Item | Value |
---|---|
geneid | 65065 |
ensemblid | ENSG00000144426.19 |
hgncid | 20681 |
symbol | NBEAL1 |
name | neurobeachin like 1 |
refseq_nuc | NM_001378026.1 |
refseq_prot | NP_001364955.1 |
ensembl_nuc | ENST00000683969.1 |
ensembl_prot | ENSP00000508055.1 |
mane_status | MANE Select |
chr | chr2 |
start | 203014875 |
end | 203225194 |
strand | + |
ver | v1.2 |
region | chr2:203014875-203225194 |
region5000 | chr2:203009875-203230194 |
regionname0 | NBEAL1_chr2_203014875_203225194 |
regionname5000 | NBEAL1_chr2_203009875_203230194 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 2723 | 208 | 38 | 43 | 98 | 8 | 21 | 70 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0002 | 1/0 | 2723 | 33 | 16 | 4 | 10 | 0 | 2 | 8 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0003 | 0/0 | 2723 | 21 | 17 | 4 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0004 | 0/0 | 2723 | 7 | 0 | 0 | 7 | 0 | 0 | 5 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0005 | 0/1 | 2723 | 5 | 0 | 2 | 0 | 0 | 2 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0006 | 0/0 | 2723 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0007 | 0/0 | 2723 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0008 | 0/0 | 2723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0009 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0010 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0011 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0012 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0013 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0014 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0015 | 0/0 | 2723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0016 | 0/0 | 704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(699): Show |
chr2 | 203009875 | 203230194 |
a0017 | 0/0 | 107 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(102): Show |
chr2 | 203009875 | 203230194 |
a0018 | 0/0 | 2723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0019 | 0/0 | 2723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0020 | 0/0 | 2723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
a0021 | 0/0 | 2723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | MASRE others(2718): Show |
chr2 | 203009875 | 203230194 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 8169 | 186 | 35 | 36 | 91 | 4 | 20 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0004 | 0/0 | 8169 | 9 | 0 | 5 | 0 | 4 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0007 | 0/0 | 8169 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0008 | 0/0 | 8169 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0017 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0018 | 0/0 | 8169 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0021 | 0/0 | 8169 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0022 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0028 | 0/0 | 8169 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0001c0029 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0002c0002 | 1/0 | 8169 | 32 | 15 | 4 | 10 | 0 | 2 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0002c0013 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0003c0003 | 0/0 | 8169 | 19 | 15 | 4 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0003c0011 | 0/0 | 8169 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0004c0005 | 0/0 | 8169 | 7 | 0 | 0 | 7 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0005c0006 | 0/1 | 8169 | 5 | 0 | 2 | 0 | 0 | 2 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0006c0009 | 0/0 | 8169 | 2 | 0 | 0 | 0 | 2 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0007c0010 | 0/0 | 8169 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0008c0024 | 0/0 | 8169 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0009c0026 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0010c0016 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0011c0025 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0012c0019 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0013c0012 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0014c0015 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0015c0023 | 0/0 | 8169 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0016c0030 | 0/0 | 7738 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(7733): Show |
chr2 | 203009875 | 203230194 | ||
a0017c0032 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8138): Show |
chr2 | 203009875 | 203230194 | ||
a0018c0031 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0019c0020 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0020c0014 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 | ||
a0021c0027 | 0/0 | 8169 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | ATGGC others(8164): Show |
chr2 | 203009875 | 203230194 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 16352 | 79 | 16 | 11 | 43 | 2 | 7 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0002 | 0/0 | 16352 | 67 | 5 | 18 | 32 | 2 | 10 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0004 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0005 | 0/0 | 16352 | 2 | 1 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0006 | 0/0 | 16351 | 7 | 0 | 6 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16346): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0013 | 0/0 | 16352 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0014 | 0/0 | 16352 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0015 | 0/0 | 16351 | 2 | 1 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16346): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0016 | 0/0 | 16352 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0018 | 0/0 | 16352 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0019 | 0/0 | 16352 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0020 | 0/0 | 16342 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16337): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0024 | 0/0 | 16350 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16345): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0025 | 0/0 | 16350 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16345): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0030 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0032 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0033 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0034 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0035 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0036 | 0/0 | 16352 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0037 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0038 | 0/0 | 16351 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16346): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0039 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0040 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0041 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0042 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0044 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0045 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0001t0047 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0004t0005 | 0/0 | 16352 | 8 | 0 | 5 | 0 | 3 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0004t0049 | 0/0 | 16352 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0007t0001 | 0/0 | 16352 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0008t0007 | 0/0 | 16352 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0017t0031 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0018t0001 | 0/0 | 16352 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0021t0002 | 0/0 | 16352 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0022t0001 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0028t0050 | 0/0 | 16352 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0001c0029t0002 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0003 | 0/0 | 16349 | 24 | 12 | 2 | 9 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0008 | 0/0 | 16349 | 3 | 2 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0022 | 0/0 | 19101 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(19096): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0026 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0027 | 0/0 | 16349 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0028 | 0/0 | 16349 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0002t0048 | 1/0 | 16349 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0002c0013t0003 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0003c0003t0004 | 0/0 | 16352 | 17 | 13 | 4 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0003c0003t0010 | 0/0 | 16352 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0003c0011t0011 | 0/0 | 16352 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0004c0005t0002 | 0/0 | 16352 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0004c0005t0009 | 0/0 | 16352 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0005c0006t0002 | 0/0 | 16352 | 4 | 0 | 2 | 0 | 0 | 2 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0005c0006t0021 | 0/1 | 16353 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16348): Show |
chr2 | 203009875 | 203230194 |
a0006c0009t0012 | 0/0 | 16352 | 2 | 0 | 0 | 0 | 2 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0007c0010t0017 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0007c0010t0046 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0008c0024t0001 | 0/0 | 16352 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0009c0026t0043 | 0/0 | 16351 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16346): Show |
chr2 | 203009875 | 203230194 |
a0010c0016t0023 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0011c0025t0007 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0012c0019t0003 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0013c0012t0003 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0014c0015t0017 | 0/0 | 16352 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0015c0023t0003 | 0/0 | 16349 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
a0016c0030t0001 | 0/0 | 15921 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(15916): Show |
chr2 | 203009875 | 203230194 |
a0017c0032t0002 | 0/0 | 16326 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16321): Show |
chr2 | 203009875 | 203230194 |
a0018c0031t0001 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0019c0020t0001 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0020c0014t0002 | 0/0 | 16352 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16347): Show |
chr2 | 203009875 | 203230194 |
a0021c0027t0029 | 0/0 | 16349 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | GCCCG others(16344): Show |
chr2 | 203009875 | 203230194 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0013g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0016g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0018g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0018g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0019g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0019g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0020g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0024g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0030g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0032g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0033g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0034g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0035g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0036g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0037g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0038g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0039g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0040g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0041g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0044g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0045g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0001t0047g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0004t0049g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0007t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0008t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0008t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0008t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0017t0031g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0018t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0021t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0022t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0028t0050g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0001c0029t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0008g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0022g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0026g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0027g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0028g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0002t0048g0286 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0002c0013t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0003t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0011t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0003c0011t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0004c0005t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0005c0006t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0005c0006t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0005c0006t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0005c0006t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0005c0006t0021g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0006c0009t0012g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0006c0009t0012g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0007c0010t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0007c0010t0046g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0008c0024t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0009c0026t0043g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0010c0016t0023g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0011c0025t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0012c0019t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0013c0012t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0014c0015t0017g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0015c0023t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0016c0030t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0017c0032t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0018c0031t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0019c0020t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0020c0014t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
a0021c0027t0029g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | FIN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00408 | hp2 | a0001 | c0022 | t0001 | g0005 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00544 | hp1 | a0001 | c0017 | t0031 | g0180 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00544 | hp2 | a0001 | c0001 | t0039 | g0003 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00597 | hp1 | a0004 | c0005 | t0002 | g0171 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00597 | hp2 | a0001 | c0001 | t0040 | g0223 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00609 | hp1 | a0001 | c0001 | t0018 | g0148 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00609 | hp2 | a0001 | c0001 | t0037 | g0207 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0232 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00673 | hp1 | a0004 | c0005 | t0009 | g0181 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00733 | hp1 | a0003 | c0003 | t0004 | g0035 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00733 | hp2 | a0001 | c0001 | t0015 | g0129 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00735 | hp1 | a0001 | c0004 | t0005 | g0281 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00735 | hp2 | a0005 | c0006 | t0002 | g0100 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00738 | hp1 | a0002 | c0002 | t0003 | g0065 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00738 | hp2 | a0001 | c0004 | t0005 | g0282 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG00741 | hp2 | a0005 | c0006 | t0002 | g0161 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01099 | hp1 | a0001 | c0004 | t0005 | g0274 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01109 | hp1 | a0003 | c0003 | t0004 | g0027 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01167 | hp1 | a0001 | c0004 | t0005 | g0278 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01168 | hp1 | a0003 | c0003 | t0004 | g0030 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01169 | hp1 | a0003 | c0003 | t0004 | g0034 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01192 | hp1 | a0008 | c0024 | t0001 | g0191 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0233 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01358 | hp2 | a0001 | c0021 | t0002 | g0169 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01361 | hp1 | a0001 | c0028 | t0050 | g0247 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01496 | hp2 | a0001 | c0004 | t0005 | g0273 | AMR | CLM | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01515 | hp1 | a0006 | c0009 | t0012 | g0101 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01515 | hp2 | a0001 | c0004 | t0049 | g0285 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01516 | hp2 | a0001 | c0004 | t0005 | g0275 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01517 | hp1 | a0001 | c0004 | t0005 | g0276 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01517 | hp2 | a0006 | c0009 | t0012 | g0102 | EUR | IBS | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01884 | hp1 | a0003 | c0003 | t0004 | g0042 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0045 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01943 | hp2 | a0002 | c0002 | t0027 | g0094 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0271 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02055 | hp1 | a0009 | c0026 | t0043 | g0250 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02055 | hp2 | a0001 | c0001 | t0025 | g0016 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02132 | hp1 | a0002 | c0002 | t0003 | g0069 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02132 | hp2 | a0001 | c0001 | t0018 | g0147 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02135 | hp1 | a0001 | c0001 | t0041 | g0012 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CDX | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CDX | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02257 | hp2 | a0012 | c0019 | t0003 | g0074 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02258 | hp2 | a0003 | c0003 | t0004 | g0026 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0259 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02293 | hp1 | a0002 | c0002 | t0008 | g0082 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02451 | hp1 | a0001 | c0001 | t0042 | g0054 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0046 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02572 | hp1 | a0003 | c0003 | t0004 | g0037 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02602 | hp1 | a0001 | c0001 | t0036 | g0256 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02622 | hp2 | a0001 | c0001 | t0035 | g0058 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0084 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02717 | hp1 | a0002 | c0002 | t0003 | g0049 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02723 | hp1 | a0002 | c0002 | t0003 | g0085 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02818 | hp2 | a0003 | c0003 | t0004 | g0038 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02886 | hp1 | a0002 | c0002 | t0008 | g0093 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02895 | hp1 | a0003 | c0003 | t0010 | g0044 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0050 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0257 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02896 | hp2 | a0003 | c0003 | t0004 | g0033 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02897 | hp1 | a0001 | c0001 | t0013 | g0251 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02897 | hp2 | a0003 | c0003 | t0010 | g0041 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0081 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02976 | hp1 | a0001 | c0008 | t0007 | g0055 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03041 | hp2 | a0003 | c0003 | t0004 | g0039 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03098 | hp2 | a0003 | c0003 | t0004 | g0032 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03130 | hp1 | a0003 | c0003 | t0004 | g0028 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03130 | hp2 | a0013 | c0012 | t0003 | g0077 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03139 | hp1 | a0001 | c0008 | t0007 | g0056 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03139 | hp2 | a0002 | c0002 | t0026 | g0075 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03195 | hp1 | a0002 | c0013 | t0003 | g0076 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03195 | hp2 | a0007 | c0010 | t0046 | g0023 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03209 | hp1 | a0001 | c0001 | t0047 | g0187 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0083 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03225 | hp1 | a0003 | c0003 | t0004 | g0025 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03225 | hp2 | a0007 | c0010 | t0017 | g0018 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03239 | hp1 | a0002 | c0002 | t0028 | g0067 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03453 | hp2 | a0014 | c0015 | t0017 | g0017 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03491 | hp1 | a0005 | c0006 | t0002 | g0179 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03491 | hp2 | a0001 | c0018 | t0001 | g0192 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03492 | hp2 | a0005 | c0006 | t0002 | g0165 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03516 | hp2 | a0003 | c0003 | t0004 | g0040 | AFR | ESN | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0086 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03540 | hp2 | a0003 | c0003 | t0004 | g0029 | AFR | GWD | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03579 | hp1 | a0015 | c0023 | t0003 | g0047 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0231 | AFR | MSL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03688 | hp1 | a0016 | c0030 | t0001 | g0246 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03710 | hp1 | a0002 | c0002 | t0003 | g0066 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03710 | hp2 | a0001 | c0001 | t0038 | g0272 | SAS | PJL | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0254 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0078 | AFR | YRI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18939 | hp1 | a0017 | c0032 | t0002 | g0116 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18939 | hp2 | a0001 | c0001 | t0045 | g0201 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18949 | hp2 | a0001 | c0001 | t0016 | g0155 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18951 | hp2 | a0001 | c0007 | t0001 | g0243 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18952 | hp2 | a0001 | c0001 | t0019 | g0280 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18965 | hp1 | a0004 | c0005 | t0009 | g0170 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18966 | hp1 | a0001 | c0001 | t0019 | g0279 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18966 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18968 | hp1 | a0001 | c0007 | t0001 | g0241 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18969 | hp1 | a0002 | c0002 | t0022 | g0072 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18977 | hp2 | a0004 | c0005 | t0009 | g0176 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18981 | hp2 | a0001 | c0001 | t0020 | g0143 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18982 | hp1 | a0018 | c0031 | t0001 | g0203 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18983 | hp1 | a0001 | c0001 | t0033 | g0144 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18988 | hp2 | a0019 | c0020 | t0001 | g0190 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18994 | hp1 | a0001 | c0029 | t0002 | g0159 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18995 | hp2 | a0001 | c0001 | t0016 | g0162 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18998 | hp1 | a0004 | c0005 | t0002 | g0175 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19010 | hp1 | a0001 | c0001 | t0044 | g0096 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19010 | hp2 | a0001 | c0007 | t0001 | g0242 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19030 | hp1 | a0001 | c0001 | t0034 | g0139 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19043 | hp1 | a0003 | c0011 | t0011 | g0043 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19057 | hp1 | a0004 | c0005 | t0002 | g0174 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19062 | hp1 | a0001 | c0007 | t0001 | g0240 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19063 | hp2 | a0020 | c0014 | t0002 | g0109 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19066 | hp2 | a0001 | c0001 | t0032 | g0115 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19077 | hp1 | a0021 | c0027 | t0029 | g0095 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19077 | hp2 | a0004 | c0005 | t0002 | g0173 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ASW | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20129 | hp2 | a0003 | c0003 | t0004 | g0031 | AFR | ASW | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | TSI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20752 | hp2 | a0001 | c0004 | t0005 | g0284 | EUR | TSI | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02109 | hp1 | a0010 | c0016 | t0023 | g0022 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02109 | hp2 | a0011 | c0025 | t0007 | g0053 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0260 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0132 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG02559 | hp2 | a0003 | c0011 | t0011 | g0024 | AFR | ACB | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG06807 | hp1 | a0003 | c0003 | t0004 | g0036 | AFR | USA | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | USA | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA20300 | hp2 | a0001 | c0008 | t0007 | g0057 | AFR | USA | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA21309 | hp1 | a0002 | c0002 | t0008 | g0088 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | LWK | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
homoSapiens | chm13v2 | a0005 | c0006 | t0021 | g0160 | REF | REF | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
homoSapiens | grch38p0 | a0002 | c0002 | t0048 | g0286 | REF | REF | NBEAL1_chr2_203009875_203230194 | NBEAL1 | chr2 | 203009875 | 203230194 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203056420 | CTCACAGA others(25): Show |
C | 1 | a0017 | 1 | NA18939.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.306-6_331delTCACAG others(26): Show |
p.Asn103fs | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 5/56 | 306/8172 | 102/2723 | chr2 | 203056420 | ||||
chr2:203083393 | C | T | 1 | a0018 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.859C>T | p.Arg287Cys | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/56 | 1196/16349 | 859/8172 | 287/2723 | chr2 | 203083393 | |||
chr2:203111919 | TTTGTCAT others(4065): Show |
T | 1 | a0016 | 1 | HG03688.hp1 | exon_loss_variant | HIGH | c.2083-55_2517del | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/56 | INFO_REALIGN_3_PRIME | chr2 | 203111919 | ||||||
chr2:203113256 | G | A | 1 | a0001 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.2444G>A | p.Gly815Glu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/56 | 2781/16349 | 2444/8172 | 815/2723 | chr2 | 203113256 | |||
chr2:203125355 | A | G | 1 | a0003 | 21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
missense_variant | MODERATE | c.2686A>G | p.Ile896Val | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 20/56 | 3023/16349 | 2686/8172 | 896/2723 | chr2 | 203125355 | |||
chr2:203126050 | T | C | 1 | a0020 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.2942T>C | p.Ile981Thr | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 21/56 | 3279/16349 | 2942/8172 | 981/2723 | chr2 | 203126050 | |||
chr2:203130423 | G | A | 1 | a0014 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3511G>A | p.Ala1171Thr | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/56 | 3848/16349 | 3511/8172 | 1171/2723 | chr2 | 203130423 | |||
chr2:203132090 | A | T | 2 | a0007 a0014 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.3682A>T | p.Thr1228Ser | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/56 | 4019/16349 | 3682/8172 | 1228/2723 | chr2 | 203132090 | |||
chr2:203135710 | G | A | 1 | a0013 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.3847G>A | p.Ala1283Thr | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4184/16349 | 3847/8172 | 1283/2723 | chr2 | 203135710 | |||
chr2:203135938 | A | C | 1 | a0021 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.4075A>C | p.Ser1359Arg | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4412/16349 | 4075/8172 | 1359/2723 | chr2 | 203135938 | |||
chr2:203136122 | C | T | 1 | a0009 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.4259C>T | p.Pro1420Leu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4596/16349 | 4259/8172 | 1420/2723 | chr2 | 203136122 | |||
chr2:203136214 | G | A | 1 | a0010 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.4351G>A | p.Gly1451Ser | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4688/16349 | 4351/8172 | 1451/2723 | chr2 | 203136214 | |||
chr2:203144736 | A | T | 1 | a0011 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4985A>T | p.Tyr1662Phe | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 32/56 | 5322/16349 | 4985/8172 | 1662/2723 | chr2 | 203144736 | |||
chr2:203149025 | G | A | 1 | a0006 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.5339G>A | p.Arg1780His | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/56 | 5676/16349 | 5339/8172 | 1780/2723 | chr2 | 203149025 | |||
chr2:203157755 | G | T | 1 | a0004 | 7 | HG00597.hp1 HG00673.hp1 NA18965.hp1 others(4): Show |
missense_variant | MODERATE | c.5644G>T | p.Val1882Leu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/56 | 5981/16349 | 5644/8172 | 1882/2723 | chr2 | 203157755 | |||
chr2:203166295 | A | C | 1 | a0008 | 1 | HG01192.hp1 | missense_variant&splice_region_variant | MODERATE | c.5861A>C | p.Asp1954Ala | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/56 | 6198/16349 | 5861/8172 | 1954/2723 | chr2 | 203166295 | |||
chr2:203167347 | A | G | 1 | a0015 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.5984A>G | p.Asn1995Ser | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/56 | 6321/16349 | 5984/8172 | 1995/2723 | chr2 | 203167347 | |||
chr2:203188550 | G | A | 1 | a0012 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.6784G>A | p.Val2262Ile | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/56 | 7121/16349 | 6784/8172 | 2262/2723 | chr2 | 203188550 | |||
chr2:203197338 | A | G | 15 | a0001 a0003 a0004 others(12): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
missense_variant | MODERATE | c.7075A>G | p.Ile2359Val | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/56 | 7412/16349 | 7075/8172 | 2359/2723 | chr2 | 203197338 | |||
chr2:203208691 | A | G | 1 | a0005 | 4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
missense_variant | MODERATE | c.7561A>G | p.Thr2521Ala | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 52/56 | 7898/16349 | 7561/8172 | 2521/2723 | chr2 | 203208691 | |||
chr2:203209297 | G | A | 1 | a0019 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.7760G>A | p.Ser2587Asn | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/56 | 8097/16349 | 7760/8172 | 2587/2723 | chr2 | 203209297 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203110255 | T | C | 2 | a0002c0013 a0013c0012 |
2 | HG03130.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.2055T>C | p.Pro685Pro | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/56 | 2392/16349 | 2055/8172 | 685/2723 | chr2 | 203110255 | |||
chr2:203113065 | T | C | 1 | a0001c0001 | 4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
synonymous_variant | LOW | c.2253T>C | p.Pro751Pro | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/56 | 2590/16349 | 2253/8172 | 751/2723 | chr2 | 203113065 | |||
chr2:203125495 | C | A | 1 | a0003c0003 | 19 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
synonymous_variant | LOW | c.2826C>A | p.Leu942Leu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 20/56 | 3163/16349 | 2826/8172 | 942/2723 | chr2 | 203125495 | |||
chr2:203126066 | T | G | 1 | a0001c0004 | 9 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(6): Show |
synonymous_variant | LOW | c.2958T>G | p.Val986Val | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 21/56 | 3295/16349 | 2958/8172 | 986/2723 | chr2 | 203126066 | |||
chr2:203132011 | G | A | 1 | a0001c0008 | 3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.3603G>A | p.Glu1201Glu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/56 | 3940/16349 | 3603/8172 | 1201/2723 | chr2 | 203132011 | |||
chr2:203135685 | A | G | 1 | a0001c0029 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.3822A>G | p.Gln1274Gln | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4159/16349 | 3822/8172 | 1274/2723 | chr2 | 203135685 | |||
chr2:203135724 | A | G | 1 | a0001c0028 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.3861A>G | p.Ser1287Ser | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 28/56 | 4198/16349 | 3861/8172 | 1287/2723 | chr2 | 203135724 | |||
chr2:203151498 | T | C | 1 | a0001c0017 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.5496T>C | p.Asn1832Asn | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/56 | 5833/16349 | 5496/8172 | 1832/2723 | chr2 | 203151498 | |||
chr2:203151543 | T | C | 1 | a0001c0007 | 4 | NA18951.hp2 NA18968.hp1 NA19010.hp2 others(1): Show |
synonymous_variant | LOW | c.5541T>C | p.Tyr1847Tyr | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/56 | 5878/16349 | 5541/8172 | 1847/2723 | chr2 | 203151543 | |||
chr2:203169836 | A | G | 1 | a0001c0022 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.6087A>G | p.Ala2029Ala | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/56 | 6424/16349 | 6087/8172 | 2029/2723 | chr2 | 203169836 | |||
chr2:203172767 | G | A | 1 | a0001c0018 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.6237G>A | p.Leu2079Leu | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/56 | 6574/16349 | 6237/8172 | 2079/2723 | chr2 | 203172767 | |||
chr2:203211029 | A | G | 1 | a0001c0021 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.7857A>G | p.Val2619Val | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/56 | 8194/16349 | 7857/8172 | 2619/2723 | chr2 | 203211029 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203014882 | C | T | 1 | a0001c0028t0050 | 1 | HG01361.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-330C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/56 | chr2 | 203014882 | |||||||
chr2:203014895 | GCGGGGTG others(3): Show |
G | 1 | a0001c0001t0020 | 1 | NA18981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-311_-302delTGACAC others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/56 | 1475 | INFO_REALIGN_3_PRIME | chr2 | 203014895 | |||||
chr2:203016269 | T | C | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(62): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
5_prime_UTR_variant | MODIFIER | c.-116T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/56 | 116 | chr2 | 203016269 | ||||||
chr2:203217528 | A | G | 1 | a0001c0001t0018 | 2 | HG00609.hp1 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*174A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 174 | chr2 | 203217528 | ||||||
chr2:203218034 | A | C | 1 | a0001c0001t0047 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 680 | chr2 | 203218034 | ||||||
chr2:203218165 | T | TAAGAGTT others(2745): Show |
1 | a0002c0002t0022 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820_*821insGGTCTC others(2746): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 821 | INFO_REALIGN_3_PRIME | chr2 | 203218165 | |||||
chr2:203218255 | A | T | 3 | a0007c0010t0017 a0007c0010t0046 a0014c0015t0017 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*901A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 901 | chr2 | 203218255 | ||||||
chr2:203218330 | T | TTA | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(52): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*977_*978dupTA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 979 | INFO_REALIGN_3_PRIME | chr2 | 203218330 | |||||
chr2:203218912 | A | G | 1 | a0001c0001t0045 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1558A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 1558 | chr2 | 203218912 | ||||||
chr2:203219333 | G | A | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1979G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 1979 | chr2 | 203219333 | ||||||
chr2:203219503 | A | C | 1 | a0001c0001t0044 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2149 | chr2 | 203219503 | ||||||
chr2:203219538 | T | C | 1 | a0010c0016t0023 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2184T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2184 | chr2 | 203219538 | ||||||
chr2:203219541 | T | G | 1 | a0001c0017t0031 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2187T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2187 | chr2 | 203219541 | ||||||
chr2:203219630 | C | T | 1 | a0009c0026t0043 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2276C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2276 | chr2 | 203219630 | ||||||
chr2:203219767 | A | G | 1 | a0001c0001t0016 | 2 | NA18949.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2413A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2413 | chr2 | 203219767 | ||||||
chr2:203219768 | G | C | 1 | a0001c0001t0016 | 2 | NA18949.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2414G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2414 | chr2 | 203219768 | ||||||
chr2:203219866 | G | GA | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(53): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*2520dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2521 | INFO_REALIGN_3_PRIME | chr2 | 203219866 | |||||
chr2:203219883 | T | G | 2 | a0007c0010t0017 a0014c0015t0017 |
2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2529T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2529 | chr2 | 203219883 | ||||||
chr2:203220054 | A | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(54): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*2700A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2700 | chr2 | 203220054 | ||||||
chr2:203220156 | A | G | 1 | a0010c0016t0023 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2802A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2802 | chr2 | 203220156 | ||||||
chr2:203220221 | C | T | 4 | a0001c0001t0014 a0001c0001t0042 a0001c0008t0007 others(1): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2867C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2867 | chr2 | 203220221 | ||||||
chr2:203220224 | G | A | 1 | a0007c0010t0046 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2870G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2870 | chr2 | 203220224 | ||||||
chr2:203220252 | G | A | 1 | a0001c0004t0049 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2898G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 2898 | chr2 | 203220252 | ||||||
chr2:203220442 | C | T | 1 | a0004c0005t0009 | 3 | HG00673.hp1 NA18965.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3088C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3088 | chr2 | 203220442 | ||||||
chr2:203220764 | C | G | 1 | a0001c0001t0013 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3410C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3410 | chr2 | 203220764 | ||||||
chr2:203220768 | G | A | 1 | a0003c0003t0010 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3414G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3414 | chr2 | 203220768 | ||||||
chr2:203220912 | C | T | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(21): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*3558C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3558 | chr2 | 203220912 | ||||||
chr2:203220972 | G | A | 1 | a0010c0016t0023 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3618G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3618 | chr2 | 203220972 | ||||||
chr2:203221188 | G | A | 1 | a0001c0001t0032 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3834G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 3834 | chr2 | 203221188 | ||||||
chr2:203221373 | A | G | 1 | a0001c0001t0041 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4019A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4019 | chr2 | 203221373 | ||||||
chr2:203221398 | T | C | 2 | a0001c0001t0020 a0001c0001t0033 |
2 | NA18981.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4044T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4044 | chr2 | 203221398 | ||||||
chr2:203221401 | G | T | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4047G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4047 | chr2 | 203221401 | ||||||
chr2:203221489 | A | G | 1 | a0021c0027t0029 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4135 | chr2 | 203221489 | ||||||
chr2:203221501 | C | T | 1 | a0002c0002t0028 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4147C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4147 | chr2 | 203221501 | ||||||
chr2:203221606 | C | A | 1 | a0003c0011t0011 | 2 | HG02559.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4252C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4252 | chr2 | 203221606 | ||||||
chr2:203221864 | T | C | 1 | a0006c0009t0012 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4510T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4510 | chr2 | 203221864 | ||||||
chr2:203222136 | G | A | 30 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(27): Show |
129 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4782G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4782 | chr2 | 203222136 | ||||||
chr2:203222255 | A | G | 1 | a0001c0001t0034 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4901A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4901 | chr2 | 203222255 | ||||||
chr2:203222290 | T | A | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4936T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4936 | chr2 | 203222290 | ||||||
chr2:203222314 | A | G | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(51): Show |
250 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*4960A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 4960 | chr2 | 203222314 | ||||||
chr2:203222366 | A | G | 2 | a0007c0010t0017 a0014c0015t0017 |
2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5012A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5012 | chr2 | 203222366 | ||||||
chr2:203222456 | G | A | 1 | a0001c0001t0037 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5102G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5102 | chr2 | 203222456 | ||||||
