0004 | c0011 | t0012 | g0198 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02970 | hp1 | a0004 | c0006 | t0009 | g0208 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02970 | hp2 | a0001 | c0001 | t0022 | g0292 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02976 | hp1 | a0010 | c0014 | t0013 | g0192 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02976 | hp2 | a0004 | c0024 | t0019 | g0261 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03041 | hp1 | a0004 | c0006 | t0009 | g0044 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03041 | hp2 | a0004 | c0006 | t0009 | g0207 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03098 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03098 | hp2 | a0004 | c0006 | t0009 | g0017 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0168 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03139 | hp1 | a0001 | c0005 | t0004 | g0096 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03139 | hp2 | a0004 | c0016 | t0014 | g0054 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03195 | hp1 | a0004 | c0008 | t0013 | g0189 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03195 | hp2 | a0004 | c0011 | t0012 | g0195 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03209 | hp1 | a0002 | c0019 | t0001 | g0045 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03209 | hp2 | a0004 | c0011 | t0012 | g0196 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03225 | hp1 | a0010 | c0014 | t0013 | g0193 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03225 | hp2 | a0002 | c0018 | t0001 | g0006 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0282 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03453 | hp2 | a0011 | c0017 | t0016 | g0276 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03486 | hp2 | a0004 | c0032 | t0012 | g0194 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03490 | hp2 | a0005 | c0004 | t0007 | g0143 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03491 | hp2 | a0006 | c0007 | t0006 | g0169 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03516 | hp1 | a0004 | c0008 | t0013 | g0190 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03516 | hp2 | a0001 | c0005 | t0004 | g0092 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03540 | hp1 | a0004 | c0015 | t0014 | g0057 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03579 | hp1 | a0017 | c0036 | t0001 | g0180 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03579 | hp2 | a0004 | c0013 | t0015 | g0204 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03654 | hp1 | a0005 | c0004 | t0007 | g0159 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03669 | hp2 | a0003 | c0003 | t0002 | g0128 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03688 | hp2 | a0018 | c0039 | t0006 | g0016 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03710 | hp1 | a0002 | c0002 | t0040 | g0003 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03831 | hp2 | a0004 | c0008 | t0001 | g0210 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03834 | hp1 | a0002 | c0002 | t0030 | g0006 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03834 | hp2 | a0006 | c0031 | t0006 | g0165 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03942 | hp1 | a0019 | c0037 | t0001 | g0229 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03942 | hp2 | a0008 | c0010 | t0006 | g0103 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04115 | hp1 | a0003 | c0003 | t0002 | g0137 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04115 | hp2 | a0003 | c0003 | t0002 | g0127 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04184 | hp1 | a0020 | c0029 | t0039 | g0222 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0224 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0256 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0212 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04228 | hp1 | a0006 | c0007 | t0006 | g0016 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0030 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18522 | hp1 | a0004 | c0013 | t0015 | g0202 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18522 | hp2 | a0004 | c0008 | t0004 | g0105 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18612 | hp2 | a0003 | c0003 | t0002 | g0038 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18747 | hp1 | a0001 | c0001 | t0010 | g0295 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18747 | hp2 | a0005 | c0004 | t0008 | g0145 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18906 | hp1 | a0021 | c0023 | t0001 | g0233 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0280 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18939 | hp2 | a0002 | c0002 | t0026 | g0004 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18940 | hp1 | a0003 | c0003 | t0002 | g0034 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18942 | hp2 | a0022 | c0035 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18946 | hp2 | a0005 | c0004 | t0008 | g0109 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18947 | hp1 | a0003 | c0042 | t0002 | g0099 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18948 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18950 | hp1 | a0001 | c0005 | t0004 | g0025 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18959 | hp1 | a0003 | c0003 | t0002 | g0133 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18962 | hp1 | a0005 | c0004 | t0008 | g0217 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18964 | hp1 | a0012 | c0021 | t0001 | g0214 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18964 | hp2 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0300 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18969 | hp2 | a0009 | c0012 | t0002 | g0163 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18970 | hp1 | a0009 | c0012 | t0002 | g0031 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18971 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18973 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18974 | hp2 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18975 | hp1 | a0001 | c0005 | t0004 | g0025 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18975 | hp2 | a0003 | c0003 | t0002 | g0108 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18979 | hp2 | a0001 | c0001 | t0010 | g0298 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18982 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18985 | hp1 | a0001 | c0005 | t0004 | g0001 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18990 | hp1 | a0003 | c0003 | t0002 | g0034 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18990 | hp2 | a0001 | c0005 | t0004 | g0026 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18993 | hp2 | a0007 | c0009 | t0004 | g0094 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18997 | hp1 | a0003 | c0003 | t0002 | g0150 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18999 | hp1 | a0003 | c0003 | t0002 | g0132 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19002 | hp1 | a0003 | c0003 | t0002 | g0110 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19002 | hp2 | a0001 | c0005 | t0004 | g0027 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19004 | hp1 | a0005 | c0004 | t0008 | g0140 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19005 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19005 | hp2 | a0007 | c0009 | t0004 | g0001 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19007 | hp1 | a0005 | c0004 | t0007 | g0160 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19007 | hp2 | a0001 | c0005 | t0004 | g0026 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19009 | hp2 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19010 | hp2 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19011 | hp1 | a0003 | c0003 | t0002 | g0120 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19011 | hp2 | a0003 | c0003 | t0002 | g0156 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19030 | hp1 | a0004 | c0008 | t0031 | g0188 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19030 | hp2 | a0001 | c0001 | t0011 | g0287 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19043 | hp1 | a0002 | c0019 | t0001 | g0045 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19055 | hp2 | a0001 | c0001 | t0010 | g0301 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19057 | hp1 | a0012 | c0021 | t0001 | g0244 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19057 | hp2 | a0003 | c0003 | t0002 | g0121 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19059 | hp2 | a0003 | c0003 | t0002 | g0175 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19060 | hp2 | a0003 | c0003 | t0002 | g0122 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19064 | hp1 | a0005 | c0004 | t0008 | g0138 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19065 | hp1 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19065 | hp2 | a0023 | c0027 | t0002 | g0186 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19066 | hp1 | a0024 | c0033 | t0003 | g0020 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19066 | hp2 | a0002 | c0002 | t0028 | g0242 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19067 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19068 | hp2 | a0003 | c0020 | t0002 | g0162 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19070 | hp2 | a0004 | c0006 | t0002 | g0157 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0119 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19075 | hp2 | a0001 | c0005 | t0004 | g0027 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19079 | hp1 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19079 | hp2 | a0001 | c0001 | t0010 | g0302 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19080 | hp1 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19081 | hp1 | a0007 | c0009 | t0004 | g0086 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19081 | hp2 | a0003 | c0003 | t0002 | g0125 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19082 | hp1 | a0001 | c0005 | t0004 | g0087 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19082 | hp2 | a0003 | c0003 | t0002 | g0154 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19083 | hp1 | a0003 | c0020 | t0002 | g0115 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19085 | hp1 | a0001 | c0005 | t0004 | g0097 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19085 | hp2 | a0001 | c0005 | t0004 | g0095 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19086 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19090 | hp2 | a0007 | c0009 | t0004 | g0085 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19091 | hp1 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19240 | hp1 | a0004 | c0011 | t0012 | g0203 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20129 | hp1 | a0004 | c0006 | t0036 | g0184 | AFR | ASW | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0118 | AFR | ASW | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20752 | hp1 | a0006 | c0007 | t0006 | g0181 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20752 | hp2 | a0003 | c0003 | t0002 | g0009 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0220 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20805 | hp2 | a0003 | c0003 | t0002 | g0164 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | GIH | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20905 | hp2 | a0006 | c0007 | t0006 | g0041 | SAS | GIH | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01123 | hp1 | a0005 | c0004 | t0007 | g0258 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG01123 | hp2 | a0008 | c0010 | t0006 | g0100 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02109 | hp1 | a0003 | c0003 | t0002 | g0158 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0254 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02486 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02486 | hp2 | a0002 | c0028 | t0001 | g0179 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02559 | hp1 | a0003 | c0003 | t0002 | g0033 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG02559 | hp2 | a0004 | c0015 | t0014 | g0058 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG03471 | hp2 | a0004 | c0008 | t0017 | g0177 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
HG06807 | hp2 | a0004 | c0015 | t0014 | g0056 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20300 | hp1 | a0004 | c0008 | t0034 | g0178 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA20300 | hp2 | a0004 | c0006 | t0009 | g0017 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA21309 | hp1 | a0025 | c0043 | t0025 | g0104 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
NA21309 | hp2 | a0004 | c0006 | t0007 | g0151 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
homoSapiens | chm13v2 | a0002 | c0022 | t0001 | g0213 | REF | REF | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0267 | REF | REF | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69049068 | C | T | 1 | a0012 | 2 | NA18964.hp1 NA19057.hp1 |
missense_variant | MODERATE | c.71C>T | p.Ala24Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 137/4969 | 71/2259 | 24/752 | chr11 | 69049068 | |||
chr11:69049077 | C | G | 1 | a0025 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.80C>G | p.Thr27Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 146/4969 | 80/2259 | 27/752 | chr11 | 69049077 | |||
chr11:69054039 | C | T | 2 | a0014 a0018 |
2 | HG02615.hp1 HG03688.hp2 |
missense_variant | MODERATE | c.116C>T | p.Ala39Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/25 | 182/4969 | 116/2259 | 39/752 | chr11 | 69054039 | |||
chr11:69054065 | C | T | 1 | a0015 | 1 | HG02622.hp1 | stop_gained | HIGH | c.142C>T | p.Gln48* | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/25 | 208/4969 | 142/2259 | 48/752 | chr11 | 69054065 | |||
chr11:69054782 | C | T | 1 | a0019 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.236C>T | p.Ser79Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 302/4969 | 236/2259 | 79/752 | chr11 | 69054782 | |||
chr11:69054787 | G | A | 1 | a0010 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.241G>A | p.Val81Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 307/4969 | 241/2259 | 81/752 | chr11 | 69054787 | |||
chr11:69054796 | C | T | 1 | a0009 | 5 | HG00544.hp1 HG00609.hp1 HG02074.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.250C>T | p.Arg84Trp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 316/4969 | 250/2259 | 84/752 | chr11 | 69054796 | |||
chr11:69055184 | C | G | 1 | a0017 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.261C>G | p.Ser87Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 327/4969 | 261/2259 | 87/752 | chr11 | 69055184 | |||
chr11:69055282 | C | T | 1 | a0022 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.359C>T | p.Pro120Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 425/4969 | 359/2259 | 120/752 | chr11 | 69055282 | |||
chr11:69055291 | G | A | 1 | a0021 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.368G>A | p.Gly123Asp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 434/4969 | 368/2259 | 123/752 | chr11 | 69055291 | |||
chr11:69057635 | G | T | 1 | a0024 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.487G>T | p.Val163Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/25 | 553/4969 | 487/2259 | 163/752 | chr11 | 69057635 | |||
chr11:69063896 | G | A | 1 | a0008 | 6 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.655G>A | p.Val219Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 721/4969 | 655/2259 | 219/752 | chr11 | 69063896 | |||
chr11:69067602 | G | A | 1 | a0016 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.826G>A | p.Asp276Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/25 | 892/4969 | 826/2259 | 276/752 | chr11 | 69067602 | |||
chr11:69072692 | A | G | 6 | a0002 a0012 a0017 others(3): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
missense_variant | MODERATE | c.1127A>G | p.Lys376Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/25 | 1193/4969 | 1127/2259 | 376/752 | chr11 | 69072692 | |||
chr11:69072931 | G | A | 2 | a0005 a0013 |
31 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(28): Show |
missense_variant | MODERATE | c.1160G>A | p.Gly387Asp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1226/4969 | 1160/2259 | 387/752 | chr11 | 69072931 | |||
chr11:69072938 | T | TCTGAAGG others(26): Show |
1 | a0013 | 1 | HG01255.hp2 | conservative_inframe_insertion | MODERATE | c.1170_1171insAAGGTG others(27): Show |
p.Leu390_Leu391insLy others(31): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1237/4969 | 1171/2259 | 391/752 | INFO_REALIGN_3_PRIME | chr11 | 69072938 | ||
chr11:69072942 | C | A | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1171C>A | p.Leu391Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1237/4969 | 1171/2259 | 391/752 | chr11 | 69072942 | |||
chr11:69072946 | C | G | 1 | a0013 | 1 | HG01255.hp2 | stop_gained | HIGH | c.1175C>G | p.Ser392* | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1241/4969 | 1175/2259 | 392/752 | chr11 | 69072946 | |||
chr11:69072949 | C | G | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1178C>G | p.Ala393Gly | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1244/4969 | 1178/2259 | 393/752 | chr11 | 69072949 | |||
chr11:69072957 | T | G | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1186T>G | p.Phe396Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1252/4969 | 1186/2259 | 396/752 | chr11 | 69072957 | |||
chr11:69072964 | A | G | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1193A>G | p.Lys398Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1259/4969 | 1193/2259 | 398/752 | chr11 | 69072964 | |||
chr11:69072986 | A | C | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1215A>C | p.Arg405Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1281/4969 | 1215/2259 | 405/752 | chr11 | 69072986 | |||
chr11:69072989 | T | G | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1218T>G | p.Ser406Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1284/4969 | 1218/2259 | 406/752 | chr11 | 69072989 | |||
chr11:69072998 | A | T | 1 | a0013 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1227A>T | p.Lys409Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1293/4969 | 1227/2259 | 409/752 | chr11 | 69072998 | |||
chr11:69073000 | A | G | 1 | a0013 | 1 | HG01255.hp2 | missense_variant&splice_region_variant | MODERATE | c.1229A>G | p.Glu410Gly | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1295/4969 | 1229/2259 | 410/752 | chr11 | 69073000 | |||
chr11:69078931 | A | T | 4 | a0006 a0008 a0018 others(1): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
missense_variant | MODERATE | c.1450A>T | p.Met484Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/25 | 1516/4969 | 1450/2259 | 484/752 | chr11 | 69078931 | |||
chr11:69081443 | C | T | 1 | a0023 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1633C>T | p.Arg545Cys | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/25 | 1699/4969 | 1633/2259 | 545/752 | chr11 | 69081443 | |||
chr11:69083946 | T | C | 19 | a0002 a0003 a0004 others(16): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
missense_variant&splice_region_variant | MODERATE | c.1691T>C | p.Leu564Pro | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/25 | 1757/4969 | 1691/2259 | 564/752 | chr11 | 69083946 | |||
chr11:69085921 | A | G | 1 | a0011 | 2 | HG02280.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1994A>G | p.Tyr665Cys | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/25 | 2060/4969 | 1994/2259 | 665/752 | chr11 | 69085921 | |||
chr11:69086561 | C | T | 1 | a0007 | 8 | HG01069.hp1 HG01192.hp2 HG02083.hp2 others(5): Show |
missense_variant | MODERATE | c.2042C>T | p.Ser681Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/25 | 2108/4969 | 2042/2259 | 681/752 | chr11 | 69086561 | |||
chr11:69087895 | G | A | 4 | a0003 a0009 a0020 others(1): Show |
71 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
missense_variant | MODERATE | c.2201G>A | p.Gly734Glu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2267/4969 | 2201/2259 | 734/752 | chr11 | 69087895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69049096 | A | G | 4 | a0001c0005 a0003c0042 a0007c0009 others(1): Show |
35 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.99A>G | p.Gln33Gln | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 165/4969 | 99/2259 | 33/752 | chr11 | 69049096 | |||
chr11:69054738 | C | T | 1 | a0004c0013 | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.192C>T | p.His64His | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 258/4969 | 192/2259 | 64/752 | chr11 | 69054738 | |||
chr11:69055190 | C | T | 2 | a0004c0015 a0014c0040 |
4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.267C>T | p.Thr89Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 333/4969 | 267/2259 | 89/752 | chr11 | 69055190 | |||
chr11:69055298 | C | G | 1 | a0002c0034 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.375C>G | p.Thr125Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 441/4969 | 375/2259 | 125/752 | chr11 | 69055298 | |||
chr11:69057667 | C | T | 1 | a0004c0032 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.519C>T | p.Thr173Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/25 | 585/4969 | 519/2259 | 173/752 | chr11 | 69057667 | |||
chr11:69063952 | G | A | 3 | a0004c0015 a0004c0016 a0014c0040 |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.711G>A | p.Leu237Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 777/4969 | 711/2259 | 237/752 | chr11 | 69063952 | |||
chr11:69063955 | C | T | 1 | a0003c0020 | 2 | NA19068.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.714C>T | p.Phe238Phe | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 780/4969 | 714/2259 | 238/752 | chr11 | 69063955 | |||
chr11:69067574 | G | A | 1 | a0004c0024 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.798G>A | p.Leu266Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/25 | 864/4969 | 798/2259 | 266/752 | chr11 | 69067574 | |||
chr11:69072687 | C | T | 1 | a0006c0031 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1122C>T | p.Ser374Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/25 | 1188/4969 | 1122/2259 | 374/752 | chr11 | 69072687 | |||
chr11:69072929 | T | C | 16 | a0002c0028 a0003c0003 a0003c0020 others(13): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
synonymous_variant | LOW | c.1158T>C | p.Tyr386Tyr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1224/4969 | 1158/2259 | 386/752 | chr11 | 69072929 | |||
chr11:69072944 | C | G | 14 | a0002c0030 a0003c0003 a0003c0020 others(11): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1173C>G | p.Leu391Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1239/4969 | 1173/2259 | 391/752 | chr11 | 69072944 | |||
chr11:69078547 | C | T | 1 | a0002c0019 | 2 | HG03209.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.1296C>T | p.Tyr432Tyr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 14/25 | 1362/4969 | 1296/2259 | 432/752 | chr11 | 69078547 | |||
chr11:69083998 | G | T | 14 | a0003c0003 a0003c0020 a0003c0026 others(11): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1743G>T | p.Ala581Ala | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/25 | 1809/4969 | 1743/2259 | 581/752 | chr11 | 69083998 | |||
chr11:69085889 | C | T | 3 | a0004c0011 a0004c0013 a0004c0032 |
12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
synonymous_variant | LOW | c.1962C>T | p.Asn654Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/25 | 2028/4969 | 1962/2259 | 654/752 | chr11 | 69085889 | |||
chr11:69086544 | A | G | 6 | a0002c0018 a0006c0007 a0006c0031 others(3): Show |
28 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(25): Show |
synonymous_variant | LOW | c.2025A>G | p.Val675Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/25 | 2091/4969 | 2025/2259 | 675/752 | chr11 | 69086544 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69048976 | G | A | 3 | a0004c0006t0019 a0004c0006t0020 a0004c0024t0019 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 22 | chr11 | 69048976 | ||||||
chr11:69087958 | C | T | 1 | a0001c0005t0041 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 5 | chr11 | 69087958 | ||||||
chr11:69087966 | C | T | 1 | a0002c0002t0040 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 13 | chr11 | 69087966 | ||||||
chr11:69088015 | G | A | 29 | a0002c0002t0001 a0002c0002t0023 a0002c0002t0026 others(26): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*62G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 62 | chr11 | 69088015 | ||||||
chr11:69088111 | G | A | 2 | a0004c0006t0019 a0004c0024t0019 |
2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 158 | chr11 | 69088111 | ||||||
chr11:69088127 | A | G | 9 | a0003c0003t0002 a0003c0003t0038 a0003c0020t0002 others(6): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*174A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 174 | chr11 | 69088127 | ||||||
chr11:69088163 | C | T | 1 | a0004c0008t0031 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 210 | chr11 | 69088163 | ||||||
chr11:69088173 | G | A | 1 | a0002c0002t0023 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 220 | chr11 | 69088173 | ||||||
chr11:69088234 | C | T | 1 | a0001c0001t0022 | 2 | HG02615.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 281 | chr11 | 69088234 | ||||||
chr11:69088247 | A | G | 1 | a0002c0002t0030 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 294 | chr11 | 69088247 | ||||||
chr11:69088373 | A | T | 3 | a0004c0011t0012 a0004c0013t0015 a0004c0032t0012 |
12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 420 | chr11 | 69088373 | ||||||
chr11:69088486 | A | G | 19 | a0002c0002t0001 a0002c0002t0023 a0002c0002t0026 others(16): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 533 | chr11 | 69088486 | ||||||
chr11:69088587 | A | G | 1 | a0002c0002t0029 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 634 | chr11 | 69088587 | ||||||
chr11:69088643 | A | G | 3 | a0004c0008t0013 a0004c0008t0031 a0010c0014t0013 |
7 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*690A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 690 | chr11 | 69088643 | ||||||
chr11:69088756 | G | T | 1 | a0001c0001t0011 | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 803 | chr11 | 69088756 | ||||||
chr11:69088804 | C | G | 1 | a0025c0043t0025 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 851 | chr11 | 69088804 | ||||||
chr11:69089119 | G | A | 3 | a0004c0006t0018 a0005c0004t0008 a0005c0004t0032 |
16 | HG00621.hp1 HG00642.hp2 HG01943.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1166G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1166 | chr11 | 69089119 | ||||||
chr11:69089139 | G | A | 1 | a0004c0006t0033 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1186G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1186 | chr11 | 69089139 | ||||||
chr11:69089158 | G | A | 2 | a0001c0001t0016 a0011c0017t0016 |
4 | HG01934.hp1 HG02280.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1205G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1205 | chr11 | 69089158 | ||||||
chr11:69089212 | G | A | 19 | a0002c0002t0001 a0002c0002t0023 a0002c0002t0026 others(16): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1259G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1259 | chr11 | 69089212 | ||||||
chr11:69089224 | C | G | 1 | a0002c0002t0028 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1271 | chr11 | 69089224 | ||||||
chr11:69089242 | TAATAAC | T | 26 | a0003c0003t0002 a0003c0003t0038 a0003c0020t0002 others(23): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1312_*1317delACAA others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1312 | INFO_REALIGN_3_PRIME | chr11 | 69089242 | |||||
chr11:69089336 | C | G | 19 | a0002c0002t0001 a0002c0002t0023 a0002c0002t0026 others(16): Show |
91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1383C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1383 | chr11 | 69089336 | ||||||
chr11:69089375 | T | A | 5 | a0004c0008t0013 a0004c0008t0017 a0004c0008t0031 others(2): Show |
11 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1422T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1422 | chr11 | 69089375 | ||||||
chr11:69089382 | G | A | 1 | a0004c0006t0035 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1429G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1429 | chr11 | 69089382 | ||||||
chr11:69089448 | C | T | 15 | a0003c0003t0002 a0003c0003t0038 a0003c0020t0002 others(12): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1495C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1495 | chr11 | 69089448 | ||||||
