Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4925 |
| ensemblid | ENSG00000070081.18 |
| hgncid | 8044 |
| symbol | NUCB2 |
| name | nucleobindin 2 |
| refseq_nuc | NM_005013.4 |
| refseq_prot | NP_005004.1 |
| ensembl_nuc | ENST00000529010.6 |
| ensembl_prot | ENSP00000436455.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 17276739 |
| end | 17332211 |
| strand | + |
| ver | v1.2 |
| region | chr11:17276739-17332211 |
| region5000 | chr11:17271739-17337211 |
| regionname0 | NUCB2_chr11_17276739_17332211 |
| regionname5000 | NUCB2_chr11_17271739_17337211 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 420 | 165 | 62 | 40 | 39 | 4 | 18 | 35 | NUCB2_chr11_17271739_17337211 | NUCB2 | MRWRT others(415): Show |
chr11 | 17271739 | 17337211 |
| a0002 | 0/0 | 419 | 100 | 8 | 13 | 71 | 2 | 6 | 54 | NUCB2_chr11_17271739_17337211 | NUCB2 | MRWRT others(414): Show |
chr11 | 17271739 | 17337211 |
| a0003 | 0/0 | 420 | 92 | 0 | 19 | 59 | 2 | 12 | 44 | NUCB2_chr11_17271739_17337211 | NUCB2 | MRWRT others(415): Show |
chr11 | 17271739 | 17337211 |
| a0004 | 0/0 | 420 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | MRWRT others(415): Show |
chr11 | 17271739 | 17337211 |
| a0005 | 0/0 | 420 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | MRWRT others(415): Show |
chr11 | 17271739 | 17337211 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1260 | 164 | 62 | 39 | 39 | 4 | 18 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 | ||
| a0001c0009 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 | ||
| a0002c0002 | 0/0 | 1257 | 95 | 4 | 13 | 70 | 2 | 6 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1252): Show |
chr11 | 17271739 | 17337211 | ||
| a0002c0004 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1252): Show |
chr11 | 17271739 | 17337211 | ||
| a0002c0008 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1252): Show |
chr11 | 17271739 | 17337211 | ||
| a0003c0003 | 0/0 | 1260 | 91 | 0 | 19 | 58 | 2 | 12 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 | ||
| a0003c0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 | ||
| a0004c0005 | 0/0 | 1260 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 | ||
| a0005c0007 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | ATGAG others(1255): Show |
chr11 | 17271739 | 17337211 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2300 | 69 | 30 | 20 | 11 | 0 | 7 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0001c0001t0002 | 1/0 | 2300 | 92 | 31 | 17 | 28 | 4 | 11 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0001c0001t0004 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0001c0001t0006 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0001c0001t0007 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0001c0009t0002 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0002c0002t0001 | 0/0 | 2297 | 62 | 2 | 1 | 55 | 0 | 4 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2292): Show |
chr11 | 17271739 | 17337211 |
| a0002c0002t0002 | 0/0 | 2297 | 33 | 2 | 12 | 15 | 2 | 2 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2292): Show |
chr11 | 17271739 | 17337211 |
| a0002c0004t0001 | 0/0 | 2297 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2292): Show |
chr11 | 17271739 | 17337211 |
| a0002c0004t0002 | 0/0 | 2297 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2292): Show |
chr11 | 17271739 | 17337211 |
| a0002c0008t0001 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2292): Show |
chr11 | 17271739 | 17337211 |
| a0003c0003t0001 | 0/0 | 2300 | 84 | 0 | 14 | 56 | 2 | 12 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0003c0003t0003 | 0/0 | 2300 | 6 | 0 | 4 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0003c0003t0005 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0003c0006t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0004c0005t0001 | 0/0 | 2300 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| a0005c0007t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | AGAGC others(2295): Show |
chr11 | 17271739 | 17337211 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0347 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0001c0009t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0002c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0003t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0003c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0004c0005t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0004c0005t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| a0005c0007t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0100 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0085 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0218 | EUR | GBR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0076 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00642 | hp1 | a0003 | c0003 | t0003 | g0032 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | CHS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00735 | hp2 | a0001 | c0009 | t0002 | g0214 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0142 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01069 | hp1 | a0004 | c0005 | t0001 | g0331 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01071 | hp1 | a0004 | c0005 | t0001 | g0006 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0071 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0080 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0197 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0156 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0327 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0141 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0087 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0163 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0191 | EUR | IBS | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0102 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01943 | hp1 | a0003 | c0003 | t0005 | g0120 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0062 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0339 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01978 | hp2 | a0003 | c0003 | t0003 | g0318 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01993 | hp1 | a0003 | c0003 | t0003 | g0293 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0335 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0338 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0083 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0098 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0329 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0140 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0275 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02273 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02572 | hp2 | a0002 | c0004 | t0002 | g0147 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0290 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0084 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0236 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0061 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03098 | hp1 | a0002 | c0004 | t0001 | g0276 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0095 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0199 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0223 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0086 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0063 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0068 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0065 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0057 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0034 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0114 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0307 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0143 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | STU | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18941 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18967 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18993 | hp1 | a0003 | c0006 | t0001 | g0090 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18997 | hp1 | a0005 | c0007 | t0001 | g0039 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18998 | hp1 | a0002 | c0008 | t0001 | g0297 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19004 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0104 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19058 | hp1 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19059 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0108 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19091 | hp2 | a0003 | c0003 | t0003 | g0043 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | YRI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ASW | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | TSI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0196 | EUR | TSI | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0070 | SAS | GIH | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | GIH | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0158 | AMR | CLM | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | USA | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0155 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | LWK | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0347 | REF | REF | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0205 | REF | REF | NUCB2_chr11_17271739_17337211 | NUCB2 | chr11 | 17271739 | 17337211 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17310862 | A | C | 1 | a0004 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.521A>C | p.His174Pro | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 766/2300 | 521/1263 | 174/420 | chr11 | 17310862 | |||
| chr11:17310872 | T | A | 1 | a0005 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.531T>A | p.Phe177Leu | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 776/2300 | 531/1263 | 177/420 | chr11 | 17310872 | |||
| chr11:17330136 | C | G | 3 | a0003 a0004 a0005 |
95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
missense_variant | MODERATE | c.1012C>G | p.Gln338Glu | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1257/2300 | 1012/1263 | 338/420 | chr11 | 17330136 | |||
| chr11:17330930 | TACA | T | 1 | a0002 | 100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
conservative_inframe_deletion | MODERATE | c.1207_1209delCAA | p.Gln403del | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/14 | 1452/2300 | 1207/1263 | 403/420 | INFO_REALIGN_3_PRIME | chr11 | 17330930 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17295398 | G | A | 1 | a0003c0006 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.75G>A | p.Val25Val | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 3/14 | 320/2300 | 75/1263 | 25/420 | chr11 | 17295398 | |||
| chr11:17310914 | T | C | 1 | a0002c0008 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.573T>C | p.Tyr191Tyr | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/14 | 818/2300 | 573/1263 | 191/420 | chr11 | 17310914 | |||
| chr11:17330174 | T | C | 1 | a0001c0009 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1050T>C | p.Tyr350Tyr | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1295/2300 | 1050/1263 | 350/420 | chr11 | 17330174 | |||
| chr11:17330201 | T | C | 1 | a0002c0004 | 4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.1077T>C | p.Asn359Asn | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/14 | 1322/2300 | 1077/1263 | 359/420 | chr11 | 17330201 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17276768 | G | A | 1 | a0001c0001t0004 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-216G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/14 | 18556 | chr11 | 17276768 | ||||||
| chr11:17276818 | G | C | 9 | a0001c0001t0001 a0002c0002t0001 a0002c0004t0001 others(6): Show |
227 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(224): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/14 | 18506 | chr11 | 17276818 | ||||||
| chr11:17331711 | C | G | 1 | a0001c0001t0007 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 292 | chr11 | 17331711 | ||||||
| chr11:17331999 | T | G | 2 | a0003c0003t0003 a0003c0003t0005 |
7 | HG00642.hp1 HG01943.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 580 | chr11 | 17331999 | ||||||
| chr11:17332202 | G | C | 1 | a0001c0001t0006 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 14/14 | 783 | chr11 | 17332202 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:17276919 | G | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.-156+91G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17276919 | |||||||
| chr11:17276993 | G | C | 1 | a0001c0001t0002g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-156+165G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17276993 | |||||||
| chr11:17277109 | C | T | 211 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(208): Show |
215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-156+281C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277109 | |||||||
| chr11:17277131 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-156+303C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277131 | |||||||
| chr11:17277267 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-156+439A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277267 | |||||||
| chr11:17277304 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-156+476C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277304 | |||||||
| chr11:17277312 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-156+484G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277312 | |||||||
| chr11:17277407 | A | C | 1 | a0002c0002t0002g0222 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-156+579A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277407 | |||||||
| chr11:17277407 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156+579A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277407 | |||||||
| chr11:17277708 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-156+880A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277708 | |||||||
| chr11:17277843 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-156+1015T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17277843 | |||||||
| chr11:17278006 | A | G | 2 | a0002c0002t0001g0007 a0002c0002t0001g0352 |
3 | NA18949.hp1 NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-156+1178A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278006 | |||||||
| chr11:17278009 | T | C | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+1181T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278009 | |||||||
| chr11:17278094 | A | G | 1 | a0001c0001t0001g0351 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-156+1266A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278094 | |||||||
| chr11:17278107 | G | T | 246 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-156+1279G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278107 | |||||||
| chr11:17278170 | C | CT | 39 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0328 others(36): Show |
39 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-156+1365dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17278170 | ||||||
| chr11:17278170 | CT | C | 100 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0081 others(97): Show |
102 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.-156+1365delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17278170 | ||||||
| chr11:17278196 | G | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(30): Show |
35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-156+1368G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278196 | |||||||
| chr11:17278214 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156+1386C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278214 | |||||||
| chr11:17278215 | A | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-156+1387A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278215 | |||||||
| chr11:17278321 | A | T | 212 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-156+1493A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278321 | |||||||
| chr11:17278422 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-156+1594T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278422 | |||||||