chr2:203222747 | AC | A | 3 | a0001c0001t0006 a0001c0001t0038 a0009c0026t0043 |
9 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5394delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5394 | chr2 | 203222747 | ||||||
chr2:203223051 | T | C | 1 | a0001c0001t0019 | 2 | NA18952.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5697T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5697 | chr2 | 203223051 | ||||||
chr2:203223057 | T | C | 1 | a0006c0009t0012 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5703T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5703 | chr2 | 203223057 | ||||||
chr2:203223239 | A | T | 1 | a0001c0001t0042 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5885A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 5885 | chr2 | 203223239 | ||||||
chr2:203223500 | G | T | 2 | a0007c0010t0017 a0014c0015t0017 |
2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6146G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 6146 | chr2 | 203223500 | ||||||
chr2:203223615 | A | T | 1 | a0002c0002t0027 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6261A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 6261 | chr2 | 203223615 | ||||||
chr2:203223799 | G | A | 18 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(15): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*6445G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 6445 | chr2 | 203223799 | ||||||
chr2:203223986 | A | G | 1 | a0001c0001t0040 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6632A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 6632 | chr2 | 203223986 | ||||||
chr2:203224336 | T | C | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6982T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 6982 | chr2 | 203224336 | ||||||
chr2:203224588 | C | T | 1 | a0001c0001t0038 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7234C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7234 | chr2 | 203224588 | ||||||
chr2:203224663 | G | C | 1 | a0001c0001t0014 | 2 | HG02486.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7309G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7309 | chr2 | 203224663 | ||||||
chr2:203224807 | C | T | 1 | a0002c0002t0026 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7453C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7453 | chr2 | 203224807 | ||||||
chr2:203225007 | G | A | 4 | a0001c0001t0014 a0001c0001t0042 a0001c0008t0007 others(1): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7653G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7653 | chr2 | 203225007 | ||||||
chr2:203225093 | T | G | 1 | a0002c0002t0008 | 3 | HG02293.hp1 HG02886.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7739T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7739 | chr2 | 203225093 | ||||||
chr2:203225191 | T | C | 1 | a0001c0001t0039 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7837T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 56/56 | 7837 | chr2 | 203225191 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203015238 | T | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-230+256T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015238 | |||||||
chr2:203015283 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-230+301G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015283 | |||||||
chr2:203015283 | G | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-230+301G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015283 | |||||||
chr2:203015512 | G | C | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-230+530G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015512 | |||||||
chr2:203015587 | A | G | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01361.hp2 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-229-569A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015587 | |||||||
chr2:203015690 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG02165.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-229-466C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203015690 | |||||||
chr2:203016101 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-229-55A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203016101 | |||||||
chr2:203016111 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(274): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.-229-45G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 1/55 | chr2 | 203016111 | |||||||
chr2:203016775 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0014g0019 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.51+340G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203016775 | |||||||
chr2:203016863 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0014g0019 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.51+428G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203016863 | |||||||
chr2:203017070 | T | C | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.51+635T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017070 | |||||||
chr2:203017229 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+794A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017229 | |||||||
chr2:203017525 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | NA18981.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.51+1090A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017525 | |||||||
chr2:203017835 | C | T | 91 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(88): Show |
91 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.51+1400C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017835 | |||||||
chr2:203017870 | A | C | 91 | a0001c0001t0001g0177 a0001c0001t0002g0097 a0001c0001t0002g0098 others(88): Show |
91 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.51+1435A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017870 | |||||||
chr2:203017975 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.51+1540C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203017975 | |||||||
chr2:203018272 | C | CT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
249 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.51+1847dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203018272 | ||||||
chr2:203018401 | G | T | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.51+1966G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203018401 | |||||||
chr2:203018433 | C | T | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.51+1998C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203018433 | |||||||
chr2:203018447 | A | AC | 135 | a0001c0001t0001g0177 a0001c0001t0002g0097 a0001c0001t0002g0098 others(132): Show |
135 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.51+2013dupC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203018447 | ||||||
chr2:203018470 | C | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2035C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203018470 | |||||||
chr2:203018943 | T | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.51+2508T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203018943 | |||||||
chr2:203018972 | C | T | 99 | a0001c0001t0001g0177 a0001c0001t0002g0097 a0001c0001t0002g0098 others(96): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.51+2537C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203018972 | |||||||
chr2:203019176 | C | G | 1 | a0001c0001t0006g0271 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.51+2741C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019176 | |||||||
chr2:203019266 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.51+2831A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019266 | |||||||
chr2:203019320 | C | G | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.51+2885C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019320 | |||||||
chr2:203019517 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.51+3082C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019517 | |||||||
chr2:203019550 | CACCTTGG others(14): Show |
C | 1 | a0002c0002t0027g0094 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.51+3118_51+3138del others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203019550 | ||||||
chr2:203019585 | A | C | 14 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+3150A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019585 | |||||||
chr2:203019632 | A | G | 1 | a0004c0005t0009g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.51+3197A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019632 | |||||||
chr2:203019722 | A | G | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.51+3287A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019722 | |||||||
chr2:203019927 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.51+3492G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019927 | |||||||
chr2:203019995 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.51+3560T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203019995 | |||||||
chr2:203020006 | GATAATTT others(10): Show |
G | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.51+3589_51+3605del others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203020006 | ||||||
chr2:203020020 | A | ATAAT | 14 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+3588_51+3589ins others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203020020 | ||||||
chr2:203020232 | A | T | 1 | a0002c0002t0003g0050 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.51+3797A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203020232 | |||||||
chr2:203020452 | T | G | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+4017T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203020452 | |||||||
chr2:203020619 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.51+4184C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203020619 | |||||||
chr2:203020670 | C | CA | 10 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(7): Show |
10 | HG00438.hp2 HG00735.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.51+4252dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203020670 | ||||||
chr2:203020670 | CA | C | 6 | a0001c0001t0001g0267 a0001c0001t0002g0178 a0001c0004t0049g0285 others(3): Show |
6 | HG01256.hp1 HG01515.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+4252delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203020670 | ||||||
chr2:203021095 | T | G | 2 | a0006c0009t0012g0101 a0006c0009t0012g0102 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.51+4660T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203021095 | |||||||
chr2:203021219 | C | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+4784C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203021219 | |||||||
chr2:203021519 | C | T | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.51+5084C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203021519 | |||||||
chr2:203021617 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.51+5182A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203021617 | |||||||
chr2:203021876 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.51+5441C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203021876 | |||||||
chr2:203022060 | A | G | 2 | a0001c0008t0007g0056 a0001c0008t0007g0057 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.51+5625A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022060 | |||||||
chr2:203022071 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+5636A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022071 | |||||||
chr2:203022382 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.51+5947A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022382 | |||||||
chr2:203022565 | C | T | 1 | a0001c0004t0005g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.51+6130C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022565 | |||||||
chr2:203022760 | A | G | 1 | a0001c0001t0005g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.51+6325A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022760 | |||||||
chr2:203022955 | G | T | 1 | a0003c0003t0004g0042 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.51+6520G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203022955 | |||||||
chr2:203023115 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+6680G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023115 | |||||||
chr2:203023165 | A | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+6730A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023165 | |||||||
chr2:203023414 | C | G | 1 | a0002c0002t0003g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.51+6979C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023414 | |||||||
chr2:203023457 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.51+7022G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023457 | |||||||
chr2:203023632 | C | CA | 15 | a0001c0001t0002g0103 a0001c0001t0005g0277 a0001c0001t0005g0283 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+7206dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203023632 | ||||||
chr2:203023892 | A | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+7457A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023892 | |||||||
chr2:203023985 | T | G | 15 | a0002c0002t0003g0060 a0002c0002t0003g0061 a0002c0002t0003g0062 others(12): Show |
15 | HG00738.hp1 HG01943.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.51+7550T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203023985 | |||||||
chr2:203024087 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0014g0019 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.51+7652T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024087 | |||||||
chr2:203024135 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.51+7700A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024135 | |||||||
chr2:203024185 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.51+7750G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024185 | |||||||
chr2:203024201 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0265 |
2 | NA18983.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.51+7766A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024201 | |||||||
chr2:203024204 | A | T | 2 | a0003c0003t0010g0041 a0003c0003t0010g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.51+7769A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024204 | |||||||
chr2:203024551 | C | CA | 95 | a0001c0001t0001g0177 a0001c0001t0001g0189 a0001c0001t0002g0097 others(92): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.51+8129dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203024551 | ||||||
chr2:203024557 | A | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.51+8122A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024557 | |||||||
chr2:203024707 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.51+8272C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024707 | |||||||
chr2:203024801 | G | A | 1 | a0019c0020t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.51+8366G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024801 | |||||||
chr2:203024879 | A | C | 9 | a0001c0001t0002g0172 a0001c0001t0024g0045 a0004c0005t0002g0171 others(6): Show |
9 | HG00597.hp1 HG00673.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+8444A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024879 | |||||||
chr2:203024908 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.51+8473C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024908 | |||||||
chr2:203024940 | AAG | A | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+8506_51+8507del others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203024940 | |||||||
chr2:203025269 | G | A | 25 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(22): Show |
25 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.51+8834G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203025269 | |||||||
chr2:203025270 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.51+8835C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203025270 | |||||||
chr2:203025499 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+9064G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203025499 | |||||||
chr2:203025983 | G | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.51+9548G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203025983 | |||||||
chr2:203026452 | G | T | 1 | a0001c0001t0006g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.51+10017G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203026452 | |||||||
chr2:203026506 | A | AT | 16 | a0001c0001t0002g0089 a0001c0001t0005g0277 a0001c0001t0005g0283 others(13): Show |
16 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.51+10087dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203026506 | ||||||
chr2:203026721 | G | A | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.51+10286G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203026721 | |||||||
chr2:203027164 | A | G | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.51+10729A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203027164 | |||||||
chr2:203027532 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.51+11097C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203027532 | |||||||
chr2:203027647 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0014g0019 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.51+11212A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203027647 | |||||||
chr2:203027915 | C | T | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.51+11480C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203027915 | |||||||
chr2:203027916 | G | A | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+11481G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203027916 | |||||||
chr2:203028044 | T | C | 14 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+11609T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028044 | |||||||
chr2:203028233 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.51+11798A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028233 | |||||||
chr2:203028268 | C | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.51+11833C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028268 | |||||||
chr2:203028335 | T | A | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+11900T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028335 | |||||||
chr2:203028336 | A | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+11901A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028336 | |||||||
chr2:203028432 | A | C | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.51+11997A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028432 | |||||||
chr2:203028471 | A | G | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.51+12036A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028471 | |||||||
chr2:203028588 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.51+12153T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028588 | |||||||
chr2:203028752 | G | A | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.51+12317G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028752 | |||||||
chr2:203028756 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51+12321T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028756 | |||||||
chr2:203028927 | C | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.51+12492C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203028927 | |||||||
chr2:203029269 | C | T | 18 | a0003c0003t0004g0026 a0003c0003t0004g0027 a0003c0003t0004g0028 others(15): Show |
18 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.52-12496C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203029269 | |||||||
chr2:203029276 | C | A | 14 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.52-12489C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203029276 | |||||||
chr2:203029504 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.52-12261G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203029504 | |||||||
chr2:203029691 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(117): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.52-12058dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203029691 | ||||||
chr2:203029691 | C | CAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0051 others(3): Show |
6 | HG00544.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-12059_52-12058d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203029691 | ||||||
chr2:203029698 | A | C | 1 | a0001c0001t0002g0089 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.52-12067A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203029698 | |||||||
chr2:203029991 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-11774G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203029991 | |||||||
chr2:203030526 | G | A | 3 | a0002c0002t0003g0046 a0002c0002t0003g0049 a0002c0002t0003g0050 |
3 | HG02451.hp2 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.52-11239G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203030526 | |||||||
chr2:203030612 | A | G | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.52-11153A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203030612 | |||||||
chr2:203030811 | G | A | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.52-10954G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203030811 | |||||||
chr2:203031083 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.52-10682T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031083 | |||||||
chr2:203031342 | T | C | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.52-10423T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031342 | |||||||
chr2:203031350 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-10415G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031350 | |||||||
chr2:203031628 | C | A | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.52-10137C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031628 | |||||||
chr2:203031697 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52-10068G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031697 | |||||||
chr2:203031934 | G | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-9831G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203031934 | |||||||
chr2:203032043 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0021t0002g0169 |
3 | HG01167.hp2 HG01169.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.52-9722C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032043 | |||||||
chr2:203032054 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.52-9711A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032054 | |||||||
chr2:203032386 | G | C | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52-9379G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032386 | |||||||
chr2:203032614 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.52-9151C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032614 | |||||||
chr2:203032614 | C | T | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.52-9151C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032614 | |||||||
chr2:203032660 | C | CT | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(172): Show |
175 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.52-9080dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203032660 | ||||||
chr2:203032660 | C | CTT | 33 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.52-9081_52-9080dup others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203032660 | ||||||
chr2:203032661 | T | C | 1 | a0001c0004t0005g0273 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-9104T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032661 | |||||||
chr2:203032881 | T | C | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.52-8884T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203032881 | |||||||
chr2:203033006 | A | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-8759A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033006 | |||||||
chr2:203033031 | C | T | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.52-8734C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033031 | |||||||
chr2:203033040 | G | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-8725G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033040 | |||||||
chr2:203033063 | C | T | 1 | a0014c0015t0017g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52-8702C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033063 | |||||||
chr2:203033149 | C | T | 1 | a0001c0001t0006g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.52-8616C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033149 | |||||||
chr2:203033154 | C | A | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.52-8611C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033154 | |||||||
chr2:203033217 | G | T | 5 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(2): Show |
5 | HG01257.hp1 HG01952.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-8548G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033217 | |||||||
chr2:203033223 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-8542A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033223 | |||||||
chr2:203033371 | A | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.52-8394A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033371 | |||||||
chr2:203033596 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.52-8169A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033596 | |||||||
chr2:203033604 | T | C | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.52-8161T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033604 | |||||||
chr2:203033708 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-8057A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033708 | |||||||
chr2:203033807 | T | C | 9 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(6): Show |
9 | HG01257.hp1 HG01952.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-7958T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033807 | |||||||
chr2:203033958 | C | A | 1 | a0019c0020t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.52-7807C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033958 | |||||||
chr2:203033958 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.52-7807C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203033958 | |||||||
chr2:203034159 | CT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0213 a0001c0001t0001g0220 others(7): Show |
10 | HG01081.hp1 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-7589delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203034159 | ||||||
chr2:203034248 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.52-7517C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203034248 | |||||||
chr2:203034348 | AGGGTTTC others(5228): Show |
A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-7409_52-2175del | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203034348 | ||||||
chr2:203034435 | G | C | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.52-7330G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203034435 | |||||||
chr2:203034457 | A | AT | 14 | a0001c0001t0001g0213 a0001c0001t0001g0262 a0001c0001t0002g0079 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.52-7290dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203034457 | ||||||
chr2:203034457 | AT | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0221 others(5): Show |
8 | HG00323.hp1 HG00323.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.52-7290delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203034457 | ||||||
chr2:203034541 | C | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52-7224C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203034541 | |||||||
chr2:203034850 | T | TG | 11 | a0002c0002t0003g0060 a0002c0002t0003g0065 a0002c0002t0003g0066 others(8): Show |
11 | HG00738.hp1 HG01943.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.52-6909dupG | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203034850 | ||||||
chr2:203035109 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18999.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.52-6656A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203035109 | |||||||
chr2:203035193 | A | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-6572A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203035193 | |||||||
chr2:203035235 | A | C | 1 | a0001c0028t0050g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.52-6530A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203035235 | |||||||
chr2:203035656 | G | C | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.52-6109G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203035656 | |||||||
chr2:203035824 | C | T | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.52-5941C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203035824 | |||||||
chr2:203036306 | G | A | 1 | a0004c0005t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.52-5459G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203036306 | |||||||
chr2:203036315 | G | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52-5450G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203036315 | |||||||
chr2:203036661 | T | C | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.52-5104T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203036661 | |||||||
chr2:203036695 | C | G | 99 | a0001c0001t0001g0177 a0001c0001t0002g0097 a0001c0001t0002g0098 others(96): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.52-5070C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203036695 | |||||||
chr2:203037202 | T | A | 2 | a0006c0009t0012g0101 a0006c0009t0012g0102 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.52-4563T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203037202 | |||||||
chr2:203037309 | A | G | 1 | a0001c0001t0002g0292 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.52-4456A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203037309 | |||||||
chr2:203037837 | C | A | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.52-3928C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203037837 | |||||||
chr2:203038030 | G | T | 98 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.52-3735G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038030 | |||||||
chr2:203038124 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.52-3641G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038124 | |||||||
chr2:203038408 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0224 |
2 | NA18974.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.52-3357T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038408 | |||||||
chr2:203038500 | C | A | 93 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0177 others(90): Show |
93 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.52-3265C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038500 | |||||||
chr2:203038640 | T | C | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.52-3125T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038640 | |||||||
chr2:203038880 | A | G | 90 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(87): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.52-2885A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203038880 | |||||||
chr2:203039184 | CCTTTT | C | 10 | a0001c0001t0002g0108 a0001c0001t0002g0157 a0001c0001t0002g0158 others(7): Show |
10 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-2576_52-2572del others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039184 | ||||||
chr2:203039189 | T | C | 86 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(83): Show |
86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.52-2576T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039189 | |||||||
chr2:203039194 | C | T | 86 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(83): Show |
86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.52-2571C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039194 | |||||||
chr2:203039199 | C | T | 10 | a0001c0001t0002g0108 a0001c0001t0002g0157 a0001c0001t0002g0158 others(7): Show |
10 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-2566C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039199 | |||||||
chr2:203039211 | TTTCCTTT others(3): Show |
T | 1 | a0001c0001t0037g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.52-2549_52-2540del others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039211 | ||||||
chr2:203039211 | TTTCCTTT others(8): Show |
T | 1 | a0001c0022t0001g0005 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.52-2549_52-2535del others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039211 | ||||||
chr2:203039211 | TTTCCTTT others(18): Show |
T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-2549_52-2525del others(25): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039211 | ||||||
chr2:203039216 | T | C | 2 | a0001c0001t0002g0110 a0002c0002t0003g0064 |
2 | NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.52-2549T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039216 | |||||||
chr2:203039216 | T | TTTCCC | 38 | a0001c0001t0001g0225 a0001c0001t0001g0238 a0001c0001t0001g0239 others(35): Show |
38 | HG00733.hp1 HG00738.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.52-2486_52-2482dup others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | T | TTTCCCTT others(3): Show |
16 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(13): Show |
16 | HG01257.hp1 HG01952.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.52-2491_52-2482dup others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | T | TTTCCCTT others(13): Show |
1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.52-2501_52-2482dup others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | TTTCCC | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0052 others(32): Show |
35 | HG00423.hp2 HG00642.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.52-2486_52-2482del others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | TTTCCCTT others(3): Show |
T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.52-2491_52-2482del others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | TTTCCCTT others(8): Show |
T | 7 | a0001c0001t0001g0204 a0001c0001t0001g0235 a0001c0001t0002g0128 others(4): Show |
7 | HG01255.hp2 HG02970.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-2496_52-2482del others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | TTTCCCTT others(13): Show |
T | 5 | a0001c0001t0041g0012 a0002c0002t0003g0046 a0002c0002t0003g0048 others(2): Show |
5 | HG02135.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-2501_52-2482del others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039216 | TTTCCCTT others(18): Show |
T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52-2506_52-2482del others(25): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039216 | ||||||
chr2:203039221 | C | T | 10 | a0001c0001t0002g0108 a0001c0001t0002g0157 a0001c0001t0002g0158 others(7): Show |
10 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.52-2544C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039221 | |||||||
chr2:203039226 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0013g0251 a0001c0001t0013g0257 |
3 | HG02083.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.52-2539C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039226 | |||||||
chr2:203039285 | C | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52-2480C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039285 | |||||||
chr2:203039306 | TC | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
99 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.52-2455delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039306 | ||||||
chr2:203039310 | C | T | 9 | a0001c0001t0001g0051 a0001c0001t0001g0212 a0001c0001t0001g0215 others(6): Show |
9 | HG00597.hp2 HG01175.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.52-2455C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039310 | |||||||
chr2:203039311 | T | C | 10 | a0001c0001t0001g0051 a0001c0001t0001g0212 a0001c0001t0001g0215 others(7): Show |
10 | HG00597.hp2 HG01175.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.52-2454T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039311 | |||||||
chr2:203039311 | T | TC | 36 | a0001c0001t0002g0059 a0001c0001t0002g0087 a0001c0001t0002g0098 others(33): Show |
36 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.52-2447dupC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039311 | ||||||
chr2:203039311 | TC | T | 9 | a0001c0001t0024g0045 a0001c0008t0007g0055 a0001c0008t0007g0057 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.52-2447delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | INFO_REALIGN_3_PRIME | chr2 | 203039311 | ||||||
chr2:203039484 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.52-2281A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039484 | |||||||
chr2:203039527 | C | G | 4 | a0001c0001t0001g0220 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01081.hp1 NA18970.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2238C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039527 | |||||||
chr2:203039625 | C | G | 1 | a0018c0031t0001g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.52-2140C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039625 | |||||||
chr2:203039827 | C | T | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.52-1938C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039827 | |||||||
chr2:203039940 | T | A | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.52-1825T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203039940 | |||||||
chr2:203040351 | C | G | 6 | a0001c0001t0002g0099 a0001c0001t0002g0150 a0001c0001t0002g0151 others(3): Show |
6 | NA18980.hp1 NA18999.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-1414C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040351 | |||||||
chr2:203040353 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.52-1412A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040353 | |||||||
chr2:203040412 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.52-1353C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040412 | |||||||
chr2:203040414 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.52-1351G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040414 | |||||||
chr2:203040452 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
250 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.52-1313G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040452 | |||||||
chr2:203040565 | G | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-1200G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040565 | |||||||
chr2:203040676 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.52-1089A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040676 | |||||||
chr2:203040995 | C | A | 98 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.52-770C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203040995 | |||||||
chr2:203041240 | A | G | 3 | a0001c0007t0001g0241 a0001c0007t0001g0242 a0001c0007t0001g0243 |
3 | NA18951.hp2 NA18968.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.52-525A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203041240 | |||||||
chr2:203041425 | C | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0149 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.52-340C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 2/55 | chr2 | 203041425 | |||||||
chr2:203042091 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.143+235A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042091 | |||||||
chr2:203042426 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.143+570C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042426 | |||||||
chr2:203042427 | G | A | 2 | a0001c0001t0002g0089 a0019c0020t0001g0190 |
2 | HG01257.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.143+571G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042427 | |||||||
chr2:203042510 | A | G | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.143+654A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042510 | |||||||
chr2:203042597 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.143+741T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042597 | |||||||
chr2:203042933 | G | A | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.143+1077G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203042933 | |||||||
chr2:203043244 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.143+1388A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203043244 | |||||||
chr2:203043531 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.143+1675A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203043531 | |||||||
chr2:203043600 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0014g0019 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.143+1744G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203043600 | |||||||
chr2:203043645 | A | G | 17 | a0002c0002t0003g0060 a0002c0002t0003g0061 a0002c0002t0003g0062 others(14): Show |
17 | HG00738.hp1 HG01943.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+1789A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203043645 | |||||||
chr2:203043728 | C | CA | 6 | a0001c0001t0001g0189 a0001c0001t0001g0248 a0001c0001t0002g0150 others(3): Show |
6 | HG01255.hp1 NA18949.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+1889dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203043728 | ||||||
chr2:203043728 | CA | C | 8 | a0001c0001t0001g0014 a0001c0001t0002g0120 a0001c0001t0002g0167 others(5): Show |
8 | HG00597.hp1 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.143+1889delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203043728 | ||||||
chr2:203043858 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.143+2002C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203043858 | |||||||
chr2:203044051 | G | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.143+2195G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203044051 | |||||||
chr2:203044397 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.143+2541A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203044397 | |||||||
chr2:203044582 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
128 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.143+2726G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203044582 | |||||||
chr2:203044694 | T | G | 4 | a0001c0001t0001g0189 a0001c0001t0001g0213 a0001c0001t0001g0224 others(1): Show |
4 | NA18974.hp2 NA18977.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+2838T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203044694 | |||||||
chr2:203045399 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.143+3543A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203045399 | |||||||
chr2:203045874 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.144-3940A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203045874 | |||||||
chr2:203046129 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.144-3685A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046129 | |||||||
chr2:203046168 | A | G | 2 | a0001c0001t0002g0097 a0001c0001t0002g0178 |
2 | HG02165.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.144-3646A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046168 | |||||||
chr2:203046208 | A | ATATT | 98 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.144-3584_144-3581d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203046208 | ||||||
chr2:203046262 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.144-3552C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046262 | |||||||