chr11:69089457 | G | A | 1 | a0004c0006t0035 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1504G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1504 | chr11 | 69089457 | ||||||
chr11:69089550 | T | G | 3 | a0004c0015t0014 a0004c0016t0014 a0014c0040t0014 |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1597 | chr11 | 69089550 | ||||||
chr11:69089566 | G | A | 1 | a0002c0002t0026 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1613 | chr11 | 69089566 | ||||||
chr11:69089570 | C | T | 60 | a0002c0002t0001 a0002c0002t0023 a0002c0002t0026 others(57): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1617 | chr11 | 69089570 | ||||||
chr11:69089753 | C | A | 3 | a0001c0001t0003 a0022c0035t0003 a0024c0033t0003 |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1800C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1800 | chr11 | 69089753 | ||||||
chr11:69089849 | T | C | 1 | a0005c0004t0037 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1896 | chr11 | 69089849 | ||||||
chr11:69089889 | G | T | 3 | a0001c0001t0003 a0022c0035t0003 a0024c0033t0003 |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1936G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1936 | chr11 | 69089889 | ||||||
chr11:69089916 | GT | G | 25 | a0003c0003t0002 a0003c0003t0038 a0003c0020t0002 others(22): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1971delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1971 | INFO_REALIGN_3_PRIME | chr11 | 69089916 | |||||
chr11:69089942 | C | T | 3 | a0001c0001t0003 a0022c0035t0003 a0024c0033t0003 |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1989C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1989 | chr11 | 69089942 | ||||||
chr11:69090125 | T | G | 1 | a0004c0006t0018 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2172T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2172 | chr11 | 69090125 | ||||||
chr11:69090172 | C | T | 1 | a0006c0007t0021 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2219C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2219 | chr11 | 69090172 | ||||||
chr11:69090194 | TCTCATCT others(27): Show |
T | 15 | a0003c0003t0002 a0003c0003t0038 a0003c0020t0002 others(12): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2245_*2278delATCT others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2245 | INFO_REALIGN_3_PRIME | chr11 | 69090194 | |||||
chr11:69090222 | C | T | 1 | a0001c0001t0010 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2269C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2269 | chr11 | 69090222 | ||||||
chr11:69090407 | G | C | 1 | a0001c0001t0010 | 9 | HG00558.hp2 HG00597.hp1 HG02015.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2454G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2454 | chr11 | 69090407 | ||||||
chr11:69090417 | T | A | 1 | a0003c0003t0038 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2464 | chr11 | 69090417 | ||||||
chr11:69090422 | T | A | 1 | a0002c0002t0027 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2469 | chr11 | 69090422 | ||||||
chr11:69090440 | T | G | 1 | a0008c0010t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2487T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2487 | chr11 | 69090440 | ||||||
chr11:69090519 | A | G | 1 | a0004c0006t0036 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2566 | chr11 | 69090519 | ||||||
chr11:69090568 | A | G | 3 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0022 |
37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2615A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2615 | chr11 | 69090568 | ||||||
chr11:69090588 | C | T | 1 | a0005c0004t0032 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2635C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2635 | chr11 | 69090588 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:69049357 | T | C | 267 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(264): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.109+251T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049357 | |||||||
chr11:69049403 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+297G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049403 | |||||||
chr11:69049407 | A | G | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+301A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049407 | |||||||
chr11:69049568 | C | T | 2 | a0005c0004t0007g0258 a0005c0004t0007g0259 |
2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.109+462C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049568 | |||||||
chr11:69049582 | C | G | 63 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(60): Show |
83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.109+476C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049582 | |||||||
chr11:69049647 | C | G | 39 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(36): Show |
44 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.109+541C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049647 | |||||||
chr11:69049761 | C | T | 208 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(205): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.109+655C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049761 | |||||||
chr11:69049973 | T | G | 6 | a0008c0010t0006g0028 a0008c0010t0006g0100 a0008c0010t0006g0101 others(3): Show |
6 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+867T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049973 | |||||||
chr11:69050256 | C | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1150C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050256 | |||||||
chr11:69050429 | G | A | 5 | a0008c0010t0006g0028 a0008c0010t0006g0100 a0008c0010t0006g0101 others(2): Show |
5 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1323G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050429 | |||||||
chr11:69050490 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1384G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050490 | |||||||
chr11:69050567 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1461G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050567 | |||||||
chr11:69050577 | T | C | 268 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(265): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.109+1471T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050577 | |||||||
chr11:69050629 | C | T | 1 | a0004c0006t0035g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+1523C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050629 | |||||||
chr11:69050638 | A | G | 21 | a0001c0005t0004g0001 a0001c0005t0004g0008 a0001c0005t0004g0025 others(18): Show |
34 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.109+1532A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050638 | |||||||
chr11:69050680 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1574G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050680 | |||||||
chr11:69050982 | T | C | 1 | a0004c0006t0020g0051 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.109+1876T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050982 | |||||||
chr11:69051025 | G | A | 1 | a0025c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+1919G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051025 | |||||||
chr11:69051028 | A | G | 216 | a0001c0001t0003g0084 a0001c0001t0004g0039 a0001c0001t0004g0155 others(213): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.109+1922A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051028 | |||||||
chr11:69051149 | A | G | 107 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(104): Show |
132 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.109+2043A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051149 | |||||||
chr11:69051267 | G | T | 213 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0005g0262 others(210): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.109+2161G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051267 | |||||||
chr11:69051468 | A | G | 64 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(61): Show |
84 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.109+2362A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051468 | |||||||
chr11:69051490 | G | C | 12 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(9): Show |
14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+2384G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051490 | |||||||
chr11:69051543 | C | T | 12 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(9): Show |
14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+2437C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051543 | |||||||
chr11:69051571 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.110-2462T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051571 | |||||||
chr11:69051590 | A | C | 2 | a0003c0003t0002g0174 a0003c0003t0002g0175 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.110-2443A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051590 | |||||||
chr11:69051629 | C | T | 65 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(62): Show |
85 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.110-2404C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051629 | |||||||
chr11:69051731 | C | T | 8 | a0001c0001t0010g0295 a0001c0001t0010g0296 a0001c0001t0010g0297 others(5): Show |
8 | HG00558.hp2 HG02015.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-2302C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051731 | |||||||
chr11:69051736 | C | T | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-2297C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051736 | |||||||
chr11:69051819 | A | T | 1 | a0005c0004t0008g0173 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110-2214A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051819 | |||||||
chr11:69051856 | G | T | 1 | a0002c0002t0001g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110-2177G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051856 | |||||||
chr11:69051966 | G | A | 2 | a0004c0011t0012g0195 a0004c0032t0012g0194 |
2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-2067G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051966 | |||||||
chr11:69052001 | G | A | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-2032G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052001 | |||||||
chr11:69052010 | G | A | 1 | a0001c0001t0003g0060 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.110-2023G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052010 | |||||||
chr11:69052030 | G | A | 1 | a0002c0030t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.110-2003G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052030 | |||||||
chr11:69052245 | C | T | 2 | a0005c0004t0007g0042 a0013c0025t0007g0172 |
3 | HG01070.hp2 HG01071.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.110-1788C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052245 | |||||||
chr11:69052352 | T | A | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1681T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052352 | |||||||
chr11:69052481 | G | A | 2 | a0002c0028t0001g0179 a0017c0036t0001g0180 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.110-1552G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052481 | |||||||
chr11:69052560 | A | G | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1473A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052560 | |||||||
chr11:69052577 | C | T | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-1456C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052577 | |||||||
chr11:69052591 | C | T | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1442C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052591 | |||||||
chr11:69052653 | C | T | 19 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.110-1380C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052653 | |||||||
chr11:69052655 | G | A | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1378G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052655 | |||||||
chr11:69052702 | G | A | 1 | a0012c0021t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.110-1331G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052702 | |||||||
chr11:69052712 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.110-1321G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052712 | |||||||
chr11:69052788 | T | C | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1245T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052788 | |||||||
chr11:69052803 | T | A | 2 | a0004c0008t0013g0187 a0004c0008t0031g0188 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-1230T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052803 | |||||||
chr11:69052931 | G | A | 1 | a0006c0031t0006g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.110-1102G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052931 | |||||||
chr11:69052948 | C | T | 1 | a0001c0005t0004g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.110-1085C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052948 | |||||||
chr11:69052961 | C | T | 62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(59): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.110-1072C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052961 | |||||||
chr11:69053014 | C | T | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1019C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053014 | |||||||
chr11:69053015 | G | A | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1018G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053015 | |||||||
chr11:69053028 | G | A | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1005G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053028 | |||||||
chr11:69053049 | T | C | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-984T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053049 | |||||||
chr11:69053101 | T | C | 209 | a0001c0001t0003g0084 a0001c0001t0004g0039 a0001c0001t0004g0155 others(206): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.110-932T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053101 | |||||||
chr11:69053148 | C | T | 84 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0003c0003t0002g0009 others(81): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.110-885C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053148 | |||||||
chr11:69053211 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110-822C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053211 | |||||||
chr11:69053358 | C | G | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.110-675C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053358 | |||||||
chr11:69053408 | A | G | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-625A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053408 | |||||||
chr11:69053455 | C | T | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-578C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053455 | |||||||
chr11:69053514 | A | G | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-519A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053514 | |||||||
chr11:69053566 | T | G | 176 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(173): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.110-467T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053566 | |||||||
chr11:69053826 | T | C | 2 | a0006c0007t0006g0166 a0006c0007t0021g0040 |
3 | HG01106.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.110-207T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053826 | |||||||
chr11:69053910 | T | C | 1 | a0001c0001t0005g0264 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-123T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053910 | |||||||
chr11:69053994 | A | T | 1 | a0004c0006t0009g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-39A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053994 | |||||||
chr11:69054148 | G | A | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+51G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054148 | |||||||
chr11:69054180 | G | C | 62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(59): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.174+83G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054180 | |||||||
chr11:69054233 | T | C | 21 | a0001c0005t0004g0001 a0001c0005t0004g0008 a0001c0005t0004g0025 others(18): Show |
34 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+136T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054233 | |||||||
chr11:69054349 | C | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+252C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054349 | |||||||
chr11:69054394 | G | A | 62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(59): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.174+297G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054394 | |||||||
chr11:69054449 | C | T | 1 | a0001c0001t0005g0294 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175-272C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054449 | |||||||
chr11:69054479 | T | C | 263 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(260): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.175-242T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054479 | |||||||
chr11:69054545 | C | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-176C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054545 | |||||||
chr11:69054555 | G | C | 52 | a0001c0001t0011g0168 a0004c0006t0009g0017 a0004c0006t0009g0044 others(49): Show |
64 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.175-166G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054555 | |||||||
chr11:69054661 | C | T | 1 | a0004c0006t0020g0051 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-60C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054661 | |||||||
chr11:69054964 | A | C | 2 | a0004c0008t0017g0106 a0004c0008t0034g0178 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.251+167A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69054964 | |||||||
chr11:69055000 | C | A | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-175C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055000 | |||||||
chr11:69055039 | G | A | 1 | a0002c0002t0001g0218 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.252-136G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055039 | |||||||
chr11:69055077 | G | A | 2 | a0003c0003t0002g0107 a0023c0027t0002g0186 |
2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.252-98G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055077 | |||||||
chr11:69055086 | C | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-89C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055086 | |||||||
chr11:69055363 | C | T | 19 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.429+11C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055363 | |||||||
chr11:69055419 | G | C | 2 | a0001c0001t0011g0168 a0006c0007t0006g0167 |
2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.429+67G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055419 | |||||||
chr11:69055501 | A | G | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+149A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055501 | |||||||
chr11:69055528 | T | TGTCAGCT others(39): Show |
119 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(116): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.429+304_429+349dup others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055528 | ||||||
chr11:69055574 | C | T | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.429+222C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055574 | |||||||
chr11:69055620 | C | T | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+268C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055620 | |||||||
chr11:69055656 | G | GCCAGTGT others(39): Show |
1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.429+343_429+388dup others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | ||||||
chr11:69055656 | G | GCCAGTGT others(85): Show |
83 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0003c0003t0002g0009 others(80): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.429+349_429+350ins others(92): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | ||||||
chr11:69055656 | G | GCCAGTGT others(177): Show |
1 | a0003c0003t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.429+349_429+350ins others(184): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | ||||||
chr11:69055656 | GCCAGTGT others(39): Show |
G | 12 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(9): Show |
14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.429+343_429+388del others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | ||||||
chr11:69055666 | C | CGTCAGCT others(39): Show |
1 | a0001c0001t0003g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.429+349_429+350ins others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055666 | ||||||
chr11:69055695 | A | AACTGAGG others(85): Show |
4 | a0002c0002t0001g0212 a0004c0008t0017g0106 a0005c0004t0008g0083 others(1): Show |
4 | HG02129.hp2 HG02630.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+349_429+350ins others(92): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055695 | ||||||
chr11:69055709 | T | G | 1 | a0005c0004t0008g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+357T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055709 | |||||||
chr11:69055779 | A | G | 214 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(211): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.429+427A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055779 | |||||||
chr11:69055965 | C | G | 1 | a0001c0001t0003g0080 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.429+613C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055965 | |||||||
chr11:69055975 | C | T | 1 | a0004c0008t0031g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+623C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055975 | |||||||
chr11:69056023 | A | G | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+671A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056023 | |||||||
chr11:69056076 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.429+724G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056076 | |||||||
chr11:69056176 | C | G | 210 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(207): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.429+824C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056176 | |||||||
chr11:69056239 | G | A | 187 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(184): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.429+887G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056239 | |||||||
chr11:69056275 | G | C | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+923G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056275 | |||||||
chr11:69056355 | C | T | 33 | a0001c0001t0004g0279 a0001c0001t0005g0012 a0001c0001t0005g0052 others(30): Show |
39 | HG00558.hp2 HG01496.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.429+1003C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056355 | |||||||
chr11:69056472 | T | C | 180 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(177): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.430-1106T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056472 | |||||||
chr11:69056511 | C | T | 6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-1067C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056511 | |||||||
chr11:69056588 | C | T | 1 | a0004c0013t0015g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430-990C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056588 | |||||||
chr11:69056636 | T | C | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-942T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056636 | |||||||
chr11:69056666 | T | TG | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-910dupG | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69056666 | ||||||
chr11:69056746 | T | G | 1 | a0002c0019t0001g0045 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430-832T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056746 | |||||||
chr11:69056819 | C | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-759C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056819 | |||||||
chr11:69056886 | A | G | 1 | a0004c0006t0035g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-692A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056886 | |||||||
chr11:69056919 | C | G | 3 | a0001c0001t0005g0289 a0001c0001t0005g0290 a0001c0001t0005g0294 |
3 | HG03130.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.430-659C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056919 | |||||||
chr11:69056923 | C | T | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.430-655C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056923 | |||||||
chr11:69056998 | C | T | 1 | a0009c0012t0002g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.430-580C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056998 | |||||||
chr11:69057046 | A | C | 212 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(209): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.430-532A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057046 | |||||||
chr11:69057065 | C | T | 218 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(215): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.430-513C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057065 | |||||||
chr11:69057118 | G | A | 1 | a0001c0001t0005g0262 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-460G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057118 | |||||||
chr11:69057128 | G | A | 12 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(9): Show |
14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-450G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057128 | |||||||
chr11:69057164 | G | A | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-414G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057164 | |||||||
chr11:69057248 | T | C | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-330T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057248 | |||||||
chr11:69057279 | C | A | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-299C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057279 | |||||||
chr11:69057286 | G | A | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-292G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057286 | |||||||
chr11:69057441 | C | T | 3 | a0010c0014t0013g0191 a0010c0014t0013g0192 a0010c0014t0013g0193 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.430-137C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057441 | |||||||
chr11:69057442 | G | A | 38 | a0001c0001t0011g0168 a0001c0005t0004g0001 a0001c0005t0004g0008 others(35): Show |
58 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.430-136G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057442 | |||||||
chr11:69057501 | G | C | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-77G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057501 | |||||||
chr11:69057521 | G | A | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-57G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057521 | |||||||
chr11:69057561 | G | T | 17 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(14): Show |
19 | HG02572.hp2 HG02622.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.430-17G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057561 | |||||||
chr11:69057569 | A | C | 212 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(209): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.430-9A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057569 | |||||||
chr11:69057870 | G | A | 32 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(29): Show |
37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.546+176G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057870 | |||||||
chr11:69057924 | G | A | 2 | a0001c0001t0022g0291 a0001c0001t0022g0292 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.546+230G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057924 | |||||||
chr11:69057983 | C | T | 16 | a0001c0005t0004g0001 a0001c0005t0004g0008 a0001c0005t0004g0025 others(13): Show |
29 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.546+289C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057983 | |||||||
chr11:69058007 | C | T | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.546+313C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058007 | |||||||
chr11:69058030 | C | T | 4 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+336C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058030 | |||||||
chr11:69058150 | C | G | 1 | a0002c0002t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.546+456C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058150 | |||||||