| chr11:17278710 | T | C | 212 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-156+1882T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278710 | |||||||
| chr11:17278870 | G | T | 212 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-156+2042G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278870 | |||||||
| chr11:17278963 | C | T | 5 | a0003c0003t0001g0088 a0003c0003t0001g0089 a0003c0003t0001g0091 others(2): Show |
5 | NA18941.hp1 NA18955.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+2135C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17278963 | |||||||
| chr11:17279022 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-156+2194G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279022 | |||||||
| chr11:17279140 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-156+2312C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279140 | |||||||
| chr11:17279157 | A | T | 1 | a0003c0003t0001g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-156+2329A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279157 | |||||||
| chr11:17279217 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-156+2389C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279217 | |||||||
| chr11:17279297 | T | G | 109 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(106): Show |
111 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-156+2469T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279297 | |||||||
| chr11:17279303 | G | A | 5 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+2475G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279303 | |||||||
| chr11:17279371 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-156+2543C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279371 | |||||||
| chr11:17279442 | C | T | 4 | a0002c0002t0002g0210 a0002c0002t0002g0211 a0002c0002t0002g0212 others(1): Show |
4 | NA18990.hp1 NA18998.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+2614C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279442 | |||||||
| chr11:17279634 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-156+2806A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17279634 | |||||||
| chr11:17279779 | AT | A | 81 | a0001c0001t0002g0116 a0001c0001t0002g0118 a0001c0001t0002g0119 others(78): Show |
81 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-156+2975delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | ||||||
| chr11:17279779 | ATT | A | 20 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(17): Show |
20 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-156+2974_-156+297 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | ||||||
| chr11:17279779 | ATTT | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156+2973_-156+297 others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | ||||||
| chr11:17279779 | ATTTT | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0244 a0001c0001t0001g0245 others(114): Show |
120 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-156+2972_-156+297 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17279779 | ||||||
| chr11:17280031 | G | A | 1 | a0003c0003t0001g0025 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-155-2758G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280031 | |||||||
| chr11:17280106 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-155-2683T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280106 | |||||||
| chr11:17280115 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-155-2674T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280115 | |||||||
| chr11:17280133 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-155-2656A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280133 | |||||||
| chr11:17280203 | T | G | 1 | a0002c0002t0001g0315 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-2586T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280203 | |||||||
| chr11:17280362 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-2427A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280362 | |||||||
| chr11:17280499 | G | A | 5 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-2290G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280499 | |||||||
| chr11:17280683 | A | G | 2 | a0002c0002t0001g0314 a0002c0002t0001g0350 |
2 | HG02135.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-155-2106A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280683 | |||||||
| chr11:17280752 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-2037C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280752 | |||||||
| chr11:17280761 | C | T | 4 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 others(1): Show |
4 | HG01109.hp1 HG01255.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-2028C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280761 | |||||||
| chr11:17280911 | C | T | 1 | a0003c0003t0001g0112 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-155-1878C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280911 | |||||||
| chr11:17280946 | C | T | 1 | a0002c0002t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-155-1843C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17280946 | |||||||
| chr11:17281002 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-155-1787A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281002 | |||||||
| chr11:17281047 | C | A | 1 | a0002c0002t0001g0315 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-1742C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281047 | |||||||
| chr11:17281048 | A | C | 1 | a0002c0002t0001g0315 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-1741A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281048 | |||||||
| chr11:17281140 | A | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-1649A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281140 | |||||||
| chr11:17281559 | T | A | 1 | a0002c0002t0001g0349 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-155-1230T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281559 | |||||||
| chr11:17281651 | AG | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
33 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-155-1137delG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281651 | |||||||
| chr11:17281858 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-931T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281858 | |||||||
| chr11:17281868 | A | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG01433.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-155-921A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281868 | |||||||
| chr11:17281996 | G | C | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-793G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17281996 | |||||||
| chr11:17282210 | A | G | 1 | a0002c0002t0001g0242 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-155-579A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282210 | |||||||
| chr11:17282214 | CTA | C | 118 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(115): Show |
120 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-155-571_-155-570d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282214 | ||||||
| chr11:17282216 | A | ATC | 86 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-155-572_-155-571i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282216 | ||||||
| chr11:17282216 | A | ATCTATC | 12 | a0001c0001t0001g0111 a0002c0002t0001g0031 a0003c0003t0001g0003 others(9): Show |
12 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-572_-155-571i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282216 | ||||||
| chr11:17282234 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0321 |
3 | HG02922.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-155-555A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282234 | |||||||
| chr11:17282236 | C | A | 1 | a0001c0001t0002g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-155-553C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282236 | |||||||
| chr11:17282236 | C | CTA | 21 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0129 others(18): Show |
21 | HG00741.hp2 HG01109.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.-155-531_-155-530d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | ||||||
| chr11:17282236 | C | CTATCTA | 17 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0177 others(14): Show |
17 | HG00621.hp1 HG00738.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-550_-155-549i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | ||||||
| chr11:17282236 | C | CTATCTAT others(3): Show |
1 | a0001c0001t0002g0207 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | ||||||
| chr11:17282236 | C | CTATCTAT others(3): Show |
1 | a0002c0002t0002g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | ||||||
| chr11:17282236 | CTA | C | 7 | a0001c0001t0001g0353 a0001c0001t0002g0194 a0002c0002t0001g0029 others(4): Show |
7 | HG01168.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-531_-155-530d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282236 | ||||||
| chr11:17282238 | A | ATC | 75 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0002g0130 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-155-550_-155-549i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | ||||||
| chr11:17282238 | A | ATCTATCT others(3): Show |
1 | a0002c0004t0002g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | ||||||
| chr11:17282238 | A | ATCTATCT others(7): Show |
1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-550_-155-549i others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | ||||||
| chr11:17282238 | A | ATCTATCT others(15): Show |
1 | a0001c0001t0001g0021 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-155-550_-155-549i others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282238 | ||||||
| chr11:17282238 | A | G | 113 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 others(110): Show |
115 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.-155-551A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282238 | |||||||
| chr11:17282240 | A | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(169): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.-155-549A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282240 | |||||||
| chr11:17282240 | A | G | 1 | a0001c0001t0001g0353 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-155-549A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282240 | |||||||
| chr11:17282242 | A | C | 74 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0067 others(71): Show |
74 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.-155-547A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282242 | |||||||
| chr11:17282242 | A | G | 13 | a0001c0001t0001g0111 a0001c0001t0001g0243 a0001c0001t0001g0345 others(10): Show |
14 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-155-547A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282242 | |||||||
| chr11:17282244 | A | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
61 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-155-545A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282244 | |||||||
| chr11:17282244 | A | G | 70 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0002c0002t0001g0023 others(67): Show |
70 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-155-545A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282244 | |||||||
| chr11:17282246 | A | ATCTGTC | 13 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0002c0002t0001g0031 others(10): Show |
13 | HG00408.hp2 HG00642.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-542_-155-541i others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282246 | ||||||
| chr11:17282246 | A | C | 73 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0067 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-155-543A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282246 | |||||||
| chr11:17282246 | A | G | 1 | a0003c0003t0001g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-155-543A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282246 | |||||||
| chr11:17282248 | A | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
34 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-155-541A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282248 | |||||||
| chr11:17282250 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0007g0223 |
2 | HG02293.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-155-539A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282250 | |||||||
| chr11:17282252 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
33 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-155-537A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282252 | |||||||
| chr11:17282254 | A | T | 1 | a0001c0001t0002g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-535A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282254 | |||||||
| chr11:17282254 | ATATAT | A | 20 | a0001c0001t0001g0259 a0001c0001t0001g0262 a0001c0001t0001g0264 others(17): Show |
20 | HG00544.hp1 HG01081.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-155-533_-155-529d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282254 | ||||||
| chr11:17282256 | A | ATT | 9 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-532_-155-531i others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | ||||||
| chr11:17282256 | A | ATTT | 8 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0173 others(5): Show |
8 | HG02027.hp1 HG02896.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-532_-155-531i others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | ||||||
| chr11:17282256 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
33 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-155-533A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282256 | |||||||
| chr11:17282256 | A | T | 4 | a0001c0001t0002g0151 a0001c0001t0002g0194 a0002c0002t0002g0222 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-533A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282256 | |||||||
| chr11:17282256 | ATATT | A | 8 | a0001c0001t0001g0341 a0002c0002t0001g0332 a0002c0002t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-531_-155-528d others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | ||||||
| chr11:17282256 | ATATTT | A | 64 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(61): Show |
66 | HG00423.hp1 HG00673.hp1 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.-155-531_-155-527d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282256 | ||||||
| chr11:17282258 | A | ATT | 16 | a0001c0001t0002g0116 a0001c0001t0002g0146 a0001c0001t0002g0150 others(13): Show |
16 | HG00597.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-155-517_-155-516d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | ||||||
| chr11:17282258 | A | T | 32 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(29): Show |
32 | HG00140.hp2 HG00738.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-155-531A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282258 | |||||||
| chr11:17282258 | AT | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0111 a0001c0001t0001g0345 others(9): Show |
12 | HG00544.hp2 HG01074.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-155-516delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | ||||||
| chr11:17282258 | ATTTTT | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0321 a0002c0002t0001g0299 others(6): Show |
10 | HG00408.hp1 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-155-520_-155-516d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr11 | 17282258 | ||||||
| chr11:17282259 | T | TA | 3 | a0001c0001t0007g0223 a0003c0003t0001g0030 a0003c0003t0001g0048 |
3 | HG02129.hp1 HG03486.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282259 | T | TCTATATA others(2): Show |
7 | a0001c0001t0001g0013 a0001c0001t0002g0008 a0001c0001t0002g0224 others(4): Show |
7 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-530_-155-529i others(11): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282259 | T | TCTATCTA others(6): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-155-530_-155-529i others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282259 | T | TCTATCTA others(6): Show |
2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282259 | T | TCTATCTA others(10): Show |
3 | a0001c0001t0001g0020 a0001c0001t0002g0230 a0001c0001t0002g0231 |
3 | HG02273.hp2 NA18961.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-155-530_-155-529i others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282259 | T | TCTATCTA others(10): Show |