chr2:203046309 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.144-3505G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046309 | |||||||
chr2:203046491 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.144-3323C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046491 | |||||||
chr2:203046549 | G | A | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.144-3265G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046549 | |||||||
chr2:203046870 | A | C | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.144-2944A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203046870 | |||||||
chr2:203047004 | G | A | 1 | a0002c0002t0003g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.144-2810G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203047004 | |||||||
chr2:203047110 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.144-2704G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203047110 | |||||||
chr2:203047507 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-2307A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203047507 | |||||||
chr2:203047741 | ATT | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
152 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.144-2054_144-2053d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203047741 | ||||||
chr2:203047741 | ATTT | A | 90 | a0001c0001t0001g0020 a0001c0001t0001g0204 a0001c0001t0001g0219 others(87): Show |
90 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.144-2055_144-2053d others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203047741 | ||||||
chr2:203047741 | ATTTT | A | 6 | a0001c0001t0002g0105 a0001c0001t0002g0108 a0001c0001t0002g0110 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-2056_144-2053d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203047741 | ||||||
chr2:203047743 | T | A | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.144-2071T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203047743 | |||||||
chr2:203047828 | C | T | 2 | a0001c0001t0001g0200 a0010c0016t0023g0022 |
2 | HG02109.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.144-1986C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203047828 | |||||||
chr2:203048330 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.144-1484T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203048330 | |||||||
chr2:203048342 | A | G | 2 | a0001c0001t0006g0259 a0001c0001t0006g0271 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.144-1472A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203048342 | |||||||
chr2:203048380 | C | CA | 12 | a0001c0001t0002g0087 a0001c0001t0004g0080 a0002c0002t0003g0060 others(9): Show |
12 | HG00738.hp1 HG01943.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.144-1414dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048380 | ||||||
chr2:203048380 | CA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.144-1414delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048380 | ||||||
chr2:203048380 | CAA | C | 84 | a0001c0001t0001g0051 a0001c0001t0002g0097 a0001c0001t0002g0098 others(81): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.144-1415_144-1414d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048380 | ||||||
chr2:203048596 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG00673.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.144-1218T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203048596 | |||||||
chr2:203048663 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0149 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.144-1151A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203048663 | |||||||
chr2:203048829 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.144-985A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203048829 | |||||||
chr2:203048882 | C | CT | 22 | a0001c0001t0002g0154 a0003c0003t0004g0025 a0003c0003t0004g0026 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-917dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048882 | ||||||
chr2:203048882 | CT | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.144-917delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048882 | ||||||
chr2:203048882 | CTT | C | 14 | a0001c0001t0001g0185 a0001c0001t0005g0277 a0001c0001t0005g0283 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.144-918_144-917del others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203048882 | ||||||
chr2:203049061 | C | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-753C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049061 | |||||||
chr2:203049110 | G | A | 10 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0001g0253 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.144-704G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049110 | |||||||
chr2:203049116 | T | C | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.144-698T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049116 | |||||||
chr2:203049219 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.144-595C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049219 | |||||||
chr2:203049252 | G | GT | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-560dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | INFO_REALIGN_3_PRIME | chr2 | 203049252 | ||||||
chr2:203049305 | C | T | 6 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0117 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-509C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049305 | |||||||
chr2:203049544 | C | G | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-270C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049544 | |||||||
chr2:203049627 | CT | C | 3 | a0001c0001t0006g0229 a0001c0001t0006g0232 a0001c0001t0006g0233 |
3 | HG00642.hp1 HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.144-186delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049627 | |||||||
chr2:203049673 | G | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.144-141G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049673 | |||||||
chr2:203049684 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.144-130G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 3/55 | chr2 | 203049684 | |||||||
chr2:203050046 | G | C | 6 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | NA18940.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.305+71G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203050046 | |||||||
chr2:203050640 | T | C | 1 | a0002c0002t0003g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.305+665T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203050640 | |||||||
chr2:203051394 | A | G | 1 | a0001c0001t0006g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.305+1419A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051394 | |||||||
chr2:203051495 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.305+1520G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051495 | |||||||
chr2:203051544 | CA | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0222 others(5): Show |
8 | HG01168.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.305+1583delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203051544 | ||||||
chr2:203051574 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.305+1599G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051574 | |||||||
chr2:203051585 | T | C | 7 | a0001c0001t0001g0188 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
7 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.305+1610T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051585 | |||||||
chr2:203051693 | A | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.305+1718A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051693 | |||||||
chr2:203051764 | T | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.305+1789T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051764 | |||||||
chr2:203051767 | G | A | 95 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(92): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.305+1792G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203051767 | |||||||
chr2:203052054 | G | T | 1 | a0001c0001t0002g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.305+2079G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203052054 | |||||||
chr2:203052255 | AT | A | 89 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(86): Show |
89 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.305+2294delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052255 | ||||||
chr2:203052627 | G | A | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.305+2652G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203052627 | |||||||
chr2:203052719 | G | GTTAT | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0220 others(8): Show |
11 | HG00642.hp2 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.305+2779_305+2782d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203052719 | G | GTTATTTA others(1): Show |
31 | a0001c0001t0001g0189 a0001c0001t0001g0199 a0001c0001t0001g0205 others(28): Show |
31 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.305+2775_305+2782d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203052719 | G | GTTATTTA others(5): Show |
54 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0186 others(51): Show |
54 | HG00323.hp2 HG00673.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.305+2771_305+2782d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203052719 | G | GTTATTTA others(9): Show |
4 | a0001c0001t0001g0200 a0001c0001t0001g0216 a0001c0001t0001g0235 others(1): Show |
4 | HG00642.hp1 HG02572.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.305+2767_305+2782d others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203052719 | GTTATTTA others(1): Show |
G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.305+2775_305+2782d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203052719 | GTTATTTA others(5): Show |
G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.305+2771_305+2782d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203052719 | ||||||
chr2:203053367 | C | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.306-3060C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053367 | |||||||
chr2:203053375 | G | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.306-3052G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053375 | |||||||
chr2:203053408 | T | A | 1 | a0001c0001t0002g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.306-3019T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053408 | |||||||
chr2:203053577 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.306-2850C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053577 | |||||||
chr2:203053735 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.306-2692C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053735 | |||||||
chr2:203053914 | G | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.306-2513G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053914 | |||||||
chr2:203053938 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-2489T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203053938 | |||||||
chr2:203054116 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.306-2311A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054116 | |||||||
chr2:203054254 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.306-2173C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054254 | |||||||
chr2:203054425 | CA | C | 6 | a0001c0001t0001g0239 a0001c0001t0002g0122 a0001c0001t0013g0257 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.306-1986delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203054425 | ||||||
chr2:203054441 | A | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0006g0259 |
3 | HG02273.hp2 NA18999.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.306-1986A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054441 | |||||||
chr2:203054536 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.306-1891T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054536 | |||||||
chr2:203054791 | C | G | 2 | a0003c0003t0010g0041 a0003c0003t0010g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.306-1636C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054791 | |||||||
chr2:203054852 | A | C | 1 | a0009c0026t0043g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306-1575A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054852 | |||||||
chr2:203054997 | C | T | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.306-1430C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203054997 | |||||||
chr2:203055148 | A | T | 1 | a0003c0003t0004g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.306-1279A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055148 | |||||||
chr2:203055178 | T | A | 1 | a0001c0004t0049g0285 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.306-1249T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055178 | |||||||
chr2:203055588 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306-839G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055588 | |||||||
chr2:203055606 | T | TA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
113 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.306-811dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203055606 | ||||||
chr2:203055606 | TA | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.306-811delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | INFO_REALIGN_3_PRIME | chr2 | 203055606 | ||||||
chr2:203055617 | C | A | 1 | a0004c0005t0009g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.306-810C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055617 | |||||||
chr2:203055848 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.306-579T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055848 | |||||||
chr2:203055897 | G | A | 1 | a0002c0002t0028g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.306-530G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 4/55 | chr2 | 203055897 | |||||||
chr2:203056547 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.387+39A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 5/55 | chr2 | 203056547 | |||||||
chr2:203056641 | A | C | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.387+133A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 5/55 | chr2 | 203056641 | |||||||
chr2:203056725 | G | A | 98 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.387+217G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 5/55 | chr2 | 203056725 | |||||||
chr2:203057011 | A | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0021t0002g0169 |
3 | HG01167.hp2 HG01169.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.388-315A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 5/55 | chr2 | 203057011 | |||||||
chr2:203057517 | A | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+64A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057517 | |||||||
chr2:203057563 | C | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.515+110C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057563 | |||||||
chr2:203057752 | A | AT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.515+305dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | INFO_REALIGN_3_PRIME | chr2 | 203057752 | ||||||
chr2:203057830 | T | C | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.515+377T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057830 | |||||||
chr2:203057832 | T | G | 3 | a0002c0002t0003g0046 a0002c0002t0003g0049 a0002c0002t0003g0050 |
3 | HG02451.hp2 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.515+379T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057832 | |||||||
chr2:203057839 | G | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.515+386G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057839 | |||||||
chr2:203057849 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.515+396C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057849 | |||||||
chr2:203057881 | G | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+428G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203057881 | |||||||
chr2:203058004 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.515+551C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058004 | |||||||
chr2:203058094 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.515+641G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058094 | |||||||
chr2:203058291 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0037g0207 a0008c0024t0001g0191 |
3 | HG00423.hp2 HG00609.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.515+838C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058291 | |||||||
chr2:203058343 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.515+890G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058343 | |||||||
chr2:203058724 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.515+1271C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058724 | |||||||
chr2:203058928 | A | G | 1 | a0001c0007t0001g0240 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.515+1475A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203058928 | |||||||
chr2:203059129 | A | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.515+1676A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059129 | |||||||
chr2:203059406 | A | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+1953A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059406 | |||||||
chr2:203059419 | A | G | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+1966A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059419 | |||||||
chr2:203059572 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.515+2119C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059572 | |||||||
chr2:203059715 | G | A | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.515+2262G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059715 | |||||||
chr2:203059895 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.515+2442C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203059895 | |||||||
chr2:203060388 | T | C | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.515+2935T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060388 | |||||||
chr2:203060513 | G | A | 1 | a0002c0002t0027g0094 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.515+3060G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060513 | |||||||
chr2:203060637 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.515+3184G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060637 | |||||||
chr2:203060651 | G | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+3198G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060651 | |||||||
chr2:203060769 | T | C | 1 | a0001c0029t0002g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.515+3316T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060769 | |||||||
chr2:203060866 | C | T | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.515+3413C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203060866 | |||||||
chr2:203061548 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.515+4095A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203061548 | |||||||
chr2:203061614 | C | T | 23 | a0001c0001t0024g0045 a0003c0003t0004g0025 a0003c0003t0004g0026 others(20): Show |
23 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.515+4161C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203061614 | |||||||
chr2:203061934 | T | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+4481T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203061934 | |||||||
chr2:203062203 | A | G | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.515+4750A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062203 | |||||||
chr2:203062230 | T | C | 5 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(2): Show |
5 | NA18939.hp1 NA18974.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+4777T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062230 | |||||||
chr2:203062419 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.515+4966A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062419 | |||||||
chr2:203062817 | G | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515+5364G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062817 | |||||||
chr2:203062828 | G | A | 90 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(87): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.515+5375G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062828 | |||||||
chr2:203062864 | T | C | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.515+5411T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203062864 | |||||||
chr2:203063013 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.516-5380T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203063013 | |||||||
chr2:203063048 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.516-5345A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203063048 | |||||||
chr2:203063438 | T | G | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.516-4955T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203063438 | |||||||
chr2:203063669 | T | C | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.516-4724T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203063669 | |||||||
chr2:203063904 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.516-4489A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203063904 | |||||||
chr2:203064045 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0235 |
2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.516-4348T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064045 | |||||||
chr2:203064095 | C | G | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.516-4298C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064095 | |||||||
chr2:203064115 | G | A | 10 | a0001c0001t0006g0227 a0001c0001t0006g0229 a0001c0001t0006g0232 others(7): Show |
10 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-4278G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064115 | |||||||
chr2:203064267 | G | C | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.516-4126G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064267 | |||||||
chr2:203064343 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.516-4050G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064343 | |||||||
chr2:203064535 | T | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.516-3858T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064535 | |||||||
chr2:203064712 | C | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.516-3681C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064712 | |||||||
chr2:203064713 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG01257.hp2 HG01258.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.516-3680G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064713 | |||||||
chr2:203064987 | G | A | 10 | a0001c0001t0006g0227 a0001c0001t0006g0229 a0001c0001t0006g0232 others(7): Show |
10 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-3406G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203064987 | |||||||
chr2:203065518 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.516-2875C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065518 | |||||||
chr2:203065564 | A | G | 3 | a0001c0001t0024g0045 a0001c0001t0025g0016 a0002c0002t0003g0021 |
3 | HG01884.hp2 HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.516-2829A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065564 | |||||||
chr2:203065611 | G | A | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.516-2782G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065611 | |||||||
chr2:203065621 | G | A | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.516-2772G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065621 | |||||||
chr2:203065662 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0013 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.516-2731G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065662 | |||||||
chr2:203065701 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.516-2692G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203065701 | |||||||
chr2:203066036 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.516-2357G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066036 | |||||||
chr2:203066150 | A | G | 2 | a0002c0002t0003g0065 a0002c0002t0027g0094 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.516-2243A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066150 | |||||||
chr2:203066180 | T | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-2213T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066180 | |||||||
chr2:203066289 | A | G | 90 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(87): Show |
90 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.516-2104A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066289 | |||||||
chr2:203066323 | C | CT | 48 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(45): Show |
48 | HG00738.hp1 HG00741.hp2 HG01257.hp1 others(45): Show |
intron_variant | MODIFIER | c.516-2053dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | INFO_REALIGN_3_PRIME | chr2 | 203066323 | ||||||
chr2:203066323 | CT | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
118 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.516-2053delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | INFO_REALIGN_3_PRIME | chr2 | 203066323 | ||||||
chr2:203066708 | C | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.516-1685C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066708 | |||||||
chr2:203066736 | C | CG | 10 | a0001c0001t0001g0215 a0001c0001t0002g0117 a0001c0001t0002g0128 others(7): Show |
10 | HG00544.hp1 HG00642.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-1653dupG | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | INFO_REALIGN_3_PRIME | chr2 | 203066736 | ||||||
chr2:203066786 | G | A | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.516-1607G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066786 | |||||||
chr2:203066859 | G | A | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG00733.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.516-1534G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066859 | |||||||
chr2:203066865 | G | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.516-1528G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066865 | |||||||
chr2:203066874 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.516-1519C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066874 | |||||||
chr2:203066897 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.516-1496C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066897 | |||||||
chr2:203066941 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.516-1452G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203066941 | |||||||
chr2:203067010 | C | T | 1 | a0002c0002t0003g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516-1383C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067010 | |||||||
chr2:203067453 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0005g0277 a0001c0001t0005g0283 others(11): Show |
14 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.516-940A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067453 | |||||||
chr2:203067546 | T | C | 2 | a0001c0001t0013g0251 a0001c0001t0013g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.516-847T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067546 | |||||||
chr2:203067604 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.516-789G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067604 | |||||||
chr2:203067649 | G | T | 1 | a0001c0001t0001g0237 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.516-744G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067649 | |||||||
chr2:203067705 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.516-688G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067705 | |||||||
chr2:203067788 | C | T | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.516-605C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067788 | |||||||
chr2:203067794 | A | G | 2 | a0001c0008t0007g0056 a0001c0008t0007g0057 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.516-599A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203067794 | |||||||
chr2:203068213 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.516-180A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203068213 | |||||||
chr2:203068253 | A | T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.516-140A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203068253 | |||||||
chr2:203068271 | A | G | 17 | a0002c0002t0003g0060 a0002c0002t0003g0061 a0002c0002t0003g0062 others(14): Show |
17 | HG00738.hp1 HG01943.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.516-122A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 6/55 | chr2 | 203068271 | |||||||
chr2:203068504 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.598+29A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203068504 | |||||||
chr2:203068616 | A | G | 9 | a0001c0004t0005g0273 a0001c0004t0005g0274 a0001c0004t0005g0275 others(6): Show |
9 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.598+141A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203068616 | |||||||
chr2:203068665 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.598+190G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203068665 | |||||||
chr2:203068762 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.598+287G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203068762 | |||||||
chr2:203069449 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+974A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203069449 | |||||||
chr2:203069961 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.598+1486G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203069961 | |||||||
chr2:203070358 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.598+1883T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070358 | |||||||
chr2:203070359 | C | CT | 15 | a0001c0001t0001g0198 a0001c0001t0001g0252 a0001c0001t0005g0277 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.598+1904dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203070359 | ||||||
chr2:203070359 | CT | C | 84 | a0001c0001t0001g0202 a0001c0001t0001g0205 a0001c0001t0001g0222 others(81): Show |
84 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.598+1904delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203070359 | ||||||
chr2:203070359 | CTT | C | 7 | a0001c0001t0002g0105 a0001c0001t0002g0124 a0001c0001t0002g0167 others(4): Show |
7 | HG00323.hp1 HG00733.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+1903_598+1904d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203070359 | ||||||
chr2:203070499 | G | T | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.598+2024G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070499 | |||||||
chr2:203070519 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+2044A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070519 | |||||||
chr2:203070824 | A | G | 2 | a0002c0002t0003g0065 a0002c0002t0027g0094 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.598+2349A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070824 | |||||||
chr2:203070841 | C | T | 74 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(71): Show |
74 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.598+2366C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070841 | |||||||
chr2:203070862 | C | G | 2 | a0003c0003t0010g0041 a0003c0003t0010g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.598+2387C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070862 | |||||||
chr2:203070896 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.598+2421G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070896 | |||||||
chr2:203070909 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.598+2434A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070909 | |||||||
chr2:203070984 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598+2509G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203070984 | |||||||
chr2:203071203 | A | G | 6 | a0001c0001t0002g0104 a0001c0001t0002g0114 a0001c0001t0002g0156 others(3): Show |
6 | HG03688.hp2 HG03942.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+2728A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203071203 | |||||||
chr2:203072414 | T | G | 1 | a0001c0001t0037g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.598+3939T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203072414 | |||||||
chr2:203072424 | A | T | 2 | a0001c0001t0024g0045 a0010c0016t0023g0022 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.598+3949A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203072424 | |||||||
chr2:203072452 | A | G | 93 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(90): Show |
93 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.598+3977A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203072452 | |||||||
chr2:203072705 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.598+4230A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203072705 | |||||||
chr2:203073185 | T | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-4567T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203073185 | |||||||
chr2:203073981 | A | T | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.599-3771A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203073981 | |||||||
chr2:203074071 | A | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.599-3681A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203074071 | |||||||
chr2:203074317 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.599-3410delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203074317 | ||||||
chr2:203074317 | CTTTTTTT | C | 25 | a0001c0001t0002g0149 a0003c0003t0004g0025 a0003c0003t0004g0026 others(22): Show |
25 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.599-3416_599-3410d others(9): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203074317 | ||||||
chr2:203074317 | CTTTTTTT others(1): Show |
C | 99 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(96): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.599-3417_599-3410d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203074317 | ||||||
chr2:203074317 | CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.599-3420_599-3410d others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203074317 | ||||||
chr2:203074574 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599-3178C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203074574 | |||||||
chr2:203074584 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.599-3168T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203074584 | |||||||
chr2:203074710 | A | G | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.599-3042A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203074710 | |||||||
chr2:203074917 | A | G | 15 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(12): Show |
15 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.599-2835A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203074917 | |||||||
chr2:203075071 | G | C | 1 | a0002c0002t0003g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.599-2681G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075071 | |||||||
chr2:203075162 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.599-2590A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075162 | |||||||
chr2:203075246 | C | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.599-2506C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075246 | |||||||
chr2:203075546 | G | A | 1 | a0003c0003t0004g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.599-2206G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075546 | |||||||
chr2:203075568 | C | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.599-2184C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075568 | |||||||
chr2:203075821 | T | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0287 |
3 | NA18970.hp2 NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.599-1931T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075821 | |||||||
chr2:203075884 | C | T | 19 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.599-1868C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203075884 | |||||||
chr2:203076014 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.599-1738T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076014 | |||||||
chr2:203076122 | C | T | 1 | a0018c0031t0001g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.599-1630C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076122 | |||||||
chr2:203076193 | A | G | 1 | a0001c0028t0050g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.599-1559A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076193 | |||||||
chr2:203076319 | C | A | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.599-1433C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076319 | |||||||
chr2:203076480 | AAC | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.599-1270_599-1269d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203076480 | ||||||
chr2:203076481 | AC | A | 10 | a0001c0001t0001g0189 a0001c0001t0001g0249 a0001c0001t0002g0059 others(7): Show |
10 | HG00597.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.599-1270delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076481 | |||||||
chr2:203076482 | C | A | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.599-1270C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076482 | |||||||
chr2:203076485 | A | C | 3 | a0001c0029t0002g0159 a0007c0010t0017g0018 a0014c0015t0017g0017 |
3 | HG03225.hp2 HG03453.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.599-1267A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076485 | |||||||
chr2:203076486 | C | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.599-1266C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076486 | |||||||
chr2:203076490 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.599-1262C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076490 | |||||||
chr2:203076491 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.599-1261A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076491 | |||||||
chr2:203076493 | AC | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
136 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.599-1258delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076493 | |||||||
chr2:203076494 | C | A | 122 | a0001c0001t0001g0268 a0001c0001t0002g0059 a0001c0001t0002g0079 others(119): Show |
122 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.599-1258C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076494 | |||||||
chr2:203076495 | A | C | 2 | a0001c0001t0002g0113 a0001c0001t0002g0182 |
2 | HG03831.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.599-1257A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076495 | |||||||
chr2:203076497 | A | C | 1 | a0019c0020t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.599-1255A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076497 | |||||||
chr2:203076589 | C | CT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(207): Show |
210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.599-1143dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203076589 | ||||||
chr2:203076589 | C | CTT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(19): Show |
22 | HG00544.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.599-1144_599-1143d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | INFO_REALIGN_3_PRIME | chr2 | 203076589 | ||||||
chr2:203076740 | C | T | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.599-1012C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076740 | |||||||
chr2:203076889 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0151 |
2 | NA18980.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.599-863G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203076889 | |||||||
chr2:203077060 | A | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-692A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077060 | |||||||
chr2:203077148 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.599-604A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077148 | |||||||
chr2:203077156 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.599-596A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077156 | |||||||
chr2:203077189 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.599-563G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077189 | |||||||
chr2:203077431 | C | G | 4 | a0001c0007t0001g0240 a0001c0007t0001g0241 a0001c0007t0001g0242 others(1): Show |
4 | NA18951.hp2 NA18968.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-321C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077431 | |||||||
chr2:203077555 | G | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.599-197G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 7/55 | chr2 | 203077555 | |||||||
chr2:203077905 | T | C | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.684+68T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203077905 | |||||||
chr2:203078445 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.684+608A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203078445 | |||||||
chr2:203078576 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.684+739C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203078576 | |||||||
chr2:203078777 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.684+940G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203078777 | |||||||
chr2:203079061 | GTTTGTTT others(3): Show |
G | 1 | a0001c0001t0002g0292 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.684+1237_684+1246d others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | INFO_REALIGN_3_PRIME | chr2 | 203079061 | ||||||
chr2:203079154 | A | C | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.684+1317A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079154 | |||||||
chr2:203079169 | T | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.684+1332T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079169 | |||||||
chr2:203079280 | T | C | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.684+1443T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079280 | |||||||
chr2:203079305 | A | G | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.684+1468A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079305 | |||||||
chr2:203079360 | G | A | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.684+1523G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079360 | |||||||
chr2:203079681 | A | T | 1 | a0001c0001t0002g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.684+1844A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079681 | |||||||
chr2:203079691 | G | A | 1 | a0001c0028t0050g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.684+1854G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079691 | |||||||
chr2:203079902 | T | C | 1 | a0001c0001t0034g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.684+2065T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203079902 | |||||||
chr2:203080026 | T | G | 1 | a0001c0001t0001g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.684+2189T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203080026 | |||||||
chr2:203080337 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.684+2500G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203080337 | |||||||
chr2:203080876 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.685-2343A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203080876 | |||||||
chr2:203081146 | A | T | 3 | a0001c0001t0035g0058 a0002c0002t0026g0075 a0012c0019t0003g0074 |
3 | HG02257.hp2 HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.685-2073A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203081146 | |||||||