chr11:69058183 | C | G | 270 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.546+489C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058183 | |||||||
chr11:69058226 | C | G | 1 | a0001c0001t0003g0060 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+532C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058226 | |||||||
chr11:69058285 | G | A | 2 | a0004c0008t0013g0187 a0004c0008t0031g0188 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.546+591G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058285 | |||||||
chr11:69058317 | A | C | 1 | a0003c0020t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.546+623A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058317 | |||||||
chr11:69058481 | G | C | 1 | a0001c0001t0010g0295 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.546+787G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058481 | |||||||
chr11:69058526 | GT | G | 221 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(218): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.546+833delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058526 | |||||||
chr11:69058683 | C | T | 1 | a0002c0002t0001g0251 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.546+989C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058683 | |||||||
chr11:69058687 | A | G | 214 | a0001c0001t0003g0079 a0001c0001t0004g0039 a0001c0001t0004g0155 others(211): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.546+993A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058687 | |||||||
chr11:69058708 | C | T | 7 | a0001c0001t0011g0288 a0002c0002t0001g0018 a0002c0002t0001g0265 others(4): Show |
9 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+1014C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058708 | |||||||
chr11:69058721 | C | T | 1 | a0005c0004t0007g0160 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.546+1027C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058721 | |||||||
chr11:69058777 | C | A | 96 | a0001c0001t0003g0060 a0001c0001t0004g0039 a0001c0001t0004g0155 others(93): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.546+1083C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058777 | |||||||
chr11:69058846 | C | T | 1 | a0004c0006t0018g0015 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.546+1152C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058846 | |||||||
chr11:69058849 | C | T | 105 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0001t0011g0168 others(102): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.546+1155C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058849 | |||||||
chr11:69058863 | G | A | 1 | a0011c0017t0016g0276 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.546+1169G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058863 | |||||||
chr11:69059028 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0080 a0024c0033t0003g0020 |
3 | NA18956.hp2 NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.546+1334G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059028 | |||||||
chr11:69059031 | G | A | 1 | a0003c0003t0002g0112 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.546+1337G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059031 | |||||||
chr11:69059063 | C | T | 1 | a0001c0005t0004g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.546+1369C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059063 | |||||||
chr11:69059064 | G | A | 43 | a0001c0001t0004g0279 a0001c0001t0005g0012 a0001c0001t0005g0052 others(40): Show |
50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.546+1370G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059064 | |||||||
chr11:69059075 | G | A | 96 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(93): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.546+1381G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059075 | |||||||
chr11:69059085 | G | C | 20 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.546+1391G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059085 | |||||||
chr11:69059101 | G | A | 2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.546+1407G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059101 | |||||||
chr11:69059145 | G | A | 1 | a0009c0012t0002g0031 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.546+1451G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059145 | |||||||
chr11:69059237 | C | A | 1 | a0004c0011t0012g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.546+1543C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059237 | |||||||
chr11:69059387 | G | T | 25 | a0001c0001t0011g0168 a0004c0015t0014g0056 a0004c0015t0014g0057 others(22): Show |
32 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.546+1693G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059387 | |||||||
chr11:69059427 | G | A | 99 | a0001c0001t0011g0168 a0002c0002t0001g0003 a0002c0002t0001g0004 others(96): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.546+1733G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059427 | |||||||
chr11:69059469 | C | G | 1 | a0002c0019t0001g0045 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.546+1775C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059469 | |||||||
chr11:69059606 | T | C | 117 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.546+1912T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059606 | |||||||
chr11:69059614 | G | A | 19 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.546+1920G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059614 | |||||||
chr11:69059707 | T | A | 51 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(48): Show |
65 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.546+2013T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059707 | |||||||
chr11:69059747 | A | C | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+2053A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059747 | |||||||
chr11:69059816 | A | G | 1 | a0002c0002t0001g0250 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.546+2122A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059816 | |||||||
chr11:69059888 | T | C | 1 | a0003c0003t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.546+2194T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059888 | |||||||
chr11:69060113 | A | G | 1 | a0001c0001t0005g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.546+2419A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060113 | |||||||
chr11:69060158 | C | G | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.546+2464C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060158 | |||||||
chr11:69060181 | G | T | 1 | a0004c0006t0009g0183 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.546+2487G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060181 | |||||||
chr11:69060187 | A | G | 118 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(115): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.546+2493A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060187 | |||||||
chr11:69060197 | T | C | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.546+2503T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060197 | |||||||
chr11:69060202 | CCA | C | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+2513_546+2514d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69060202 | ||||||
chr11:69060249 | T | C | 248 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(245): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.546+2555T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060249 | |||||||
chr11:69060391 | C | T | 16 | a0002c0002t0001g0004 a0002c0002t0001g0049 a0002c0002t0001g0234 others(13): Show |
21 | HG00408.hp2 HG00621.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.547-2493C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060391 | |||||||
chr11:69060692 | G | A | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-2192G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060692 | |||||||
chr11:69060749 | A | C | 1 | a0017c0036t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-2135A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060749 | |||||||
chr11:69060750 | G | T | 1 | a0017c0036t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-2134G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060750 | |||||||
chr11:69060770 | T | C | 116 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-2114T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060770 | |||||||
chr11:69060856 | T | C | 3 | a0001c0001t0005g0052 a0001c0001t0005g0277 a0001c0001t0005g0278 |
4 | NA18612.hp1 NA18947.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2028T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060856 | |||||||
chr11:69060860 | T | C | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-2024T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060860 | |||||||
chr11:69060866 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.547-2018C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060866 | |||||||
chr11:69060952 | G | A | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-1932G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060952 | |||||||
chr11:69060995 | G | A | 1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.547-1889G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060995 | |||||||
chr11:69061008 | A | C | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-1876A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061008 | |||||||
chr11:69061210 | G | A | 116 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-1674G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061210 | |||||||
chr11:69061330 | T | TC | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.547-1552dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69061330 | ||||||
chr11:69061413 | G | A | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-1471G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061413 | |||||||
chr11:69061461 | G | A | 65 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(62): Show |
87 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.547-1423G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061461 | |||||||
chr11:69061481 | C | T | 20 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-1403C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061481 | |||||||
chr11:69061580 | C | T | 1 | a0001c0001t0005g0264 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.547-1304C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061580 | |||||||
chr11:69061636 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.547-1248G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061636 | |||||||
chr11:69061776 | A | T | 1 | a0025c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.547-1108A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061776 | |||||||
chr11:69061854 | GGTGGT | G | 116 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-1023_547-1019d others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69061854 | ||||||
chr11:69061920 | T | C | 116 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-964T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061920 | |||||||
chr11:69062048 | T | C | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-836T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062048 | |||||||
chr11:69062066 | C | T | 116 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(113): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-818C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062066 | |||||||
chr11:69062067 | G | A | 1 | a0006c0007t0006g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.547-817G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062067 | |||||||
chr11:69062103 | A | C | 2 | a0012c0021t0001g0214 a0012c0021t0001g0244 |
2 | NA18964.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.547-781A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062103 | |||||||
chr11:69062170 | C | T | 96 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(93): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.547-714C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062170 | |||||||
chr11:69062349 | G | T | 20 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-535G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062349 | |||||||
chr11:69062422 | G | A | 1 | a0009c0012t0002g0114 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.547-462G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062422 | |||||||
chr11:69062486 | C | T | 19 | a0001c0001t0011g0168 a0006c0007t0006g0005 a0006c0007t0006g0016 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.547-398C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062486 | |||||||
chr11:69062555 | AC | A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.547-327delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69062555 | ||||||
chr11:69062601 | T | TTGGACA | 117 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.547-283_547-282ins others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062601 | |||||||
chr11:69062645 | C | T | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547-239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062645 | |||||||
chr11:69062649 | C | T | 1 | a0002c0002t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.547-235C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062649 | |||||||
chr11:69062758 | G | A | 117 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(114): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.547-126G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062758 | |||||||
chr11:69062805 | C | T | 5 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-79C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062805 | |||||||
chr11:69063044 | C | T | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.653+54C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063044 | |||||||
chr11:69063160 | T | G | 182 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(179): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.653+170T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063160 | |||||||
chr11:69063197 | T | C | 3 | a0010c0014t0013g0191 a0010c0014t0013g0192 a0010c0014t0013g0193 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.653+207T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063197 | |||||||
chr11:69063222 | C | T | 1 | a0010c0014t0013g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.653+232C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063222 | |||||||
chr11:69063239 | G | A | 77 | a0002c0002t0001g0221 a0002c0002t0001g0255 a0003c0003t0002g0009 others(74): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.653+249G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063239 | |||||||
chr11:69063260 | G | C | 9 | a0001c0001t0011g0168 a0001c0001t0011g0280 a0001c0001t0011g0287 others(6): Show |
9 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+270G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063260 | |||||||
chr11:69063260 | G | GC | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+271dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | 69063260 | ||||||
chr11:69063290 | C | T | 1 | a0005c0004t0007g0160 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.653+300C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063290 | |||||||
chr11:69063323 | C | T | 5 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0016t0014g0054 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+333C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063323 | |||||||
chr11:69063390 | C | T | 3 | a0004c0008t0017g0106 a0004c0008t0017g0177 a0004c0008t0034g0178 |
3 | HG02630.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+400C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063390 | |||||||
chr11:69063456 | G | A | 29 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(26): Show |
40 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.654-439G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063456 | |||||||
chr11:69063467 | A | G | 1 | a0001c0001t0010g0302 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.654-428A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063467 | |||||||
chr11:69063501 | G | A | 2 | a0002c0002t0001g0182 a0002c0002t0001g0246 |
2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.654-394G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063501 | |||||||
chr11:69063514 | C | T | 1 | a0002c0028t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.654-381C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063514 | |||||||
chr11:69063698 | C | G | 143 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(140): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.654-197C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063698 | |||||||
chr11:69063699 | G | A | 2 | a0002c0028t0001g0179 a0017c0036t0001g0180 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.654-196G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063699 | |||||||
chr11:69063755 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.654-140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063755 | |||||||
chr11:69063825 | C | G | 90 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(87): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.654-70C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063825 | |||||||
chr11:69063828 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.654-67G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063828 | |||||||
chr11:69063997 | T | C | 1 | a0001c0001t0022g0291 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.726+30T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69063997 | |||||||
chr11:69064068 | C | T | 1 | a0001c0001t0003g0022 | 2 | NA18986.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.726+101C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064068 | |||||||
chr11:69064175 | G | A | 1 | a0006c0007t0021g0040 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.726+208G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064175 | |||||||
chr11:69064285 | C | CT | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+318_726+319ins others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064285 | |||||||
chr11:69064317 | C | T | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+350C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064317 | |||||||
chr11:69064431 | C | T | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.726+464C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064431 | |||||||
chr11:69064441 | C | T | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.726+474C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064441 | |||||||
chr11:69064452 | C | T | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+485C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064452 | |||||||
chr11:69064562 | A | C | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+595A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064562 | |||||||
chr11:69064663 | A | C | 1 | a0002c0002t0001g0048 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.726+696A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064663 | |||||||
chr11:69064753 | G | A | 21 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(18): Show |
35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.726+786G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064753 | |||||||
chr11:69064883 | T | TTGTC | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.726+919_726+920ins others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064883 | ||||||
chr11:69064929 | CTG | C | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.726+972_726+973del others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064929 | ||||||
chr11:69064945 | A | T | 1 | a0005c0004t0037g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.726+978A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064945 | |||||||
chr11:69064959 | AGTGTCTG others(33): Show |
A | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.726+1002_726+1041d others(42): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064959 | ||||||
chr11:69064964 | C | CTG | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.726+1000_726+1001d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064964 | ||||||
chr11:69064981 | A | G | 66 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(63): Show |
88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.726+1014A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064981 | |||||||
chr11:69064981 | ATGTC | A | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.726+1018_726+1021d others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064981 | ||||||
chr11:69065020 | T | G | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1053T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065020 | |||||||
chr11:69065034 | T | C | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.726+1067T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065034 | |||||||
chr11:69065037 | G | A | 93 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(90): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.726+1070G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065037 | |||||||
chr11:69065062 | CTA | C | 172 | a0001c0001t0003g0084 a0001c0001t0004g0039 a0001c0001t0004g0155 others(169): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.726+1097_726+1098d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69065062 | ||||||
chr11:69065062 | CTATG | C | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+1097_726+1100d others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69065062 | ||||||
chr11:69065126 | G | A | 1 | a0005c0004t0008g0140 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.726+1159G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065126 | |||||||
chr11:69065155 | T | C | 1 | a0001c0001t0005g0281 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.726+1188T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065155 | |||||||
chr11:69065236 | C | T | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.726+1269C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065236 | |||||||
chr11:69065247 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.726+1280G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065247 | |||||||
chr11:69065262 | C | G | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+1295C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065262 | |||||||
chr11:69065366 | A | G | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.726+1399A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065366 | |||||||
chr11:69065380 | G | A | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(65): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.726+1413G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065380 | |||||||
chr11:69065419 | C | T | 1 | a0003c0003t0002g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.726+1452C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065419 | |||||||
chr11:69065507 | G | A | 2 | a0001c0005t0041g0091 a0016c0041t0004g0090 |
2 | HG00639.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.726+1540G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065507 | |||||||
chr11:69065605 | C | G | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.726+1638C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065605 | |||||||
chr11:69065925 | G | C | 2 | a0001c0005t0004g0025 a0001c0005t0004g0087 |
3 | NA18950.hp1 NA18975.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.727-1578G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065925 | |||||||
chr11:69065953 | G | T | 1 | a0002c0002t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.727-1550G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065953 | |||||||
chr11:69065988 | G | C | 1 | a0001c0001t0005g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.727-1515G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065988 | |||||||
chr11:69065994 | C | T | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1509C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065994 | |||||||
chr11:69066027 | T | A | 1 | a0003c0020t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.727-1476T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066027 | |||||||
chr11:69066028 | G | T | 1 | a0003c0020t0002g0162 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.727-1475G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066028 | |||||||
chr11:69066045 | C | T | 1 | a0002c0002t0028g0242 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.727-1458C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066045 | |||||||
chr11:69066053 | A | G | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.727-1450A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066053 | |||||||
chr11:69066069 | T | A | 1 | a0001c0001t0003g0060 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.727-1434T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066069 | |||||||
chr11:69066097 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.727-1406T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066097 | |||||||
chr11:69066127 | A | G | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1376A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066127 | |||||||
chr11:69066140 | T | C | 2 | a0001c0001t0011g0282 a0001c0001t0011g0283 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.727-1363T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066140 | |||||||
chr11:69066164 | A | G | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1339A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066164 | |||||||
chr11:69066213 | C | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0080 others(1): Show |
4 | NA18956.hp2 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-1290C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066213 | |||||||
chr11:69066235 | G | C | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1268G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066235 | |||||||
chr11:69066258 | T | C | 264 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(261): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.727-1245T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066258 | |||||||
chr11:69066327 | A | T | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.727-1176A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066327 | |||||||
chr11:69066380 | C | T | 1 | a0006c0007t0006g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.727-1123C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066380 | |||||||
chr11:69066415 | A | G | 148 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(145): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.727-1088A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066415 | |||||||
chr11:69066568 | C | A | 4 | a0003c0003t0002g0009 a0003c0003t0002g0112 a0003c0003t0002g0117 others(1): Show |
7 | HG00733.hp1 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-935C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066568 | |||||||
chr11:69066636 | C | T | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-867C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066636 | |||||||
chr11:69066643 | G | T | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.727-860G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066643 | |||||||
chr11:69066648 | G | C | 1 | a0004c0011t0012g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727-855G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066648 | |||||||
chr11:69066713 | G | C | 6 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0005g0270 others(3): Show |
6 | HG00544.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-790G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066713 | |||||||
chr11:69066771 | C | T | 1 | a0025c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.727-732C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066771 | |||||||
chr11:69066799 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.727-704G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066799 | |||||||
chr11:69066873 | A | G | 110 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(107): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-630A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066873 | |||||||
chr11:69066905 | G | A | 126 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(123): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.727-598G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066905 | |||||||
chr11:69066923 | C | G | 1 | a0001c0001t0011g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727-580C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066923 | |||||||