1 | a0001c0001t0002g0234 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-155-530_-155-529i others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282259 | |||||||
| chr11:17282260 | T | A | 31 | a0001c0001t0002g0134 a0002c0002t0001g0023 a0002c0002t0001g0024 others(28): Show |
31 | HG00642.hp1 HG00673.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.-155-529T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282260 | |||||||
| chr11:17282261 | T | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
42 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-155-528T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282261 | |||||||
| chr11:17282262 | T | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0322 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-155-527T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282262 | |||||||
| chr11:17282263 | T | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(31): Show |
36 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-526T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282263 | |||||||
| chr11:17282273 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-155-516T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282273 | |||||||
| chr11:17282419 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-370C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282419 | |||||||
| chr11:17282541 | A | G | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-155-248A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282541 | |||||||
| chr11:17282557 | G | A | 6 | a0003c0003t0001g0049 a0003c0003t0001g0050 a0003c0003t0001g0051 others(3): Show |
6 | HG00423.hp2 HG00621.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-232G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282557 | |||||||
| chr11:17282579 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-155-210G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282579 | |||||||
| chr11:17282592 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-155-197G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282592 | |||||||
| chr11:17282770 | T | A | 1 | a0002c0002t0001g0315 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-19T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282770 | |||||||
| chr11:17282770 | T | C | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-155-19T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282770 | |||||||
| chr11:17282771 | A | T | 1 | a0002c0002t0001g0315 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-155-18A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 1/13 | chr11 | 17282771 | |||||||
| chr11:17283055 | T | TG | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0004g0010 |
3 | HG00642.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-1+113dupG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17283055 | ||||||
| chr11:17283096 | A | T | 1 | a0002c0002t0001g0312 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-1+153A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283096 | |||||||
| chr11:17283207 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-1+264A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283207 | |||||||
| chr11:17283256 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-1+313A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283256 | |||||||
| chr11:17283369 | T | C | 1 | a0002c0002t0001g0249 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-1+426T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283369 | |||||||
| chr11:17283723 | C | T | 92 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0081 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+780C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283723 | |||||||
| chr11:17283747 | T | G | 212 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-1+804T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283747 | |||||||
| chr11:17283770 | T | A | 92 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0081 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+827T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283770 | |||||||
| chr11:17283830 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+887A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17283830 | |||||||
| chr11:17284053 | G | A | 212 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-1+1110G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284053 | |||||||
| chr11:17284067 | C | G | 1 | a0001c0001t0002g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1+1124C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284067 | |||||||
| chr11:17284085 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-1+1142A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284085 | |||||||
| chr11:17284103 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-1+1160T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284103 | |||||||
| chr11:17284284 | A | C | 213 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1+1341A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284284 | |||||||
| chr11:17284307 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1+1364C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284307 | |||||||
| chr11:17284451 | T | A | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+1508T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284451 | |||||||
| chr11:17284706 | A | AGTTTT | 213 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-1+1764_-1+1768dup others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17284706 | ||||||
| chr11:17284767 | C | G | 1 | a0001c0001t0002g0175 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-1+1824C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284767 | |||||||
| chr11:17284863 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+1920A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284863 | |||||||
| chr11:17284872 | CTTCCTCA others(690): Show |
C | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+1930_-1+2626del | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284872 | |||||||
| chr11:17284911 | T | A | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+1968T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17284911 | |||||||
| chr11:17285014 | AATAC | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0111 others(221): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.-1+2096_-1+2099del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285014 | ||||||
| chr11:17285107 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1+2164G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285107 | |||||||
| chr11:17285165 | T | C | 10 | a0001c0001t0007g0223 a0003c0003t0001g0026 a0003c0003t0001g0045 others(7): Show |
10 | HG00673.hp2 HG02129.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+2222T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285165 | |||||||
| chr11:17285166 | G | A | 9 | a0003c0003t0001g0026 a0003c0003t0001g0045 a0003c0003t0001g0048 others(6): Show |
9 | HG00673.hp2 HG02129.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+2223G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285166 | |||||||
| chr11:17285194 | A | G | 1 | a0003c0003t0001g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-1+2251A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285194 | |||||||
| chr11:17285203 | A | G | 1 | a0002c0002t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-1+2260A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285203 | |||||||
| chr11:17285356 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+2413C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285356 | |||||||
| chr11:17285450 | G | A | 6 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+2507G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285450 | |||||||
| chr11:17285502 | A | G | 1 | a0002c0002t0001g0284 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-1+2559A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285502 | |||||||
| chr11:17285508 | C | T | 1 | a0002c0002t0002g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-1+2565C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285508 | |||||||
| chr11:17285564 | G | A | 2 | a0003c0003t0001g0049 a0003c0003t0001g0052 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-1+2621G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285564 | |||||||
| chr11:17285576 | C | CA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
38 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1+2651dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285576 | ||||||
| chr11:17285577 | A | T | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2634A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285577 | |||||||
| chr11:17285579 | A | C | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2636A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285579 | |||||||
| chr11:17285580 | A | T | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2637A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285580 | |||||||
| chr11:17285586 | A | T | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2643A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285586 | |||||||
| chr11:17285588 | A | C | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2645A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285588 | |||||||
| chr11:17285600 | T | A | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2657T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285600 | |||||||
| chr11:17285605 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2662G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285605 | |||||||
| chr11:17285614 | G | C | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2671G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285614 | |||||||
| chr11:17285615 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2672G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285615 | |||||||
| chr11:17285619 | C | T | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2676C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285619 | |||||||
| chr11:17285627 | C | A | 1 | a0003c0003t0001g0088 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-1+2684C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285627 | |||||||
| chr11:17285628 | C | T | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-1+2685C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285628 | |||||||
| chr11:17285661 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1+2718G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285661 | |||||||
| chr11:17285701 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+2758G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285701 | |||||||
| chr11:17285743 | C | CA | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0326 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1+2823dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | ||||||
| chr11:17285743 | CA | C | 67 | a0001c0001t0001g0020 a0001c0001t0001g0274 a0001c0001t0001g0295 others(64): Show |
68 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.-1+2823delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | ||||||
| chr11:17285743 | CAA | C | 6 | a0001c0001t0007g0223 a0002c0002t0001g0007 a0002c0002t0001g0249 others(3): Show |
7 | HG03486.hp1 NA18942.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+2822_-1+2823del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285743 | ||||||
| chr11:17285829 | T | C | 2 | a0001c0001t0001g0351 a0001c0001t0002g0127 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-1+2886T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285829 | |||||||
| chr11:17285867 | C | T | 1 | a0002c0002t0001g0308 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-1+2924C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285867 | |||||||
| chr11:17285934 | T | TAC | 35 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(32): Show |
35 | HG00597.hp2 HG00735.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-1+3023_-1+3024dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | T | TACAC | 22 | a0001c0001t0001g0272 a0001c0001t0001g0311 a0002c0002t0001g0007 others(19): Show |
23 | HG00544.hp1 HG02027.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.-1+3021_-1+3024dup others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | T | TACACAC | 4 | a0002c0002t0001g0287 a0002c0002t0001g0288 a0002c0002t0001g0289 others(1): Show |
4 | HG00423.hp1 NA18963.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3019_-1+3024dup others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | T | TACACACA others(1): Show |
31 | a0001c0001t0001g0295 a0002c0002t0001g0004 a0002c0002t0001g0241 others(28): Show |
32 | HG00408.hp1 HG00673.hp1 HG01978.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1+3017_-1+3024dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | T | TACACACA others(3): Show |
1 | a0003c0003t0005g0120 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1+3015_-1+3024dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | T | TACACACA others(5): Show |
1 | a0002c0002t0001g0307 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-1+3013_-1+3024dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | TAC | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0243 a0001c0001t0001g0244 others(46): Show |
50 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-1+3023_-1+3024del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285934 | TACAC | T | 8 | a0001c0001t0001g0255 a0001c0001t0002g0136 a0001c0001t0002g0150 others(5): Show |
8 | HG00639.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+3021_-1+3024del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17285934 | ||||||
| chr11:17285964 | C | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0045 a0003c0003t0001g0093 |
3 | HG00673.hp2 NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-1+3021C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17285964 | |||||||
| chr11:17286095 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+3152G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286095 | |||||||
| chr11:17286141 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3198T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286141 | |||||||
| chr11:17286241 | T | G | 1 | a0002c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1+3298T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286241 | |||||||
| chr11:17286583 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3640T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286583 | |||||||
| chr11:17286602 | C | T | 2 | a0002c0002t0001g0306 a0002c0002t0001g0349 |
2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-1+3659C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286602 | |||||||
| chr11:17286726 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.-1+3783T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286726 | |||||||
| chr11:17286921 | A | G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+3978A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17286921 | |||||||
| chr11:17287113 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4170T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287113 | |||||||
| chr11:17287172 | A | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+4229A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287172 | |||||||
| chr11:17287174 | T | A | 1 | a0001c0001t0001g0348 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-1+4231T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287174 | |||||||
| chr11:17287193 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+4250G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287193 | |||||||
| chr11:17287287 | T | G | 1 | a0002c0002t0002g0156 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-1+4344T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287287 | |||||||
| chr11:17287339 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4396A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287339 | |||||||
| chr11:17287400 | G | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4457G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287400 | |||||||
| chr11:17287422 | G | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+4479G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287422 | |||||||
| chr11:17287490 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4547G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287490 | |||||||