chr2:203081273 | T | A | 3 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 |
3 | HG02970.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.685-1946T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203081273 | |||||||
chr2:203081414 | C | T | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.685-1805C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203081414 | |||||||
chr2:203081870 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.685-1349G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203081870 | |||||||
chr2:203081997 | A | G | 1 | a0002c0002t0026g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.685-1222A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203081997 | |||||||
chr2:203082161 | G | T | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.685-1058G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203082161 | |||||||
chr2:203082547 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.685-672A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203082547 | |||||||
chr2:203082672 | A | G | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.685-547A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203082672 | |||||||
chr2:203082870 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.685-349T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203082870 | |||||||
chr2:203082986 | A | G | 1 | a0002c0002t0028g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.685-233A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 8/55 | chr2 | 203082986 | |||||||
chr2:203083770 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.991+245C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203083770 | |||||||
chr2:203083804 | G | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.991+279G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203083804 | |||||||
chr2:203083848 | A | T | 1 | a0001c0001t0045g0201 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.991+323A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203083848 | |||||||
chr2:203083976 | C | CTG | 42 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.992-443_992-442dup others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTG | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(43): Show |
46 | HG00544.hp2 HG00741.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.992-445_992-442dup others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTGTG | 15 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0224 others(12): Show |
15 | HG00738.hp1 HG02055.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.992-447_992-442dup others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTGTGT others(1): Show |
22 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0001g0228 others(19): Show |
22 | HG00408.hp2 HG01192.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.992-449_992-442dup others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTGTGT others(3): Show |
6 | a0001c0001t0001g0185 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG01516.hp1 HG03579.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-451_992-442dup others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0220 |
3 | HG01081.hp1 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.992-453_992-442dup others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0006g0254 a0002c0002t0008g0082 |
2 | HG02293.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.992-455_992-442dup others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | CTG | C | 82 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0252 others(79): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.992-443_992-442del others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | CTGTG | C | 11 | a0001c0001t0002g0103 a0001c0001t0002g0119 a0001c0001t0002g0120 others(8): Show |
11 | HG01361.hp2 HG02602.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.992-445_992-442del others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0040g0223 |
3 | HG00597.hp2 HG00673.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.992-451_992-442del others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203083976 | CTGTGTGT others(7): Show |
C | 1 | a0002c0002t0003g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.992-455_992-442del others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | INFO_REALIGN_3_PRIME | chr2 | 203083976 | ||||||
chr2:203084021 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0006g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.992-442_992-441ins others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203084021 | |||||||
chr2:203084269 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.992-194G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203084269 | |||||||
chr2:203084378 | T | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.992-85T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 9/55 | chr2 | 203084378 | |||||||
chr2:203084952 | C | T | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1098+383C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203084952 | |||||||
chr2:203085096 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1098+527A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085096 | |||||||
chr2:203085214 | G | A | 18 | a0003c0003t0004g0026 a0003c0003t0004g0027 a0003c0003t0004g0028 others(15): Show |
18 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1098+645G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085214 | |||||||
chr2:203085233 | C | T | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+664C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085233 | |||||||
chr2:203085240 | C | G | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1098+671C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085240 | |||||||
chr2:203085353 | G | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1098+784G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085353 | |||||||
chr2:203085869 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1098+1300G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085869 | |||||||
chr2:203085877 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1098+1308G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203085877 | |||||||
chr2:203086162 | C | G | 1 | a0007c0010t0017g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1098+1593C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203086162 | |||||||
chr2:203086449 | T | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1098+1880T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203086449 | |||||||
chr2:203086615 | A | C | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1098+2046A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203086615 | |||||||
chr2:203086703 | C | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1098+2134C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203086703 | |||||||
chr2:203086827 | G | C | 104 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1098+2258G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203086827 | |||||||
chr2:203087019 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1098+2450A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087019 | |||||||
chr2:203087090 | C | CT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(26): Show |
29 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1098+2543dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203087090 | ||||||
chr2:203087123 | T | C | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2554T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087123 | |||||||
chr2:203087336 | C | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+2767C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087336 | |||||||
chr2:203087371 | G | A | 6 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0001t0042g0054 others(3): Show |
6 | HG02451.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+2802G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087371 | |||||||
chr2:203087609 | A | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1098+3040A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087609 | |||||||
chr2:203087693 | A | G | 3 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 |
3 | HG02970.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1098+3124A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087693 | |||||||
chr2:203087800 | A | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+3231A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087800 | |||||||
chr2:203087903 | G | A | 2 | a0001c0001t0001g0198 a0001c0018t0001g0192 |
2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1098+3334G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203087903 | |||||||
chr2:203088015 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1098+3446C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088015 | |||||||
chr2:203088214 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1098+3645A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088214 | |||||||
chr2:203088299 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1098+3730G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088299 | |||||||
chr2:203088339 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1098+3770A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088339 | |||||||
chr2:203088511 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1098+3942G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088511 | |||||||
chr2:203088731 | A | G | 55 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1098+4162A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088731 | |||||||
chr2:203088768 | T | G | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1098+4199T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088768 | |||||||
chr2:203088777 | C | T | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1098+4208C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088777 | |||||||
chr2:203088905 | G | A | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1098+4336G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088905 | |||||||
chr2:203088932 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1098+4363G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203088932 | |||||||
chr2:203089266 | A | C | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+4697A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089266 | |||||||
chr2:203089307 | C | T | 1 | a0001c0008t0007g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1098+4738C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089307 | |||||||
chr2:203089374 | G | A | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+4805G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089374 | |||||||
chr2:203089380 | C | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+4811C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089380 | |||||||
chr2:203089449 | A | G | 23 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(20): Show |
23 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1098+4880A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089449 | |||||||
chr2:203089640 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1098+5071A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203089640 | |||||||
chr2:203090219 | A | T | 1 | a0014c0015t0017g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+5650A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090219 | |||||||
chr2:203090310 | T | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1098+5741T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090310 | |||||||
chr2:203090550 | T | C | 102 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(99): Show |
102 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1098+5981T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090550 | |||||||
chr2:203090725 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1098+6156A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090725 | |||||||
chr2:203090753 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1098+6184G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090753 | |||||||
chr2:203090756 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1098+6187G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203090756 | |||||||
chr2:203090953 | GAGAAAGG others(6): Show |
G | 1 | a0001c0001t0002g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1098+6399_1098+641 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203090953 | ||||||
chr2:203091192 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1099-6355A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091192 | |||||||
chr2:203091204 | T | C | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1099-6343T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091204 | |||||||
chr2:203091283 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1099-6264G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091283 | |||||||
chr2:203091416 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(260): Show |
263 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1099-6131G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091416 | |||||||
chr2:203091525 | T | C | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1099-6022T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091525 | |||||||
chr2:203091823 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1099-5724T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091823 | |||||||
chr2:203091962 | A | G | 1 | a0001c0001t0006g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1099-5585A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203091962 | |||||||
chr2:203092195 | C | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0235 |
2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1099-5352C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092195 | |||||||
chr2:203092361 | C | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-5186C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092361 | |||||||
chr2:203092399 | C | CA | 9 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0212 others(6): Show |
9 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-5132dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203092399 | ||||||
chr2:203092435 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-5112C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092435 | |||||||
chr2:203092635 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1099-4912A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092635 | |||||||
chr2:203092662 | C | G | 19 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-4885C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092662 | |||||||
chr2:203092780 | A | T | 1 | a0015c0023t0003g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-4767A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203092780 | |||||||
chr2:203093060 | G | A | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1099-4487G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093060 | |||||||
chr2:203093125 | G | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1099-4422G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093125 | |||||||
chr2:203093230 | TA | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(61): Show |
64 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1099-4289delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203093230 | ||||||
chr2:203093230 | TAA | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1099-4290_1099-428 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203093230 | ||||||
chr2:203093230 | TAAA | T | 146 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(143): Show |
146 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1099-4291_1099-428 others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203093230 | ||||||
chr2:203093230 | TAAAAAAA others(10): Show |
T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0261 others(4): Show |
7 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-4305_1099-428 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203093230 | ||||||
chr2:203093233 | A | T | 1 | a0003c0003t0004g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-4314A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093233 | |||||||
chr2:203093258 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0230 others(7): Show |
10 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-4289A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093258 | |||||||
chr2:203093305 | T | C | 1 | a0002c0002t0027g0094 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1099-4242T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093305 | |||||||
chr2:203093317 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1099-4230G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093317 | |||||||
chr2:203093418 | G | A | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1099-4129G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093418 | |||||||
chr2:203093547 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0287 |
3 | NA18970.hp2 NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1099-4000A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093547 | |||||||
chr2:203093704 | A | C | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099-3843A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093704 | |||||||
chr2:203093840 | G | T | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1099-3707G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093840 | |||||||
chr2:203093909 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1099-3638G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203093909 | |||||||
chr2:203094358 | A | C | 1 | a0001c0001t0002g0112 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1099-3189A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094358 | |||||||
chr2:203094375 | G | A | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1099-3172G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094375 | |||||||
chr2:203094597 | T | G | 2 | a0001c0004t0005g0275 a0001c0004t0005g0276 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1099-2950T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094597 | |||||||
chr2:203094605 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1099-2942T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094605 | |||||||
chr2:203094614 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1099-2933A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094614 | |||||||
chr2:203094738 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1099-2809G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094738 | |||||||
chr2:203094847 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1099-2700C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094847 | |||||||
chr2:203094941 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1099-2606G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094941 | |||||||
chr2:203094985 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-2562G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203094985 | |||||||
chr2:203095287 | A | ATTGT | 6 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-2241_1099-223 others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | INFO_REALIGN_3_PRIME | chr2 | 203095287 | ||||||
chr2:203095412 | A | G | 1 | a0001c0001t0002g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1099-2135A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203095412 | |||||||
chr2:203095760 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1099-1787T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203095760 | |||||||
chr2:203095767 | T | G | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1099-1780T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203095767 | |||||||
chr2:203095864 | C | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
109 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1099-1683C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203095864 | |||||||
chr2:203095898 | A | G | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1099-1649A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203095898 | |||||||
chr2:203096223 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1099-1324C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203096223 | |||||||
chr2:203096646 | T | C | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-901T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203096646 | |||||||
chr2:203096746 | C | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-801C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203096746 | |||||||
chr2:203096963 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1099-584A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203096963 | |||||||
chr2:203097006 | C | A | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1099-541C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097006 | |||||||
chr2:203097113 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1099-434T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097113 | |||||||
chr2:203097140 | T | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1099-407T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097140 | |||||||
chr2:203097168 | G | A | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1099-379G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097168 | |||||||
chr2:203097307 | A | G | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1099-240A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097307 | |||||||
chr2:203097369 | C | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1099-178C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097369 | |||||||
chr2:203097423 | T | C | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1099-124T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097423 | |||||||
chr2:203097530 | G | A | 1 | a0001c0001t0014g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1099-17G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 10/55 | chr2 | 203097530 | |||||||
chr2:203097749 | A | G | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1185+116A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203097749 | |||||||
chr2:203097802 | T | C | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1185+169T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203097802 | |||||||
chr2:203097828 | T | C | 6 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0117 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1185+195T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203097828 | |||||||
chr2:203097928 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1185+295C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203097928 | |||||||
chr2:203098247 | C | T | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1185+614C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203098247 | |||||||
chr2:203098427 | A | G | 1 | a0001c0001t0005g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1185+794A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203098427 | |||||||
chr2:203099005 | T | C | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1186-624T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203099005 | |||||||
chr2:203099041 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1186-588G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203099041 | |||||||
chr2:203099224 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1186-405C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203099224 | |||||||
chr2:203099302 | A | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1186-327A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203099302 | |||||||
chr2:203099414 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1186-215T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 11/55 | chr2 | 203099414 | |||||||
chr2:203099935 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1269+223C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203099935 | |||||||
chr2:203099993 | G | A | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1269+281G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203099993 | |||||||
chr2:203100548 | C | CT | 97 | a0001c0001t0001g0186 a0001c0001t0002g0059 a0001c0001t0002g0079 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1269+851dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | INFO_REALIGN_3_PRIME | chr2 | 203100548 | ||||||
chr2:203100552 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1269+840T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100552 | |||||||
chr2:203100602 | A | G | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1269+890A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100602 | |||||||
chr2:203100632 | C | T | 2 | a0003c0003t0010g0041 a0003c0003t0010g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1269+920C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100632 | |||||||
chr2:203100665 | G | A | 3 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 |
3 | HG02970.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1269+953G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100665 | |||||||
chr2:203100800 | G | A | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1269+1088G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100800 | |||||||
chr2:203100807 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
259 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1269+1095A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100807 | |||||||
chr2:203100981 | A | G | 1 | a0008c0024t0001g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1269+1269A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203100981 | |||||||
chr2:203102086 | G | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1269+2374G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203102086 | |||||||
chr2:203102118 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1269+2406G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203102118 | |||||||
chr2:203102474 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1269+2762A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203102474 | |||||||
chr2:203102787 | G | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1269+3075G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203102787 | |||||||
chr2:203103259 | A | G | 5 | a0001c0001t0002g0131 a0005c0006t0002g0100 a0005c0006t0002g0161 others(2): Show |
5 | HG00735.hp2 HG00741.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269+3547A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203103259 | |||||||
chr2:203103334 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1269+3622C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203103334 | |||||||
chr2:203103366 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1269+3654C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203103366 | |||||||
chr2:203103642 | T | TGCTA | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270-3774_1270-377 others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | INFO_REALIGN_3_PRIME | chr2 | 203103642 | ||||||
chr2:203103757 | C | T | 3 | a0001c0004t0005g0275 a0001c0004t0005g0276 a0001c0004t0005g0278 |
3 | HG01167.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1270-3663C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203103757 | |||||||
chr2:203104230 | G | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1270-3190G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104230 | |||||||
chr2:203104250 | T | C | 8 | a0001c0004t0005g0273 a0001c0004t0005g0274 a0001c0004t0005g0275 others(5): Show |
8 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270-3170T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104250 | |||||||
chr2:203104386 | G | C | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1270-3034G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104386 | |||||||
chr2:203104424 | A | G | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1270-2996A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104424 | |||||||
chr2:203104538 | A | ATTCAAGG others(9): Show |
1 | a0001c0001t0039g0003 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1270-2867_1270-286 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | INFO_REALIGN_3_PRIME | chr2 | 203104538 | ||||||
chr2:203104713 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1270-2707C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104713 | |||||||
chr2:203104781 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1270-2639G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104781 | |||||||
chr2:203104841 | T | C | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270-2579T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104841 | |||||||
chr2:203104864 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270-2556T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104864 | |||||||
chr2:203104867 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270-2553C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104867 | |||||||
chr2:203104868 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270-2552T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203104868 | |||||||
chr2:203105102 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1270-2318C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105102 | |||||||
chr2:203105120 | G | T | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1270-2300G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105120 | |||||||
chr2:203105183 | A | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1270-2237A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105183 | |||||||
chr2:203105195 | G | A | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1270-2225G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105195 | |||||||
chr2:203105268 | G | C | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1270-2152G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105268 | |||||||
chr2:203105275 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270-2145A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105275 | |||||||
chr2:203105334 | C | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | NA18940.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270-2086C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105334 | |||||||
chr2:203105405 | G | A | 1 | a0001c0001t0019g0279 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1270-2015G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105405 | |||||||
chr2:203105560 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1270-1860A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105560 | |||||||
chr2:203105855 | A | G | 1 | a0002c0002t0003g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1270-1565A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105855 | |||||||
chr2:203105888 | A | G | 1 | a0002c0002t0003g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1270-1532A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105888 | |||||||
chr2:203105960 | A | G | 22 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1270-1460A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203105960 | |||||||
chr2:203106327 | C | T | 1 | a0002c0002t0008g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1270-1093C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203106327 | |||||||
chr2:203106364 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
107 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1270-1056G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203106364 | |||||||
chr2:203106607 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1270-813T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203106607 | |||||||
chr2:203106704 | C | A | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1270-716C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203106704 | |||||||
chr2:203106996 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0219 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1270-424A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 12/55 | chr2 | 203106996 | |||||||
chr2:203108251 | A | G | 1 | a0019c0020t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1949+63A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203108251 | |||||||
chr2:203108396 | GT | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1949+220delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | INFO_REALIGN_3_PRIME | chr2 | 203108396 | ||||||
chr2:203108408 | T | G | 1 | a0001c0001t0002g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1949+220T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203108408 | |||||||
chr2:203108409 | G | T | 1 | a0001c0001t0002g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1949+221G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203108409 | |||||||
chr2:203108655 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0039g0003 |
2 | HG00544.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1949+467G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203108655 | |||||||
chr2:203108693 | G | A | 1 | a0002c0002t0026g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1949+505G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203108693 | |||||||
chr2:203109078 | C | T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1949+890C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203109078 | |||||||
chr2:203109537 | TAGAC | T | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1950-609_1950-606d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | INFO_REALIGN_3_PRIME | chr2 | 203109537 | ||||||
chr2:203109677 | G | A | 1 | a0001c0004t0005g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1950-473G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203109677 | |||||||
chr2:203109718 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0261 others(4): Show |
7 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1950-432C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203109718 | |||||||
chr2:203109788 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1950-362A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203109788 | |||||||
chr2:203109813 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1950-337C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203109813 | |||||||
chr2:203110068 | G | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1950-82G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203110068 | |||||||
chr2:203110090 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1950-60T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203110090 | |||||||
chr2:203110137 | G | A | 1 | a0004c0005t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1950-13G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 14/55 | chr2 | 203110137 | |||||||
chr2:203110674 | A | AAAAT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(87): Show |
90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2082+430_2082+433d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | A | AAAATAAA others(1): Show |
93 | a0001c0001t0001g0177 a0001c0001t0001g0186 a0001c0001t0001g0193 others(90): Show |
93 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2082+426_2082+433d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | A | AAAATAAA others(5): Show |
31 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0188 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.2082+422_2082+433d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | A | AAAATAAA others(9): Show |
5 | a0001c0001t0001g0185 a0001c0001t0001g0211 a0001c0001t0001g0220 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+418_2082+433d others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | A | AAAATAAA others(13): Show |
1 | a0001c0001t0001g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2082+414_2082+433d others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | AAAAT | A | 24 | a0001c0001t0001g0010 a0001c0001t0024g0045 a0003c0003t0004g0025 others(21): Show |
24 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2082+430_2082+433d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110674 | AAAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0002g0149 a0001c0001t0002g0153 |
3 | HG03942.hp2 HG04228.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2082+426_2082+433d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110674 | ||||||
chr2:203110716 | T | A | 3 | a0001c0001t0005g0283 a0001c0001t0014g0019 a0001c0001t0025g0016 |
3 | HG00438.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2082+434T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203110716 | |||||||
chr2:203110767 | C | CT | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
216 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.2082+502dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110767 | ||||||
chr2:203110767 | C | CTT | 37 | a0001c0001t0001g0010 a0001c0001t0001g0198 a0001c0001t0005g0277 others(34): Show |
37 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2082+501_2082+502d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | INFO_REALIGN_3_PRIME | chr2 | 203110767 | ||||||
chr2:203110811 | T | G | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2082+529T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203110811 | |||||||
chr2:203111151 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2083-828G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111151 | |||||||
chr2:203111235 | G | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2083-744G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111235 | |||||||
chr2:203111368 | T | G | 1 | a0001c0001t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2083-611T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111368 | |||||||
chr2:203111403 | G | C | 6 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 others(3): Show |
6 | HG02293.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2083-576G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111403 | |||||||
chr2:203111531 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2083-448C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111531 | |||||||
chr2:203111575 | T | A | 1 | a0001c0001t0041g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2083-404T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111575 | |||||||
chr2:203111605 | G | T | 1 | a0001c0008t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2083-374G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111605 | |||||||
chr2:203111716 | T | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0287 |
3 | NA18970.hp2 NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2083-263T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111716 | |||||||
chr2:203111944 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2083-35A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 15/55 | chr2 | 203111944 | |||||||
chr2:203112133 | T | C | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2202+35T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112133 | |||||||
chr2:203112159 | A | G | 3 | a0002c0002t0003g0068 a0002c0002t0003g0071 a0002c0002t0022g0072 |
3 | NA18968.hp2 NA18969.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2202+61A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112159 | |||||||
chr2:203112371 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2202+273G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112371 | |||||||
chr2:203112436 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2202+338T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112436 | |||||||
chr2:203112614 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2203-401A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112614 | |||||||
chr2:203112622 | T | C | 1 | a0001c0001t0018g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2203-393T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112622 | |||||||
chr2:203112792 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2203-223A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112792 | |||||||
chr2:203112845 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2203-170G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 16/55 | chr2 | 203112845 | |||||||
chr2:203113358 | T | G | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2506+40T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203113358 | |||||||
chr2:203113361 | T | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2506+43T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203113361 | |||||||
chr2:203113821 | CT | C | 227 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(224): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.2506+521delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | INFO_REALIGN_3_PRIME | chr2 | 203113821 | ||||||
chr2:203113971 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
250 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.2506+653G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203113971 | |||||||
chr2:203113981 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
250 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.2506+663C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203113981 | |||||||
chr2:203114064 | C | T | 3 | a0001c0001t0002g0140 a0007c0010t0017g0018 a0014c0015t0017g0017 |
3 | HG00408.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2506+746C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114064 | |||||||
chr2:203114065 | G | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2506+747G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114065 | |||||||
chr2:203114152 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2506+834C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114152 | |||||||
chr2:203114298 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2506+980T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114298 | |||||||
chr2:203114755 | G | T | 6 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 others(3): Show |
6 | HG02293.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2507-1230G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114755 | |||||||
chr2:203114855 | GTT | G | 101 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(98): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2507-1128_2507-112 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | INFO_REALIGN_3_PRIME | chr2 | 203114855 | ||||||
chr2:203114932 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2507-1053A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203114932 | |||||||
chr2:203115076 | A | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2507-909A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115076 | |||||||
chr2:203115130 | CT | C | 7 | a0001c0001t0001g0235 a0001c0004t0005g0278 a0002c0002t0003g0046 others(4): Show |
7 | HG01167.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2507-840delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | INFO_REALIGN_3_PRIME | chr2 | 203115130 | ||||||
chr2:203115231 | G | A | 2 | a0001c0001t0004g0080 a0002c0002t0003g0078 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2507-754G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115231 | |||||||
chr2:203115310 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2507-675G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115310 | |||||||
chr2:203115341 | C | G | 3 | a0001c0001t0035g0058 a0002c0002t0026g0075 a0012c0019t0003g0074 |
3 | HG02257.hp2 HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2507-644C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115341 | |||||||
chr2:203115382 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.2507-603T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115382 | |||||||
chr2:203115474 | T | A | 74 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(71): Show |
74 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2507-511T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115474 | |||||||