chr11:69066961 | C | T | 1 | a0004c0006t0020g0051 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.727-542C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066961 | |||||||
chr11:69067039 | A | G | 4 | a0002c0002t0001g0018 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-464A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067039 | |||||||
chr11:69067112 | C | A | 3 | a0001c0001t0005g0012 a0001c0001t0005g0284 a0001c0001t0005g0285 |
6 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-391C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067112 | |||||||
chr11:69067176 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.727-327A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067176 | |||||||
chr11:69067205 | C | T | 4 | a0001c0001t0010g0275 a0001c0001t0010g0295 a0001c0001t0010g0300 others(1): Show |
4 | HG00597.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-298C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067205 | |||||||
chr11:69067363 | G | A | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(65): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.727-140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067363 | |||||||
chr11:69067500 | T | C | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
splice_region_variant&intron_variant | LOW | c.727-3T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067500 | |||||||
chr11:69067714 | T | A | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+109T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067714 | |||||||
chr11:69067845 | T | G | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+240T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067845 | |||||||
chr11:69067904 | A | T | 236 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(233): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.829+299A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067904 | |||||||
chr11:69068017 | G | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+412G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068017 | |||||||
chr11:69068132 | G | T | 1 | a0004c0008t0013g0190 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.829+527G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068132 | |||||||
chr11:69068159 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.829+554C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068159 | |||||||
chr11:69068160 | G | A | 12 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.829+555G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068160 | |||||||
chr11:69068289 | A | C | 1 | a0009c0012t0002g0031 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.829+684A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068289 | |||||||
chr11:69068303 | C | G | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+698C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068303 | |||||||
chr11:69068314 | G | GCCGTCTG others(71): Show |
1 | a0004c0016t0014g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+736_829+737ins others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068314 | ||||||
chr11:69068316 | CGTCTGAG others(734): Show |
C | 1 | a0001c0001t0011g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.829+734_830-1351de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068316 | ||||||
chr11:69068329 | G | GGAAGTGA others(32): Show |
2 | a0005c0004t0007g0111 a0005c0004t0007g0141 |
2 | HG01168.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.829+736_829+737ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068329 | ||||||
chr11:69068342 | C | CTGGGAGC others(1045): Show |
2 | a0001c0001t0004g0039 a0001c0001t0004g0155 |
3 | HG00438.hp2 NA18945.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.829+853_829+854ins others(1052): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068342 | ||||||
chr11:69068342 | C | CTGGGAGC others(149): Show |
1 | a0001c0001t0003g0077 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.829+771_829+772ins others(156): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068342 | ||||||
chr11:69068342 | C | G | 117 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(114): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.829+737C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068342 | |||||||
chr11:69068353 | A | G | 2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.829+748A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068353 | |||||||
chr11:69068354 | C | T | 1 | a0010c0014t0013g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.829+749C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068354 | |||||||
chr11:69068364 | C | T | 12 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.829+759C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068364 | |||||||
chr11:69068368 | G | T | 82 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(79): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.829+763G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068368 | |||||||
chr11:69068381 | G | C | 9 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0015t0014g0056 others(6): Show |
10 | HG01168.hp2 HG02080.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+776G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068381 | |||||||
chr11:69068381 | G | GTGGGAGC others(32): Show |
4 | a0001c0001t0010g0299 a0004c0006t0009g0017 a0004c0006t0009g0183 others(1): Show |
6 | HG00558.hp2 HG01346.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.829+815_829+853dup others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068381 | ||||||
chr11:69068381 | GTGGGAGC others(32): Show |
G | 1 | a0002c0002t0001g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.829+815_829+853del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068381 | ||||||
chr11:69068420 | C | CTGGGAGC others(188): Show |
4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.829+853_829+854ins others(195): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | ||||||
chr11:69068420 | C | CTGGGAGC others(227): Show |
2 | a0004c0011t0012g0198 a0004c0011t0012g0203 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.829+853_829+854ins others(234): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | ||||||
chr11:69068420 | C | G | 1 | a0001c0001t0003g0077 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.829+815C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068420 | |||||||
chr11:69068420 | CTGGGAGC others(32): Show |
C | 59 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(56): Show |
79 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.829+893_829+931del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | ||||||
chr11:69068434 | G | GTCTGAGT others(32): Show |
1 | a0003c0003t0002g0124 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.829+853_829+854ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068434 | ||||||
chr11:69068456 | G | C | 31 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(28): Show |
44 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.829+851G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068456 | |||||||
chr11:69068459 | G | C | 203 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(200): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.829+854G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068459 | |||||||
chr11:69068473 | G | A | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.829+868G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068473 | |||||||
chr11:69068498 | G | C | 15 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0230 others(12): Show |
17 | HG00741.hp2 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.829+893G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068498 | |||||||
chr11:69068498 | G | GTGGGAGC others(188): Show |
6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+931_829+932ins others(195): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068498 | ||||||
chr11:69068537 | C | CTGGGAGC others(32): Show |
74 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(71): Show |
93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.829+1016_829+1054d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068537 | ||||||
chr11:69068537 | C | G | 74 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(71): Show |
94 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.829+932C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068537 | |||||||
chr11:69068538 | T | TGGGAGCA others(110): Show |
1 | a0004c0016t0014g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+1005_829+1006i others(119): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068538 | ||||||
chr11:69068548 | A | G | 6 | a0002c0002t0001g0049 a0002c0002t0001g0230 a0002c0002t0001g0234 others(3): Show |
7 | HG01192.hp1 NA18956.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+943A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068548 | |||||||
chr11:69068576 | G | C | 4 | a0001c0001t0010g0275 a0001c0001t0010g0295 a0001c0001t0010g0300 others(1): Show |
4 | HG00597.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+971G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068576 | |||||||
chr11:69068577 | T | TGGGAGCA others(149): Show |
4 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1022_829+1023i others(158): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068577 | ||||||
chr11:69068587 | A | G | 59 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(56): Show |
77 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.829+982A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068587 | |||||||
chr11:69068611 | C | G | 1 | a0001c0005t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1006C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068611 | |||||||
chr11:69068615 | G | GTGGGAGC others(691): Show |
1 | a0003c0003t0002g0033 | 2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.829+1054_829+1055i others(700): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068615 | ||||||
chr11:69068621 | GCAGGACC others(32): Show |
G | 1 | a0002c0002t0001g0048 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.829+1055_829+1093d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068621 | ||||||
chr11:69068629 | G | A | 4 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1024G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068629 | |||||||
chr11:69068629 | G | GTCTGAGT others(149): Show |
1 | a0004c0016t0014g0054 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.829+1054_829+1055i others(158): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068629 | ||||||
chr11:69068651 | G | A | 1 | a0001c0005t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1046G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068651 | |||||||
chr11:69068654 | G | C | 7 | a0002c0002t0001g0049 a0002c0002t0001g0230 a0002c0002t0001g0234 others(4): Show |
8 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1049G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068654 | |||||||
chr11:69068655 | T | G | 1 | a0001c0005t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1050T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068655 | |||||||
chr11:69068660 | A | G | 269 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(266): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.829+1055A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068660 | |||||||
chr11:69068686 | G | GACCGCAG others(227): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.829+1123_829+1124i others(236): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068686 | ||||||
chr11:69068693 | G | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(58): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.829+1088G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068693 | |||||||
chr11:69068694 | TGGGAGCA others(71): Show |
T | 1 | a0001c0005t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1163_829+1240d others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068694 | ||||||
chr11:69068725 | G | T | 5 | a0002c0002t0001g0018 a0002c0002t0001g0265 a0002c0002t0001g0266 others(2): Show |
7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+1120G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068725 | |||||||
chr11:69068728 | C | CGCAGTGG others(32): Show |
4 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1161_829+1162i others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068728 | ||||||
chr11:69068728 | C | G | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.829+1123C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068728 | |||||||
chr11:69068729 | G | A | 6 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(3): Show |
7 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.829+1124G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068729 | |||||||
chr11:69068733 | T | G | 6 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(3): Show |
7 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.829+1128T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068733 | |||||||
chr11:69068768 | A | G | 26 | a0001c0005t0004g0061 a0002c0002t0001g0049 a0002c0002t0001g0234 others(23): Show |
30 | HG00323.hp2 HG01192.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.829+1163A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068768 | |||||||
chr11:69068772 | G | T | 24 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(21): Show |
28 | HG00323.hp2 HG01192.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.829+1167G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068772 | |||||||
chr11:69068785 | G | A | 7 | a0001c0005t0004g0027 a0002c0002t0001g0049 a0002c0002t0001g0234 others(4): Show |
8 | HG01192.hp1 HG02257.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1180G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068785 | |||||||
chr11:69068807 | G | A | 8 | a0003c0003t0002g0014 a0003c0003t0002g0135 a0003c0003t0002g0137 others(5): Show |
10 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.829+1202G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068807 | |||||||
chr11:69068810 | G | C | 1 | a0020c0029t0039g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829+1205G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068810 | |||||||
chr11:69068811 | T | G | 8 | a0003c0003t0002g0014 a0003c0003t0002g0135 a0003c0003t0002g0137 others(5): Show |
10 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.829+1206T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068811 | |||||||
chr11:69068821 | ACCGTCTG others(538): Show |
A | 1 | a0020c0029t0039g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829+1244_830-1037d others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068821 | ||||||
chr11:69068823 | C | T | 56 | a0001c0001t0004g0279 a0003c0003t0002g0009 a0003c0003t0002g0013 others(53): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.829+1218C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068823 | |||||||
chr11:69068824 | G | A | 146 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(143): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.829+1219G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068824 | |||||||
chr11:69068849 | C | G | 228 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(225): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.829+1244C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068849 | |||||||
chr11:69068862 | C | T | 4 | a0003c0003t0002g0014 a0003c0003t0002g0135 a0003c0003t0002g0137 others(1): Show |
6 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.829+1257C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068862 | |||||||
chr11:69068885 | GCACTGGG others(304): Show |
G | 2 | a0003c0003t0002g0014 a0004c0006t0009g0185 |
4 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+1283_830-1232d others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068885 | ||||||
chr11:69068888 | C | G | 148 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(145): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.829+1283C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068888 | |||||||
chr11:69068889 | T | TGGGAGCA others(31): Show |
2 | a0005c0004t0008g0083 a0005c0004t0008g0145 |
2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.829+1309_829+1310i others(40): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068889 | ||||||
chr11:69068920 | G | T | 7 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(4): Show |
8 | HG01192.hp1 HG02257.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1315G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068920 | |||||||
chr11:69068923 | C | A | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.829+1318C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068923 | |||||||
chr11:69068927 | C | G | 40 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(37): Show |
56 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.829+1322C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068927 | |||||||
chr11:69068940 | CGTCTGAG others(32): Show |
C | 1 | a0001c0005t0004g0027 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1354_829+1392d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068940 | ||||||
chr11:69068959 | T | G | 149 | a0001c0001t0003g0073 a0001c0001t0004g0039 a0001c0001t0004g0155 others(146): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.829+1354T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068959 | |||||||
chr11:69068962 | C | A | 3 | a0003c0003t0002g0135 a0003c0003t0002g0137 a0003c0003t0002g0158 |
3 | HG00323.hp2 HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.829+1357C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068962 | |||||||
chr11:69068966 | C | G | 263 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(260): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.829+1361C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068966 | |||||||
chr11:69068979 | T | C | 173 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(170): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.829+1374T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068979 | |||||||
chr11:69069002 | G | A | 1 | a0004c0011t0012g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.829+1397G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069002 | |||||||
chr11:69069006 | T | G | 5 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.829+1401T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069006 | |||||||
chr11:69069018 | T | C | 28 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0008t0017g0106 others(25): Show |
36 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.830-1412T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069018 | |||||||
chr11:69069019 | GTCTGAGT others(71): Show |
G | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1350_830-1273d others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069019 | ||||||
chr11:69069041 | G | A | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1389G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069041 | |||||||
chr11:69069045 | T | G | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1385T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069045 | |||||||
chr11:69069057 | T | C | 8 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0011t0012g0195 others(5): Show |
9 | HG02145.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-1373T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069057 | |||||||
chr11:69069058 | G | A | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1372G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069058 | |||||||
chr11:69069058 | G | C | 96 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(93): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.830-1372G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069058 | |||||||
chr11:69069076 | GACC | G | 90 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(87): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.830-1351_830-1349d others(5): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069076 | ||||||
chr11:69069078 | C | CACGGGGA others(1232): Show |
1 | a0004c0006t0009g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1241): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(299): Show |
1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(308): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(1312): Show |
1 | a0004c0006t0009g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1321): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(1234): Show |
1 | a0004c0006t0009g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(1273): Show |
1 | a0004c0006t0009g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1282): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(1234): Show |
1 | a0015c0038t0009g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069078 | C | CACGGGGA others(1234): Show |
1 | a0004c0006t0009g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | |||||||
chr11:69069079 | C | CGCACTGG others(146): Show |
2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.830-1351_830-1350i others(155): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | |||||||
chr11:69069079 | C | CGCAGTGG others(185): Show |
1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-1351_830-1350i others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | |||||||
chr11:69069079 | C | CGCAGTGG others(223): Show |
5 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-1351_830-1350i others(232): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | |||||||
chr11:69069079 | C | CGCAGTGG others(29): Show |
1 | a0003c0003t0002g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.830-1351_830-1350i others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | |||||||
chr11:69069079 | C | G | 6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-1351C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | |||||||
chr11:69069080 | A | G | 11 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(8): Show |
12 | HG01192.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.830-1350A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069080 | |||||||
chr11:69069083 | G | C | 105 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(102): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.830-1347G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069083 | |||||||
chr11:69069084 | G | T | 11 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(8): Show |
12 | HG01192.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.830-1346G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069084 | |||||||
chr11:69069097 | A | C | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1333A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069097 | |||||||
chr11:69069097 | A | G | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1333A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069097 | |||||||
chr11:69069097 | ATCTGAGT others(538): Show |
A | 1 | a0011c0017t0016g0276 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.830-1295_830-751de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069097 | ||||||
chr11:69069122 | G | C | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1308G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069122 | |||||||
chr11:69069123 | T | G | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1307T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069123 | |||||||
chr11:69069135 | T | C | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1295T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069135 | |||||||
chr11:69069135 | TGTCTGAG others(70): Show |
T | 2 | a0001c0001t0011g0282 a0001c0001t0011g0283 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.830-1256_830-1180d others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069135 | ||||||
chr11:69069136 | G | A | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1294G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069136 | |||||||
chr11:69069149 | G | C | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1281G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069149 | |||||||
chr11:69069154 | G | T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1276G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069154 | |||||||
chr11:69069155 | AC | A | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1273delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069155 | ||||||
chr11:69069157 | C | T | 1 | a0004c0006t0007g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.830-1273C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069157 | |||||||
chr11:69069158 | G | A | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1272G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069158 | |||||||
chr11:69069162 | T | G | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1268T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069162 | |||||||
chr11:69069174 | T | C | 116 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(113): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.830-1256T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069174 | |||||||
chr11:69069174 | TGTCTGAG others(265): Show |
T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1242_830-971de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069174 | ||||||
chr11:69069188 | C | G | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1242C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069188 | |||||||
chr11:69069194 | A | AC | 13 | a0001c0001t0005g0289 a0001c0001t0005g0290 a0001c0001t0005g0294 others(10): Show |
14 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.830-1235dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069194 | ||||||
chr11:69069196 | A | G | 13 | a0001c0001t0005g0289 a0001c0001t0005g0290 a0001c0001t0005g0294 others(10): Show |
14 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.830-1234A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069196 | |||||||
chr11:69069200 | G | T | 12 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(9): Show |
15 | HG01192.hp1 HG01243.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-1230G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069200 | |||||||
chr11:69069200 | GGGGAGCA others(305): Show |
G | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1192_830-881de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069200 | ||||||
chr11:69069210 | A | G | 1 | a0005c0004t0007g0042 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.830-1220A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069210 | |||||||
chr11:69069234 | C | T | 1 | a0006c0007t0006g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069234 | |||||||
chr11:69069238 | G | A | 1 | a0006c0007t0006g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1192G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069238 | |||||||
chr11:69069238 | G | C | 9 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(6): Show |
10 | HG01168.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1192G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069238 | |||||||
chr11:69069251 | C | T | 4 | a0002c0002t0001g0239 a0002c0002t0001g0240 a0002c0002t0001g0241 others(1): Show |
4 | NA18941.hp2 NA18979.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-1179C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069251 | |||||||
chr11:69069265 | G | T | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.830-1165G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069265 | |||||||
chr11:69069270 | G | C | 11 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(8): Show |
12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.830-1160G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069270 | |||||||
chr11:69069273 | C | A | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1157C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069273 | |||||||
chr11:69069277 | C | CTGGGAGC others(32): Show |
1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-1139_830-1101d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069277 | ||||||
chr11:69069277 | C | G | 31 | a0001c0001t0003g0073 a0002c0002t0001g0018 a0002c0002t0001g0265 others(28): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.830-1153C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069277 | |||||||
chr11:69069288 | A | G | 1 | a0006c0007t0006g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1142A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069288 | |||||||
chr11:69069290 | C | T | 1 | a0017c0036t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.830-1140C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069290 | |||||||
chr11:69069309 | G | T | 8 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(5): Show |
9 | HG01192.hp1 HG02258.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-1121G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069309 | |||||||
chr11:69069320 | G | A | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1110G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069320 | |||||||