| chr11:17287493 | A | G | 5 | a0001c0001t0001g0243 a0001c0001t0002g0239 a0002c0002t0001g0023 others(2): Show |
5 | HG00639.hp2 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+4550A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287493 | |||||||
| chr11:17287602 | A | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+4659A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287602 | |||||||
| chr11:17287630 | AC | A | 26 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.-1+4689delC | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287630 | ||||||
| chr11:17287672 | C | CA | 102 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0244 others(99): Show |
105 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-1+4749dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | ||||||
| chr11:17287672 | C | CAA | 6 | a0001c0001t0002g0234 a0002c0002t0001g0290 a0002c0002t0001g0291 others(3): Show |
6 | HG00673.hp1 HG00735.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+4748_-1+4749dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | ||||||
| chr11:17287672 | CA | C | 13 | a0001c0001t0002g0130 a0001c0001t0002g0172 a0001c0001t0002g0218 others(10): Show |
13 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+4749delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17287672 | ||||||
| chr11:17287698 | G | T | 1 | a0002c0002t0001g0286 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1+4755G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287698 | |||||||
| chr11:17287768 | G | A | 1 | a0003c0003t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-1+4825G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287768 | |||||||
| chr11:17287807 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+4864T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287807 | |||||||
| chr11:17287913 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+4970G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287913 | |||||||
| chr11:17287954 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+5011C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287954 | |||||||
| chr11:17287966 | C | T | 1 | a0003c0003t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-1+5023C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17287966 | |||||||
| chr11:17288165 | GT | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+5225delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288165 | ||||||
| chr11:17288190 | A | C | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-1+5247A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288190 | |||||||
| chr11:17288273 | G | C | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+5330G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288273 | |||||||
| chr11:17288314 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1+5371A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288314 | |||||||
| chr11:17288401 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5458C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288401 | |||||||
| chr11:17288546 | C | CTTTT | 4 | a0002c0002t0001g0004 a0002c0002t0001g0241 a0002c0002t0001g0319 others(1): Show |
5 | NA18956.hp1 NA18983.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+5605_-1+5606ins others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288546 | ||||||
| chr11:17288549 | C | T | 5 | a0002c0002t0001g0004 a0002c0002t0001g0241 a0002c0002t0001g0292 others(2): Show |
6 | NA18956.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5606C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288549 | |||||||
| chr11:17288552 | C | CTTCTTTT others(5): Show |
1 | a0001c0001t0001g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTCTTTT others(6): Show |
12 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0261 others(9): Show |
12 | HG00735.hp1 HG01243.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTCTTTT others(7): Show |
2 | a0001c0001t0001g0260 a0001c0001t0001g0264 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-1+5611_-1+5612ins others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0243 a0001c0001t0001g0328 a0002c0002t0001g0024 others(5): Show |
8 | HG01081.hp1 HG01168.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+5618_-1+5625dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(2): Show |
97 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0256 others(94): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-1+5617_-1+5625dup others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(3): Show |
62 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(59): Show |
63 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-1+5616_-1+5625dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(4): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0022 others(19): Show |
23 | HG00423.hp1 HG01070.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-1+5615_-1+5625dup others(11): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(5): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.-1+5614_-1+5625dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0021 |
2 | HG01255.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-1+5613_-1+5625dup others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288552 | ||||||
| chr11:17288552 | C | T | 5 | a0002c0002t0001g0004 a0002c0002t0001g0241 a0002c0002t0001g0292 others(2): Show |
6 | NA18956.hp1 NA18979.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5609C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288552 | |||||||
| chr11:17288679 | C | T | 1 | a0001c0009t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-1+5736C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288679 | |||||||
| chr11:17288703 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-1+5760C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288703 | |||||||
| chr11:17288844 | C | T | 85 | a0002c0002t0001g0031 a0003c0003t0001g0003 a0003c0003t0001g0025 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-1+5901C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288844 | |||||||
| chr11:17288845 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1+5902G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288845 | |||||||
| chr11:17288877 | GTA | G | 9 | a0002c0002t0002g0208 a0003c0003t0001g0045 a0003c0003t0001g0050 others(6): Show |
9 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5940del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288877 | ||||||
| chr11:17288880 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-1+5937T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288880 | |||||||
| chr11:17288880 | T | TAC | 6 | a0001c0001t0002g0219 a0003c0003t0001g0049 a0003c0003t0001g0058 others(3): Show |
6 | HG00621.hp2 HG02080.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | T | TACACACA others(1): Show |
3 | a0003c0003t0001g0047 a0003c0003t0001g0057 a0003c0003t0001g0078 |
3 | HG02132.hp2 HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | T | TACACACA others(17): Show |
1 | a0001c0001t0002g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | T | TACACACA others(27): Show |
1 | a0001c0001t0001g0271 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-1+5938_-1+5939ins others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATAC | T | 12 | a0001c0001t0002g0231 a0003c0003t0001g0025 a0003c0003t0001g0027 others(9): Show |
12 | HG01261.hp1 HG02056.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5942del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACAC | T | 12 | a0001c0001t0002g0224 a0001c0001t0002g0228 a0002c0002t0002g0210 others(9): Show |
12 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5944del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(1): Show |
T | 12 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0238 others(9): Show |
12 | HG01074.hp2 HG01175.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5946del others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(3): Show |
T | 16 | a0001c0001t0001g0323 a0001c0001t0002g0218 a0001c0001t0002g0237 others(13): Show |
16 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5948del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(5): Show |
T | 10 | a0001c0001t0001g0353 a0003c0003t0001g0053 a0003c0003t0001g0069 others(7): Show |
10 | HG02109.hp2 HG03492.hp2 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5950del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(7): Show |
T | 6 | a0001c0001t0001g0322 a0003c0003t0001g0046 a0003c0003t0001g0054 others(3): Show |
6 | HG00639.hp1 HG01884.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5952del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(9): Show |
T | 3 | a0001c0001t0001g0320 a0002c0002t0001g0031 a0003c0003t0001g0026 |
3 | HG02083.hp2 HG02257.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5954del others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(11): Show |
T | 2 | a0003c0003t0001g0033 a0003c0003t0001g0042 |
2 | HG02129.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5956del others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(13): Show |
T | 1 | a0003c0003t0003g0038 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-1+5939_-1+5958del others(20): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(15): Show |
T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0321 a0003c0003t0001g0065 |
4 | HG02922.hp2 HG02970.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5939_-1+5960del others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(17): Show |
T | 1 | a0001c0001t0001g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1+5939_-1+5962del others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288880 | TATACACA others(21): Show |
T | 2 | a0001c0001t0001g0244 a0003c0003t0001g0108 |
2 | HG03579.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-1+5939_-1+5966del others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288880 | ||||||
| chr11:17288882 | T | C | 26 | a0001c0001t0001g0271 a0001c0001t0002g0150 a0001c0001t0002g0152 others(23): Show |
27 | HG00099.hp1 HG00621.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+5939T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288882 | |||||||
| chr11:17288882 | T | TAC | 6 | a0001c0001t0002g0116 a0001c0001t0002g0168 a0001c0001t0002g0181 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+6007_-1+6008dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACAC | 11 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0002g0119 others(8): Show |
12 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6008dup others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACAC | 8 | a0001c0001t0001g0013 a0001c0001t0001g0096 a0001c0001t0001g0255 others(5): Show |
8 | HG01192.hp1 HG01261.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6008dup others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0336 a0001c0001t0002g0118 a0001c0001t0002g0133 others(5): Show |
8 | HG01123.hp2 HG02004.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+6001_-1+6008dup others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0263 a0001c0001t0002g0183 |
2 | HG02895.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6008dup others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0341 a0001c0001t0002g0117 others(3): Show |
6 | HG01255.hp1 HG02293.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5997_-1+6008dup others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(7): Show |
4 | a0001c0001t0002g0164 a0001c0001t0002g0173 a0002c0002t0002g0121 others(1): Show |
4 | HG00597.hp1 HG03688.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+5995_-1+6008dup others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(9): Show |
2 | a0001c0001t0002g0207 a0002c0002t0002g0145 |
2 | HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-1+5993_-1+6008dup others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(11): Show |
1 | a0001c0001t0002g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+5991_-1+6008dup others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(15): Show |
1 | a0001c0001t0002g0178 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-1+5987_-1+6008dup others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(19): Show |
1 | a0001c0001t0002g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1+5983_-1+6008dup others(26): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(21): Show |
1 | a0002c0002t0002g0144 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-1+5981_-1+6008dup others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(25): Show |
4 | a0001c0001t0002g0132 a0001c0001t0002g0153 a0001c0001t0002g0179 others(1): Show |
4 | HG03453.hp1 NA18948.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5977_-1+6008dup others(32): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(27): Show |
4 | a0001c0001t0001g0111 a0001c0001t0002g0012 a0001c0001t0002g0188 others(1): Show |
4 | HG01928.hp2 HG02559.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5975_-1+6008dup others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(31): Show |
1 | a0001c0001t0002g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-1+5971_-1+6008dup others(38): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(33): Show |
1 | a0002c0002t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1+5969_-1+6008dup others(40): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(35): Show |
3 | a0001c0001t0002g0186 a0001c0001t0002g0203 a0001c0001t0006g0163 |
3 | HG01433.hp1 HG02055.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-1+5967_-1+6008dup others(42): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(37): Show |
2 | a0001c0001t0002g0177 a0002c0002t0002g0220 |
2 | HG00621.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-1+5965_-1+6008dup others(44): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(41): Show |
3 | a0001c0001t0002g0146 a0002c0002t0002g0160 a0002c0002t0002g0195 |
3 | HG01496.hp2 HG02300.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-1+5961_-1+6008dup others(48): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | T | TACACACA others(43): Show |
1 | a0001c0001t0002g0157 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-1+5959_-1+6008dup others(50): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TAC | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0328 a0003c0003t0001g0338 |
3 | HG01168.hp1 HG02040.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-1+6007_-1+6008del others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACAC | T | 7 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0262 others(4): Show |
7 | HG02258.hp2 HG02293.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6008del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACAC | T | 6 | a0001c0001t0001g0252 a0001c0001t0001g0272 a0001c0001t0001g0330 others(3): Show |
6 | HG01099.hp2 HG01243.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6008del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0268 a0002c0002t0001g0281 |
2 | HG02155.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6008del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0270 a0002c0002t0001g0301 |
3 | HG02055.hp1 NA18966.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-1+5997_-1+6008del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0261 a0001c0001t0001g0264 a0001c0001t0001g0267 others(1): Show |
4 | HG02602.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+5995_-1+6008del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0002g0189 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+5993_-1+6008del others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(11): Show |
T | 10 | a0001c0001t0002g0130 a0001c0001t0002g0190 a0002c0002t0001g0280 others(7): Show |
10 | HG00673.hp1 HG01070.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1+5991_-1+6008del others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(13): Show |
T | 1 | a0002c0002t0001g0300 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-1+5989_-1+6008del others(20): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(15): Show |
T | 20 | a0001c0001t0001g0274 a0002c0002t0001g0004 a0002c0002t0001g0007 others(17): Show |
22 | HG00423.hp1 HG01934.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1+5987_-1+6008del others(22): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(17): Show |
T | 21 | a0001c0001t0001g0248 a0001c0001t0001g0295 a0001c0001t0001g0324 others(18): Show |