chr2:203115524 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2507-461C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 17/55 | chr2 | 203115524 | |||||||
chr2:203116319 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2592+249G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116319 | |||||||
chr2:203116502 | C | CAGTGGCT others(46): Show |
1 | a0001c0004t0005g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2592+435_2592+487d others(55): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116502 | ||||||
chr2:203116550 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2592+480C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116550 | |||||||
chr2:203116617 | T | C | 3 | a0004c0005t0002g0173 a0004c0005t0002g0174 a0004c0005t0002g0175 |
3 | NA18998.hp1 NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2592+547T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116617 | |||||||
chr2:203116620 | A | G | 6 | a0001c0001t0001g0189 a0001c0001t0001g0213 a0001c0001t0001g0224 others(3): Show |
6 | HG02523.hp1 NA18949.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.2592+550A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116620 | |||||||
chr2:203116627 | C | CA | 6 | a0001c0001t0001g0001 a0001c0001t0002g0166 a0001c0001t0024g0045 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2592+571dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116627 | ||||||
chr2:203116627 | C | CAA | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.2592+570_2592+571d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116627 | ||||||
chr2:203116627 | C | CAAA | 98 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0177 others(95): Show |
98 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.2592+569_2592+571d others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116627 | ||||||
chr2:203116708 | T | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2592+638T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116708 | |||||||
chr2:203116789 | C | CA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2592+737dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116789 | ||||||
chr2:203116789 | C | CAA | 20 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(17): Show |
20 | HG00741.hp1 HG01175.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.2592+736_2592+737d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203116789 | ||||||
chr2:203116804 | A | G | 1 | a0001c0004t0005g0281 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2592+734A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116804 | |||||||
chr2:203116808 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
153 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.2592+738G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116808 | |||||||
chr2:203116814 | G | A | 22 | a0001c0004t0005g0274 a0003c0003t0004g0025 a0003c0003t0004g0026 others(19): Show |
22 | HG00733.hp1 HG01099.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2592+744G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116814 | |||||||
chr2:203116900 | G | A | 1 | a0002c0002t0003g0132 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2592+830G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203116900 | |||||||
chr2:203117006 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2592+936G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117006 | |||||||
chr2:203117025 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2592+955C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117025 | |||||||
chr2:203117057 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2592+987G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117057 | |||||||
chr2:203117158 | A | G | 1 | a0001c0001t0002g0141 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2592+1088A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117158 | |||||||
chr2:203117167 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2592+1097C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117167 | |||||||
chr2:203117183 | C | T | 2 | a0001c0001t0002g0158 a0001c0017t0031g0180 |
2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2592+1113C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117183 | |||||||
chr2:203117219 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2592+1149C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117219 | |||||||
chr2:203117239 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2592+1169C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117239 | |||||||
chr2:203117292 | G | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2592+1222G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117292 | |||||||
chr2:203117297 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2592+1227T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117297 | |||||||
chr2:203117459 | T | TC | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.2592+1389_2592+139 others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117459 | |||||||
chr2:203117594 | C | A | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2592+1524C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117594 | |||||||
chr2:203117752 | G | A | 1 | a0019c0020t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2592+1682G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117752 | |||||||
chr2:203117860 | T | G | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2592+1790T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203117860 | |||||||
chr2:203118109 | A | C | 1 | a0001c0001t0001g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2592+2039A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203118109 | |||||||
chr2:203118294 | ACT | A | 4 | a0005c0006t0002g0100 a0005c0006t0002g0161 a0005c0006t0002g0165 others(1): Show |
4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+2227_2592+222 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203118294 | ||||||
chr2:203118594 | C | CT | 98 | a0001c0001t0001g0189 a0001c0001t0001g0218 a0001c0001t0002g0059 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.2592+2539dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203118594 | ||||||
chr2:203118926 | T | G | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2592+2856T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203118926 | |||||||
chr2:203118941 | T | G | 3 | a0001c0001t0030g0231 a0002c0002t0026g0075 a0012c0019t0003g0074 |
3 | HG02257.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2592+2871T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203118941 | |||||||
chr2:203118965 | AT | A | 116 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2592+2910delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203118965 | ||||||
chr2:203119005 | A | T | 1 | a0001c0001t0002g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2592+2935A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119005 | |||||||
chr2:203119095 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2592+3025G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119095 | |||||||
chr2:203119169 | AT | A | 9 | a0001c0001t0001g0214 a0001c0001t0001g0248 a0001c0001t0002g0292 others(6): Show |
9 | HG01516.hp1 HG01884.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.2593-3071delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119169 | ||||||
chr2:203119217 | C | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2593-3037C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119217 | |||||||
chr2:203119308 | A | G | 1 | a0002c0002t0008g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2593-2946A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119308 | |||||||
chr2:203119394 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2593-2860C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119394 | |||||||
chr2:203119410 | C | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2593-2844C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119410 | |||||||
chr2:203119424 | C | CTT | 18 | a0002c0002t0003g0021 a0003c0003t0004g0025 a0003c0003t0004g0026 others(15): Show |
18 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.2593-2811_2593-281 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTT | 8 | a0001c0001t0001g0228 a0001c0001t0002g0110 a0001c0001t0002g0125 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.2593-2814_2593-281 others(9): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTT | 81 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(78): Show |
81 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2593-2815_2593-281 others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT | 19 | a0001c0001t0002g0059 a0001c0001t0002g0092 a0001c0001t0002g0103 others(16): Show |
19 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2593-2816_2593-281 others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0019g0279 a0001c0001t0019g0280 |
2 | NA18952.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2593-2819_2593-281 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0004t0005g0273 others(4): Show |
7 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.2593-2820_2593-281 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(5): Show |
4 | a0001c0004t0005g0275 a0001c0004t0005g0276 a0001c0004t0005g0278 others(1): Show |
4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2593-2821_2593-281 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(10): Show |
1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2593-2826_2593-281 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(11): Show |
2 | a0001c0008t0007g0055 a0001c0008t0007g0056 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2593-2827_2593-281 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(12): Show |
1 | a0001c0008t0007g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2593-2828_2593-281 others(23): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0014g0260 a0018c0031t0001g0203 |
2 | HG02486.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2593-2829_2593-281 others(24): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(14): Show |
25 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0193 others(22): Show |
25 | HG00673.hp2 HG01255.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.2593-2810_2593-280 others(25): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(15): Show |
48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(45): Show |
48 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.2593-2810_2593-280 others(26): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(16): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
15 | HG00597.hp2 HG02083.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.2593-2810_2593-280 others(27): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0255 a0001c0001t0041g0012 |
3 | HG02135.hp1 HG02135.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.2593-2810_2593-280 others(28): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0186 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2593-2810_2593-280 others(29): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(20): Show |
1 | a0001c0007t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2593-2810_2593-280 others(31): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0039g0003 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2593-2810_2593-280 others(33): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119424 | CT | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(4): Show |
7 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.2593-2810delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203119424 | ||||||
chr2:203119451 | G | A | 1 | a0001c0004t0005g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2593-2803G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119451 | |||||||
chr2:203119508 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2593-2746C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119508 | |||||||
chr2:203119575 | G | A | 1 | a0001c0001t0006g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2593-2679G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119575 | |||||||
chr2:203119614 | C | G | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2593-2640C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119614 | |||||||
chr2:203119653 | T | A | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2593-2601T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119653 | |||||||
chr2:203119703 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2593-2551G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119703 | |||||||
chr2:203119773 | A | C | 1 | a0002c0002t0003g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2593-2481A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119773 | |||||||
chr2:203119812 | C | T | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2593-2442C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119812 | |||||||
chr2:203119942 | A | G | 7 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0117 others(4): Show |
7 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2593-2312A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203119942 | |||||||
chr2:203120092 | T | A | 1 | a0001c0001t0001g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2593-2162T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120092 | |||||||
chr2:203120254 | C | A | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2593-2000C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120254 | |||||||
chr2:203120464 | G | T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2593-1790G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120464 | |||||||
chr2:203120486 | T | C | 1 | a0016c0030t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2593-1768T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120486 | |||||||
chr2:203120756 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2593-1498G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120756 | |||||||
chr2:203120921 | A | G | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2593-1333A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120921 | |||||||
chr2:203120947 | C | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2593-1307C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203120947 | |||||||
chr2:203121086 | C | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2593-1168C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121086 | |||||||
chr2:203121183 | A | G | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.2593-1071A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121183 | |||||||
chr2:203121197 | A | AT | 22 | a0001c0001t0002g0103 a0003c0003t0004g0025 a0003c0003t0004g0026 others(19): Show |
22 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.2593-1047dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203121197 | ||||||
chr2:203121520 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2593-734C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121520 | |||||||
chr2:203121558 | A | G | 1 | a0002c0002t0008g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2593-696A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121558 | |||||||
chr2:203121588 | G | A | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2593-666G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121588 | |||||||
chr2:203121653 | C | CA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(30): Show |
33 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2593-585dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | 203121653 | ||||||
chr2:203121855 | G | A | 1 | a0002c0002t0003g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2593-399G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121855 | |||||||
chr2:203121872 | G | A | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2593-382G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121872 | |||||||
chr2:203121977 | G | A | 1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2593-277G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121977 | |||||||
chr2:203121988 | G | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2593-266G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203121988 | |||||||
chr2:203122078 | G | A | 25 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(22): Show |
25 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.2593-176G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | chr2 | 203122078 | |||||||
chr2:203122473 | C | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2682+130C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203122473 | |||||||
chr2:203122831 | C | T | 98 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2682+488C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203122831 | |||||||
chr2:203122874 | G | T | 1 | a0001c0008t0007g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2682+531G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203122874 | |||||||
chr2:203122981 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2682+638C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203122981 | |||||||
chr2:203123044 | A | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2682+701A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203123044 | |||||||
chr2:203123083 | C | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2682+740C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203123083 | |||||||
chr2:203123136 | G | GA | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(280): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.2682+806dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | INFO_REALIGN_3_PRIME | chr2 | 203123136 | ||||||
chr2:203123342 | C | CT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0189 a0001c0001t0002g0103 others(3): Show |
6 | HG01081.hp2 HG02055.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.2682+1013dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | INFO_REALIGN_3_PRIME | chr2 | 203123342 | ||||||
chr2:203123342 | CT | C | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2682+1013delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | INFO_REALIGN_3_PRIME | chr2 | 203123342 | ||||||
chr2:203123401 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2682+1058C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203123401 | |||||||
chr2:203123629 | C | T | 5 | a0001c0001t0024g0045 a0001c0001t0025g0016 a0001c0008t0007g0055 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2682+1286C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203123629 | |||||||
chr2:203123648 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2682+1305T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203123648 | |||||||
chr2:203124094 | T | A | 91 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0177 others(88): Show |
91 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2683-1258T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124094 | |||||||
chr2:203124095 | G | T | 91 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0177 others(88): Show |
91 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2683-1257G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124095 | |||||||
chr2:203124183 | G | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2683-1169G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124183 | |||||||
chr2:203124590 | A | G | 7 | a0001c0001t0006g0227 a0001c0001t0006g0229 a0001c0001t0006g0232 others(4): Show |
7 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2683-762A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124590 | |||||||
chr2:203124624 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.2683-728G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124624 | |||||||
chr2:203124641 | A | C | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2683-711A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124641 | |||||||
chr2:203124675 | A | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2683-677A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124675 | |||||||
chr2:203124730 | G | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2683-622G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124730 | |||||||
chr2:203124997 | C | T | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2683-355C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203124997 | |||||||
chr2:203125065 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2683-287C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 19/55 | chr2 | 203125065 | |||||||
chr2:203125546 | T | C | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2851+26T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 20/55 | chr2 | 203125546 | |||||||
chr2:203125700 | A | C | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2851+180A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 20/55 | chr2 | 203125700 | |||||||
chr2:203126469 | T | C | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2986-88T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 21/55 | chr2 | 203126469 | |||||||
chr2:203126765 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.3145+49A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 22/55 | chr2 | 203126765 | |||||||
chr2:203127017 | A | G | 1 | a0002c0002t0003g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3248+91A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127017 | |||||||
chr2:203127095 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.3248+169T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127095 | |||||||
chr2:203127213 | T | G | 106 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3248+287T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127213 | |||||||
chr2:203127482 | G | A | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249-299G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127482 | |||||||
chr2:203127494 | T | C | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3249-287T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127494 | |||||||
chr2:203127496 | G | A | 1 | a0002c0002t0008g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3249-285G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127496 | |||||||
chr2:203127580 | G | A | 1 | a0002c0002t0003g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3249-201G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127580 | |||||||
chr2:203127637 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3249-144G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 23/55 | chr2 | 203127637 | |||||||
chr2:203127984 | T | G | 4 | a0005c0006t0002g0100 a0005c0006t0002g0161 a0005c0006t0002g0165 others(1): Show |
4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3405+47T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203127984 | |||||||
chr2:203128004 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3405+67G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128004 | |||||||
chr2:203128262 | C | CT | 7 | a0001c0001t0002g0059 a0001c0001t0024g0045 a0002c0002t0003g0063 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3405+348dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128262 | ||||||
chr2:203128262 | CT | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
142 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.3405+348delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128262 | ||||||
chr2:203128262 | CTT | C | 85 | a0001c0001t0001g0010 a0001c0001t0002g0079 a0001c0001t0002g0089 others(82): Show |
85 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3405+347_3405+348d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128262 | ||||||
chr2:203128489 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3405+552T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128489 | |||||||
chr2:203128516 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0149 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3405+579A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128516 | |||||||
chr2:203128601 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.3405+679dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128601 | ||||||
chr2:203128601 | C | CTT | 74 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(71): Show |
74 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.3405+678_3405+679d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128601 | ||||||
chr2:203128601 | C | CTTT | 12 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0118 others(9): Show |
12 | HG00423.hp1 HG02083.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.3405+677_3405+679d others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128601 | ||||||
chr2:203128601 | C | CTTTT | 6 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0117 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.3405+676_3405+679d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | INFO_REALIGN_3_PRIME | chr2 | 203128601 | ||||||
chr2:203128619 | G | C | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3405+682G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128619 | |||||||
chr2:203128775 | G | A | 1 | a0001c0004t0049g0285 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3405+838G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128775 | |||||||
chr2:203128786 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.3405+849T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128786 | |||||||
chr2:203128787 | G | A | 1 | a0003c0003t0004g0038 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3405+850G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128787 | |||||||
chr2:203128789 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.3405+852G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128789 | |||||||
chr2:203128842 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3405+905C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128842 | |||||||
chr2:203128985 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3405+1048G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203128985 | |||||||
chr2:203129077 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3405+1140A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129077 | |||||||
chr2:203129111 | A | G | 18 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0112 others(15): Show |
18 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.3405+1174A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129111 | |||||||
chr2:203129182 | C | T | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3406-1136C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129182 | |||||||
chr2:203129453 | A | C | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3406-865A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129453 | |||||||
chr2:203129513 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18999.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3406-805A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129513 | |||||||
chr2:203129602 | C | T | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3406-716C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203129602 | |||||||
chr2:203130091 | A | G | 95 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(92): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3406-227A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 24/55 | chr2 | 203130091 | |||||||
chr2:203130637 | A | G | 23 | a0001c0001t0034g0139 a0002c0002t0003g0132 a0003c0003t0004g0025 others(20): Show |
23 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.3564+161A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203130637 | |||||||
chr2:203130682 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.3564+206G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203130682 | |||||||
chr2:203130785 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3564+309G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203130785 | |||||||
chr2:203130808 | A | G | 1 | a0001c0004t0005g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3564+332A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203130808 | |||||||
chr2:203130850 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3564+374G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203130850 | |||||||
chr2:203131102 | A | C | 1 | a0004c0005t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3564+626A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131102 | |||||||
chr2:203131119 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3564+643A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131119 | |||||||
chr2:203131208 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3564+732C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131208 | |||||||
chr2:203131243 | T | C | 1 | a0002c0002t0003g0081 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3565-730T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131243 | |||||||
chr2:203131545 | A | G | 1 | a0001c0001t0005g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3565-428A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131545 | |||||||
chr2:203131678 | C | G | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3565-295C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131678 | |||||||
chr2:203131695 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0149 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3565-278C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131695 | |||||||
chr2:203131696 | G | A | 2 | a0001c0001t0024g0045 a0003c0003t0004g0039 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3565-277G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131696 | |||||||
chr2:203131767 | C | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3565-206C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131767 | |||||||
chr2:203131791 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3565-182G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131791 | |||||||
chr2:203131912 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.3565-61T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131912 | |||||||
chr2:203131927 | T | C | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3565-46T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 25/55 | chr2 | 203131927 | |||||||
chr2:203132147 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
260 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.3724+15A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/55 | chr2 | 203132147 | |||||||
chr2:203132324 | T | C | 1 | a0003c0003t0004g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3724+192T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/55 | chr2 | 203132324 | |||||||
chr2:203132403 | A | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3724+271A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/55 | chr2 | 203132403 | |||||||
chr2:203132941 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3725-117A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 26/55 | chr2 | 203132941 | |||||||
chr2:203133244 | A | C | 1 | a0001c0001t0006g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3813+98A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133244 | |||||||
chr2:203133421 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3813+275C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133421 | |||||||
chr2:203133421 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3813+275C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133421 | |||||||
chr2:203133556 | A | G | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0249 |
3 | NA18986.hp1 NA19066.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.3813+410A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133556 | |||||||
chr2:203133613 | C | G | 93 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(90): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.3813+467C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133613 | |||||||
chr2:203133704 | G | GAT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(24): Show |
27 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.3813+575_3813+576d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | INFO_REALIGN_3_PRIME | chr2 | 203133704 | ||||||
chr2:203133870 | T | C | 1 | a0003c0003t0004g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3813+724T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203133870 | |||||||
chr2:203134048 | T | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3813+902T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134048 | |||||||
chr2:203134517 | A | G | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3814-1160A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134517 | |||||||
chr2:203134667 | C | G | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3814-1010C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134667 | |||||||
chr2:203134730 | A | G | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3814-947A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134730 | |||||||
chr2:203134754 | T | G | 1 | a0002c0002t0003g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3814-923T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134754 | |||||||
chr2:203134759 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00408.hp2 HG02083.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.3814-918T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203134759 | |||||||
chr2:203135043 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3814-634C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135043 | |||||||
chr2:203135169 | C | CA | 6 | a0001c0001t0001g0266 a0001c0001t0001g0288 a0001c0001t0002g0104 others(3): Show |
6 | HG01109.hp2 HG02523.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.3814-492dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | INFO_REALIGN_3_PRIME | chr2 | 203135169 | ||||||
chr2:203135181 | A | C | 1 | a0001c0001t0006g0229 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3814-496A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135181 | |||||||
chr2:203135254 | TTATGTGT others(2): Show |
T | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.3814-419_3814-411d others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | INFO_REALIGN_3_PRIME | chr2 | 203135254 | ||||||
chr2:203135419 | A | C | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3814-258A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135419 | |||||||
chr2:203135480 | A | G | 1 | a0001c0001t0006g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3814-197A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135480 | |||||||
chr2:203135542 | T | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3814-135T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135542 | |||||||
chr2:203135582 | A | T | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3814-95A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135582 | |||||||
chr2:203135622 | G | C | 3 | a0007c0010t0017g0018 a0007c0010t0046g0023 a0014c0015t0017g0017 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3814-55G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 27/55 | chr2 | 203135622 | |||||||
chr2:203136775 | G | A | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | splice_donor_variant&intron_variant | HIGH | c.4565+1G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203136775 | |||||||
chr2:203136798 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4565+24C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203136798 | |||||||
chr2:203136856 | T | C | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4565+82T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203136856 | |||||||
chr2:203137001 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(266): Show |
269 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.4565+227G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137001 | |||||||
chr2:203137018 | A | G | 5 | a0001c0001t0002g0131 a0005c0006t0002g0100 a0005c0006t0002g0161 others(2): Show |
5 | HG00735.hp2 HG00741.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4565+244A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137018 | |||||||
chr2:203137145 | T | G | 1 | a0002c0002t0008g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4565+371T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137145 | |||||||
chr2:203137383 | G | C | 1 | a0001c0001t0016g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.4565+609G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137383 | |||||||
chr2:203137422 | G | C | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4565+648G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137422 | |||||||
chr2:203137445 | G | A | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4565+671G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137445 | |||||||
chr2:203137767 | T | G | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4566-395T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137767 | |||||||
chr2:203137798 | A | G | 1 | a0001c0008t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4566-364A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203137798 | |||||||
chr2:203137990 | CA | C | 141 | a0001c0001t0001g0222 a0001c0001t0002g0079 a0001c0001t0002g0087 others(138): Show |
141 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.4566-157delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | INFO_REALIGN_3_PRIME | chr2 | 203137990 | ||||||
chr2:203138005 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.4566-157A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203138005 | |||||||
chr2:203138086 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.4566-76A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 29/55 | chr2 | 203138086 | |||||||
chr2:203138384 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4719+69C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 30/55 | chr2 | 203138384 | |||||||
chr2:203138960 | C | T | 3 | a0002c0002t0008g0082 a0002c0002t0008g0088 a0002c0002t0008g0093 |
3 | HG02293.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4848+212C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203138960 | |||||||
chr2:203139222 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0224 |
2 | NA18974.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.4848+474A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203139222 | |||||||
chr2:203139342 | A | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4848+594A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203139342 | |||||||
chr2:203139557 | C | CT | 27 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0111 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.4848+838dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTT | 10 | a0001c0001t0005g0277 a0001c0001t0033g0144 a0001c0004t0005g0273 others(7): Show |
10 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.4848+837_4848+838d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTTT | 17 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0217 others(14): Show |
17 | HG00438.hp1 HG00642.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.4848+836_4848+838d others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTTTT | 67 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(64): Show |
67 | HG00597.hp2 HG00673.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.4848+835_4848+838d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTTTTT | 14 | a0001c0001t0001g0177 a0001c0001t0001g0196 a0001c0001t0001g0205 others(11): Show |
14 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.4848+834_4848+838d others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTTTTTT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(8): Show |
11 | HG00544.hp2 HG01175.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4848+833_4848+838d others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | C | CTTTTTTT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
9 | HG00408.hp2 HG02083.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.4848+832_4848+838d others(9): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139557 | CT | C | 33 | a0001c0001t0002g0089 a0001c0001t0002g0097 a0001c0001t0002g0133 others(30): Show |
33 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.4848+838delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203139557 | ||||||
chr2:203139608 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4848+860T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203139608 | |||||||
chr2:203139853 | A | G | 1 | a0001c0001t0006g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4848+1105A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203139853 | |||||||
chr2:203140349 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4848+1601A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140349 | |||||||
chr2:203140363 | C | T | 1 | a0001c0001t0006g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4848+1615C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140363 | |||||||
chr2:203140431 | C | T | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4848+1683C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140431 | |||||||
chr2:203140686 | T | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.4848+1938T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140686 | |||||||
chr2:203140715 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4848+1967T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140715 | |||||||
chr2:203140809 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
260 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.4848+2061A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140809 | |||||||
chr2:203140825 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4848+2077G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140825 | |||||||
chr2:203140894 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.4848+2146G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140894 | |||||||
chr2:203140969 | A | T | 1 | a0001c0001t0006g0233 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4848+2221A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140969 | |||||||
chr2:203140988 | A | T | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4848+2240A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140988 | |||||||
chr2:203140992 | T | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.4848+2244T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140992 | |||||||
chr2:203140996 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4848+2248T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203140996 | |||||||
chr2:203141154 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.4848+2406T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141154 | |||||||
chr2:203141182 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4848+2434A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141182 | |||||||
chr2:203141197 | A | G | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG00733.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4848+2449A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141197 | |||||||
chr2:203141238 | T | TC | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.4848+2492dupC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141238 | ||||||
chr2:203141341 | G | GATTATT | 6 | a0001c0001t0002g0090 a0001c0001t0005g0277 a0001c0001t0014g0019 others(3): Show |
6 | HG02257.hp1 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4848+2615_4848+262 others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141341 | ||||||
chr2:203141341 | G | GATTATTA others(2): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0234 others(3): Show |
6 | HG02293.hp2 HG02523.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4848+2612_4848+262 others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141341 | ||||||
chr2:203141341 | G | GATTATTA others(5): Show |
1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4848+2609_4848+262 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141341 | ||||||
chr2:203141357 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4848+2611_4848+261 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141357 | ||||||