chr11:69069327 | A | G | 5 | a0004c0008t0004g0105 a0004c0008t0017g0176 a0006c0007t0006g0167 others(2): Show |
5 | HG02257.hp2 HG02258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-1103A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069327 | |||||||
chr11:69069327 | ACCATCTG others(32): Show |
A | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1100_830-1062d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069327 | ||||||
chr11:69069329 | C | T | 1 | a0002c0028t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.830-1101C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069329 | |||||||
chr11:69069330 | A | G | 263 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(260): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.830-1100A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069330 | |||||||
chr11:69069348 | T | G | 132 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(129): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.830-1082T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069348 | |||||||
chr11:69069355 | G | C | 19 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(16): Show |
22 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.830-1075G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069355 | |||||||
chr11:69069366 | G | A | 114 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(111): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.830-1064G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069366 | |||||||
chr11:69069366 | G | GCCGTCTG others(71): Show |
1 | a0004c0008t0017g0177 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.830-1026_830-1025i others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069366 | ||||||
chr11:69069366 | GCCGTCTG others(32): Show |
G | 1 | a0001c0001t0010g0296 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.830-997_830-959del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069366 | ||||||
chr11:69069368 | C | T | 1 | a0004c0006t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1062C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069368 | |||||||
chr11:69069369 | G | A | 68 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(65): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.830-1061G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069369 | |||||||
chr11:69069381 | G | A | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.830-1049G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069381 | |||||||
chr11:69069394 | G | C | 1 | a0006c0007t0006g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1036G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069394 | |||||||
chr11:69069405 | A | G | 41 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(38): Show |
54 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.830-1025A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069405 | |||||||
chr11:69069412 | G | C | 1 | a0004c0006t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1018G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069412 | |||||||
chr11:69069421 | G | C | 1 | a0004c0006t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1009G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069421 | |||||||
chr11:69069426 | G | T | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1004G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069426 | |||||||
chr11:69069426 | GACCGCAG others(71): Show |
G | 1 | a0002c0002t0029g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.830-926_830-849del others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069426 | ||||||
chr11:69069427 | ACCGCAGT others(72): Show |
A | 1 | a0004c0006t0009g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1001_830-923de others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069427 | ||||||
chr11:69069433 | G | C | 7 | a0004c0008t0004g0105 a0004c0008t0017g0176 a0005c0004t0007g0141 others(4): Show |
7 | HG01168.hp2 HG01255.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-997G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069433 | |||||||
chr11:69069446 | C | T | 1 | a0003c0003t0002g0014 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-984C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069446 | |||||||
chr11:69069465 | G | T | 3 | a0004c0008t0004g0105 a0004c0008t0017g0176 a0017c0036t0001g0180 |
3 | HG02258.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.830-965G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069465 | |||||||
chr11:69069472 | C | G | 37 | a0001c0001t0005g0052 a0002c0002t0001g0049 a0002c0002t0001g0234 others(34): Show |
43 | HG01168.hp2 HG01192.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.830-958C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069472 | |||||||
chr11:69069490 | G | C | 3 | a0003c0003t0002g0014 a0003c0003t0002g0137 a0003c0003t0002g0158 |
5 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-940G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069490 | |||||||
chr11:69069499 | G | C | 4 | a0003c0003t0002g0014 a0003c0003t0002g0137 a0003c0003t0002g0158 others(1): Show |
6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-931G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069499 | |||||||
chr11:69069499 | G | GAAGTGAC others(265): Show |
1 | a0006c0007t0006g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.830-927_830-926ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069499 | ||||||
chr11:69069504 | T | G | 119 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(116): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.830-926T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069504 | |||||||
chr11:69069505 | AC | A | 4 | a0003c0003t0002g0014 a0003c0003t0002g0137 a0003c0003t0002g0158 others(1): Show |
6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-923delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069505 | ||||||
chr11:69069508 | G | A | 5 | a0003c0003t0002g0014 a0003c0003t0002g0137 a0003c0003t0002g0158 others(2): Show |
7 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-922G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069508 | |||||||
chr11:69069508 | G | GCACTGGG others(265): Show |
1 | a0003c0003t0002g0119 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.830-920_830-919ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069508 | ||||||
chr11:69069511 | G | C | 19 | a0004c0008t0004g0105 a0004c0008t0017g0176 a0006c0007t0006g0005 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.830-919G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069511 | |||||||
chr11:69069512 | T | G | 6 | a0003c0003t0002g0014 a0003c0003t0002g0119 a0003c0003t0002g0137 others(3): Show |
8 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.830-918T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069512 | |||||||
chr11:69069512 | T | TGGGAGCA others(31): Show |
5 | a0002c0002t0001g0049 a0002c0002t0001g0234 a0002c0002t0001g0235 others(2): Show |
6 | HG01192.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-893_830-892ins others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(263): Show |
1 | a0002c0002t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.830-881_830-880ins others(270): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(265): Show |
1 | a0002c0002t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(265): Show |
50 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0011 others(47): Show |
67 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(226): Show |
68 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0030 others(65): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(226): Show |
5 | a0002c0002t0001g0004 a0002c0002t0023g0004 a0002c0002t0026g0004 others(2): Show |
9 | HG00621.hp2 HG02071.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(265): Show |
1 | a0021c0023t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069512 | T | TGGGAGCA others(187): Show |
1 | a0009c0012t0002g0163 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | ||||||
chr11:69069543 | G | A | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-887G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069543 | |||||||
chr11:69069546 | C | CGCAGTGG others(226): Show |
1 | a0006c0007t0006g0170 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069546 | ||||||
chr11:69069546 | C | T | 1 | a0006c0007t0006g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.830-884C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069546 | |||||||
chr11:69069550 | C | A | 141 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(138): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.830-880C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | |||||||
chr11:69069550 | C | CTGGGAGC others(304): Show |
6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-764_830-763ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | CTGGGAGC others(32): Show |
2 | a0004c0008t0013g0189 a0010c0014t0013g0193 |
2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.830-842_830-841ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | CTGGGAGC others(304): Show |
6 | a0004c0008t0013g0187 a0004c0008t0013g0190 a0004c0008t0031g0188 others(3): Show |
6 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | CTGGGAGC others(304): Show |
1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | CTGGGAGC others(304): Show |
2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | CTGGGAGC others(304): Show |
11 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(8): Show |
12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | ||||||
chr11:69069550 | C | G | 51 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(48): Show |
66 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.830-880C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | |||||||
chr11:69069550 | C | GTGGGAGC others(265): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.830-880delCinsGTGG others(269): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | |||||||
chr11:69069551 | T | TGGAAGCA others(148): Show |
1 | a0005c0004t0007g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.830-877_830-876ins others(155): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069551 | ||||||
chr11:69069551 | T | TGGGAGCA others(187): Show |
13 | a0005c0004t0007g0029 a0005c0004t0007g0042 a0005c0004t0007g0111 others(10): Show |
15 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069551 | ||||||
chr11:69069554 | G | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-876G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069554 | |||||||
chr11:69069563 | C | T | 16 | a0001c0001t0004g0039 a0001c0005t0004g0001 a0001c0005t0004g0025 others(13): Show |
27 | HG00423.hp1 HG01069.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.830-867C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069563 | |||||||
chr11:69069589 | C | A | 14 | a0005c0004t0007g0029 a0005c0004t0007g0042 a0005c0004t0007g0111 others(11): Show |
16 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.830-841C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069589 | |||||||
chr11:69069589 | C | CTGGGAGC others(343): Show |
4 | a0004c0006t0009g0044 a0004c0006t0009g0207 a0004c0006t0009g0208 others(1): Show |
5 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(350): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069589 | ||||||
chr11:69069589 | C | CTGGGAGC others(32): Show |
1 | a0002c0028t0001g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.830-829_830-828ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069589 | ||||||
chr11:69069589 | C | G | 119 | a0001c0001t0003g0007 a0001c0001t0003g0071 a0001c0001t0003g0072 others(116): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.830-841C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069589 | |||||||
chr11:69069590 | T | TGGGAGCA others(109): Show |
1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-810_830-809ins others(116): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069590 | ||||||
chr11:69069628 | G | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-802G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069628 | |||||||
chr11:69069634 | G | A | 1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.830-796G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069634 | |||||||
chr11:69069663 | C | T | 39 | a0001c0001t0004g0279 a0001c0001t0005g0012 a0001c0001t0005g0052 others(36): Show |
45 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.830-767C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069663 | |||||||
chr11:69069664 | G | A | 41 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(38): Show |
54 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.830-766G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069664 | |||||||
chr11:69069664 | G | GCAGTGGG others(226): Show |
3 | a0002c0028t0001g0179 a0004c0008t0017g0177 a0017c0036t0001g0180 |
3 | HG02486.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.830-725_830-724ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | ||||||
chr11:69069664 | G | GCAGTGGG others(265): Show |
4 | a0004c0008t0004g0105 a0004c0008t0013g0189 a0004c0008t0017g0176 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | ||||||
chr11:69069664 | G | GCAGTGGG others(304): Show |
17 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(14): Show |
24 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | ||||||
chr11:69069667 | G | C | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.830-763G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069667 | |||||||
chr11:69069706 | C | G | 83 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(80): Show |
105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.830-724C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069706 | |||||||
chr11:69069707 | T | TGGGAGCA others(345): Show |
1 | a0004c0006t0009g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.830-686_830-685ins others(352): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069707 | ||||||
chr11:69069742 | G | T | 1 | a0001c0005t0041g0091 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.830-688G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069742 | |||||||
chr11:69069745 | C | G | 2 | a0003c0003t0002g0134 a0004c0024t0019g0261 |
2 | HG01099.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.830-685C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069745 | |||||||
chr11:69069780 | C | G | 1 | a0002c0002t0001g0232 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.830-650C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069780 | |||||||
chr11:69069784 | C | G | 214 | a0001c0001t0003g0079 a0001c0005t0004g0096 a0002c0002t0001g0003 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.830-646C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069784 | |||||||
chr11:69069788 | G | A | 107 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(104): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.830-642G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069788 | |||||||
chr11:69069797 | C | CGTCTCAG others(304): Show |
1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-629_830-628ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069797 | ||||||
chr11:69069797 | C | CGTCTGAG others(32): Show |
1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-612_830-611ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069797 | ||||||
chr11:69069797 | C | T | 212 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(209): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.830-633C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069797 | |||||||
chr11:69069833 | G | C | 3 | a0001c0001t0016g0019 a0011c0017t0016g0019 a0011c0017t0016g0276 |
4 | HG01934.hp1 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-597G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069833 | |||||||
chr11:69069861 | G | C | 1 | a0001c0001t0010g0300 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.830-569G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069861 | |||||||
chr11:69069900 | G | A | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.830-530G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069900 | |||||||
chr11:69069951 | G | C | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-479G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069951 | |||||||
chr11:69070026 | CT | C | 108 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(105): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.830-392delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69070026 | ||||||
chr11:69070046 | A | G | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-384A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070046 | |||||||
chr11:69070089 | G | A | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.830-341G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070089 | |||||||
chr11:69070093 | C | T | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-337C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070093 | |||||||
chr11:69070094 | G | A | 1 | a0002c0002t0001g0265 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.830-336G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070094 | |||||||
chr11:69070184 | C | T | 1 | a0003c0003t0002g0037 | 2 | NA19010.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.830-246C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070184 | |||||||
chr11:69070280 | C | G | 1 | a0001c0001t0005g0273 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.830-150C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070280 | |||||||
chr11:69070326 | A | G | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(65): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.830-104A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070326 | |||||||
chr11:69070407 | C | A | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-23C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070407 | |||||||
chr11:69070409 | G | A | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-21G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070409 | |||||||
chr11:69070413 | T | C | 2 | a0003c0020t0002g0115 a0003c0020t0002g0162 |
2 | NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.830-17T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070413 | |||||||
chr11:69070514 | G | A | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.895+19G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070514 | |||||||
chr11:69070552 | C | A | 1 | a0001c0001t0005g0277 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.895+57C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070552 | |||||||
chr11:69070560 | C | T | 105 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(102): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.895+65C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070560 | |||||||
chr11:69070716 | C | T | 1 | a0002c0002t0001g0236 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.895+221C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070716 | |||||||
chr11:69070779 | A | T | 1 | a0003c0003t0002g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.895+284A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070779 | |||||||
chr11:69070826 | C | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.895+331C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070826 | |||||||
chr11:69070852 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+357C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070852 | |||||||
chr11:69070954 | A | C | 1 | a0002c0002t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.896-402A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070954 | |||||||
chr11:69070962 | G | A | 1 | a0001c0005t0004g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.896-394G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070962 | |||||||
chr11:69070995 | C | G | 1 | a0004c0008t0001g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.896-361C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070995 | |||||||
chr11:69071003 | C | G | 105 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(102): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.896-353C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071003 | |||||||
chr11:69071089 | GGCTTCAC others(21): Show |
G | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.896-214_896-187del others(28): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr11 | 69071089 | ||||||
chr11:69071130 | G | A | 17 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(14): Show |
24 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.896-226G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071130 | |||||||
chr11:69071269 | C | T | 2 | a0002c0002t0001g0215 a0002c0002t0001g0254 |
2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.896-87C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071269 | |||||||
chr11:69071344 | C | G | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.896-12C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071344 | |||||||
chr11:69071461 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.960+41G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071461 | |||||||
chr11:69071519 | C | G | 2 | a0004c0006t0009g0185 a0004c0006t0036g0184 |
2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.960+99C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071519 | |||||||
chr11:69071553 | C | T | 1 | a0005c0004t0008g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.960+133C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071553 | |||||||
chr11:69071645 | G | A | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+225G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071645 | |||||||
chr11:69071659 | C | T | 12 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071659 | |||||||
chr11:69071701 | G | T | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-222G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071701 | |||||||
chr11:69071712 | G | A | 3 | a0004c0006t0009g0017 a0004c0006t0009g0185 a0004c0006t0036g0184 |
5 | HG01891.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.961-211G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071712 | |||||||
chr11:69071719 | T | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.961-204T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071719 | |||||||
chr11:69071806 | G | GC | 16 | a0001c0001t0011g0283 a0001c0005t0004g0095 a0002c0002t0001g0238 others(13): Show |
16 | HG01934.hp2 HG02055.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.961-108dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr11 | 69071806 | ||||||
chr11:69071808 | C | G | 1 | a0001c0005t0041g0091 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.961-115C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071808 | |||||||
chr11:69071814 | C | G | 1 | a0002c0002t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.961-109C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071814 | |||||||
chr11:69071843 | G | A | 1 | a0005c0004t0037g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.961-80G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071843 | |||||||
chr11:69071866 | G | A | 50 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(47): Show |
64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.961-57G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071866 | |||||||
chr11:69072024 | G | GTGAGTGC others(6): Show |
1 | a0002c0002t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1061+4_1061+16dupA others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr11 | 69072024 | ||||||
chr11:69072077 | G | A | 1 | a0005c0004t0008g0138 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1061+54G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072077 | |||||||
chr11:69072087 | C | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1061+64C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072087 | |||||||
chr11:69072175 | C | A | 6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061+152C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072175 | |||||||
chr11:69072191 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+168G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072191 | |||||||
chr11:69072192 | C | T | 2 | a0003c0042t0002g0099 a0006c0031t0006g0165 |
2 | HG03834.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1061+169C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072192 | |||||||
chr11:69072226 | G | GC | 89 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(86): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1061+209dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr11 | 69072226 | ||||||
chr11:69072233 | G | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1061+210G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072233 | |||||||
chr11:69072254 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+231G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072254 | |||||||
chr11:69072257 | C | T | 1 | a0001c0001t0005g0262 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1061+234C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072257 | |||||||
chr11:69072378 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1062-249C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072378 | |||||||
chr11:69072442 | G | C | 19 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(16): Show |
30 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1062-185G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072442 | |||||||
chr11:69072455 | C | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1062-172C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072455 | |||||||
chr11:69072481 | C | T | 105 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(102): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1062-146C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072481 | |||||||
chr11:69072546 | G | A | 101 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(98): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1062-81G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072546 | |||||||
chr11:69072600 | C | T | 3 | a0010c0014t0013g0191 a0010c0014t0013g0192 a0010c0014t0013g0193 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1062-27C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072600 | |||||||
chr11:69072603 | C | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1062-24C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072603 | |||||||
chr11:69072775 | T | C | 1 | a0003c0003t0002g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1143+67T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | chr11 | 69072775 | |||||||
chr11:69072846 | GGGGCGCT others(9): Show |
G | 2 | a0004c0008t0013g0189 a0004c0008t0013g0190 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1144-54_1144-39del others(16): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | 69072846 | ||||||
chr11:69072854 | C | T | 1 | a0001c0001t0004g0039 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1144-61C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | chr11 | 69072854 | |||||||
chr11:69073022 | C | T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0158 |
2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1230+21C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073022 | |||||||
chr11:69073041 | C | G | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+40C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073041 | |||||||
chr11:69073046 | C | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+45C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073046 | |||||||
chr11:69073051 | T | G | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+50T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073051 | |||||||
chr11:69073052 | C | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+51C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073052 | |||||||
chr11:69073053 | C | T | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+52C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073053 | |||||||
chr11:69073058 | C | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+57C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073058 | |||||||
chr11:69073076 | A | T | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+75A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073076 | |||||||
chr11:69073081 | T | G | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+80T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073081 | |||||||
chr11:69073085 | A | C | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+84A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073085 | |||||||
chr11:69073095 | C | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+94C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073095 | |||||||