21 | HG00544.hp1 HG01943.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1+5985_-1+6008del others(24): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288882 | TACACACA others(19): Show |
T | 4 | a0001c0001t0001g0247 a0002c0002t0001g0304 a0002c0002t0001g0315 others(1): Show |
4 | HG01978.hp2 HG02280.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5983_-1+6008del others(26): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288882 | ||||||
| chr11:17288884 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+5941C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288884 | |||||||
| chr11:17288920 | CACACACA others(25): Show |
C | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+5979_-1+6010del others(32): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288920 | ||||||
| chr11:17288924 | CACACACA others(27): Show |
C | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+5983_-1+6016del others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288924 | ||||||
| chr11:17288940 | CACACACA others(5): Show |
C | 1 | a0001c0001t0002g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-1+5999_-1+6010del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288940 | ||||||
| chr11:17288940 | CACACACA others(7): Show |
C | 2 | a0001c0001t0002g0129 a0001c0001t0007g0223 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-1+5999_-1+6012del others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288940 | ||||||
| chr11:17288942 | CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0194 a0001c0001t0002g0240 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+6001_-1+6010del others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288942 | ||||||
| chr11:17288942 | CACACACA others(5): Show |
C | 1 | a0001c0001t0002g0001 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-1+6001_-1+6012del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288942 | ||||||
| chr11:17288944 | CACACACA others(1): Show |
C | 4 | a0001c0001t0002g0187 a0001c0001t0002g0192 a0002c0002t0002g0148 others(1): Show |
4 | HG00738.hp2 HG02027.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+6003_-1+6010del others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288944 | ||||||
| chr11:17288944 | CACACACA others(5): Show |
C | 2 | a0003c0003t0001g0003 a0003c0003t0001g0080 |
2 | HG01074.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-1+6003_-1+6014del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288944 | ||||||
| chr11:17288946 | C | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0330 a0001c0001t0001g0334 others(1): Show |
4 | HG01099.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+6003C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288946 | |||||||
| chr11:17288946 | CACACAT | C | 4 | a0001c0001t0002g0171 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
4 | HG00741.hp1 HG01516.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+6005_-1+6010del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288946 | ||||||
| chr11:17288948 | C | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
34 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1+6005C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288948 | |||||||
| chr11:17288948 | CACATAT | C | 3 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0126 |
3 | HG01243.hp1 HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+6007_-1+6012del others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288948 | ||||||
| chr11:17288950 | C | CACACACA others(27): Show |
1 | a0002c0002t0002g0161 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(34): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | ||||||
| chr11:17288950 | C | CACACACA others(9): Show |
1 | a0003c0003t0001g0339 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | ||||||
| chr11:17288950 | C | CACACACA others(3): Show |
1 | a0001c0001t0001g0340 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | ||||||
| chr11:17288950 | C | CACACACA others(1): Show |
5 | a0002c0002t0002g0193 a0002c0002t0002g0211 a0002c0002t0002g0222 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+6008_-1+6009ins others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | ||||||
| chr11:17288950 | C | T | 88 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-1+6007C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288950 | |||||||
| chr11:17288950 | CATAT | C | 3 | a0001c0001t0001g0066 a0001c0001t0002g0011 a0001c0001t0002g0123 |
3 | HG01258.hp2 HG02572.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1+6018_-1+6021del others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288950 | ||||||
| chr11:17288951 | A | G | 4 | a0001c0001t0001g0320 a0001c0001t0001g0322 a0001c0001t0001g0323 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+6008A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288951 | |||||||
| chr11:17288952 | T | C | 79 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0081 others(76): Show |
79 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.-1+6009T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288952 | |||||||
| chr11:17288954 | T | C | 27 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0111 others(24): Show |
27 | HG00621.hp1 HG00642.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1+6011T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288954 | |||||||
| chr11:17288955 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
5 | HG02922.hp2 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+6012A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288955 | |||||||
| chr11:17288956 | T | C | 8 | a0001c0001t0001g0243 a0001c0001t0001g0341 a0001c0001t0002g0128 others(5): Show |
8 | HG01516.hp1 HG02602.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+6013T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288956 | |||||||
| chr11:17288958 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+6015T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288958 | |||||||
| chr11:17288958 | TA | T | 32 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1+6016delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288958 | |||||||
| chr11:17288959 | A | AT | 28 | a0001c0001t0001g0274 a0001c0001t0001g0295 a0002c0002t0001g0004 others(25): Show |
30 | HG00423.hp1 HG01934.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.-1+6017dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288959 | ||||||
| chr11:17288959 | A | ATT | 3 | a0001c0001t0001g0337 a0001c0001t0001g0346 a0003c0003t0001g0329 |
3 | HG02148.hp1 HG02735.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-1+6017_-1+6018ins others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288959 | ||||||
| chr11:17288959 | A | T | 22 | a0001c0001t0001g0256 a0001c0001t0001g0328 a0001c0001t0001g0330 others(19): Show |
22 | HG00408.hp1 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1+6016A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288959 | |||||||
| chr11:17288960 | TA | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(21): Show |
24 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-1+6018delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288960 | |||||||
| chr11:17288961 | A | AT | 14 | a0001c0001t0001g0022 a0001c0001t0001g0324 a0001c0001t0002g0215 others(11): Show |
14 | HG00544.hp1 HG01943.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+6019dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288961 | ||||||
| chr11:17288961 | A | ATTT | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0002c0004t0002g0236 |
3 | HG02818.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1+6019_-1+6020ins others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288961 | ||||||
| chr11:17288961 | A | T | 175 | a0001c0001t0001g0256 a0001c0001t0001g0261 a0001c0001t0001g0264 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-1+6018A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288961 | |||||||
| chr11:17288962 | TA | T | 5 | a0001c0001t0002g0157 a0001c0001t0002g0229 a0002c0002t0001g0023 others(2): Show |
5 | HG01516.hp1 HG02922.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+6020delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288962 | |||||||
| chr11:17288963 | A | ATATTTTT others(8): Show |
1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1+6021_-1+6022ins others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288963 | ||||||
| chr11:17288963 | A | ATTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(4): Show |
9 | HG01257.hp1 HG01258.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+6030_-1+6032dup others(3): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17288963 | ||||||
| chr11:17288963 | A | T | 315 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(312): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-1+6020A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17288963 | |||||||
| chr11:17289133 | T | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1+6190T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289133 | |||||||
| chr11:17289294 | A | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-6030A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289294 | |||||||
| chr11:17289320 | C | T | 5 | a0001c0001t0001g0259 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | NA18943.hp1 NA18973.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1-6004C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289320 | |||||||
| chr11:17289502 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0217 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1-5822G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289502 | |||||||
| chr11:17289562 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-5762T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289562 | |||||||
| chr11:17289615 | T | A | 1 | a0002c0002t0001g0099 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1-5709T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289615 | |||||||
| chr11:17289645 | A | G | 1 | a0003c0003t0001g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1-5679A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17289645 | |||||||
| chr11:17290091 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-5233C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290091 | |||||||
| chr11:17290113 | G | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-5211G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290113 | |||||||
| chr11:17290264 | G | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(232): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1-5060G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290264 | |||||||
| chr11:17290280 | A | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-5044A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290280 | |||||||
| chr11:17290553 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1-4771A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290553 | |||||||
| chr11:17290649 | T | C | 2 | a0002c0002t0002g0140 a0002c0002t0002g0158 |
2 | HG01123.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1-4675T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290649 | |||||||
| chr11:17290652 | C | G | 1 | a0003c0003t0001g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1-4672C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290652 | |||||||
| chr11:17290841 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1-4483T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290841 | |||||||
| chr11:17290999 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1-4325C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17290999 | |||||||
| chr11:17291081 | C | G | 1 | a0003c0003t0001g0051 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1-4243C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291081 | |||||||
| chr11:17291229 | T | A | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1-4095T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291229 | |||||||
| chr11:17291323 | G | A | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-4001G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291323 | |||||||
| chr11:17291462 | C | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3862C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291462 | |||||||
| chr11:17291471 | G | A | 1 | a0002c0002t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1-3853G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291471 | |||||||
| chr11:17291545 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0130 a0001c0001t0002g0190 |
2 | HG01070.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1-3773_1-3764dupAA others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-3774_1-3764dupAA others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0325 a0001c0001t0002g0186 a0001c0001t0002g0226 others(1): Show |
4 | HG02683.hp2 HG03017.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-3777_1-3764dupAA others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(8): Show |
89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(86): Show |
92 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1-3778_1-3764dupAA others(13): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(9): Show |
110 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0066 others(107): Show |
112 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(14): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(10): Show |
82 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0260 others(79): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(15): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(11): Show |
26 | a0002c0002t0001g0031 a0002c0002t0001g0280 a0003c0003t0001g0027 others(23): Show |
26 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(12): Show |
11 | a0001c0001t0001g0274 a0003c0003t0001g0059 a0003c0003t0001g0076 others(8): Show |
11 | HG00544.hp2 HG01934.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(17): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(13): Show |
3 | a0003c0003t0001g0060 a0003c0003t0001g0094 a0003c0003t0001g0108 |
3 | HG01993.hp2 NA18956.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(18): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291545 | C | CAAAAAAA others(14): Show |
2 | a0003c0003t0001g0102 a0003c0003t0001g0115 |
2 | HG01928.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1-3764_1-3763insAA others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17291545 | ||||||
| chr11:17291628 | C | G | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-3696C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291628 | |||||||
| chr11:17291663 | C | G | 1 | a0001c0001t0002g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1-3661C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291663 | |||||||
| chr11:17291734 | A | G | 26 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0259 others(23): Show |
26 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-3590A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291734 | |||||||
| chr11:17291893 | C | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3431C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291893 | |||||||
| chr11:17291974 | A | G | 85 | a0002c0002t0001g0031 a0003c0003t0001g0003 a0003c0003t0001g0025 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1-3350A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17291974 | |||||||
| chr11:17292029 | T | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-3295T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292029 | |||||||
| chr11:17292609 | C | T | 1 | a0003c0003t0001g0327 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1-2715C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292609 | |||||||
| chr11:17292798 | T | A | 85 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(82): Show |
87 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1-2526T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292798 | |||||||
| chr11:17292820 | G | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2504G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292820 | |||||||
| chr11:17292979 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-2345T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17292979 | |||||||
| chr11:17293041 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1-2283G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293041 | |||||||
| chr11:17293232 | C | T | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2092C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293232 | |||||||