chr2:203141360 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0039g0003 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4848+2614_4848+261 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141360 | ||||||
chr2:203141360 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0002g0138 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4848+2614_4848+261 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141360 | ||||||
chr2:203141360 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0002g0114 a0001c0001t0002g0121 |
2 | HG03942.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.4848+2614_4848+261 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141360 | ||||||
chr2:203141360 | A | ATTTTTTT others(11): Show |
1 | a0001c0029t0002g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4848+2614_4848+261 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141360 | ||||||
chr2:203141360 | A | T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4848+2612A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141360 | |||||||
chr2:203141363 | A | ATTTTT | 3 | a0003c0003t0004g0039 a0006c0009t0012g0101 a0006c0009t0012g0102 |
3 | HG01515.hp1 HG01517.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(9): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(3): Show |
1 | a0011c0025t0007g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4848+2617_4848+261 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(4): Show |
1 | a0003c0003t0010g0041 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4848+2617_4848+261 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(5): Show |
2 | a0003c0003t0004g0026 a0003c0003t0004g0031 |
2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(6): Show |
4 | a0003c0003t0004g0027 a0003c0003t0004g0032 a0003c0003t0004g0033 others(1): Show |
4 | HG01109.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0002g0087 a0001c0001t0002g0110 a0001c0001t0006g0233 |
3 | HG01358.hp1 HG03669.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0002g0122 a0001c0001t0020g0143 a0001c0001t0033g0144 others(1): Show |
4 | HG02818.hp2 NA18951.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0002g0107 a0001c0001t0002g0120 a0001c0001t0002g0145 others(1): Show |
4 | NA18747.hp2 NA18970.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0103 a0001c0001t0002g0152 a0001c0001t0018g0147 |
3 | HG02132.hp2 NA18991.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.4848+2617_4848+261 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | ATTTTTTT others(12): Show |
1 | a0020c0014t0002g0109 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4848+2617_4848+261 others(23): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | A | T | 10 | a0001c0001t0002g0114 a0001c0001t0002g0121 a0001c0001t0002g0138 others(7): Show |
10 | HG00544.hp2 HG02976.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.4848+2615A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141363 | |||||||
chr2:203141363 | ATTATTTT | A | 8 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0125 others(5): Show |
8 | HG02083.hp1 HG02523.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.4848+2618_4848+262 others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | ATTATTTT others(2): Show |
A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0230 others(4): Show |
7 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4848+2618_4848+262 others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141363 | ATTATTTT others(5): Show |
A | 1 | a0001c0001t0018g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4848+2618_4848+262 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141363 | ||||||
chr2:203141366 | A | ATTATTAT | 13 | a0001c0001t0001g0226 a0001c0001t0002g0108 a0001c0001t0005g0283 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(3): Show |
2 | a0001c0001t0001g0195 a0019c0020t0001g0190 |
2 | HG02129.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(4): Show |
4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0289 others(1): Show |
4 | HG00673.hp2 HG00735.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(7): Show |
1 | a0004c0005t0009g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(11): Show |
1 | a0001c0001t0002g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(16): Show |
1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(27): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(8): Show |
3 | a0001c0001t0002g0182 a0002c0002t0003g0046 a0004c0005t0002g0174 |
3 | HG02451.hp2 HG03831.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(9): Show |
1 | a0015c0023t0003g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(11): Show |
1 | a0001c0001t0002g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(5): Show |
2 | a0001c0001t0001g0196 a0001c0001t0036g0256 |
2 | HG02056.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(6): Show |
1 | a0004c0005t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(7): Show |
1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(8): Show |
1 | a0004c0005t0002g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(9): Show |
3 | a0002c0002t0003g0049 a0002c0002t0003g0050 a0004c0005t0002g0173 |
3 | HG02717.hp1 HG02895.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(10): Show |
1 | a0002c0002t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(2): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG00408.hp2 HG01256.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(3): Show |
13 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0220 others(10): Show |
13 | HG01081.hp1 HG01358.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(4): Show |
3 | a0001c0001t0001g0238 a0001c0001t0001g0288 a0018c0031t0001g0203 |
3 | NA18982.hp1 NA18994.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(5): Show |
7 | a0001c0001t0001g0197 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | HG00423.hp2 HG00609.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(6): Show |
4 | a0001c0001t0001g0177 a0001c0001t0030g0231 a0001c0001t0041g0012 others(1): Show |
4 | HG02135.hp1 HG03225.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(7): Show |
4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0172 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTAT others(11): Show |
1 | a0001c0001t0002g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(3): Show |
13 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0189 others(10): Show |
13 | HG00323.hp2 HG00741.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(4): Show |
6 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0219 others(3): Show |
6 | HG01169.hp1 HG02723.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(5): Show |
8 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0268 others(5): Show |
8 | HG00733.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(7): Show |
5 | a0001c0001t0002g0106 a0001c0001t0002g0140 a0001c0001t0006g0232 others(2): Show |
5 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(8): Show |
5 | a0001c0001t0002g0119 a0001c0001t0002g0157 a0001c0001t0032g0115 others(2): Show |
5 | HG01175.hp2 HG02055.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(9): Show |
1 | a0003c0003t0004g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(10): Show |
1 | a0001c0001t0002g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTATTTT others(11): Show |
1 | a0001c0001t0002g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTAT others(7): Show |
2 | a0001c0008t0007g0056 a0001c0008t0007g0057 |
2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4848+2623_4848+262 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0270 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4848+2641_4848+265 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0266 |
2 | HG04228.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.4848+2640_4848+265 others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(5): Show |
2 | a0003c0003t0004g0036 a0003c0003t0004g0042 |
2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4848+2639_4848+265 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(6): Show |
5 | a0001c0001t0001g0204 a0001c0001t0001g0252 a0001c0001t0006g0259 others(2): Show |
5 | HG02273.hp2 HG03516.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.4848+2638_4848+265 others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(7): Show |
9 | a0001c0001t0002g0111 a0001c0001t0002g0134 a0001c0001t0002g0156 others(6): Show |
9 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.4848+2637_4848+265 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0002g0099 a0001c0001t0002g0292 a0001c0001t0016g0155 others(1): Show |
4 | HG02273.hp1 NA18949.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.4848+2636_4848+265 others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(9): Show |
6 | a0001c0001t0002g0104 a0001c0001t0002g0117 a0001c0001t0002g0150 others(3): Show |
6 | HG01361.hp2 HG02080.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.4848+2635_4848+265 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0098 a0001c0001t0002g0163 a0001c0001t0006g0254 |
3 | HG00438.hp2 HG04115.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.4848+2634_4848+265 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141366 | ||||||
chr2:203141366 | A | T | 37 | a0001c0001t0002g0087 a0001c0001t0002g0103 a0001c0001t0002g0107 others(34): Show |
37 | HG00544.hp2 HG01109.hp1 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.4848+2618A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141366 | |||||||
chr2:203141367 | T | TTATTATT others(10): Show |
1 | a0004c0005t0009g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4848+2620_4848+262 others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203141367 | ||||||
chr2:203141368 | T | TA | 3 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0008g0088 |
3 | NA18906.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141368 | |||||||
chr2:203141368 | T | TATTATTA others(3): Show |
3 | a0001c0001t0001g0186 a0001c0001t0001g0255 a0001c0007t0001g0240 |
3 | HG02135.hp2 HG03834.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.4848+2620_4848+262 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141368 | |||||||
chr2:203141369 | T | A | 11 | a0001c0001t0002g0090 a0001c0001t0019g0279 a0001c0001t0019g0280 others(8): Show |
11 | HG02257.hp1 HG02622.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.4848+2621T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141369 | |||||||
chr2:203141370 | T | A | 3 | a0002c0002t0003g0061 a0002c0002t0003g0066 a0002c0002t0008g0093 |
3 | HG01975.hp2 HG02886.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.4848+2622T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141370 | |||||||
chr2:203141372 | T | A | 3 | a0001c0001t0035g0058 a0002c0002t0003g0068 a0002c0002t0026g0075 |
3 | HG02622.hp2 HG03139.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.4848+2624T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141372 | |||||||
chr2:203141373 | T | A | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4848+2625T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141373 | |||||||
chr2:203141375 | T | A | 3 | a0001c0001t0035g0058 a0002c0002t0026g0075 a0007c0010t0046g0023 |
3 | HG02622.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4848+2627T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141375 | |||||||
chr2:203141376 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0248 a0001c0001t0040g0223 |
3 | HG00597.hp2 HG03942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.4848+2628T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141376 | |||||||
chr2:203141379 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0248 |
2 | HG03942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.4848+2631T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141379 | |||||||
chr2:203141398 | T | C | 1 | a0001c0001t0045g0201 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4848+2650T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141398 | |||||||
chr2:203141519 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
259 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.4848+2771G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141519 | |||||||
chr2:203141625 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0258 |
2 | NA18945.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.4848+2877C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141625 | |||||||
chr2:203141731 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4849-2869C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141731 | |||||||
chr2:203141849 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4849-2751C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141849 | |||||||
chr2:203141914 | T | G | 103 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0079 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4849-2686T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203141914 | |||||||
chr2:203142224 | C | T | 1 | a0002c0002t0003g0068 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4849-2376C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142224 | |||||||
chr2:203142402 | C | T | 1 | a0001c0001t0016g0162 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4849-2198C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142402 | |||||||
chr2:203142481 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0287 |
3 | NA18970.hp2 NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.4849-2119C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142481 | |||||||
chr2:203142569 | G | A | 2 | a0006c0009t0012g0101 a0006c0009t0012g0102 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4849-2031G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142569 | |||||||
chr2:203142828 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4849-1772C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142828 | |||||||
chr2:203142872 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4849-1728A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142872 | |||||||
chr2:203142890 | G | T | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4849-1710G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203142890 | |||||||
chr2:203143016 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.4849-1584G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143016 | |||||||
chr2:203143396 | A | AAAATATT others(46): Show |
6 | a0001c0001t0001g0215 a0002c0002t0003g0046 a0002c0002t0003g0048 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4849-1201_4849-114 others(57): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203143396 | ||||||
chr2:203143470 | G | T | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.4849-1130G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143470 | |||||||
chr2:203143520 | C | T | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4849-1080C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143520 | |||||||
chr2:203143676 | A | G | 1 | a0001c0001t0002g0122 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4849-924A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143676 | |||||||
chr2:203143711 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(104): Show |
107 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.4849-889C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143711 | |||||||
chr2:203143873 | C | A | 1 | a0004c0005t0002g0171 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4849-727C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143873 | |||||||
chr2:203143931 | G | A | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4849-669G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203143931 | |||||||
chr2:203144126 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4849-474G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203144126 | |||||||
chr2:203144210 | C | CA | 17 | a0001c0001t0005g0277 a0001c0001t0019g0279 a0001c0001t0019g0280 others(14): Show |
17 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.4849-368dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203144210 | ||||||
chr2:203144210 | CA | C | 38 | a0001c0001t0001g0014 a0001c0001t0001g0221 a0001c0001t0001g0224 others(35): Show |
38 | HG00323.hp2 HG00733.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.4849-368delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | INFO_REALIGN_3_PRIME | chr2 | 203144210 | ||||||
chr2:203144334 | T | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4849-266T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 31/55 | chr2 | 203144334 | |||||||
chr2:203145215 | TATTG | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0252 |
3 | NA18747.hp1 NA18965.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.5304+59_5304+62del others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | INFO_REALIGN_3_PRIME | chr2 | 203145215 | ||||||
chr2:203145363 | A | G | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.5304+203A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145363 | |||||||
chr2:203145386 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5304+226G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145386 | |||||||
chr2:203145550 | C | G | 2 | a0001c0001t0034g0139 a0002c0002t0003g0132 |
2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.5304+390C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145550 | |||||||
chr2:203145781 | G | C | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5304+621G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145781 | |||||||
chr2:203145797 | CA | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
160 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.5304+656delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | INFO_REALIGN_3_PRIME | chr2 | 203145797 | ||||||
chr2:203145813 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5304+653A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145813 | |||||||
chr2:203145938 | A | C | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.5304+778A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203145938 | |||||||
chr2:203146043 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5304+883A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146043 | |||||||
chr2:203146156 | A | G | 1 | a0002c0002t0008g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5304+996A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146156 | |||||||
chr2:203146359 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00408.hp2 HG02083.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.5304+1199A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146359 | |||||||
chr2:203146372 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5304+1212T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146372 | |||||||
chr2:203146866 | G | T | 1 | a0001c0001t0006g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5304+1706G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146866 | |||||||
chr2:203146921 | A | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5304+1761A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203146921 | |||||||
chr2:203147068 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.5304+1908G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203147068 | |||||||
chr2:203147377 | T | G | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5305-1614T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203147377 | |||||||
chr2:203147569 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5305-1422A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203147569 | |||||||
chr2:203147571 | A | G | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5305-1420A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203147571 | |||||||
chr2:203147987 | A | C | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5305-1004A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203147987 | |||||||
chr2:203148067 | A | G | 105 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.5305-924A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148067 | |||||||
chr2:203148148 | CA | C | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5305-841delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | INFO_REALIGN_3_PRIME | chr2 | 203148148 | ||||||
chr2:203148182 | A | G | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5305-809A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148182 | |||||||
chr2:203148300 | A | C | 1 | a0001c0001t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5305-691A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148300 | |||||||
chr2:203148387 | T | C | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5305-604T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148387 | |||||||
chr2:203148389 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.5305-602A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148389 | |||||||
chr2:203148730 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5305-261A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148730 | |||||||
chr2:203148776 | A | G | 1 | a0002c0002t0003g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5305-215A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 33/55 | chr2 | 203148776 | |||||||
chr2:203149223 | C | T | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5462+75C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203149223 | |||||||
chr2:203149547 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5462+399C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203149547 | |||||||
chr2:203149588 | C | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0287 |
3 | NA18970.hp2 NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.5462+440C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203149588 | |||||||
chr2:203149932 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.5462+784G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203149932 | |||||||
chr2:203149941 | C | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5462+793C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203149941 | |||||||
chr2:203150542 | T | C | 1 | a0002c0002t0003g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.5463-923T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203150542 | |||||||
chr2:203150608 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.5463-857G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203150608 | |||||||
chr2:203150645 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0089 |
2 | HG01257.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.5463-820T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203150645 | |||||||
chr2:203150820 | C | G | 1 | a0001c0001t0015g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5463-645C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203150820 | |||||||
chr2:203151067 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5463-398C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203151067 | |||||||
chr2:203151103 | G | A | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5463-362G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203151103 | |||||||
chr2:203151249 | T | C | 12 | a0001c0001t0005g0283 a0001c0001t0019g0279 a0001c0001t0019g0280 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.5463-216T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203151249 | |||||||
chr2:203151258 | G | C | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5463-207G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203151258 | |||||||
chr2:203151365 | C | T | 1 | a0002c0002t0008g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5463-100C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 34/55 | chr2 | 203151365 | |||||||
chr2:203151826 | G | C | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5587+237G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203151826 | |||||||
chr2:203151996 | C | T | 2 | a0006c0009t0012g0101 a0006c0009t0012g0102 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.5587+407C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203151996 | |||||||
chr2:203152235 | G | A | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5587+646G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203152235 | |||||||
chr2:203152352 | GA | G | 73 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(70): Show |
73 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.5587+777delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203152352 | ||||||
chr2:203152586 | G | A | 1 | a0001c0001t0044g0096 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5587+997G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203152586 | |||||||
chr2:203152915 | G | A | 1 | a0014c0015t0017g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5587+1326G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203152915 | |||||||
chr2:203152954 | C | A | 1 | a0001c0001t0015g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5587+1365C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203152954 | |||||||
chr2:203152987 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5587+1398G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203152987 | |||||||
chr2:203153037 | TCAA | T | 38 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0098 others(35): Show |
38 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.5587+1467_5587+146 others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203153037 | ||||||
chr2:203153070 | T | C | 6 | a0001c0001t0002g0131 a0001c0001t0002g0136 a0005c0006t0002g0100 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.5587+1481T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153070 | |||||||
chr2:203153089 | T | C | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5587+1500T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153089 | |||||||
chr2:203153174 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5587+1585C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153174 | |||||||
chr2:203153180 | T | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5587+1591T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153180 | |||||||
chr2:203153200 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5587+1611A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153200 | |||||||
chr2:203153214 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.5587+1625C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153214 | |||||||
chr2:203153302 | A | AT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
214 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.5587+1732dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203153302 | ||||||
chr2:203153302 | A | ATT | 18 | a0001c0001t0001g0208 a0001c0001t0001g0245 a0001c0001t0001g0248 others(15): Show |
18 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.5587+1731_5587+173 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203153302 | ||||||
chr2:203153302 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5587+1723_5587+173 others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203153302 | ||||||
chr2:203153330 | C | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5587+1741C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153330 | |||||||
chr2:203153430 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5587+1841C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153430 | |||||||
chr2:203153722 | G | C | 1 | a0001c0004t0005g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5587+2133G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153722 | |||||||
chr2:203153806 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.5587+2217C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153806 | |||||||
chr2:203153929 | T | G | 1 | a0001c0001t0001g0266 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5587+2340T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203153929 | |||||||
chr2:203154137 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5587+2548G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154137 | |||||||
chr2:203154142 | A | AGGAGAAT others(18): Show |
21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5587+2558_5587+258 others(29): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203154142 | ||||||
chr2:203154160 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5587+2571C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154160 | |||||||
chr2:203154168 | G | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.5587+2579G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154168 | |||||||
chr2:203154235 | CA | C | 28 | a0001c0001t0001g0265 a0001c0001t0024g0045 a0002c0002t0003g0046 others(25): Show |
28 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.5587+2663delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203154235 | ||||||
chr2:203154608 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.5587+3019T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154608 | |||||||
chr2:203154640 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5587+3051C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154640 | |||||||
chr2:203154705 | A | G | 1 | a0018c0031t0001g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.5588-2994A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154705 | |||||||
chr2:203154852 | T | A | 4 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(1): Show |
4 | HG02630.hp1 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5588-2847T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203154852 | |||||||
chr2:203154934 | C | CA | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(231): Show |
234 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.5588-2746dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203154934 | ||||||
chr2:203154934 | C | CAA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0225 others(13): Show |
16 | HG00438.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.5588-2747_5588-274 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203154934 | ||||||
chr2:203155039 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.5588-2660G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155039 | |||||||
chr2:203155121 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.5588-2578G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155121 | |||||||
chr2:203155133 | A | T | 1 | a0004c0005t0009g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5588-2566A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155133 | |||||||
chr2:203155247 | C | CA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
163 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.5588-2436dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203155247 | ||||||
chr2:203155247 | C | CAA | 86 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(83): Show |
86 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.5588-2437_5588-243 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | INFO_REALIGN_3_PRIME | chr2 | 203155247 | ||||||
chr2:203155571 | G | A | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5588-2128G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155571 | |||||||
chr2:203155658 | G | C | 1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5588-2041G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155658 | |||||||
chr2:203155676 | G | C | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5588-2023G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155676 | |||||||
chr2:203155894 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5588-1805G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155894 | |||||||
chr2:203155968 | A | G | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5588-1731A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203155968 | |||||||
chr2:203156064 | C | A | 2 | a0003c0003t0010g0041 a0003c0003t0010g0044 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5588-1635C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156064 | |||||||
chr2:203156074 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
115 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.5588-1625A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156074 | |||||||
chr2:203156196 | G | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5588-1503G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156196 | |||||||
chr2:203156241 | T | C | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5588-1458T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156241 | |||||||
chr2:203156383 | C | T | 1 | a0001c0001t0040g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5588-1316C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156383 | |||||||
chr2:203156478 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5588-1221C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156478 | |||||||
chr2:203156666 | G | A | 1 | a0001c0004t0005g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5588-1033G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156666 | |||||||
chr2:203156713 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.5588-986A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156713 | |||||||
chr2:203156987 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.5588-712C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203156987 | |||||||
chr2:203157051 | C | T | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5588-648C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203157051 | |||||||
chr2:203157249 | A | G | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5588-450A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203157249 | |||||||
chr2:203157297 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.5588-402G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203157297 | |||||||
chr2:203157532 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5588-167C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 35/55 | chr2 | 203157532 | |||||||
chr2:203158269 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5714+444C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203158269 | |||||||
chr2:203158782 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.5714+957T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203158782 | |||||||
chr2:203158815 | G | GT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.5714+1012dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203158815 | ||||||
chr2:203158815 | G | GTT | 36 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0189 others(33): Show |
36 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.5714+1011_5714+101 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203158815 | ||||||
chr2:203158815 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5714+990G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203158815 | |||||||
chr2:203158881 | G | A | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5714+1056G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203158881 | |||||||
chr2:203159001 | C | T | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5714+1176C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203159001 | |||||||
chr2:203159141 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5714+1316A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203159141 | |||||||
chr2:203159332 | C | A | 1 | a0001c0001t0002g0164 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5714+1507C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203159332 | |||||||
chr2:203159509 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5714+1684C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203159509 | |||||||
chr2:203159646 | A | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5714+1821A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203159646 | |||||||
chr2:203160077 | A | T | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5714+2252A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203160077 | |||||||
chr2:203160077 | AT | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
130 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.5714+2272delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203160077 | ||||||
chr2:203160144 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5714+2319A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203160144 | |||||||
chr2:203160328 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.5714+2503G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203160328 | |||||||
chr2:203160665 | A | G | 92 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(89): Show |
92 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.5714+2840A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203160665 | |||||||
chr2:203161009 | A | G | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5714+3184A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161009 | |||||||
chr2:203161055 | C | T | 73 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(70): Show |
73 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.5714+3230C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161055 | |||||||
chr2:203161093 | C | T | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5714+3268C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161093 | |||||||
chr2:203161308 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.5714+3483T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161308 | |||||||
chr2:203161326 | C | CA | 9 | a0001c0001t0001g0188 a0001c0001t0002g0114 a0001c0001t0002g0157 others(6): Show |
9 | HG00408.hp2 HG01175.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.5714+3521dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161326 | ||||||
chr2:203161326 | CA | C | 8 | a0001c0001t0001g0249 a0001c0001t0002g0059 a0001c0001t0002g0090 others(5): Show |
8 | HG01515.hp1 HG01515.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.5714+3521delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161326 | ||||||
chr2:203161628 | CAAAT | C | 14 | a0001c0001t0005g0283 a0001c0001t0019g0280 a0001c0004t0005g0273 others(11): Show |
14 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.5714+3855_5714+385 others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161628 | ||||||
chr2:203161628 | CAAATAAA others(1): Show |
C | 32 | a0001c0001t0004g0080 a0001c0001t0005g0277 a0001c0001t0019g0279 others(29): Show |
32 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.5714+3851_5714+385 others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161628 | ||||||
chr2:203161628 | CAAATAAA others(5): Show |
C | 36 | a0001c0001t0001g0193 a0001c0001t0001g0202 a0001c0001t0001g0234 others(33): Show |
36 | HG00423.hp1 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.5714+3847_5714+385 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161628 | ||||||
chr2:203161628 | CAAATAAA others(9): Show |
C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.5714+3843_5714+385 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161628 | ||||||
chr2:203161628 | CAAATAAA others(21): Show |
C | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5714+3831_5714+385 others(32): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203161628 | ||||||
chr2:203161781 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.5714+3956T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161781 | |||||||
chr2:203161853 | G | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.5714+4028G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161853 | |||||||
chr2:203161929 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0002g0133 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5714+4104C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203161929 | |||||||
chr2:203162019 | A | AT | 23 | a0001c0001t0001g0020 a0001c0001t0001g0258 a0001c0001t0002g0059 others(20): Show |
23 | HG00408.hp1 HG00642.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.5715-4108dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203162019 | ||||||
chr2:203162019 | AT | A | 14 | a0001c0001t0001g0235 a0001c0001t0001g0244 a0001c0001t0001g0261 others(11): Show |
14 | HG01167.hp1 HG01168.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.5715-4108delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203162019 | ||||||
chr2:203162330 | T | G | 1 | a0001c0007t0001g0240 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5715-3819T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203162330 | |||||||
chr2:203162448 | T | C | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5715-3701T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203162448 | |||||||
chr2:203162517 | C | T | 1 | a0001c0001t0005g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5715-3632C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203162517 | |||||||
chr2:203162978 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.5715-3171G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203162978 | |||||||
chr2:203163027 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(270): Show |
273 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.5715-3122A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163027 | |||||||
chr2:203163154 | C | T | 1 | a0003c0003t0004g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5715-2995C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163154 | |||||||
chr2:203163309 | C | T | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5715-2840C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163309 | |||||||
chr2:203163347 | A | G | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5715-2802A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163347 | |||||||
chr2:203163436 | T | G | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5715-2713T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163436 | |||||||
chr2:203163841 | C | T | 138 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(135): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.5715-2308C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203163841 | |||||||
chr2:203164263 | A | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.5715-1886A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164263 | |||||||
chr2:203164430 | T | C | 138 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(135): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.5715-1719T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164430 | |||||||
chr2:203164464 | G | A | 1 | a0001c0021t0002g0169 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5715-1685G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164464 | |||||||
chr2:203164572 | G | T | 138 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(135): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.5715-1577G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164572 | |||||||
chr2:203164667 | A | G | 3 | a0003c0003t0004g0026 a0003c0003t0004g0031 a0003c0003t0004g0038 |
3 | HG02258.hp2 HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5715-1482A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164667 | |||||||
chr2:203164861 | C | CT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): Show |
119 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.5715-1271dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203164861 | ||||||
chr2:203164861 | CT | C | 9 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0125 others(6): Show |
9 | HG01081.hp2 HG01099.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.5715-1271delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | INFO_REALIGN_3_PRIME | chr2 | 203164861 | ||||||
chr2:203164938 | C | T | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5715-1211C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203164938 | |||||||
chr2:203165018 | C | T | 4 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | NA18974.hp1 NA18984.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.5715-1131C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165018 | |||||||
chr2:203165103 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5715-1046C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165103 | |||||||