chr11:69073103 | C | A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+102C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073103 | |||||||
chr11:69073104 | ACCTGCCA others(21): Show |
A | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+104_1230+131d others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073104 | |||||||
chr11:69073149 | T | A | 111 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0003c0003t0002g0009 others(108): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1230+148T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073149 | |||||||
chr11:69073179 | T | G | 1 | a0001c0001t0003g0078 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1230+178T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073179 | |||||||
chr11:69073236 | G | T | 1 | a0004c0006t0007g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+235G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073236 | |||||||
chr11:69073399 | A | G | 12 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1230+398A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073399 | |||||||
chr11:69073448 | T | C | 118 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(115): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1230+447T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073448 | |||||||
chr11:69073671 | G | A | 1 | a0003c0003t0002g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1230+670G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073671 | |||||||
chr11:69073774 | C | T | 1 | a0001c0001t0010g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1230+773C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073774 | |||||||
chr11:69073780 | CTGTAGAT others(45): Show |
C | 1 | a0003c0003t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1230+826_1230+877d others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69073780 | ||||||
chr11:69073789 | C | A | 11 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0063 others(8): Show |
14 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1230+788C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073789 | |||||||
chr11:69073834 | G | A | 1 | a0001c0001t0003g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1230+833G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073834 | |||||||
chr11:69073844 | G | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+843G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073844 | |||||||
chr11:69073974 | AG | A | 85 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(82): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1230+976delG | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69073974 | ||||||
chr11:69074103 | A | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1230+1102A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074103 | |||||||
chr11:69074205 | C | T | 1 | a0004c0006t0007g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+1204C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074205 | |||||||
chr11:69074219 | T | G | 312 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(309): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1230+1218T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074219 | |||||||
chr11:69074262 | G | C | 1 | a0001c0001t0005g0284 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1230+1261G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074262 | |||||||
chr11:69074340 | G | A | 1 | a0004c0013t0015g0201 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1230+1339G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074340 | |||||||
chr11:69074341 | C | T | 1 | a0002c0002t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1230+1340C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074341 | |||||||
chr11:69074421 | T | C | 2 | a0003c0003t0002g0120 a0003c0003t0002g0133 |
2 | NA18959.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1230+1420T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074421 | |||||||
chr11:69074428 | T | C | 1 | a0001c0001t0003g0023 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1230+1427T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074428 | |||||||
chr11:69074451 | T | TA | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+1451dupA | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69074451 | ||||||
chr11:69074490 | T | C | 8 | a0003c0003t0002g0032 a0003c0003t0002g0113 a0003c0003t0002g0119 others(5): Show |
9 | HG00558.hp1 NA18947.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+1489T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074490 | |||||||
chr11:69074525 | A | G | 105 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(102): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1230+1524A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074525 | |||||||
chr11:69074553 | C | T | 6 | a0003c0003t0002g0013 a0003c0003t0002g0030 a0003c0003t0002g0128 others(3): Show |
9 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+1552C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074553 | |||||||
chr11:69074560 | C | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1559C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074560 | |||||||
chr11:69074580 | GA | G | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1581delA | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69074580 | ||||||
chr11:69074630 | A | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1629A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074630 | |||||||
chr11:69074654 | G | C | 1 | a0004c0006t0007g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+1653G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074654 | |||||||
chr11:69074715 | T | G | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+1714T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074715 | |||||||
chr11:69074982 | C | T | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1230+1981C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074982 | |||||||
chr11:69075004 | C | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+2003C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075004 | |||||||
chr11:69075023 | G | A | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+2022G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075023 | |||||||
chr11:69075127 | T | C | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2126T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075127 | |||||||
chr11:69075153 | G | A | 6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+2152G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075153 | |||||||
chr11:69075229 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1230+2228T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075229 | |||||||
chr11:69075236 | A | G | 20 | a0004c0008t0017g0177 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+2235A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075236 | |||||||
chr11:69075418 | A | G | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2417A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075418 | |||||||
chr11:69075433 | A | G | 270 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1230+2432A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075433 | |||||||
chr11:69075451 | A | G | 1 | a0002c0002t0001g0231 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1230+2450A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075451 | |||||||
chr11:69075535 | G | A | 25 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(22): Show |
32 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1230+2534G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075535 | |||||||
chr11:69075544 | G | C | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2543G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075544 | |||||||
chr11:69075651 | G | A | 115 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(112): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1230+2650G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075651 | |||||||
chr11:69075720 | C | T | 7 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(4): Show |
7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+2719C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075720 | |||||||
chr11:69075743 | C | T | 1 | a0021c0023t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1231-2739C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075743 | |||||||
chr11:69075744 | G | A | 1 | a0004c0006t0019g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1231-2738G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075744 | |||||||
chr11:69075760 | C | T | 2 | a0002c0002t0001g0046 a0002c0034t0001g0046 |
2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1231-2722C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075760 | |||||||
chr11:69075802 | T | G | 1 | a0002c0002t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1231-2680T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075802 | |||||||
chr11:69075892 | C | T | 1 | a0003c0003t0002g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1231-2590C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075892 | |||||||
chr11:69075946 | G | A | 9 | a0005c0004t0007g0042 a0005c0004t0007g0141 a0005c0004t0007g0142 others(6): Show |
10 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-2536G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075946 | |||||||
chr11:69075955 | T | C | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2527T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075955 | |||||||
chr11:69076138 | A | G | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2344A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076138 | |||||||
chr11:69076239 | C | T | 2 | a0003c0003t0002g0174 a0003c0003t0002g0175 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1231-2243C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076239 | |||||||
chr11:69076240 | G | A | 7 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(4): Show |
7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-2242G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076240 | |||||||
chr11:69076243 | C | T | 89 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(86): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1231-2239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076243 | |||||||
chr11:69076247 | G | A | 3 | a0005c0004t0007g0029 a0005c0004t0007g0258 a0005c0004t0007g0259 |
4 | HG00741.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-2235G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076247 | |||||||
chr11:69076272 | C | G | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2210C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076272 | |||||||
chr11:69076280 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1231-2202G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076280 | |||||||
chr11:69076324 | C | T | 1 | a0003c0003t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1231-2158C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076324 | |||||||
chr11:69076378 | T | G | 1 | a0001c0005t0004g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1231-2104T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076378 | |||||||
chr11:69076445 | C | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1231-2037C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076445 | |||||||
chr11:69076464 | C | T | 66 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(63): Show |
88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1231-2018C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076464 | |||||||
chr11:69076522 | G | A | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1231-1960G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076522 | |||||||
chr11:69076528 | C | G | 1 | a0002c0030t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-1954C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076528 | |||||||
chr11:69076538 | GCCTGCCC others(18): Show |
G | 1 | a0005c0004t0007g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1231-1905_1231-188 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076538 | ||||||
chr11:69076553 | C | CTGTCCCT others(358): Show |
2 | a0006c0007t0006g0041 a0006c0007t0006g0170 |
3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1231-1906_1231-190 others(369): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076553 | ||||||
chr11:69076553 | C | CTGTCCCT others(383): Show |
16 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0166 others(13): Show |
22 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1231-1906_1231-190 others(394): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076553 | ||||||
chr11:69076555 | G | A | 12 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(9): Show |
12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-1927G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076555 | |||||||
chr11:69076575 | G | C | 64 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(61): Show |
85 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1231-1907G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076575 | |||||||
chr11:69076577 | T | C | 131 | a0002c0002t0001g0048 a0002c0002t0001g0212 a0002c0028t0001g0179 others(128): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1231-1905T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076577 | |||||||
chr11:69076578 | C | A | 20 | a0002c0028t0001g0179 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1231-1904C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076578 | |||||||
chr11:69076578 | C | G | 111 | a0002c0002t0001g0048 a0002c0002t0001g0212 a0003c0003t0002g0009 others(108): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1231-1904C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076578 | |||||||
chr11:69076579 | T | C | 2 | a0002c0028t0001g0179 a0017c0036t0001g0180 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1231-1903T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076579 | |||||||
chr11:69076588 | A | ACCTGCCC others(308): Show |
1 | a0025c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-1881_1231-188 others(319): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076588 | ||||||
chr11:69076602 | C | G | 110 | a0002c0002t0001g0048 a0002c0002t0001g0212 a0003c0003t0002g0009 others(107): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1231-1880C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076602 | |||||||
chr11:69076627 | G | A | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1231-1855G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076627 | |||||||
chr11:69076627 | G | C | 128 | a0002c0002t0001g0048 a0002c0002t0001g0212 a0003c0003t0002g0009 others(125): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1231-1855G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076627 | |||||||
chr11:69076627 | GGTGTCCC others(18): Show |
G | 43 | a0001c0001t0004g0279 a0001c0001t0005g0012 a0001c0001t0005g0052 others(40): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1231-1780_1231-175 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076627 | ||||||
chr11:69076638 | A | ACCTGCCC others(100): Show |
2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1830_1231-182 others(111): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076638 | ||||||
chr11:69076648 | C | CTGCCCTC others(67): Show |
1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-1830_1231-182 others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076648 | ||||||
chr11:69076653 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1829G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076653 | |||||||
chr11:69076663 | A | ACTTGCCC others(1): Show |
3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1818_1231-181 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076663 | ||||||
chr11:69076677 | C | T | 2 | a0004c0008t0004g0105 a0004c0008t0017g0176 |
2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1231-1805C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076677 | |||||||
chr11:69076678 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1804G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076678 | |||||||
chr11:69076690 | C | T | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1792C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076690 | |||||||
chr11:69076701 | C | G | 1 | a0004c0006t0009g0207 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1231-1781C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076701 | |||||||
chr11:69076702 | C | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1231-1780C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076702 | |||||||
chr11:69076702 | CGTGTCCC others(18): Show |
C | 7 | a0004c0008t0013g0190 a0004c0015t0014g0056 a0004c0015t0014g0057 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-1730_1231-170 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076702 | ||||||
chr11:69076703 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1779G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076703 | |||||||
chr11:69076706 | T | C | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1776T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076706 | |||||||
chr11:69076706 | T | TCCCTCCA others(150): Show |
82 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(79): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(161): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | ||||||
chr11:69076706 | T | TCCCTCCA others(142): Show |
1 | a0005c0004t0007g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1231-1756_1231-175 others(153): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | ||||||
chr11:69076706 | T | TCCCTCCA others(175): Show |
6 | a0004c0011t0012g0196 a0004c0011t0012g0197 a0004c0011t0012g0198 others(3): Show |
6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(186): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | ||||||
chr11:69076721 | TCCTGCTG others(60): Show |
T | 9 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(6): Show |
12 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1231-1755_1231-168 others(71): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076721 | ||||||
chr11:69076725 | G | GCCCTCCT others(122): Show |
5 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(2): Show |
6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(133): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076725 | ||||||
chr11:69076727 | T | C | 124 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(121): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1231-1755T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076727 | |||||||
chr11:69076728 | G | A | 24 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(21): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1754G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076728 | |||||||
chr11:69076728 | G | GCCA | 6 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(3): Show |
7 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1754_1231-175 others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076728 | |||||||
chr11:69076729 | T | C | 24 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(21): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1753T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076729 | |||||||
chr11:69076731 | T | C | 5 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(2): Show |
6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1751T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076731 | |||||||
chr11:69076746 | TCCTGCTG others(10): Show |
T | 1 | a0004c0011t0012g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1730_1231-171 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076746 | ||||||
chr11:69076750 | G | GCCCTC | 24 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(21): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1731_1231-173 others(9): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076750 | ||||||
chr11:69076752 | T | C | 229 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(226): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1231-1730T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076752 | |||||||
chr11:69076753 | G | A | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1729G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076753 | |||||||
chr11:69076753 | G | GCCA | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1729_1231-172 others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076753 | |||||||
chr11:69076754 | T | C | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1728T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076754 | |||||||
chr11:69076771 | TCCTGCCG others(10): Show |
T | 6 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0002c0002t0001g0048 others(3): Show |
7 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1704_1231-168 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076771 | ||||||
chr11:69076773 | C | G | 24 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(21): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1709C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076773 | |||||||
chr11:69076778 | G | A | 158 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(155): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1231-1704G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076778 | |||||||
chr11:69076779 | T | C | 91 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(88): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1231-1703T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076779 | |||||||
chr11:69076788 | A | ACCTGCCC others(1): Show |
91 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(88): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1231-1687_1231-168 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076788 | ||||||
chr11:69076788 | A | ACTTGCCC others(1): Show |
25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1693_1231-169 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076788 | ||||||
chr11:69076789 | C | CCTGCCCT others(607): Show |
1 | a0006c0007t0006g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1231-1532_1231-153 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | ||||||
chr11:69076789 | C | CCTGCCCT others(922): Show |
3 | a0008c0010t0006g0100 a0008c0010t0006g0101 a0008c0010t0006g0102 |
3 | HG00099.hp1 HG00323.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1231-1456_1231-145 others(933): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | ||||||
chr11:69076789 | C | CCTGCCCT others(607): Show |
1 | a0006c0007t0006g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1231-1456_1231-145 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | ||||||
chr11:69076789 | C | CCTGCCCT others(607): Show |
13 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(10): Show |
20 | HG00735.hp2 HG01167.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-1456_1231-145 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | ||||||
chr11:69076789 | C | CCTGCCCT others(682): Show |
1 | a0025c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-1680_1231-167 others(693): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | ||||||
chr11:69076798 | C | CTGCCCTC others(1): Show |
104 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(101): Show |
138 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1231-1680_1231-167 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076798 | ||||||
chr11:69076798 | C | CTGCCCTC others(34): Show |
1 | a0002c0002t0001g0182 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1231-1680_1231-167 others(45): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076798 | ||||||
chr11:69076798 | C | G | 6 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0002c0002t0001g0048 others(3): Show |
7 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1684C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076798 | |||||||
chr11:69076804 | T | C | 6 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(3): Show |
7 | HG02523.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1678T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076804 | |||||||
chr11:69076815 | C | T | 136 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(133): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1231-1667C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076815 | |||||||
chr11:69076831 | G | A | 54 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(51): Show |
70 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1231-1651G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076831 | |||||||
chr11:69076831 | G | C | 30 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(27): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1231-1651G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076831 | |||||||
chr11:69076848 | T | C | 30 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(27): Show |
45 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1231-1634T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076848 | |||||||
chr11:69076854 | T | TCCTGCCA others(10): Show |
24 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(21): Show |
38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1622_1231-162 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076854 | ||||||
chr11:69076856 | C | CTGCCCTC others(18): Show |
4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1619_1231-161 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076856 | ||||||
chr11:69076864 | A | C | 152 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(149): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1231-1618A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076864 | |||||||
chr11:69076864 | A | G | 5 | a0002c0002t0001g0182 a0002c0002t0001g0221 a0002c0002t0001g0248 others(2): Show |
5 | HG00642.hp1 HG01099.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-1618A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076864 | |||||||
chr11:69076869 | A | G | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1613A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076869 | |||||||
chr11:69076897 | C | A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1231-1585C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076897 | |||||||
chr11:69076900 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1582C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076900 | |||||||
chr11:69076901 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1581C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076901 | |||||||
chr11:69076902 | A | G | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1580A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076902 | |||||||
chr11:69076907 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1575C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076907 | |||||||
chr11:69076908 | C | G | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1574C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076908 | |||||||
chr11:69076914 | T | C | 95 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(92): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1231-1568T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076914 | |||||||
chr11:69076914 | T | TTGCCCTC others(1): Show |
34 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(31): Show |
47 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1231-1563_1231-155 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076914 | ||||||
chr11:69076914 | T | TTTCCCTC others(1): Show |
25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1567_1231-156 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076914 | ||||||
chr11:69076930 | C | T | 122 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(119): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1231-1552C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076930 | |||||||
chr11:69076942 | C | T | 1 | a0001c0001t0003g0070 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1231-1540C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076942 | |||||||
chr11:69076951 | T | C | 122 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(119): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1231-1531T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076951 | |||||||
chr11:69076952 | G | A | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1530G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076952 | |||||||
chr11:69076952 | G | GTGTCCCT others(134): Show |
15 | a0003c0003t0002g0033 a0003c0003t0002g0123 a0003c0003t0002g0128 others(12): Show |
18 | HG01243.hp2 HG01346.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1231-1519_1231-151 others(145): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076952 | ||||||
chr11:69076962 | A | ACTTGCCC others(34): Show |