| chr11:17293237 | G | A | 85 | a0002c0002t0001g0031 a0003c0003t0001g0003 a0003c0003t0001g0025 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1-2087G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293237 | |||||||
| chr11:17293253 | CA | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(220): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1-2052delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17293253 | ||||||
| chr11:17293408 | G | GA | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1915dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17293408 | ||||||
| chr11:17293887 | G | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1-1437G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17293887 | |||||||
| chr11:17294078 | T | C | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-1246T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294078 | |||||||
| chr11:17294194 | A | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-1130A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294194 | |||||||
| chr11:17294482 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1-842C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294482 | |||||||
| chr11:17294529 | CA | C | 8 | a0003c0003t0001g0026 a0003c0003t0001g0045 a0003c0003t0001g0088 others(5): Show |
8 | HG00673.hp2 NA18941.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-793delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294529 | ||||||
| chr11:17294622 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-702A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294622 | |||||||
| chr11:17294678 | T | TA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(26): Show |
30 | HG00099.hp2 HG00544.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1-623dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294678 | ||||||
| chr11:17294678 | TA | T | 115 | a0001c0001t0001g0243 a0001c0001t0001g0256 a0001c0001t0001g0257 others(112): Show |
116 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1-623delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17294678 | ||||||
| chr11:17294701 | A | G | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1-623A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294701 | |||||||
| chr11:17294823 | G | A | 2 | a0003c0003t0001g0048 a0003c0003t0001g0058 |
2 | HG02129.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1-501G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294823 | |||||||
| chr11:17294838 | A | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1-486A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17294838 | |||||||
| chr11:17295143 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1-181G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | chr11 | 17295143 | |||||||
| chr11:17295201 | AT | A | 42 | a0001c0001t0001g0066 a0001c0001t0001g0111 a0001c0001t0001g0271 others(39): Show |
43 | HG00621.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1-113delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr11 | 17295201 | ||||||
| chr11:17295993 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.145-111T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 3/13 | chr11 | 17295993 | |||||||
| chr11:17296386 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+175A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296386 | |||||||
| chr11:17296387 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+176T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296387 | |||||||
| chr11:17296389 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+178T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296389 | |||||||
| chr11:17296390 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+179T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296390 | |||||||
| chr11:17296391 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+180T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296391 | |||||||
| chr11:17296392 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+181A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296392 | |||||||
| chr11:17296396 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+185A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296396 | |||||||
| chr11:17296398 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+187C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296398 | |||||||
| chr11:17296399 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.252+188A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296399 | |||||||
| chr11:17296582 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.252+371G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296582 | |||||||
| chr11:17296601 | C | T | 3 | a0003c0003t0001g0025 a0003c0003t0001g0027 a0003c0003t0001g0028 |
3 | NA18964.hp1 NA18965.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.252+390C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296601 | |||||||
| chr11:17296689 | A | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+478A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296689 | |||||||
| chr11:17296760 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+549G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296760 | |||||||
| chr11:17296981 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.252+770A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17296981 | |||||||
| chr11:17297231 | T | TAAAAAAT others(313): Show |
1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1036_252+1037i others(322): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17297231 | ||||||
| chr11:17297242 | G | A | 1 | a0002c0002t0001g0099 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.252+1031G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297242 | |||||||
| chr11:17297642 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.252+1431A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297642 | |||||||
| chr11:17297688 | G | C | 1 | a0001c0009t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.252+1477G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297688 | |||||||
| chr11:17297807 | T | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+1596T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297807 | |||||||
| chr11:17297845 | A | G | 1 | a0001c0001t0001g0336 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.252+1634A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297845 | |||||||
| chr11:17297971 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+1760A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17297971 | |||||||
| chr11:17298040 | C | G | 1 | a0002c0002t0001g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.252+1829C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298040 | |||||||
| chr11:17298040 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.252+1829C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298040 | |||||||
| chr11:17298081 | CA | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(211): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.252+1891delA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17298081 | ||||||
| chr11:17298081 | CAA | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0274 a0001c0001t0002g0239 others(6): Show |
9 | HG00639.hp2 HG01934.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+1890_252+1891d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17298081 | ||||||
| chr11:17298091 | A | G | 1 | a0003c0003t0001g0033 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.252+1880A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298091 | |||||||
| chr11:17298102 | A | G | 5 | a0001c0001t0001g0256 a0001c0001t0002g0200 a0001c0001t0002g0237 others(2): Show |
5 | HG00408.hp1 HG01175.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1891A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298102 | |||||||
| chr11:17298128 | G | A | 1 | a0003c0003t0001g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.252+1917G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298128 | |||||||
| chr11:17298337 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.252+2126G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298337 | |||||||
| chr11:17298487 | G | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252+2276G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298487 | |||||||
| chr11:17298785 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.252+2574G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17298785 | |||||||
| chr11:17299083 | G | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.253-2661G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299083 | |||||||
| chr11:17299250 | G | T | 233 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(230): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.253-2494G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299250 | |||||||
| chr11:17299280 | A | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.253-2464A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299280 | |||||||
| chr11:17299820 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.253-1924C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299820 | |||||||
| chr11:17299875 | T | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.253-1869T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17299875 | |||||||
| chr11:17299902 | C | CATAAA | 86 | a0001c0001t0007g0223 a0002c0002t0001g0031 a0003c0003t0001g0003 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.253-1820_253-1816d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17299902 | ||||||
| chr11:17299902 | CATAAA | C | 3 | a0001c0001t0001g0268 a0002c0002t0002g0135 a0002c0002t0002g0141 |
3 | HG01346.hp2 HG02293.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-1820_253-1816d others(7): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17299902 | ||||||
| chr11:17300019 | G | GT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-1716dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300019 | ||||||
| chr11:17300180 | T | G | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253-1564T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300180 | |||||||
| chr11:17300231 | A | C | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-1513A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300231 | |||||||
| chr11:17300451 | C | T | 1 | a0003c0003t0001g0109 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.253-1293C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300451 | |||||||
| chr11:17300520 | C | T | 2 | a0002c0002t0001g0286 a0002c0002t0001g0316 |
2 | NA18940.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.253-1224C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300520 | |||||||
| chr11:17300650 | A | G | 1 | a0001c0001t0002g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-1094A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300650 | |||||||
| chr11:17300664 | C | T | 2 | a0001c0001t0001g0243 a0003c0003t0001g0335 |
2 | HG02004.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-1080C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300664 | |||||||
| chr11:17300706 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.253-1038G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300706 | |||||||
| chr11:17300749 | G | A | 5 | a0003c0003t0001g0049 a0003c0003t0001g0050 a0003c0003t0001g0052 others(2): Show |
5 | HG00423.hp2 HG00621.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-995G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300749 | |||||||
| chr11:17300849 | T | C | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.253-895T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300849 | |||||||
| chr11:17300862 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253-882C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300862 | |||||||
| chr11:17300918 | C | A | 1 | a0001c0001t0001g0266 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-826C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17300918 | |||||||
| chr11:17300967 | C | CT | 99 | a0001c0001t0001g0013 a0001c0001t0001g0066 a0001c0001t0001g0081 others(96): Show |
100 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.253-755dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | ||||||
| chr11:17300967 | C | CTT | 7 | a0001c0001t0002g0159 a0001c0001t0002g0175 a0001c0001t0002g0185 others(4): Show |
7 | HG00741.hp1 HG01109.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-756_253-755dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | ||||||
| chr11:17300967 | CT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01975.hp1 HG02273.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-755delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17300967 | ||||||
| chr11:17301248 | C | T | 1 | a0002c0002t0001g0291 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.253-496C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301248 | |||||||
| chr11:17301272 | C | CT | 55 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0244 others(52): Show |
56 | HG00673.hp1 HG00735.hp1 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.253-449dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17301272 | ||||||
| chr11:17301272 | CT | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.253-449delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr11 | 17301272 | ||||||
| chr11:17301295 | T | G | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-449T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301295 | |||||||
| chr11:17301296 | G | A | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-448G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301296 | |||||||
| chr11:17301297 | A | G | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-447A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301297 | |||||||
| chr11:17301476 | C | T | 58 | a0001c0001t0001g0274 a0002c0002t0001g0004 a0002c0002t0001g0007 others(55): Show |
60 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.253-268C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301476 | |||||||
| chr11:17301579 | C | G | 1 | a0003c0003t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.253-165C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301579 | |||||||
| chr11:17301632 | A | G | 1 | a0003c0003t0001g0075 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.253-112A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301632 | |||||||
| chr11:17301673 | T | A | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.253-71T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 4/13 | chr11 | 17301673 | |||||||
| chr11:17302237 | C | T | 1 | a0003c0003t0001g0051 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.379+367C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302237 | |||||||
| chr11:17302245 | C | A | 4 | a0003c0003t0001g0061 a0003c0003t0001g0084 a0003c0003t0001g0085 others(1): Show |
4 | HG00140.hp1 HG02273.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+375C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302245 | |||||||
| chr11:17302308 | T | G | 1 | a0002c0002t0002g0142 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.379+438T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302308 | |||||||
| chr11:17302384 | G | A | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+514G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302384 | |||||||
| chr11:17302385 | A | G | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+515A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302385 | |||||||
| chr11:17302738 | AT | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.379+885delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17302738 | ||||||
| chr11:17302765 | A | G | 1 | a0003c0003t0001g0036 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.379+895A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302765 | |||||||
| chr11:17302770 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.379+900C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302770 | |||||||
| chr11:17302779 | G | A | 6 | a0001c0001t0002g0146 a0001c0001t0002g0162 a0001c0001t0006g0163 others(3): Show |
6 | HG01433.hp1 HG02004.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.379+909G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302779 | |||||||
| chr11:17302800 | C | T | 1 | a0002c0002t0002g0208 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.379+930C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302800 | |||||||