chr2:203165151 | G | A | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5715-998G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165151 | |||||||
chr2:203165293 | T | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.5715-856T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165293 | |||||||
chr2:203165694 | C | T | 1 | a0002c0002t0003g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5715-455C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165694 | |||||||
chr2:203165742 | A | G | 1 | a0001c0001t0019g0280 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5715-407A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165742 | |||||||
chr2:203165743 | T | A | 1 | a0001c0001t0019g0280 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5715-406T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165743 | |||||||
chr2:203165745 | A | ATTTATAT others(28): Show |
1 | a0001c0001t0019g0280 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5715-404_5715-403i others(37): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165745 | |||||||
chr2:203165939 | A | C | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5715-210A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203165939 | |||||||
chr2:203166020 | C | G | 21 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.5715-129C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203166020 | |||||||
chr2:203166043 | T | G | 1 | a0001c0001t0002g0111 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5715-106T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 36/55 | chr2 | 203166043 | |||||||
chr2:203166363 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | NA18986.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.5863+66A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166363 | |||||||
chr2:203166414 | G | A | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.5863+117G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166414 | |||||||
chr2:203166507 | A | T | 4 | a0005c0006t0002g0100 a0005c0006t0002g0161 a0005c0006t0002g0165 others(1): Show |
4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.5863+210A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166507 | |||||||
chr2:203166559 | T | A | 2 | a0001c0001t0001g0052 a0007c0010t0046g0023 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5863+262T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166559 | |||||||
chr2:203166637 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5863+340C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166637 | |||||||
chr2:203166785 | A | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
249 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.5864-442A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203166785 | |||||||
chr2:203167045 | G | C | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5864-182G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203167045 | |||||||
chr2:203167173 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5864-54T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203167173 | |||||||
chr2:203167202 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5864-25G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203167202 | |||||||
chr2:203167219 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.5864-8G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 37/55 | chr2 | 203167219 | |||||||
chr2:203167383 | A | G | 1 | a0002c0002t0008g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5997+23A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167383 | |||||||
chr2:203167505 | G | A | 2 | a0001c0001t0024g0045 a0001c0001t0025g0016 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.5997+145G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167505 | |||||||
chr2:203167511 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5997+151A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167511 | |||||||
chr2:203167600 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.5997+240C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167600 | |||||||
chr2:203167831 | G | T | 1 | a0001c0017t0031g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5997+471G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167831 | |||||||
chr2:203167976 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.5997+616G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203167976 | |||||||
chr2:203168155 | A | T | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.5997+795A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168155 | |||||||
chr2:203168302 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5997+942T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168302 | |||||||
chr2:203168446 | G | A | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5997+1086G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168446 | |||||||
chr2:203168801 | G | A | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5998-946G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168801 | |||||||
chr2:203168823 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5998-924G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168823 | |||||||
chr2:203168870 | G | A | 1 | a0002c0002t0003g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5998-877G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168870 | |||||||
chr2:203168881 | G | A | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5998-866G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203168881 | |||||||
chr2:203168893 | C | CA | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
231 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.5998-834dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | INFO_REALIGN_3_PRIME | chr2 | 203168893 | ||||||
chr2:203168893 | C | CAA | 14 | a0001c0001t0001g0189 a0001c0001t0001g0194 a0001c0001t0001g0199 others(11): Show |
14 | HG00673.hp1 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.5998-835_5998-834d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | INFO_REALIGN_3_PRIME | chr2 | 203168893 | ||||||
chr2:203169128 | A | G | 7 | a0001c0001t0006g0227 a0001c0001t0006g0229 a0001c0001t0006g0232 others(4): Show |
7 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.5998-619A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203169128 | |||||||
chr2:203169388 | T | TA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): Show |
123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.5998-336dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | INFO_REALIGN_3_PRIME | chr2 | 203169388 | ||||||
chr2:203169388 | T | TAA | 25 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0210 others(22): Show |
25 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.5998-337_5998-336d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | INFO_REALIGN_3_PRIME | chr2 | 203169388 | ||||||
chr2:203169412 | C | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.5998-335C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203169412 | |||||||
chr2:203169460 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
249 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.5998-287A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203169460 | |||||||
chr2:203169555 | T | A | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5998-192T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 38/55 | chr2 | 203169555 | |||||||
chr2:203170059 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0041g0012 a0001c0022t0001g0005 |
3 | HG00408.hp2 HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.6102+208C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203170059 | |||||||
chr2:203170244 | C | T | 138 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(135): Show |
138 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.6102+393C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203170244 | |||||||
chr2:203170304 | G | A | 3 | a0007c0010t0017g0018 a0010c0016t0023g0022 a0014c0015t0017g0017 |
3 | HG02109.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6102+453G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203170304 | |||||||
chr2:203170856 | TA | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG02080.hp1 NA18986.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.6102+1007delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203170856 | ||||||
chr2:203170992 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(251): Show |
254 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.6103-936T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203170992 | |||||||
chr2:203171119 | A | G | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.6103-809A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203171119 | |||||||
chr2:203171124 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6103-804G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203171124 | |||||||
chr2:203171289 | TAATAA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.6103-630_6103-626d others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203171289 | ||||||
chr2:203171340 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.6103-588T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203171340 | |||||||
chr2:203171634 | T | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.6103-294T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | chr2 | 203171634 | |||||||
chr2:203171677 | G | GT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.6103-239dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203171677 | ||||||
chr2:203171677 | G | GTT | 24 | a0001c0001t0002g0152 a0001c0001t0002g0182 a0001c0001t0016g0155 others(21): Show |
24 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.6103-240_6103-239d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203171677 | ||||||
chr2:203171822 | C | CT | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(239): Show |
242 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.6103-92dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203171822 | ||||||
chr2:203171822 | C | CTT | 8 | a0001c0001t0001g0212 a0001c0001t0001g0222 a0001c0001t0001g0269 others(5): Show |
8 | HG01168.hp2 HG01175.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.6103-93_6103-92dup others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 39/55 | INFO_REALIGN_3_PRIME | chr2 | 203171822 | ||||||
chr2:203172291 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6198+268C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 40/55 | chr2 | 203172291 | |||||||
chr2:203172324 | G | A | 98 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.6198+301G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 40/55 | chr2 | 203172324 | |||||||
chr2:203172409 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.6199-320A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 40/55 | chr2 | 203172409 | |||||||
chr2:203172514 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | NA18981.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.6199-215T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 40/55 | chr2 | 203172514 | |||||||
chr2:203172937 | T | A | 3 | a0001c0001t0006g0254 a0001c0001t0018g0148 a0001c0017t0031g0180 |
3 | HG00544.hp1 HG00609.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.6323+84T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203172937 | |||||||
chr2:203173327 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.6323+474A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203173327 | |||||||
chr2:203173353 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6323+500C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203173353 | |||||||
chr2:203173507 | T | A | 14 | a0002c0002t0003g0060 a0002c0002t0003g0062 a0002c0002t0003g0063 others(11): Show |
14 | HG00738.hp1 HG01943.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.6323+654T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203173507 | |||||||
chr2:203173516 | G | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.6323+663G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203173516 | |||||||
chr2:203174216 | C | CA | 52 | a0001c0001t0001g0214 a0001c0001t0002g0079 a0001c0001t0002g0090 others(49): Show |
52 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.6324-904dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174216 | C | CAA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): Show |
85 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.6324-905_6324-904d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174216 | C | CAAA | 32 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(29): Show |
32 | HG00597.hp2 HG01081.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.6324-906_6324-904d others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174216 | CA | C | 12 | a0001c0001t0005g0283 a0001c0001t0019g0280 a0001c0004t0005g0273 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.6324-904delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174216 | CAAAAAAA others(2): Show |
C | 21 | a0001c0001t0001g0215 a0003c0003t0004g0025 a0003c0003t0004g0026 others(18): Show |
21 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.6324-912_6324-904d others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174216 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6324-914_6324-904d others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174216 | ||||||
chr2:203174465 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6324-682G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174465 | |||||||
chr2:203174502 | C | G | 6 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 others(3): Show |
6 | HG02293.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.6324-645C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174502 | |||||||
chr2:203174551 | C | G | 1 | a0001c0029t0002g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.6324-596C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174551 | |||||||
chr2:203174675 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.6324-472A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174675 | |||||||
chr2:203174751 | C | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6324-396C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174751 | |||||||
chr2:203174762 | G | A | 3 | a0001c0001t0004g0080 a0002c0002t0003g0078 a0002c0002t0003g0081 |
3 | HG02970.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6324-385G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174762 | |||||||
chr2:203174789 | G | T | 1 | a0001c0008t0007g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6324-358G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174789 | |||||||
chr2:203174808 | G | A | 2 | a0001c0004t0005g0275 a0001c0004t0005g0276 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6324-339G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174808 | |||||||
chr2:203174816 | A | G | 1 | a0003c0003t0004g0035 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6324-331A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174816 | |||||||
chr2:203174858 | C | CAAAT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.6324-253_6324-250d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174858 | ||||||
chr2:203174858 | C | CAAATAAA others(1): Show |
3 | a0001c0001t0001g0200 a0001c0001t0001g0208 a0001c0001t0001g0225 |
3 | HG02080.hp1 NA18946.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.6324-257_6324-250d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174858 | ||||||
chr2:203174858 | C | CAAATAAA others(5): Show |
1 | a0001c0001t0001g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.6324-261_6324-250d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174858 | ||||||
chr2:203174858 | CAAAT | C | 126 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(123): Show |
126 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.6324-253_6324-250d others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174858 | ||||||
chr2:203174858 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6324-261_6324-250d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | INFO_REALIGN_3_PRIME | chr2 | 203174858 | ||||||
chr2:203174948 | T | C | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6324-199T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174948 | |||||||
chr2:203174984 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.6324-163T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 41/55 | chr2 | 203174984 | |||||||
chr2:203175483 | G | A | 143 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(140): Show |
143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.6464+196G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203175483 | |||||||
chr2:203175573 | G | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.6464+286G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203175573 | |||||||
chr2:203175794 | T | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6464+507T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203175794 | |||||||
chr2:203176171 | C | CT | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
106 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.6464+904dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203176171 | ||||||
chr2:203176171 | CT | C | 7 | a0001c0001t0002g0124 a0001c0008t0007g0055 a0001c0008t0007g0056 others(4): Show |
7 | HG01169.hp1 HG01256.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.6464+904delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203176171 | ||||||
chr2:203176257 | C | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6464+970C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176257 | |||||||
chr2:203176343 | T | C | 17 | a0002c0002t0003g0060 a0002c0002t0003g0061 a0002c0002t0003g0062 others(14): Show |
17 | HG00738.hp1 HG01943.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.6464+1056T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176343 | |||||||
chr2:203176375 | C | A | 95 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(92): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.6464+1088C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176375 | |||||||
chr2:203176559 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6464+1272G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176559 | |||||||
chr2:203176645 | T | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.6464+1358T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176645 | |||||||
chr2:203176666 | A | T | 1 | a0001c0001t0002g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.6464+1379A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176666 | |||||||
chr2:203176729 | C | CA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
158 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.6464+1457dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203176729 | ||||||
chr2:203176729 | C | CAA | 7 | a0001c0001t0001g0205 a0001c0001t0015g0129 a0001c0001t0015g0130 others(4): Show |
7 | HG00733.hp2 HG01496.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.6464+1456_6464+145 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203176729 | ||||||
chr2:203176729 | C | CAAA | 12 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.6464+1455_6464+145 others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203176729 | ||||||
chr2:203176910 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6464+1623G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203176910 | |||||||
chr2:203177025 | C | G | 6 | a0001c0001t0001g0215 a0002c0002t0003g0046 a0002c0002t0003g0048 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.6464+1738C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203177025 | |||||||
chr2:203177150 | CA | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0002g0107 others(17): Show |
20 | HG00738.hp1 HG01256.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.6464+1880delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203177150 | ||||||
chr2:203177178 | AGAAAT | A | 3 | a0001c0008t0007g0055 a0001c0008t0007g0056 a0001c0008t0007g0057 |
3 | HG02976.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.6464+1901_6464+190 others(9): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203177178 | ||||||
chr2:203177373 | T | TA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
113 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.6464+2101dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203177373 | ||||||
chr2:203177616 | C | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6464+2329C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203177616 | |||||||
chr2:203177845 | C | G | 139 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(136): Show |
139 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.6465-2537C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203177845 | |||||||
chr2:203177935 | C | A | 1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6465-2447C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203177935 | |||||||
chr2:203178018 | CA | C | 127 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(124): Show |
127 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.6465-2352delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203178018 | ||||||
chr2:203178025 | A | T | 4 | a0001c0001t0001g0239 a0002c0002t0003g0062 a0002c0002t0003g0063 others(1): Show |
4 | NA18948.hp2 NA18986.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.6465-2357A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203178025 | |||||||
chr2:203178149 | CT | C | 139 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(136): Show |
139 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.6465-2223delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | INFO_REALIGN_3_PRIME | chr2 | 203178149 | ||||||
chr2:203178343 | A | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.6465-2039A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203178343 | |||||||
chr2:203178437 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.6465-1945G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203178437 | |||||||
chr2:203178883 | T | C | 74 | a0001c0001t0001g0020 a0001c0001t0001g0177 a0001c0001t0001g0185 others(71): Show |
74 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.6465-1499T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203178883 | |||||||
chr2:203178953 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.6465-1429G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203178953 | |||||||
chr2:203179293 | C | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.6465-1089C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179293 | |||||||
chr2:203179326 | G | A | 93 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(90): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.6465-1056G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179326 | |||||||
chr2:203179490 | G | A | 139 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(136): Show |
139 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.6465-892G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179490 | |||||||
chr2:203179662 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0252 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.6465-720G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179662 | |||||||
chr2:203179771 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6465-611A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179771 | |||||||
chr2:203179896 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6465-486C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179896 | |||||||
chr2:203179962 | C | T | 2 | a0006c0009t0012g0101 a0006c0009t0012g0102 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.6465-420C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203179962 | |||||||
chr2:203180012 | A | G | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6465-370A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180012 | |||||||
chr2:203180021 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(251): Show |
254 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.6465-361A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180021 | |||||||
chr2:203180049 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.6465-333T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180049 | |||||||
chr2:203180053 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6465-329C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180053 | |||||||
chr2:203180076 | A | C | 1 | a0002c0002t0008g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6465-306A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180076 | |||||||
chr2:203180152 | A | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6465-230A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180152 | |||||||
chr2:203180377 | T | A | 2 | a0002c0013t0003g0076 a0013c0012t0003g0077 |
2 | HG03130.hp2 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.6465-5T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 42/55 | chr2 | 203180377 | |||||||
chr2:203180545 | A | G | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6595+33A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203180545 | |||||||
chr2:203180652 | A | C | 1 | a0001c0001t0004g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6595+140A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203180652 | |||||||
chr2:203180816 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.6595+304T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203180816 | |||||||
chr2:203180933 | A | ATTTTTTT others(2): Show |
7 | a0001c0001t0042g0054 a0001c0008t0007g0055 a0001c0008t0007g0056 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.6595+435_6595+443d others(11): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(3): Show |
17 | a0001c0001t0002g0168 a0003c0003t0004g0027 a0003c0003t0004g0028 others(14): Show |
17 | HG00733.hp1 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.6595+434_6595+443d others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(4): Show |
78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
78 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.6595+433_6595+443d others(13): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(5): Show |
77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(74): Show |
77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.6595+432_6595+443d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(6): Show |
45 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0198 others(42): Show |
45 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.6595+431_6595+443d others(15): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(7): Show |
10 | a0001c0001t0001g0212 a0001c0001t0002g0112 a0001c0001t0002g0113 others(7): Show |
10 | HG00423.hp1 HG01175.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.6595+430_6595+443d others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0002g0154 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG01361.hp2 HG01515.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.6595+429_6595+443d others(17): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0019g0279 a0001c0001t0030g0231 a0001c0004t0005g0282 others(1): Show |
4 | HG00738.hp2 HG03579.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.6595+428_6595+443d others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(10): Show |
6 | a0001c0001t0005g0283 a0001c0001t0019g0280 a0001c0004t0005g0274 others(3): Show |
6 | HG00438.hp1 HG01099.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.6595+427_6595+443d others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(11): Show |
3 | a0001c0004t0005g0273 a0001c0004t0005g0278 a0001c0004t0005g0281 |
3 | HG00735.hp1 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.6595+426_6595+443d others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203180933 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6595+424_6595+443d others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | INFO_REALIGN_3_PRIME | chr2 | 203180933 | ||||||
chr2:203181077 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6595+565C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181077 | |||||||
chr2:203181078 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0037g0207 |
2 | HG00423.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.6595+566A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181078 | |||||||
chr2:203181133 | T | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6595+621T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181133 | |||||||
chr2:203181433 | T | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0149 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.6595+921T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181433 | |||||||
chr2:203181440 | T | G | 1 | a0012c0019t0003g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6595+928T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181440 | |||||||
chr2:203181530 | A | C | 19 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.6595+1018A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181530 | |||||||
chr2:203181673 | C | T | 6 | a0002c0002t0003g0021 a0002c0002t0003g0046 a0002c0002t0003g0048 others(3): Show |
6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.6595+1161C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181673 | |||||||
chr2:203181737 | C | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.6595+1225C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181737 | |||||||
chr2:203181803 | A | G | 98 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(95): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.6595+1291A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181803 | |||||||
chr2:203181938 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.6596-1341T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203181938 | |||||||
chr2:203182223 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6596-1056G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182223 | |||||||
chr2:203182479 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6596-800A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182479 | |||||||
chr2:203182554 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.6596-725G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182554 | |||||||
chr2:203182731 | C | G | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6596-548C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182731 | |||||||
chr2:203182865 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.6596-414A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182865 | |||||||
chr2:203182882 | A | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.6596-397A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 43/55 | chr2 | 203182882 | |||||||
chr2:203183684 | G | A | 1 | a0002c0002t0003g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6705+296G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203183684 | |||||||
chr2:203183868 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6705+480G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203183868 | |||||||
chr2:203184038 | G | A | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6705+650G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184038 | |||||||
chr2:203184074 | T | TA | 10 | a0001c0001t0002g0149 a0001c0001t0015g0130 a0001c0001t0035g0058 others(7): Show |
10 | HG00597.hp1 HG00735.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.6705+711dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203184074 | ||||||
chr2:203184074 | TA | T | 9 | a0001c0001t0001g0224 a0001c0001t0002g0126 a0001c0001t0002g0168 others(6): Show |
9 | HG01167.hp2 HG02559.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.6705+711delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203184074 | ||||||
chr2:203184074 | TAA | T | 22 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0014g0019 others(19): Show |
22 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.6705+710_6705+711d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203184074 | ||||||
chr2:203184090 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.6705+702A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184090 | |||||||
chr2:203184096 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.6705+708A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184096 | |||||||
chr2:203184100 | G | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
109 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6705+712G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184100 | |||||||
chr2:203184117 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
224 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.6705+729G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184117 | |||||||
chr2:203184218 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6705+830G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184218 | |||||||
chr2:203184417 | C | T | 1 | a0002c0002t0003g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6705+1029C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184417 | |||||||
chr2:203184471 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0041g0012 a0001c0022t0001g0005 |
3 | HG00408.hp2 HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.6705+1083T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184471 | |||||||
chr2:203184614 | T | G | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6705+1226T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184614 | |||||||
chr2:203184896 | TA | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0202 others(18): Show |
21 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.6705+1525delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203184896 | ||||||
chr2:203184897 | A | T | 132 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(129): Show |
132 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.6705+1509A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184897 | |||||||
chr2:203184898 | A | T | 6 | a0001c0001t0002g0167 a0001c0001t0002g0291 a0003c0003t0004g0042 others(3): Show |
6 | HG01169.hp2 HG01517.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.6705+1510A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203184898 | |||||||
chr2:203185093 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6705+1705A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185093 | |||||||
chr2:203185173 | T | G | 1 | a0001c0001t0014g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6705+1785T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185173 | |||||||
chr2:203185381 | A | T | 1 | a0002c0002t0003g0063 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.6705+1993A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185381 | |||||||
chr2:203185506 | A | G | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.6705+2118A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185506 | |||||||
chr2:203185553 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6705+2165A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185553 | |||||||
chr2:203185751 | T | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.6705+2363T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203185751 | |||||||
chr2:203186025 | C | G | 2 | a0001c0008t0007g0056 a0011c0025t0007g0053 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.6706-2447C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186025 | |||||||
chr2:203186095 | T | C | 1 | a0002c0002t0008g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.6706-2377T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186095 | |||||||
chr2:203186165 | T | G | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6706-2307T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186165 | |||||||
chr2:203186286 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.6706-2186G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186286 | |||||||
chr2:203186347 | G | A | 10 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0001t0024g0045 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.6706-2125G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186347 | |||||||
chr2:203186617 | A | AAAAT | 4 | a0001c0001t0001g0002 a0001c0007t0001g0241 a0001c0007t0001g0242 others(1): Show |
4 | HG03831.hp2 NA18951.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.6706-1832_6706-182 others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203186617 | ||||||
chr2:203186617 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6706-1844_6706-182 others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203186617 | ||||||
chr2:203186788 | T | C | 1 | a0014c0015t0017g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6706-1684T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203186788 | |||||||
chr2:203187073 | GCCCTCTA others(5): Show |
G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6706-1395_6706-138 others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187073 | ||||||
chr2:203187101 | T | C | 1 | a0015c0023t0003g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6706-1371T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187101 | |||||||
chr2:203187105 | C | G | 4 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0008t0007g0056 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6706-1367C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187105 | |||||||
chr2:203187108 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6706-1364C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187108 | |||||||
chr2:203187109 | G | C | 2 | a0005c0006t0002g0165 a0005c0006t0002g0179 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6706-1363G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187109 | |||||||
chr2:203187173 | TC | T | 7 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0001t0042g0054 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.6706-1296delC | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187173 | ||||||
chr2:203187207 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.6706-1265G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187207 | |||||||
chr2:203187232 | A | AT | 20 | a0001c0001t0004g0080 a0003c0003t0004g0025 a0003c0003t0004g0026 others(17): Show |
20 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.6706-1234dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187232 | ||||||
chr2:203187338 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.6706-1134A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187338 | |||||||
chr2:203187367 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
109 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.6706-1084dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187367 | ||||||
chr2:203187367 | G | GTT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0209 others(130): Show |
133 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.6706-1085_6706-108 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187367 | ||||||
chr2:203187367 | G | GTTT | 20 | a0001c0001t0002g0104 a0001c0001t0002g0114 a0001c0001t0002g0119 others(17): Show |
20 | HG00544.hp1 HG00597.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.6706-1086_6706-108 others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187367 | ||||||
chr2:203187433 | C | T | 3 | a0003c0003t0004g0028 a0003c0003t0004g0036 a0003c0003t0004g0040 |
3 | HG03130.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6706-1039C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187433 | |||||||
chr2:203187471 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00408.hp2 HG02083.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.6706-1001G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187471 | |||||||
chr2:203187716 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6706-756C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203187716 | |||||||
chr2:203187744 | C | CA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.6706-715dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | INFO_REALIGN_3_PRIME | chr2 | 203187744 | ||||||
chr2:203188148 | A | G | 4 | a0003c0003t0004g0029 a0003c0003t0004g0032 a0003c0003t0004g0033 others(1): Show |
4 | HG02572.hp1 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6706-324A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203188148 | |||||||
chr2:203188185 | G | A | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6706-287G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203188185 | |||||||
chr2:203188267 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
249 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.6706-205T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 44/55 | chr2 | 203188267 | |||||||
chr2:203188940 | G | A | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.6823+351G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203188940 | |||||||
chr2:203189019 | A | G | 93 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(90): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.6823+430A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189019 | |||||||
chr2:203189323 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6823+734A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189323 | |||||||
chr2:203189418 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.6823+829C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189418 | |||||||
chr2:203189629 | C | T | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6824-663C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189629 | |||||||
chr2:203189676 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.6824-616C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189676 | |||||||
chr2:203189851 | A | G | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6824-441A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189851 | |||||||
chr2:203189874 | G | A | 142 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(139): Show |
142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.6824-418G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189874 | |||||||
chr2:203189899 | G | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6824-393G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189899 | |||||||
chr2:203189905 | G | T | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6824-387G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189905 | |||||||
chr2:203189930 | G | A | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6824-362G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203189930 | |||||||
chr2:203190098 | T | C | 5 | a0001c0001t0002g0131 a0005c0006t0002g0100 a0005c0006t0002g0161 others(2): Show |
5 | HG00735.hp2 HG00741.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.6824-194T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203190098 | |||||||
chr2:203190111 | G | A | 142 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(139): Show |
142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.6824-181G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203190111 | |||||||
chr2:203190150 | A | C | 1 | a0001c0001t0035g0058 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6824-142A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203190150 | |||||||
chr2:203190159 | T | TAC | 10 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(7): Show |
10 | HG02083.hp2 HG02129.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.6824-84_6824-83dup others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | T | TACAC | 4 | a0001c0001t0001g0013 a0002c0002t0003g0086 a0013c0012t0003g0077 others(1): Show |
4 | HG03130.hp2 HG03540.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.6824-86_6824-83dup others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | T | TACACAC | 3 | a0002c0002t0003g0078 a0002c0002t0003g0132 a0002c0013t0003g0076 |
3 | HG02559.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6824-88_6824-83dup others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | T | TACACACA others(5): Show |