81 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(78): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1231-1519_1231-151 others(45): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076962 | ||||||
chr11:69076975 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1507C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076975 | |||||||
chr11:69076976 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1506C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076976 | |||||||
chr11:69076977 | A | G | 37 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(34): Show |
54 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1231-1505A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076977 | |||||||
chr11:69076982 | C | T | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1500C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076982 | |||||||
chr11:69076983 | C | G | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1499C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076983 | |||||||
chr11:69076989 | C | T | 26 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(23): Show |
40 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1231-1493C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076989 | |||||||
chr11:69077002 | A | G | 82 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(79): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1231-1480A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077002 | |||||||
chr11:69077003 | C | T | 107 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(104): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1231-1479C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077003 | |||||||
chr11:69077007 | C | T | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1475C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077007 | |||||||
chr11:69077008 | C | G | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1474C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077008 | |||||||
chr11:69077012 | ACCTGCCC others(1): Show |
A | 25 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(22): Show |
39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1455_1231-144 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077012 | ||||||
chr11:69077014 | C | T | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1468C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077014 | |||||||
chr11:69077016 | G | T | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1466G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077016 | |||||||
chr11:69077020 | T | TCCTGTTG others(35): Show |
28 | a0004c0006t0007g0151 a0004c0006t0019g0260 a0004c0006t0033g0200 others(25): Show |
33 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1231-1458_1231-145 others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077020 | ||||||
chr11:69077022 | C | CTGTTGTG others(10): Show |
53 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(50): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1231-1458_1231-145 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077022 | ||||||
chr11:69077045 | A | ACCTGCCC others(1): Show |
11 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(8): Show |
14 | HG01106.hp1 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1231-1435_1231-142 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077045 | ||||||
chr11:69077055 | G | C | 108 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(105): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1231-1427G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077055 | |||||||
chr11:69077055 | G | T | 14 | a0003c0003t0002g0033 a0003c0003t0002g0123 a0003c0003t0002g0128 others(11): Show |
17 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1231-1427G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077055 | |||||||
chr11:69077060 | A | G | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1422A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077060 | |||||||
chr11:69077061 | T | C | 68 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(65): Show |
90 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1231-1421T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077061 | |||||||
chr11:69077070 | ACTTGCCC others(1): Show |
A | 52 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(49): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1231-1410_1231-140 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077070 | ||||||
chr11:69077072 | T | C | 70 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(67): Show |
93 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1231-1410T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077072 | |||||||
chr11:69077078 | T | TCCTGCCA others(43): Show |
1 | a0003c0003t0002g0032 | 2 | NA18973.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1231-1398_1231-139 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | ||||||
chr11:69077078 | T | TCCTGCCA others(110): Show |
3 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0204 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1398_1231-139 others(121): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | ||||||
chr11:69077078 | T | TCCTGTTG others(60): Show |
1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1400_1231-139 others(71): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | ||||||
chr11:69077094 | T | C | 58 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(55): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-1388T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077094 | |||||||
chr11:69077094 | T | TGTCCCTC others(68): Show |
1 | a0003c0003t0002g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-1378_1231-137 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | ||||||
chr11:69077094 | T | TGTCCCTC others(284): Show |
1 | a0001c0001t0003g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1231-1378_1231-137 others(295): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | ||||||
chr11:69077094 | T | TGTCCCTC others(18): Show |
49 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(46): Show |
68 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1231-1378_1231-137 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | ||||||
chr11:69077103 | ACTTGCCC others(1): Show |
A | 3 | a0001c0005t0004g0097 a0004c0006t0035g0209 a0016c0041t0004g0090 |
3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1377_1231-137 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077103 | ||||||
chr11:69077105 | T | C | 120 | a0001c0001t0003g0066 a0001c0001t0004g0039 a0001c0001t0004g0155 others(117): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1231-1377T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077105 | |||||||
chr11:69077105 | T | TTGCCCTC others(301): Show |
1 | a0001c0001t0005g0278 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(312): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(432): Show |
1 | a0002c0002t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(443): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(317): Show |
25 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0021 others(22): Show |
37 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(328): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(317): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0075 |
2 | HG02074.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(328): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(342): Show |
6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(353): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(408): Show |
18 | a0006c0007t0006g0016 a0006c0007t0006g0041 a0006c0007t0006g0166 others(15): Show |
20 | HG00099.hp1 HG00323.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(419): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(1007): Show |
1 | a0006c0007t0006g0005 | 5 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(1018): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(350): Show |
1 | a0006c0007t0006g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(361): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(325): Show |
38 | a0001c0001t0004g0279 a0001c0001t0005g0262 a0001c0001t0005g0268 others(35): Show |
39 | HG00544.hp2 HG01106.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(300): Show |
6 | a0001c0001t0005g0012 a0001c0001t0005g0052 a0001c0001t0005g0277 others(3): Show |
10 | NA18612.hp1 NA18942.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(325): Show |
10 | a0001c0001t0005g0053 a0001c0001t0010g0275 a0001c0001t0010g0295 others(7): Show |
11 | HG00558.hp2 HG00597.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(341): Show |
5 | a0002c0002t0001g0018 a0002c0002t0001g0253 a0002c0002t0001g0265 others(2): Show |
7 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(352): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(457): Show |
55 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(52): Show |
75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(468): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(456): Show |
1 | a0002c0002t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(467): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(458): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(469): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(482): Show |
1 | a0002c0002t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(493): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077105 | T | TTGCCCTC others(325): Show |
3 | a0010c0014t0013g0191 a0010c0014t0013g0192 a0010c0014t0013g0193 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | ||||||
chr11:69077111 | T | TCCTGCCA others(10): Show |
3 | a0003c0003t0002g0033 a0003c0003t0002g0123 a0003c0003t0002g0164 |
4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | ||||||
chr11:69077111 | T | TCCTGCCC others(325): Show |
1 | a0001c0001t0005g0264 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | ||||||
chr11:69077111 | T | TCCTGCCG others(10): Show |
6 | a0004c0011t0012g0196 a0004c0011t0012g0197 a0004c0011t0012g0198 others(3): Show |
6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | ||||||
chr11:69077111 | T | TCCTGCCG others(143): Show |
1 | a0004c0006t0020g0051 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(154): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | ||||||
chr11:69077111 | T | TCTTGCCA others(10): Show |
1 | a0004c0013t0015g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1231-1370_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | ||||||
chr11:69077121 | C | T | 3 | a0001c0005t0004g0097 a0004c0006t0035g0209 a0016c0041t0004g0090 |
3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1361C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077121 | |||||||
chr11:69077126 | A | G | 7 | a0004c0006t0020g0051 a0004c0011t0012g0196 a0004c0011t0012g0197 others(4): Show |
8 | HG02809.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-1356A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077126 | |||||||
chr11:69077127 | T | C | 3 | a0001c0005t0004g0097 a0004c0006t0035g0209 a0016c0041t0004g0090 |
3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1355T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077127 | |||||||
chr11:69077129 | T | TCCCTCCA others(459): Show |
1 | a0002c0002t0001g0234 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(470): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077129 | ||||||
chr11:69077134 | C | T | 6 | a0004c0011t0012g0196 a0004c0011t0012g0197 a0004c0011t0012g0198 others(3): Show |
6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1348C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077134 | |||||||
chr11:69077136 | A | ACCTGCCC others(1): Show |
3 | a0001c0005t0004g0097 a0004c0006t0035g0209 a0016c0041t0004g0090 |
3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1339_1231-133 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077136 | ||||||
chr11:69077136 | A | ACCTGCCC others(26): Show |
1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1337_1231-133 others(37): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077136 | ||||||
chr11:69077144 | T | TCCTGCCA others(319): Show |
1 | a0001c0001t0003g0077 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(330): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077144 | ||||||
chr11:69077146 | C | T | 53 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(50): Show |
69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1231-1336C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077146 | |||||||
chr11:69077151 | G | A | 79 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0080 others(76): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231-1331G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077151 | |||||||
chr11:69077152 | T | C | 56 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(53): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1231-1330T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077152 | |||||||
chr11:69077161 | A | ACCTGCCC others(1): Show |
56 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(53): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1231-1314_1231-130 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077161 | ||||||
chr11:69077161 | A | ACCTGCCC others(12): Show |
1 | a0001c0005t0004g0026 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1231-1317_1231-129 others(23): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077161 | ||||||
chr11:69077176 | G | A | 62 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(59): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1231-1306G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077176 | |||||||
chr11:69077176 | G | GTGTCCCT others(525): Show |
4 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0080 others(1): Show |
4 | NA18956.hp2 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(536): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | ||||||
chr11:69077176 | G | GTGTCCCT others(159): Show |
5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(170): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | ||||||
chr11:69077176 | G | GTGTCCCT others(159): Show |
4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(170): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | ||||||
chr11:69077184 | T | C | 79 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0080 others(76): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231-1298T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077184 | |||||||
chr11:69077184 | T | TCACCTGC others(43): Show |
1 | a0003c0003t0002g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-1280_1231-123 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077184 | ||||||
chr11:69077186 | A | ACTTGCCC others(125): Show |
1 | a0002c0002t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1231-1295_1231-129 others(136): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077186 | ||||||
chr11:69077201 | A | G | 18 | a0001c0001t0011g0282 a0001c0001t0011g0283 a0001c0005t0004g0097 others(15): Show |
22 | HG01346.hp1 HG01515.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1231-1281A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077201 | |||||||
chr11:69077202 | T | C | 15 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(12): Show |
18 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-1280T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077202 | |||||||
chr11:69077209 | C | T | 3 | a0001c0005t0004g0097 a0005c0004t0007g0147 a0016c0041t0004g0090 |
3 | HG02523.hp1 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1273C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077209 | |||||||
chr11:69077211 | A | ACCTGCCC others(1): Show |
15 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(12): Show |
18 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-1264_1231-125 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077211 | ||||||
chr11:69077226 | A | G | 6 | a0003c0003t0002g0033 a0003c0003t0002g0038 a0003c0003t0002g0123 others(3): Show |
8 | HG01346.hp1 HG01515.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1256A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077226 | |||||||
chr11:69077227 | T | C | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-1255T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077227 | |||||||
chr11:69077227 | T | TGTCCCTC others(176): Show |
1 | a0004c0006t0020g0051 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1245_1231-124 others(187): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077227 | ||||||
chr11:69077228 | G | A | 1 | a0001c0001t0005g0264 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1231-1254G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077228 | |||||||
chr11:69077234 | C | T | 3 | a0003c0003t0002g0033 a0003c0003t0002g0123 a0003c0003t0002g0164 |
4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1248C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077234 | |||||||
chr11:69077246 | C | T | 9 | a0004c0006t0009g0017 a0004c0006t0009g0044 a0004c0006t0009g0183 others(6): Show |
12 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1231-1236C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077246 | |||||||
chr11:69077251 | A | G | 3 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0204 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1231A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077251 | |||||||
chr11:69077252 | C | T | 7 | a0001c0005t0004g0097 a0003c0003t0002g0033 a0003c0003t0002g0123 others(4): Show |
9 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-1230C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077252 | |||||||
chr11:69077253 | G | A | 65 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(62): Show |
87 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1231-1229G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077253 | |||||||
chr11:69077261 | ACCTGCCC others(1): Show |
A | 23 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(20): Show |
37 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1231-1206_1231-119 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077261 | ||||||
chr11:69077263 | C | T | 3 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0204 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1219C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077263 | |||||||
chr11:69077269 | T | TCCTGCCA others(10): Show |
1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1231-1207_1231-120 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077269 | T | TCCTGCCA others(10): Show |
3 | a0003c0003t0002g0033 a0003c0003t0002g0123 a0003c0003t0002g0164 |
4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1207_1231-120 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077269 | T | TCCTGCCC others(267): Show |
1 | a0002c0002t0001g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1231-1187_1231-118 others(278): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077269 | T | TCCTGCCC others(243): Show |
1 | a0004c0013t0015g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1231-1199_1231-119 others(254): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077269 | T | TCCTGCCC others(95): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-1204_1231-120 others(106): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077269 | T | TCCTGCCG others(260): Show |
3 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0204 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1207_1231-120 others(271): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | ||||||
chr11:69077284 | A | G | 4 | a0004c0013t0015g0043 a0004c0013t0015g0201 a0004c0013t0015g0202 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1198A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077284 | |||||||
chr11:69077285 | T | C | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1197T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077285 | |||||||
chr11:69077292 | C | CCACCTGC others(101): Show |
1 | a0004c0011t0012g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1187_1231-118 others(112): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077292 | ||||||
chr11:69077296 | T | C | 215 | a0001c0005t0004g0097 a0002c0002t0001g0003 a0002c0002t0001g0004 others(212): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1231-1186T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077296 | |||||||
chr11:69077309 | G | A | 8 | a0001c0005t0004g0097 a0004c0008t0013g0187 a0004c0008t0013g0189 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1173G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077309 | |||||||
chr11:69077317 | C | T | 1 | a0004c0011t0012g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1165C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077317 | |||||||
chr11:69077321 | C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1161C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077321 | |||||||
chr11:69077333 | T | C | 108 | a0001c0001t0005g0285 a0001c0005t0004g0097 a0003c0003t0002g0009 others(105): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1231-1149T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077333 | |||||||
chr11:69077334 | G | A | 2 | a0001c0001t0005g0285 a0004c0011t0012g0195 |
2 | HG03195.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1231-1148G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077334 | |||||||
chr11:69077342 | T | C | 20 | a0001c0001t0005g0285 a0001c0005t0004g0097 a0001c0005t0041g0091 others(17): Show |
21 | HG00639.hp1 HG01884.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1231-1140T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077342 | |||||||
chr11:69077342 | T | TCACCTGC others(19): Show |
1 | a0001c0001t0005g0278 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1231-1117_1231-111 others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | ||||||
chr11:69077342 | T | TCACCTGC others(18): Show |
1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1231-1123_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | ||||||
chr11:69077342 | T | TCACCTGC others(18): Show |
1 | a0005c0004t0008g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1231-1124_1231-112 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | ||||||
chr11:69077342 | T | TCACCTGC others(43): Show |
4 | a0004c0011t0012g0196 a0004c0011t0012g0198 a0004c0011t0012g0199 others(1): Show |
4 | HG02080.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1124_1231-112 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | ||||||
chr11:69077342 | T | TCACCTGC others(68): Show |
3 | a0004c0011t0012g0197 a0004c0011t0012g0203 a0004c0032t0012g0194 |
3 | HG02809.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1231-1124_1231-112 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | ||||||
chr11:69077358 | C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1124C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077358 | |||||||
chr11:69077359 | A | G | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1123A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077359 | |||||||
chr11:69077360 | T | TGTCCCTC others(18): Show |
5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077360 | ||||||
chr11:69077363 | C | CCTCCACC others(90): Show |
1 | a0002c0002t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1231-1118_1231-111 others(101): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077363 | ||||||
chr11:69077371 | C | CTGCCCTC others(93): Show |
10 | a0004c0008t0004g0105 a0004c0008t0013g0187 a0004c0008t0013g0189 others(7): Show |
10 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(104): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(68): Show |
7 | a0001c0001t0005g0289 a0004c0008t0017g0177 a0004c0008t0034g0178 others(4): Show |
8 | HG00099.hp2 HG00642.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(43): Show |
112 | a0001c0001t0003g0067 a0001c0001t0011g0168 a0001c0001t0011g0280 others(109): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(68): Show |
1 | a0003c0003t0002g0037 | 2 | NA19010.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(143): Show |
1 | a0002c0002t0001g0224 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1231-1099_1231-109 others(154): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(409): Show |
1 | a0001c0001t0003g0021 | 2 | NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(420): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(93): Show |
62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(59): Show |
84 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(104): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(18): Show |
70 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0023 others(67): Show |
89 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | CTGCCCTC others(392): Show |
3 | a0001c0001t0003g0022 a0001c0001t0003g0069 a0001c0001t0003g0070 |
4 | NA18986.hp1 NA18998.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(403): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | ||||||
chr11:69077371 | C | T | 40 | a0001c0001t0003g0020 a0001c0001t0003g0076 a0001c0001t0003g0080 others(37): Show |
59 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1231-1111C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077371 | |||||||
chr11:69077474 | G | T | 1 | a0003c0003t0002g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1231-1008G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077474 | |||||||
chr11:69077498 | G | A | 246 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(243): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1231-984G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077498 | |||||||
chr11:69077500 | C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-982C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077500 | |||||||
chr11:69077519 | C | G | 7 | a0004c0008t0013g0187 a0004c0008t0013g0189 a0004c0008t0013g0190 others(4): Show |
7 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-963C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077519 | |||||||
chr11:69077647 | A | G | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1231-835A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077647 | |||||||
chr11:69077689 | G | A | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-793G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077689 | |||||||
chr11:69077712 | G | T | 1 | a0001c0001t0005g0281 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1231-770G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077712 | |||||||
chr11:69077847 | T | G | 1 | a0021c0023t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1231-635T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077847 | |||||||
chr11:69077928 | C | T | 1 | a0004c0024t0019g0261 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-554C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077928 | |||||||
chr11:69077974 | A | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1231-508A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077974 | |||||||
chr11:69078050 | C | T | 1 | a0001c0001t0010g0297 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1231-432C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078050 | |||||||
chr11:69078159 | C | CT | 87 | a0001c0001t0003g0079 a0001c0001t0011g0283 a0003c0003t0002g0009 others(84): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1231-310dupT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69078159 | ||||||
chr11:69078199 | A | C | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1231-283A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078199 | |||||||
chr11:69078268 | A | G | 1 | a0003c0003t0038g0126 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1231-214A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078268 | |||||||
chr11:69078395 | C | T | 1 | a0003c0003t0002g0033 | 2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1231-87C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078395 | |||||||
chr11:69078399 | G | A | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1231-83G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078399 | |||||||
chr11:69078630 | A | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1350+29A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 14/24 | chr11 | 69078630 | |||||||
chr11:69079051 | A | C | 270 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1539+31A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079051 | |||||||
chr11:69079069 | C | T | 7 | a0004c0011t0012g0195 a0004c0011t0012g0196 a0004c0011t0012g0197 others(4): Show |
7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+49C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079069 | |||||||
chr11:69079110 | G | A | 2 | a0003c0003t0002g0014 a0003c0003t0002g0124 |
4 | HG01074.hp2 HG01243.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+90G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079110 | |||||||