| chr11:17302835 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.379+965G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302835 | |||||||
| chr11:17302890 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+1020T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302890 | |||||||
| chr11:17302954 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+1084G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17302954 | |||||||
| chr11:17303018 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+1148G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303018 | |||||||
| chr11:17303027 | C | T | 1 | a0002c0002t0001g0343 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.379+1157C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303027 | |||||||
| chr11:17303083 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379+1213G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303083 | |||||||
| chr11:17303367 | A | C | 1 | a0003c0003t0001g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.379+1497A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303367 | |||||||
| chr11:17303401 | A | G | 86 | a0001c0001t0007g0223 a0002c0002t0001g0031 a0003c0003t0001g0003 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.379+1531A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303401 | |||||||
| chr11:17303506 | A | C | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+1636A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303506 | |||||||
| chr11:17303656 | G | A | 1 | a0003c0003t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.379+1786G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303656 | |||||||
| chr11:17303659 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.379+1789T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303659 | |||||||
| chr11:17303884 | C | CA | 37 | a0001c0001t0001g0066 a0001c0001t0001g0244 a0001c0001t0001g0266 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.379+2032dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17303884 | ||||||
| chr11:17303952 | T | A | 1 | a0005c0007t0001g0039 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.379+2082T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17303952 | |||||||
| chr11:17304225 | C | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2355C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304225 | |||||||
| chr11:17304243 | A | T | 1 | a0003c0003t0001g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.379+2373A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304243 | |||||||
| chr11:17304246 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.379+2376A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304246 | |||||||
| chr11:17304355 | C | A | 1 | a0001c0001t0002g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379+2485C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304355 | |||||||
| chr11:17304551 | G | A | 4 | a0002c0002t0002g0142 a0002c0002t0002g0143 a0002c0002t0002g0165 others(1): Show |
4 | HG00741.hp2 HG01099.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+2681G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304551 | |||||||
| chr11:17304571 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379+2701C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304571 | |||||||
| chr11:17304642 | C | T | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0004t0002g0147 |
3 | HG02572.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2772C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304642 | |||||||
| chr11:17304715 | C | T | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.379+2845C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17304715 | |||||||
| chr11:17305062 | G | A | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.379+3192G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305062 | |||||||
| chr11:17305091 | A | T | 32 | a0001c0001t0001g0295 a0002c0002t0001g0029 a0002c0002t0001g0056 others(29): Show |
32 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.379+3221A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305091 | |||||||
| chr11:17305282 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.379+3412C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305282 | |||||||
| chr11:17305513 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0002g0151 |
2 | HG01496.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379+3643G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305513 | |||||||
| chr11:17305566 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.379+3696T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305566 | |||||||
| chr11:17305862 | A | G | 1 | a0002c0002t0001g0304 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.380-3710A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17305862 | |||||||
| chr11:17306328 | T | C | 1 | a0002c0002t0001g0282 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-3244T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306328 | |||||||
| chr11:17306352 | A | G | 71 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0274 others(68): Show |
73 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.380-3220A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306352 | |||||||
| chr11:17306554 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.380-3018A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306554 | |||||||
| chr11:17306682 | C | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380-2890C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306682 | |||||||
| chr11:17306706 | C | T | 67 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0323 others(64): Show |
69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.380-2866C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306706 | |||||||
| chr11:17306820 | G | A | 1 | a0003c0003t0001g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.380-2752G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306820 | |||||||
| chr11:17306868 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.380-2704T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306868 | |||||||
| chr11:17306895 | G | T | 1 | a0002c0004t0002g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.380-2677G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306895 | |||||||
| chr11:17306911 | C | CA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01978.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-2646dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17306911 | ||||||
| chr11:17306911 | C | CAA | 59 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(56): Show |
61 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.380-2647_380-2646d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr11 | 17306911 | ||||||
| chr11:17306927 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(15): Show |
19 | HG00140.hp2 HG01071.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.380-2645G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306927 | |||||||
| chr11:17306929 | A | C | 1 | a0002c0002t0001g0282 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-2643A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306929 | |||||||
| chr11:17306970 | G | A | 67 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0323 others(64): Show |
69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.380-2602G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17306970 | |||||||
| chr11:17307023 | T | A | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.380-2549T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307023 | |||||||
| chr11:17307157 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.380-2415G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307157 | |||||||
| chr11:17307197 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2375C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307197 | |||||||
| chr11:17307211 | G | A | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2361G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307211 | |||||||
| chr11:17307237 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-2335C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307237 | |||||||
| chr11:17307315 | G | A | 3 | a0001c0001t0002g0130 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.380-2257G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307315 | |||||||
| chr11:17307355 | T | C | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0002g0123 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-2217T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307355 | |||||||
| chr11:17307451 | T | G | 1 | a0002c0008t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.380-2121T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307451 | |||||||
| chr11:17307665 | A | G | 2 | a0002c0004t0001g0275 a0002c0004t0001g0276 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.380-1907A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307665 | |||||||
| chr11:17307688 | C | T | 4 | a0001c0001t0002g0149 a0001c0001t0002g0164 a0001c0001t0002g0204 others(1): Show |
4 | HG02056.hp1 HG03688.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-1884C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307688 | |||||||
| chr11:17307831 | A | G | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380-1741A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17307831 | |||||||
| chr11:17308251 | G | T | 95 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(92): Show |
97 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.380-1321G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308251 | |||||||
| chr11:17308512 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.380-1060A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308512 | |||||||
| chr11:17308562 | A | G | 91 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.380-1010A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308562 | |||||||
| chr11:17308567 | T | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0238 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.380-1005T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308567 | |||||||
| chr11:17308634 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.380-938A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17308634 | |||||||
| chr11:17309069 | T | C | 2 | a0001c0001t0002g0137 a0001c0001t0002g0139 |
2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.380-503T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17309069 | |||||||
| chr11:17309508 | G | A | 1 | a0002c0002t0001g0302 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.380-64G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 5/13 | chr11 | 17309508 | |||||||
| chr11:17309810 | TTATTAAT others(5): Show |
T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+144_483+155del others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17309810 | ||||||
| chr11:17309813 | T | G | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483+138T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309813 | |||||||
| chr11:17309851 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483+176C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309851 | |||||||
| chr11:17309879 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.483+204G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309879 | |||||||
| chr11:17309895 | C | G | 1 | a0003c0003t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.483+220C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309895 | |||||||
| chr11:17309928 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.483+253T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309928 | |||||||
| chr11:17309952 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.483+277T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309952 | |||||||
| chr11:17309989 | A | C | 1 | a0003c0003t0001g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.483+314A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17309989 | |||||||
| chr11:17310236 | CT | C | 95 | a0001c0001t0001g0014 a0001c0001t0002g0119 a0001c0001t0002g0182 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.483+573delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17310236 | ||||||
| chr11:17310261 | A | G | 18 | a0003c0003t0001g0006 a0003c0003t0001g0060 a0003c0003t0001g0094 others(15): Show |
18 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.484-564A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310261 | |||||||
| chr11:17310493 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.484-332C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310493 | |||||||
| chr11:17310644 | C | CAA | 96 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(93): Show |
98 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.484-173_484-172dup others(2): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr11 | 17310644 | ||||||
| chr11:17310741 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.484-84G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310741 | |||||||
| chr11:17310796 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.484-29T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 6/13 | chr11 | 17310796 | |||||||
| chr11:17311038 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.669+28T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/13 | chr11 | 17311038 | |||||||
| chr11:17311067 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.669+57C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 7/13 | chr11 | 17311067 | |||||||
| chr11:17311636 | G | A | 93 | a0003c0003t0001g0003 a0003c0003t0001g0006 a0003c0003t0001g0025 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.761-236G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311636 | |||||||
| chr11:17311651 | A | G | 31 | a0002c0002t0001g0029 a0002c0002t0001g0056 a0002c0002t0002g0135 others(28): Show |
31 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.761-221A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311651 | |||||||
| chr11:17311830 | T | G | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.761-42T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 8/13 | chr11 | 17311830 | |||||||
| chr11:17312229 | C | T | 2 | a0001c0001t0001g0323 a0001c0001t0001g0353 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.912+109C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312229 | |||||||
| chr11:17312344 | T | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.912+224T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312344 | |||||||
| chr11:17312372 | G | A | 1 | a0002c0002t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+252G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312372 | |||||||
| chr11:17312373 | A | C | 1 | a0002c0002t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+253A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312373 | |||||||
| chr11:17312405 | AT | A | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+301delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17312405 | ||||||
| chr11:17312466 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0001c0001t0002g0116 others(5): Show |
8 | HG01175.hp2 HG03710.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.912+346C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312466 | |||||||
| chr11:17312467 | G | A | 1 | a0002c0002t0001g0300 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.912+347G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312467 | |||||||
| chr11:17312511 | CTCTGCCT others(12): Show |
C | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+393_912+411del others(19): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17312511 | ||||||
| chr11:17312695 | A | G | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+575A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312695 | |||||||
| chr11:17312781 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.912+661G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312781 | |||||||
| chr11:17312799 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.912+679C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312799 | |||||||
| chr11:17312863 | C | G | 1 | a0002c0002t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+743C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312863 | |||||||
| chr11:17312864 | G | C | 1 | a0002c0002t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.912+744G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312864 | |||||||