1 | a0002c0002t0008g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6824-94_6824-83dup others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TAC | T | 10 | a0002c0002t0003g0021 a0002c0002t0003g0049 a0002c0002t0003g0050 others(7): Show |
10 | HG02109.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.6824-84_6824-83del others(2): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACAC | T | 3 | a0001c0001t0001g0002 a0001c0001t0024g0045 a0002c0002t0003g0061 |
3 | HG01884.hp2 HG01975.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.6824-86_6824-83del others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(3): Show |
T | 3 | a0001c0001t0014g0260 a0001c0008t0007g0057 a0012c0019t0003g0074 |
3 | HG02257.hp2 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6824-92_6824-83del others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(5): Show |
T | 7 | a0001c0001t0014g0019 a0001c0001t0042g0054 a0001c0008t0007g0055 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.6824-94_6824-83del others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0220 a0016c0030t0001g0246 |
2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.6824-96_6824-83del others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(9): Show |
T | 91 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(88): Show |
91 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.6824-98_6824-83del others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(11): Show |
T | 11 | a0001c0001t0001g0196 a0001c0001t0001g0204 a0001c0001t0002g0104 others(8): Show |
11 | HG00597.hp1 HG00673.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.6824-100_6824-83de others(19): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190159 | TACACACA others(13): Show |
T | 124 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(121): Show |
124 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.6824-102_6824-83de others(21): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | INFO_REALIGN_3_PRIME | chr2 | 203190159 | ||||||
chr2:203190224 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.6824-68C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 45/55 | chr2 | 203190224 | |||||||
chr2:203190490 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.6921+101C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190490 | |||||||
chr2:203190735 | C | T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6921+346C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190735 | |||||||
chr2:203190794 | C | T | 19 | a0003c0003t0004g0025 a0003c0003t0004g0026 a0003c0003t0004g0027 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+405C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190794 | |||||||
chr2:203190844 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6921+455T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190844 | |||||||
chr2:203190954 | A | G | 2 | a0002c0002t0003g0083 a0002c0002t0003g0085 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6921+565A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190954 | |||||||
chr2:203190984 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6921+595G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203190984 | |||||||
chr2:203191106 | C | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.6921+717C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191106 | |||||||
chr2:203191177 | T | C | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6921+788T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191177 | |||||||
chr2:203191319 | G | GA | 99 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(96): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.6921+946dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203191319 | ||||||
chr2:203191406 | A | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6921+1017A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191406 | |||||||
chr2:203191765 | T | C | 8 | a0001c0001t0006g0227 a0001c0001t0006g0229 a0001c0001t0006g0232 others(5): Show |
8 | HG00642.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.6921+1376T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191765 | |||||||
chr2:203191788 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6921+1399G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191788 | |||||||
chr2:203191790 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6921+1401C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191790 | |||||||
chr2:203191924 | C | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.6921+1535C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191924 | |||||||
chr2:203191955 | T | C | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.6921+1566T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203191955 | |||||||
chr2:203192152 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.6922-1643A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192152 | |||||||
chr2:203192299 | G | T | 1 | a0001c0001t0038g0272 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6922-1496G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192299 | |||||||
chr2:203192351 | T | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6922-1444T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192351 | |||||||
chr2:203192382 | A | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(251): Show |
254 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.6922-1413A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192382 | |||||||
chr2:203192385 | AT | A | 47 | a0001c0001t0001g0234 a0001c0001t0002g0135 a0001c0001t0004g0080 others(44): Show |
47 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.6922-1394delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203192385 | ||||||
chr2:203192487 | C | T | 1 | a0010c0016t0023g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6922-1308C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192487 | |||||||
chr2:203192625 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6922-1170A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192625 | |||||||
chr2:203192640 | C | G | 1 | a0003c0011t0011g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6922-1155C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192640 | |||||||
chr2:203192716 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6922-1079T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192716 | |||||||
chr2:203192878 | G | T | 142 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(139): Show |
142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.6922-917G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192878 | |||||||
chr2:203192951 | T | C | 6 | a0002c0002t0003g0078 a0002c0002t0003g0081 a0002c0002t0003g0132 others(3): Show |
6 | HG02293.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.6922-844T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192951 | |||||||
chr2:203192963 | C | CT | 13 | a0001c0001t0002g0092 a0001c0001t0002g0114 a0001c0001t0002g0118 others(10): Show |
13 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.6922-806dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203192963 | ||||||
chr2:203192963 | CT | C | 7 | a0001c0001t0002g0079 a0001c0001t0002g0091 a0001c0001t0002g0120 others(4): Show |
7 | HG01167.hp1 HG01256.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.6922-806delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203192963 | ||||||
chr2:203192964 | T | TTTC | 6 | a0001c0001t0001g0211 a0001c0001t0001g0225 a0001c0001t0001g0253 others(3): Show |
6 | HG02080.hp1 HG02165.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6922-829_6922-828i others(5): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203192964 | ||||||
chr2:203192965 | T | C | 10 | a0001c0001t0005g0283 a0001c0001t0019g0279 a0001c0001t0019g0280 others(7): Show |
10 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.6922-830T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192965 | |||||||
chr2:203192965 | T | TTC | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
93 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.6922-829_6922-828i others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | INFO_REALIGN_3_PRIME | chr2 | 203192965 | ||||||
chr2:203192966 | T | C | 2 | a0001c0001t0005g0277 a0001c0004t0005g0278 |
2 | HG01167.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.6922-829T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192966 | |||||||
chr2:203192966 | T | TC | 6 | a0001c0001t0001g0193 a0001c0001t0001g0206 a0001c0001t0001g0235 others(3): Show |
6 | HG01975.hp1 HG02055.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.6922-829_6922-828i others(3): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192966 | |||||||
chr2:203192972 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6922-823T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192972 | |||||||
chr2:203192992 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.6922-803G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203192992 | |||||||
chr2:203193152 | A | T | 1 | a0001c0001t0016g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6922-643A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203193152 | |||||||
chr2:203193206 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6922-589A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203193206 | |||||||
chr2:203193387 | G | C | 2 | a0002c0002t0003g0065 a0002c0002t0027g0094 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.6922-408G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 46/55 | chr2 | 203193387 | |||||||
chr2:203194265 | G | T | 1 | a0001c0001t0034g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7038+354G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203194265 | |||||||
chr2:203194566 | TAATAACT others(11): Show |
T | 4 | a0003c0003t0004g0029 a0003c0003t0004g0032 a0003c0003t0004g0033 others(1): Show |
4 | HG02572.hp1 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.7038+656_7038+673d others(20): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203194566 | |||||||
chr2:203194737 | A | C | 1 | a0021c0027t0029g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.7038+826A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203194737 | |||||||
chr2:203194809 | C | T | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7038+898C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203194809 | |||||||
chr2:203195054 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.7038+1143A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195054 | |||||||
chr2:203195156 | T | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.7038+1245T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195156 | |||||||
chr2:203195159 | A | T | 2 | a0002c0002t0003g0062 a0002c0002t0003g0063 |
2 | NA18988.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.7038+1248A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195159 | |||||||
chr2:203195168 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7038+1257G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195168 | |||||||
chr2:203195425 | G | T | 143 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(140): Show |
143 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.7038+1514G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195425 | |||||||
chr2:203195585 | G | A | 2 | a0001c0008t0007g0055 a0001c0008t0007g0057 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.7038+1674G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195585 | |||||||
chr2:203195957 | A | G | 2 | a0001c0001t0001g0051 a0001c0004t0005g0273 |
2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.7039-1345A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203195957 | |||||||
chr2:203196112 | CCATAATC others(7): Show |
C | 1 | a0002c0002t0003g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.7039-1186_7039-117 others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | INFO_REALIGN_3_PRIME | chr2 | 203196112 | ||||||
chr2:203196166 | A | G | 134 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(131): Show |
134 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.7039-1136A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196166 | |||||||
chr2:203196186 | T | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7039-1116T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196186 | |||||||
chr2:203196209 | G | C | 5 | a0003c0003t0004g0027 a0003c0003t0004g0030 a0003c0003t0004g0034 others(2): Show |
5 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.7039-1093G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196209 | |||||||
chr2:203196252 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7039-1050C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196252 | |||||||
chr2:203196499 | T | G | 2 | a0001c0008t0007g0056 a0011c0025t0007g0053 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7039-803T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196499 | |||||||
chr2:203196521 | T | G | 1 | a0001c0004t0005g0278 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.7039-781T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196521 | |||||||
chr2:203196973 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7039-329G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203196973 | |||||||
chr2:203197115 | A | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7039-187A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203197115 | |||||||
chr2:203197234 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG00673.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.7039-68C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 47/55 | chr2 | 203197234 | |||||||
chr2:203197501 | G | A | 1 | a0001c0001t0004g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7128+110G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203197501 | |||||||
chr2:203197521 | C | T | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7128+130C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203197521 | |||||||
chr2:203197606 | T | C | 97 | a0001c0001t0002g0059 a0001c0001t0002g0079 a0001c0001t0002g0087 others(94): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.7128+215T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203197606 | |||||||
chr2:203197722 | A | T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7128+331A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203197722 | |||||||
chr2:203197751 | T | C | 2 | a0001c0001t0015g0129 a0001c0001t0015g0130 |
2 | HG00733.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7128+360T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203197751 | |||||||
chr2:203198005 | A | T | 11 | a0001c0001t0005g0283 a0001c0001t0019g0279 a0001c0001t0019g0280 others(8): Show |
11 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.7128+614A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198005 | |||||||
chr2:203198007 | T | A | 142 | a0001c0001t0001g0188 a0001c0001t0001g0214 a0001c0001t0001g0219 others(139): Show |
142 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.7128+616T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198007 | |||||||
chr2:203198020 | C | CT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.7128+646dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | INFO_REALIGN_3_PRIME | chr2 | 203198020 | ||||||
chr2:203198283 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7128+892C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198283 | |||||||
chr2:203198549 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.7129-789G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198549 | |||||||
chr2:203198582 | T | A | 2 | a0001c0001t0013g0251 a0001c0001t0013g0257 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7129-756T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198582 | |||||||
chr2:203198627 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.7129-711G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198627 | |||||||
chr2:203198847 | ACT | A | 4 | a0001c0001t0001g0220 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01081.hp1 NA18970.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.7129-488_7129-487d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | INFO_REALIGN_3_PRIME | chr2 | 203198847 | ||||||
chr2:203198856 | CA | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(11): Show |
14 | HG00408.hp2 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.7129-465delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | INFO_REALIGN_3_PRIME | chr2 | 203198856 | ||||||
chr2:203198925 | C | T | 92 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 others(89): Show |
92 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.7129-413C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198925 | |||||||
chr2:203198978 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7129-360G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 48/55 | chr2 | 203198978 | |||||||
chr2:203199544 | A | AT | 10 | a0001c0001t0002g0059 a0001c0001t0002g0090 a0001c0001t0002g0091 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.7238+115dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | INFO_REALIGN_3_PRIME | chr2 | 203199544 | ||||||
chr2:203199544 | AT | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0193 others(16): Show |
19 | HG01099.hp2 HG01168.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.7238+115delT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | INFO_REALIGN_3_PRIME | chr2 | 203199544 | ||||||
chr2:203199759 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.7238+312G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203199759 | |||||||
chr2:203200116 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.7238+669C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203200116 | |||||||
chr2:203200203 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7238+756C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203200203 | |||||||
chr2:203200353 | A | C | 16 | a0001c0001t0004g0080 a0003c0003t0004g0025 a0003c0003t0004g0026 others(13): Show |
16 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.7238+906A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203200353 | |||||||
chr2:203200930 | A | G | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7239-613A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203200930 | |||||||
chr2:203201122 | A | G | 2 | a0001c0008t0007g0055 a0001c0008t0007g0057 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.7239-421A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203201122 | |||||||
chr2:203201533 | G | A | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7239-10G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 49/55 | chr2 | 203201533 | |||||||
chr2:203201948 | G | A | 5 | a0001c0001t0001g0212 a0001c0001t0001g0221 a0001c0001t0001g0222 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.7411+233G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203201948 | |||||||
chr2:203202121 | T | C | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7411+406T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203202121 | |||||||
chr2:203202545 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.7412-142A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203202545 | |||||||
chr2:203202640 | T | G | 18 | a0001c0001t0002g0098 a0001c0001t0002g0107 a0001c0001t0002g0112 others(15): Show |
18 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.7412-47T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203202640 | |||||||
chr2:203202660 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7412-27C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203202660 | |||||||
chr2:203202680 | C | A | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.7412-7C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 50/55 | chr2 | 203202680 | |||||||
chr2:203203186 | T | C | 1 | a0003c0003t0004g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7506+405T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203186 | |||||||
chr2:203203235 | G | A | 1 | a0003c0003t0004g0031 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7506+454G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203235 | |||||||
chr2:203203307 | A | AT | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(237): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.7506+536dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | INFO_REALIGN_3_PRIME | chr2 | 203203307 | ||||||
chr2:203203307 | A | ATT | 7 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0199 others(4): Show |
7 | HG00741.hp1 HG01256.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.7506+535_7506+536d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | INFO_REALIGN_3_PRIME | chr2 | 203203307 | ||||||
chr2:203203320 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.7506+539T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203320 | |||||||
chr2:203203470 | C | T | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7506+689C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203470 | |||||||
chr2:203203612 | G | A | 3 | a0001c0001t0035g0058 a0002c0002t0026g0075 a0012c0019t0003g0074 |
3 | HG02257.hp2 HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7506+831G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203612 | |||||||
chr2:203203825 | A | G | 1 | a0007c0010t0046g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.7506+1044A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203825 | |||||||
chr2:203203886 | T | C | 3 | a0007c0010t0017g0018 a0007c0010t0046g0023 a0014c0015t0017g0017 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7506+1105T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203886 | |||||||
chr2:203203915 | G | GT | 3 | a0001c0001t0001g0234 a0001c0001t0001g0238 a0001c0001t0001g0253 |
3 | HG04228.hp2 NA19003.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.7506+1135dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | INFO_REALIGN_3_PRIME | chr2 | 203203915 | ||||||
chr2:203203917 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.7506+1136G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203917 | |||||||
chr2:203203918 | T | G | 1 | a0002c0002t0003g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.7506+1137T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203918 | |||||||
chr2:203203970 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.7506+1189C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203970 | |||||||
chr2:203203971 | C | T | 2 | a0002c0002t0003g0065 a0002c0002t0027g0094 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.7506+1190C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203971 | |||||||
chr2:203203974 | G | C | 2 | a0002c0002t0003g0065 a0002c0002t0027g0094 |
2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.7506+1193G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203203974 | |||||||
chr2:203204074 | G | A | 1 | a0003c0003t0004g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7506+1293G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204074 | |||||||
chr2:203204244 | T | A | 3 | a0001c0001t0005g0277 a0003c0011t0011g0024 a0003c0011t0011g0043 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7506+1463T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204244 | |||||||
chr2:203204245 | A | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0230 others(6): Show |
9 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.7506+1464A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204245 | |||||||
chr2:203204322 | T | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA18946.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.7506+1541T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204322 | |||||||
chr2:203204324 | G | GT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0210 others(9): Show |
12 | HG00423.hp2 HG01081.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.7506+1561dupT | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | INFO_REALIGN_3_PRIME | chr2 | 203204324 | ||||||
chr2:203204324 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0235 |
2 | HG03834.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.7506+1543G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204324 | |||||||
chr2:203204421 | C | T | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7506+1640C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204421 | |||||||
chr2:203204620 | G | A | 1 | a0002c0002t0003g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7506+1839G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204620 | |||||||
chr2:203204678 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.7506+1897G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204678 | |||||||
chr2:203204883 | T | C | 19 | a0001c0001t0004g0080 a0003c0003t0004g0025 a0003c0003t0004g0026 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.7506+2102T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203204883 | |||||||
chr2:203205032 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7506+2251G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203205032 | |||||||
chr2:203205750 | TCTTTACC others(15): Show |
T | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7507-2886_7507-286 others(26): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203205750 | |||||||
chr2:203205764 | A | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.7507-2873A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203205764 | |||||||
chr2:203205780 | T | C | 1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.7507-2857T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203205780 | |||||||
chr2:203206233 | A | G | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.7507-2404A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206233 | |||||||
chr2:203206604 | GAAC | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.7507-2031_7507-202 others(7): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | INFO_REALIGN_3_PRIME | chr2 | 203206604 | ||||||
chr2:203206708 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7507-1929C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206708 | |||||||
chr2:203206709 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7507-1928C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206709 | |||||||
chr2:203206743 | T | G | 19 | a0001c0001t0004g0080 a0003c0003t0004g0025 a0003c0003t0004g0026 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.7507-1894T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206743 | |||||||
chr2:203206812 | C | T | 3 | a0007c0010t0017g0018 a0007c0010t0046g0023 a0014c0015t0017g0017 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7507-1825C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206812 | |||||||
chr2:203206835 | C | T | 120 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(117): Show |
120 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.7507-1802C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206835 | |||||||
chr2:203206887 | A | G | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.7507-1750A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206887 | |||||||
chr2:203206901 | C | G | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7507-1736C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206901 | |||||||
chr2:203206961 | A | T | 1 | a0001c0001t0020g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7507-1676A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206961 | |||||||
chr2:203206998 | C | A | 1 | a0001c0001t0020g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7507-1639C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203206998 | |||||||
chr2:203207004 | A | G | 1 | a0001c0001t0020g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7507-1633A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207004 | |||||||
chr2:203207025 | T | C | 1 | a0001c0001t0020g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7507-1612T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207025 | |||||||
chr2:203207028 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7507-1609G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207028 | |||||||
chr2:203207039 | A | G | 1 | a0001c0001t0020g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7507-1598A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207039 | |||||||
chr2:203207104 | G | A | 2 | a0001c0008t0007g0055 a0001c0008t0007g0057 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.7507-1533G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207104 | |||||||
chr2:203207170 | C | A | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.7507-1467C>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207170 | |||||||
chr2:203207176 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.7507-1461C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207176 | |||||||
chr2:203207187 | C | T | 1 | a0001c0008t0007g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7507-1450C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207187 | |||||||
chr2:203207220 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
249 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.7507-1417T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207220 | |||||||
chr2:203207251 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.7507-1386A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207251 | |||||||
chr2:203207267 | C | G | 114 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(111): Show |
114 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.7507-1370C>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207267 | |||||||
chr2:203207297 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.7507-1340A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207297 | |||||||
chr2:203207340 | G | A | 1 | a0007c0010t0017g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7507-1297G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207340 | |||||||
chr2:203207454 | T | C | 1 | a0001c0001t0006g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7507-1183T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207454 | |||||||
chr2:203207580 | C | T | 1 | a0003c0011t0011g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7507-1057C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207580 | |||||||
chr2:203207640 | C | T | 1 | a0001c0001t0005g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.7507-997C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207640 | |||||||
chr2:203207775 | C | T | 2 | a0002c0002t0026g0075 a0012c0019t0003g0074 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7507-862C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207775 | |||||||
chr2:203207784 | G | A | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7507-853G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203207784 | |||||||
chr2:203208111 | C | T | 1 | a0001c0029t0002g0159 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.7507-526C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208111 | |||||||
chr2:203208148 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.7507-489G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208148 | |||||||
chr2:203208237 | G | A | 1 | a0001c0001t0014g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7507-400G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208237 | |||||||
chr2:203208306 | A | G | 3 | a0007c0010t0017g0018 a0007c0010t0046g0023 a0014c0015t0017g0017 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7507-331A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208306 | |||||||
chr2:203208449 | T | G | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7507-188T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208449 | |||||||
chr2:203208497 | G | A | 1 | a0002c0002t0003g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7507-140G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 51/55 | chr2 | 203208497 | |||||||
chr2:203208811 | C | T | 1 | a0001c0001t0030g0231 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.7623+58C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 52/55 | chr2 | 203208811 | |||||||
chr2:203209007 | G | C | 4 | a0003c0003t0004g0028 a0003c0003t0004g0036 a0003c0003t0004g0040 others(1): Show |
4 | HG01884.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.7624-154G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 52/55 | chr2 | 203209007 | |||||||
chr2:203209096 | C | T | 1 | a0001c0001t0042g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7624-65C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 52/55 | chr2 | 203209096 | |||||||
chr2:203209355 | C | T | 1 | a0013c0012t0003g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7785+33C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209355 | |||||||
chr2:203209356 | C | T | 2 | a0001c0001t0014g0019 a0001c0001t0014g0260 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.7785+34C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209356 | |||||||
chr2:203209380 | A | G | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7785+58A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209380 | |||||||
chr2:203209494 | C | T | 4 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0008t0007g0056 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7785+172C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209494 | |||||||
chr2:203209500 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.7785+178C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209500 | |||||||
chr2:203209563 | T | C | 1 | a0002c0002t0003g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7785+241T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209563 | |||||||
chr2:203209711 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7785+390_7785+391i others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209711 | ||||||
chr2:203209713 | A | ATG | 17 | a0001c0001t0002g0099 a0001c0001t0002g0151 a0002c0002t0003g0049 others(14): Show |
17 | HG02109.hp1 HG02129.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.7785+423_7785+424d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTG | 30 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0236 others(27): Show |
30 | HG00408.hp2 HG00438.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.7785+419_7785+424d others(8): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(1): Show |
41 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(38): Show |
41 | HG00323.hp1 HG00609.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.7785+417_7785+424d others(10): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(3): Show |
92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
92 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.7785+415_7785+424d others(12): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(5): Show |
53 | a0001c0001t0001g0002 a0001c0001t0001g0206 a0001c0001t0001g0210 others(50): Show |
53 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.7785+413_7785+424d others(14): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(7): Show |
15 | a0001c0001t0001g0239 a0001c0001t0002g0098 a0001c0001t0002g0111 others(12): Show |
15 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.7785+411_7785+424d others(16): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(9): Show |
8 | a0001c0001t0002g0107 a0001c0001t0002g0119 a0001c0001t0002g0140 others(5): Show |
8 | HG00408.hp1 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.7785+409_7785+424d others(18): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(13): Show |
3 | a0001c0001t0001g0249 a0001c0001t0042g0054 a0001c0008t0007g0055 |
3 | HG02451.hp1 HG02976.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.7785+405_7785+424d others(22): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | ATGTGTGT others(15): Show |
1 | a0001c0008t0007g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7785+403_7785+424d others(24): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203209713 | ||||||
chr2:203209713 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7785+391A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203209713 | |||||||
chr2:203210136 | G | A | 1 | a0001c0001t0036g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.7785+814G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210136 | |||||||
chr2:203210362 | C | CA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
115 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.7786-579dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203210362 | ||||||
chr2:203210362 | C | CAA | 10 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0210 others(7): Show |
10 | HG00423.hp2 HG02135.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.7786-580_7786-579d others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | INFO_REALIGN_3_PRIME | chr2 | 203210362 | ||||||
chr2:203210379 | A | AAG | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(3): Show |
6 | HG00408.hp2 HG02083.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.7786-579_7786-578i others(4): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210379 | |||||||
chr2:203210474 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.7786-484A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210474 | |||||||
chr2:203210624 | A | G | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7786-334A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210624 | |||||||
chr2:203210778 | G | A | 3 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 |
3 | HG01257.hp1 HG01952.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.7786-180G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210778 | |||||||
chr2:203210785 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.7786-173G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210785 | |||||||
chr2:203210933 | T | G | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7786-25T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 53/55 | chr2 | 203210933 | |||||||
chr2:203211168 | T | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7934+62T>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211168 | |||||||
chr2:203211271 | G | A | 1 | a0001c0001t0025g0016 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7934+165G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211271 | |||||||
chr2:203211373 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.7934+267A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211373 | |||||||
chr2:203211373 | A | T | 2 | a0007c0010t0017g0018 a0014c0015t0017g0017 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.7934+267A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211373 | |||||||
chr2:203211644 | A | G | 1 | a0002c0002t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7934+538A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211644 | |||||||
chr2:203211924 | G | C | 5 | a0002c0002t0003g0046 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.7934+818G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211924 | |||||||
chr2:203211956 | T | G | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7934+850T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203211956 | |||||||
chr2:203212023 | A | C | 2 | a0003c0011t0011g0024 a0003c0011t0011g0043 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7934+917A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203212023 | |||||||
chr2:203212606 | C | CA | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(33): Show |
36 | HG00408.hp2 HG00642.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.7935-895dupA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | INFO_REALIGN_3_PRIME | chr2 | 203212606 | ||||||
chr2:203212606 | CA | C | 16 | a0001c0001t0001g0185 a0001c0001t0002g0110 a0001c0001t0005g0277 others(13): Show |
16 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.7935-895delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | INFO_REALIGN_3_PRIME | chr2 | 203212606 | ||||||
chr2:203212707 | G | A | 1 | a0002c0002t0003g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.7935-811G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203212707 | |||||||
chr2:203213108 | G | T | 1 | a0002c0002t0008g0088 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7935-410G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 54/55 | chr2 | 203213108 | |||||||
chr2:203214372 | A | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.8070+719A>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203214372 | |||||||
chr2:203214550 | G | C | 2 | a0001c0008t0007g0055 a0001c0008t0007g0057 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.8070+897G>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203214550 | |||||||
chr2:203214590 | C | T | 126 | a0001c0001t0002g0079 a0001c0001t0002g0087 a0001c0001t0002g0089 others(123): Show |
126 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.8070+937C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203214590 | |||||||
chr2:203214723 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8070+1070G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203214723 | |||||||
chr2:203215133 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8070+1480G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215133 | |||||||
chr2:203215139 | T | C | 1 | a0001c0001t0024g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.8070+1486T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215139 | |||||||
chr2:203215165 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.8070+1512A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215165 | |||||||
chr2:203215276 | G | A | 1 | a0001c0001t0004g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8070+1623G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215276 | |||||||
chr2:203215352 | A | T | 7 | a0001c0001t0014g0019 a0001c0001t0014g0260 a0001c0001t0042g0054 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.8070+1699A>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215352 | |||||||
chr2:203215861 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.8071-1392A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215861 | |||||||
chr2:203215877 | G | T | 6 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0121 others(3): Show |
6 | NA18940.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.8071-1376G>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203215877 | |||||||
chr2:203216009 | TA | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
174 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.8071-1225delA | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | INFO_REALIGN_3_PRIME | chr2 | 203216009 | ||||||
chr2:203216009 | TAA | T | 108 | a0001c0001t0001g0186 a0001c0001t0001g0265 a0001c0001t0002g0059 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.8071-1226_8071-122 others(6): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | INFO_REALIGN_3_PRIME | chr2 | 203216009 | ||||||
chr2:203216119 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.8071-1134A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216119 | |||||||
chr2:203216293 | T | C | 1 | a0001c0001t0006g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.8071-960T>C | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216293 | |||||||
chr2:203216352 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.8071-901T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216352 | |||||||
chr2:203216377 | T | G | 1 | a0004c0005t0009g0170 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.8071-876T>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216377 | |||||||
chr2:203216588 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.8071-665A>G | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216588 | |||||||
chr2:203216952 | C | T | 13 | a0001c0001t0005g0277 a0001c0001t0005g0283 a0001c0001t0019g0279 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.8071-301C>T | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216952 | |||||||
chr2:203216953 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.8071-300G>A | NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 55/55 | chr2 | 203216953 |