chr11:69079418 | T | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1539+398T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079418 | |||||||
chr11:69079537 | A | G | 270 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1540-297A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079537 | |||||||
chr11:69079582 | C | T | 1 | a0002c0002t0001g0234 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1540-252C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079582 | |||||||
chr11:69079628 | C | T | 1 | a0001c0005t0004g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1540-206C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079628 | |||||||
chr11:69079670 | T | C | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1540-164T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079670 | |||||||
chr11:69079688 | C | T | 80 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(77): Show |
102 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1540-146C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079688 | |||||||
chr11:69080219 | C | G | 32 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(29): Show |
45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1589+336C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080219 | |||||||
chr11:69080353 | A | T | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589+470A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080353 | |||||||
chr11:69080498 | G | T | 7 | a0003c0003t0002g0032 a0003c0003t0002g0113 a0003c0003t0002g0119 others(4): Show |
8 | HG00558.hp1 NA18973.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+615G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080498 | |||||||
chr11:69080499 | C | T | 7 | a0003c0003t0002g0032 a0003c0003t0002g0113 a0003c0003t0002g0119 others(4): Show |
8 | HG00558.hp1 NA18973.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+616C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080499 | |||||||
chr11:69080520 | G | A | 1 | a0003c0003t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1589+637G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080520 | |||||||
chr11:69080561 | C | T | 2 | a0004c0006t0019g0260 a0004c0006t0020g0051 |
3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1589+678C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080561 | |||||||
chr11:69080606 | T | C | 1 | a0004c0008t0017g0177 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1589+723T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080606 | |||||||
chr11:69080665 | T | G | 1 | a0001c0001t0003g0072 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1590-735T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080665 | |||||||
chr11:69080764 | C | T | 1 | a0001c0001t0011g0282 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1590-636C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080764 | |||||||
chr11:69080918 | C | T | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1590-482C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080918 | |||||||
chr11:69081004 | C | T | 1 | a0006c0007t0021g0040 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1590-396C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081004 | |||||||
chr11:69081136 | C | T | 1 | a0007c0009t0004g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1590-264C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081136 | |||||||
chr11:69081144 | A | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1590-256A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081144 | |||||||
chr11:69081281 | A | G | 2 | a0004c0008t0004g0105 a0004c0008t0017g0176 |
2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1590-119A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081281 | |||||||
chr11:69081317 | G | A | 1 | a0007c0009t0004g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1590-83G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081317 | |||||||
chr11:69081368 | C | T | 3 | a0004c0011t0012g0196 a0004c0011t0012g0198 a0004c0011t0012g0203 |
3 | HG02965.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1590-32C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081368 | |||||||
chr11:69081592 | G | A | 6 | a0001c0001t0004g0279 a0001c0001t0011g0168 a0001c0001t0011g0280 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+93G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081592 | |||||||
chr11:69081605 | G | A | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1689+106G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081605 | |||||||
chr11:69081644 | C | T | 2 | a0004c0008t0013g0189 a0004c0008t0013g0190 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1689+145C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081644 | |||||||
chr11:69081670 | T | G | 1 | a0004c0006t0007g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1689+171T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081670 | |||||||
chr11:69081722 | C | T | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1689+223C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081722 | |||||||
chr11:69081816 | G | C | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+317G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081816 | |||||||
chr11:69081852 | C | T | 1 | a0003c0003t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1689+353C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081852 | |||||||
chr11:69081874 | T | C | 215 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(212): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1689+375T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081874 | |||||||
chr11:69081936 | C | T | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(30): Show |
46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1689+437C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081936 | |||||||
chr11:69082010 | G | A | 4 | a0001c0001t0005g0012 a0001c0001t0005g0281 a0001c0001t0005g0284 others(1): Show |
7 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+511G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082010 | |||||||
chr11:69082133 | G | A | 2 | a0003c0003t0002g0129 a0003c0003t0002g0130 |
2 | HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1689+634G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082133 | |||||||
chr11:69082177 | G | A | 1 | a0002c0002t0001g0256 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1689+678G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082177 | |||||||
chr11:69082218 | C | T | 1 | a0004c0006t0018g0015 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1689+719C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082218 | |||||||
chr11:69082350 | A | G | 1 | a0019c0037t0001g0229 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1689+851A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082350 | |||||||
chr11:69082360 | A | G | 1 | a0001c0001t0004g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+861A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082360 | |||||||
chr11:69082377 | A | G | 20 | a0002c0002t0001g0228 a0006c0007t0006g0005 a0006c0007t0006g0016 others(17): Show |
27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1689+878A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082377 | |||||||
chr11:69082501 | C | T | 1 | a0003c0003t0002g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1689+1002C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082501 | |||||||
chr11:69082525 | G | A | 2 | a0003c0003t0002g0120 a0003c0003t0002g0133 |
2 | NA18959.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1689+1026G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082525 | |||||||
chr11:69082556 | GGTAAGAC others(117): Show |
G | 1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1689+1090_1689+121 others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082556 | ||||||
chr11:69082564 | G | T | 1 | a0005c0004t0007g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1689+1065G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082564 | |||||||
chr11:69082572 | G | A | 2 | a0005c0004t0007g0141 a0005c0004t0007g0144 |
2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1689+1073G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082572 | |||||||
chr11:69082589 | A | C | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1090A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082589 | |||||||
chr11:69082618 | GGTAAGAC others(55): Show |
G | 171 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(168): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1690-1172_1690-111 others(66): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082618 | ||||||
chr11:69082651 | G | A | 91 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(88): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1689+1152G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082651 | |||||||
chr11:69082680 | T | G | 91 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(88): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1689+1181T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082680 | |||||||
chr11:69082695 | C | T | 1 | a0003c0003t0002g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1689+1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082695 | |||||||
chr11:69082708 | A | G | 1 | a0013c0025t0007g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1689+1209A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082708 | |||||||
chr11:69082713 | G | A | 1 | a0003c0003t0002g0125 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1214G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082713 | |||||||
chr11:69082734 | C | T | 1 | a0003c0003t0002g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1690-1211C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082734 | |||||||
chr11:69082742 | T | G | 8 | a0003c0003t0002g0149 a0004c0015t0014g0056 a0004c0015t0014g0057 others(5): Show |
8 | HG00423.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-1203T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082742 | |||||||
chr11:69082749 | C | T | 4 | a0004c0006t0009g0017 a0004c0006t0009g0183 a0004c0006t0009g0185 others(1): Show |
6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082749 | |||||||
chr11:69082763 | T | C | 7 | a0002c0002t0001g0225 a0004c0015t0014g0056 a0004c0015t0014g0057 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690-1182T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082763 | |||||||
chr11:69082773 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1172G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082773 | |||||||
chr11:69082773 | GCGTGCAG others(55): Show |
G | 1 | a0003c0003t0002g0149 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1690-1141_1690-108 others(66): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082773 | ||||||
chr11:69082775 | G | A | 6 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(3): Show |
7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690-1170G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082775 | |||||||
chr11:69082796 | C | G | 1 | a0004c0011t0012g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690-1149C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082796 | |||||||
chr11:69082796 | C | T | 107 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(104): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1690-1149C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082796 | |||||||
chr11:69082804 | T | G | 214 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(211): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1690-1141T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082804 | |||||||
chr11:69082805 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082805 | |||||||
chr11:69082812 | G | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1133G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082812 | |||||||
chr11:69082825 | T | C | 100 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(97): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1690-1120T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082825 | |||||||
chr11:69082835 | A | G | 105 | a0001c0001t0004g0279 a0001c0001t0011g0168 a0001c0001t0011g0280 others(102): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1690-1110A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082835 | |||||||
chr11:69082837 | G | A | 8 | a0001c0001t0005g0264 a0001c0001t0005g0268 a0001c0001t0005g0269 others(5): Show |
8 | HG00544.hp2 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-1108G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082837 | |||||||
chr11:69082850 | T | C | 8 | a0002c0002t0001g0011 a0002c0002t0001g0245 a0004c0015t0014g0056 others(5): Show |
11 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690-1095T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082850 | |||||||
chr11:69082858 | C | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1087C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082858 | |||||||
chr11:69082866 | G | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1079G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082866 | |||||||
chr11:69082867 | A | G | 7 | a0001c0001t0010g0295 a0004c0015t0014g0056 a0004c0015t0014g0057 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690-1078A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082867 | |||||||
chr11:69082873 | C | T | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1072C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082873 | |||||||
chr11:69082874 | G | T | 100 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(97): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1690-1071G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082874 | |||||||
chr11:69082874 | GCATGATC others(179): Show |
G | 3 | a0001c0001t0005g0012 a0001c0001t0005g0284 a0001c0001t0005g0285 |
6 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1046_1690-861 others(3): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082874 | ||||||
chr11:69082899 | G | A | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1046G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082899 | |||||||
chr11:69082912 | C | T | 41 | a0001c0001t0004g0279 a0001c0001t0005g0052 a0001c0001t0005g0053 others(38): Show |
44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1690-1033C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082912 | |||||||
chr11:69082922 | T | C | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1023T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082922 | |||||||
chr11:69082935 | TGCATGAT others(55): Show |
T | 1 | a0004c0008t0017g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1690-947_1690-886d others(64): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082935 | ||||||
chr11:69082961 | A | G | 1 | a0001c0001t0003g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1690-984A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082961 | |||||||
chr11:69082982 | C | T | 1 | a0017c0036t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1690-963C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082982 | |||||||
chr11:69082998 | GCATGATC others(55): Show |
G | 23 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(20): Show |
37 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1690-910_1690-849d others(64): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082998 | ||||||
chr11:69083060 | A | G | 1 | a0006c0007t0006g0041 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1690-885A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083060 | |||||||
chr11:69083082 | C | T | 1 | a0002c0002t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1690-863C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083082 | |||||||
chr11:69083096 | C | T | 2 | a0004c0011t0012g0198 a0004c0011t0012g0203 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1690-849C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083096 | |||||||
chr11:69083141 | C | T | 6 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0060 others(3): Show |
8 | HG00408.hp1 HG00609.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-804C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083141 | |||||||
chr11:69083305 | G | C | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1690-640G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083305 | |||||||
chr11:69083347 | G | A | 3 | a0004c0006t0019g0260 a0004c0006t0020g0051 a0004c0024t0019g0261 |
4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690-598G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083347 | |||||||
chr11:69083650 | C | T | 1 | a0003c0003t0002g0036 | 2 | NA18954.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1690-295C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083650 | |||||||
chr11:69083670 | C | T | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-275C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083670 | |||||||
chr11:69083703 | G | A | 6 | a0004c0015t0014g0056 a0004c0015t0014g0057 a0004c0015t0014g0058 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-242G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083703 | |||||||
chr11:69083768 | T | A | 1 | a0002c0002t0001g0228 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1690-177T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083768 | |||||||
chr11:69083873 | G | T | 1 | a0008c0010t0006g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1690-72G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083873 | |||||||
chr11:69084079 | G | A | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1761+63G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084079 | |||||||
chr11:69084125 | C | G | 3 | a0001c0001t0005g0052 a0001c0001t0005g0277 a0001c0001t0005g0278 |
4 | NA18612.hp1 NA18947.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+109C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084125 | |||||||
chr11:69084137 | C | T | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1761+121C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084137 | |||||||
chr11:69084238 | G | C | 2 | a0001c0001t0022g0291 a0001c0001t0022g0292 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1761+222G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084238 | |||||||
chr11:69084322 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1761+306G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084322 | |||||||
chr11:69084438 | A | G | 1 | a0005c0004t0007g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1761+422A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084438 | |||||||
chr11:69084589 | G | A | 84 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(81): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1761+573G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084589 | |||||||
chr11:69084613 | G | C | 1 | a0006c0007t0006g0171 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1761+597G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084613 | |||||||
chr11:69084630 | C | T | 22 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(19): Show |
36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1762-580C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084630 | |||||||
chr11:69084647 | G | A | 1 | a0002c0002t0001g0047 | 2 | HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1762-563G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084647 | |||||||
chr11:69084713 | C | T | 81 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(78): Show |
103 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1762-497C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084713 | |||||||
chr11:69084748 | C | G | 4 | a0004c0008t0004g0105 a0004c0008t0017g0106 a0004c0008t0017g0176 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-462C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084748 | |||||||
chr11:69084847 | G | A | 109 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(106): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1762-363G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084847 | |||||||
chr11:69084854 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1762-356G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084854 | |||||||
chr11:69084868 | T | C | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1762-342T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084868 | |||||||
chr11:69084890 | C | T | 19 | a0006c0007t0006g0005 a0006c0007t0006g0016 a0006c0007t0006g0041 others(16): Show |
26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1762-320C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084890 | |||||||
chr11:69085029 | G | A | 20 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(17): Show |
23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.1762-181G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085029 | |||||||
chr11:69085176 | G | A | 5 | a0004c0006t0009g0044 a0004c0006t0009g0206 a0004c0006t0009g0207 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1762-34G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085176 | |||||||
chr11:69085192 | C | T | 32 | a0001c0001t0005g0012 a0001c0001t0005g0052 a0001c0001t0005g0053 others(29): Show |
37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1762-18C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085192 | |||||||
chr11:69085338 | G | A | 1 | a0005c0004t0008g0131 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1838+52G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085338 | |||||||
chr11:69085460 | C | T | 1 | a0005c0004t0007g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1838+174C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085460 | |||||||
chr11:69085550 | C | T | 1 | a0003c0003t0002g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1839-121C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085550 | |||||||
chr11:69085565 | T | G | 215 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(212): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1839-106T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085565 | |||||||
chr11:69085616 | C | A | 2 | a0003c0003t0002g0112 a0003c0003t0002g0117 |
2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1839-55C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085616 | |||||||
chr11:69085640 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1839-31G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085640 | |||||||
chr11:69085774 | AGCACCCT others(3): Show |
A | 1 | a0002c0002t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1920+23_1920+32del others(10): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 21/24 | chr11 | 69085774 | |||||||
chr11:69085964 | C | T | 1 | a0020c0029t0039g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2003+34C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69085964 | |||||||
chr11:69085993 | G | A | 1 | a0004c0008t0031g0188 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2003+63G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69085993 | |||||||
chr11:69086036 | C | T | 93 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(90): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2003+106C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086036 | |||||||
chr11:69086064 | G | A | 21 | a0001c0001t0004g0279 a0004c0006t0009g0044 a0004c0006t0009g0206 others(18): Show |
24 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.2003+134G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086064 | |||||||
chr11:69086219 | G | A | 8 | a0002c0028t0001g0179 a0004c0015t0014g0056 a0004c0015t0014g0057 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+289G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086219 | |||||||
chr11:69086309 | C | T | 1 | a0010c0014t0013g0192 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2004-214C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086309 | |||||||
chr11:69086381 | T | C | 2 | a0002c0028t0001g0179 a0017c0036t0001g0180 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2004-142T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086381 | |||||||
chr11:69086623 | C | G | 1 | a0001c0001t0005g0289 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2085+19C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086623 | |||||||
chr11:69086662 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2085+58C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086662 | |||||||
chr11:69086714 | C | A | 1 | a0005c0004t0007g0029 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2085+110C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086714 | |||||||
chr11:69086794 | T | C | 1 | a0004c0006t0033g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2085+190T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086794 | |||||||
chr11:69086800 | A | AGTGCTCC others(29): Show |
4 | a0001c0001t0005g0012 a0001c0001t0005g0281 a0001c0001t0005g0284 others(1): Show |
7 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085+254_2086-219d others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086800 | ||||||
chr11:69086800 | A | G | 1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2085+196A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086800 | |||||||
chr11:69086800 | AGTGCTCC others(29): Show |
A | 2 | a0004c0006t0033g0200 a0006c0007t0006g0171 |
2 | HG02155.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2085+254_2086-219d others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086800 | ||||||
chr11:69086833 | G | GGGGGTGC others(29): Show |
267 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0020 others(264): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2086-244_2086-243i others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086833 | ||||||
chr11:69086833 | G | GGGGGTGC others(101): Show |
3 | a0003c0003t0002g0034 a0003c0003t0002g0125 a0003c0003t0002g0132 |
4 | NA18940.hp1 NA18990.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2086-244_2086-243i others(110): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086833 | ||||||
chr11:69086833 | G | T | 1 | a0016c0041t0004g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2085+229G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086833 | |||||||
chr11:69086980 | C | T | 2 | a0001c0001t0004g0039 a0001c0001t0004g0155 |
3 | HG00438.hp2 NA18945.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2086-132C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086980 | |||||||
chr11:69087032 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2086-80G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087032 | |||||||
chr11:69087076 | G | C | 25 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0268 others(22): Show |
28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2086-36G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087076 | |||||||
chr11:69087087 | A | G | 1 | a0002c0002t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2086-25A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087087 | |||||||
chr11:69087284 | C | T | 1 | a0002c0002t0001g0215 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2180+78C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087284 | |||||||
chr11:69087287 | C | T | 1 | a0002c0002t0001g0266 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2180+81C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087287 | |||||||
chr11:69087368 | C | T | 1 | a0004c0006t0035g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2180+162C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087368 | |||||||
chr11:69087625 | G | A | 2 | a0005c0004t0008g0109 a0005c0004t0008g0140 |
2 | NA18946.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2181-250G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087625 | |||||||
chr11:69087644 | C | T | 17 | a0001c0001t0004g0039 a0001c0001t0004g0155 a0001c0005t0004g0001 others(14): Show |
28 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.2181-231C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087644 | |||||||
chr11:69087729 | T | G | 108 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0006 others(105): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2181-146T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087729 | |||||||
chr11:69087765 | G | A | 113 | a0003c0003t0002g0009 a0003c0003t0002g0013 a0003c0003t0002g0014 others(110): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2181-110G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087765 | |||||||
chr11:69087846 | C | A | 2 | a0004c0016t0014g0054 a0004c0016t0014g0055 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2181-29C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087846 | |||||||
chr11:69087864 | C | G | 6 | a0001c0001t0005g0268 a0001c0001t0005g0269 a0001c0001t0005g0270 others(3): Show |
6 | HG00544.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-11C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087864 |