| chr11:17312893 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+773_912+774ins others(10): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312893 | |||||||
| chr11:17312894 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+774A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17312894 | |||||||
| chr11:17313012 | A | AT | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.912+897dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr11 | 17313012 | ||||||
| chr11:17313018 | A | T | 114 | a0001c0001t0001g0243 a0001c0001t0001g0256 a0001c0001t0001g0257 others(111): Show |
116 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.912+898A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313018 | |||||||
| chr11:17313049 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.912+929C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313049 | |||||||
| chr11:17313075 | T | C | 1 | a0002c0002t0001g0298 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.912+955T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313075 | |||||||
| chr11:17313106 | T | G | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.912+986T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313106 | |||||||
| chr11:17313146 | T | C | 1 | a0003c0003t0001g0051 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.912+1026T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313146 | |||||||
| chr11:17313153 | T | C | 1 | a0002c0002t0001g0288 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.912+1033T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313153 | |||||||
| chr11:17313233 | A | C | 25 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(22): Show |
25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.912+1113A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313233 | |||||||
| chr11:17313444 | C | T | 1 | a0002c0004t0001g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.912+1324C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313444 | |||||||
| chr11:17313469 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.912+1349G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313469 | |||||||
| chr11:17313657 | C | G | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.912+1537C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313657 | |||||||
| chr11:17313832 | G | A | 1 | a0002c0002t0001g0287 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.913-1554G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313832 | |||||||
| chr11:17313849 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1537G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313849 | |||||||
| chr11:17313868 | T | C | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.913-1518T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313868 | |||||||
| chr11:17313919 | A | T | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1467A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17313919 | |||||||
| chr11:17314278 | C | A | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.913-1108C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314278 | |||||||
| chr11:17314370 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.913-1016G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314370 | |||||||
| chr11:17314515 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-871A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314515 | |||||||
| chr11:17314598 | A | G | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0325 others(11): Show |
14 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.913-788A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314598 | |||||||
| chr11:17314599 | T | A | 1 | a0002c0002t0001g0284 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.913-787T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314599 | |||||||
| chr11:17314784 | G | A | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.913-602G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314784 | |||||||
| chr11:17314796 | T | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.913-590T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314796 | |||||||
| chr11:17314864 | C | T | 94 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0029 others(91): Show |
96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.913-522C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17314864 | |||||||
| chr11:17315228 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.913-158C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17315228 | |||||||
| chr11:17315288 | A | G | 2 | a0003c0003t0001g0101 a0003c0003t0001g0106 |
2 | NA19080.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.913-98A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 10/13 | chr11 | 17315288 | |||||||
| chr11:17315480 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02300.hp2 | splice_region_variant&intron_variant | LOW | c.1002+5T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315480 | |||||||
| chr11:17315683 | T | C | 97 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(94): Show |
99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1002+208T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315683 | |||||||
| chr11:17315732 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+257C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315732 | |||||||
| chr11:17315788 | T | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0001g0320 others(14): Show |
18 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1002+313T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315788 | |||||||
| chr11:17315849 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1002+374G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315849 | |||||||
| chr11:17315866 | A | G | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1002+391A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315866 | |||||||
| chr11:17315874 | T | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1002+399T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17315874 | |||||||
| chr11:17315897 | ATG | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1002+424_1002+425d others(4): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17315897 | ||||||
| chr11:17316004 | G | A | 2 | a0002c0004t0001g0275 a0002c0004t0001g0276 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1002+529G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316004 | |||||||
| chr11:17316035 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1002+560C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316035 | |||||||
| chr11:17316077 | A | G | 1 | a0003c0003t0001g0094 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1002+602A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316077 | |||||||
| chr11:17316132 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+657C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316132 | |||||||
| chr11:17316140 | T | G | 1 | a0001c0001t0002g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1002+665T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316140 | |||||||
| chr11:17316172 | A | G | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+697A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316172 | |||||||
| chr11:17316383 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1002+908T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316383 | |||||||
| chr11:17316387 | C | T | 2 | a0002c0002t0001g0273 a0002c0002t0001g0283 |
2 | HG00544.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1002+912C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316387 | |||||||
| chr11:17316520 | A | G | 8 | a0003c0003t0001g0055 a0003c0003t0001g0059 a0003c0003t0001g0064 others(5): Show |
8 | HG00597.hp2 NA18940.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1002+1045A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316520 | |||||||
| chr11:17316829 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+1354T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17316829 | |||||||
| chr11:17317021 | T | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0217 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1002+1546T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317021 | |||||||
| chr11:17317045 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0018 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1002+1570T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317045 | |||||||
| chr11:17317068 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1002+1593G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317068 | |||||||
| chr11:17317139 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1002+1664A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317139 | |||||||
| chr11:17317147 | A | C | 1 | a0002c0002t0001g0277 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1002+1672A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317147 | |||||||
| chr11:17317185 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0235 |
2 | NA18946.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1002+1710G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317185 | |||||||
| chr11:17317232 | T | C | 1 | a0003c0003t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1002+1757T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317232 | |||||||
| chr11:17317332 | A | G | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1002+1857A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317332 | |||||||
| chr11:17317401 | G | A | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+1926G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317401 | |||||||
| chr11:17317459 | A | G | 1 | a0002c0002t0001g0287 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1002+1984A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317459 | |||||||
| chr11:17317504 | G | A | 1 | a0003c0003t0001g0030 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1002+2029G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317504 | |||||||
| chr11:17317514 | C | T | 1 | a0002c0002t0001g0007 | 2 | NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1002+2039C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317514 | |||||||
| chr11:17317520 | A | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1002+2045A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317520 | |||||||
| chr11:17317580 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1002+2105T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317580 | |||||||
| chr11:17317700 | A | G | 1 | a0003c0003t0001g0109 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002+2225A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317700 | |||||||
| chr11:17317718 | T | C | 1 | a0003c0003t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1002+2243T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317718 | |||||||
| chr11:17317764 | C | T | 2 | a0003c0003t0001g0072 a0003c0003t0001g0073 |
2 | NA18940.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1002+2289C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317764 | |||||||
| chr11:17317815 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1002+2340T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317815 | |||||||
| chr11:17317872 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1002+2397C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317872 | |||||||
| chr11:17317946 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0002g0128 |
2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1002+2471T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317946 | |||||||
| chr11:17317973 | G | GT | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0325 others(11): Show |
14 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1002+2498_1002+249 others(5): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317973 | |||||||
| chr11:17317974 | C | CT | 100 | a0001c0001t0001g0258 a0001c0001t0001g0265 a0001c0001t0001g0272 others(97): Show |
102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1002+2521dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17317974 | ||||||
| chr11:17317974 | C | T | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0325 others(11): Show |
14 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1002+2499C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17317974 | |||||||
| chr11:17317974 | CT | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0263 a0001c0001t0001g0324 others(7): Show |
10 | HG01934.hp2 HG02109.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002+2521delT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17317974 | ||||||
| chr11:17318085 | C | T | 1 | a0002c0002t0001g0300 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1002+2610C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17318085 | |||||||
| chr11:17318329 | T | TA | 97 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(94): Show |
99 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1002+2864dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17318329 | ||||||
| chr11:17318654 | T | C | 1 | a0003c0003t0001g0338 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1002+3179T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17318654 | |||||||
| chr11:17319021 | A | T | 3 | a0001c0001t0001g0245 a0002c0002t0002g0221 a0003c0003t0001g0049 |
3 | HG00621.hp2 HG02027.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1002+3546A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319021 | |||||||
| chr11:17319022 | T | A | 3 | a0001c0001t0002g0129 a0002c0002t0001g0296 a0002c0002t0001g0303 |
3 | HG02723.hp1 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1002+3547T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319022 | |||||||
| chr11:17319029 | A | T | 5 | a0001c0001t0002g0129 a0001c0001t0002g0154 a0001c0001t0002g0174 others(2): Show |
5 | HG02109.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+3554A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319029 | |||||||
| chr11:17319150 | G | A | 24 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0250 others(21): Show |
24 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1002+3675G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319150 | |||||||
| chr11:17319319 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1002+3844T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319319 | |||||||
| chr11:17319655 | T | C | 3 | a0001c0001t0002g0146 a0001c0001t0002g0162 a0001c0001t0006g0163 |
3 | HG01433.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1002+4180T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319655 | |||||||
| chr11:17319684 | A | G | 1 | a0003c0003t0001g0051 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1002+4209A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319684 | |||||||
| chr11:17319934 | A | G | 1 | a0003c0003t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1002+4459A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17319934 | |||||||
| chr11:17320009 | A | G | 1 | a0002c0002t0002g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1002+4534A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320009 | |||||||
| chr11:17320030 | T | G | 98 | a0001c0001t0007g0223 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+4555T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320030 | |||||||
| chr11:17320059 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002+4584G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320059 | |||||||
| chr11:17320074 | C | CT | 94 | a0003c0003t0001g0003 a0003c0003t0001g0006 a0003c0003t0001g0025 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1002+4606dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17320074 | ||||||
| chr11:17320605 | C | T | 4 | a0002c0002t0002g0210 a0002c0002t0002g0211 a0002c0002t0002g0212 others(1): Show |
4 | NA18990.hp1 NA18998.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+5130C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17320605 | |||||||
| chr11:17321050 | TG | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1002+5577delG | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17321050 | ||||||
| chr11:17321066 | C | G | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+5591C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321066 | |||||||
| chr11:17321176 | A | G | 2 | a0002c0002t0001g0023 a0002c0002t0001g0024 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1002+5701A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321176 | |||||||
| chr11:17321202 | A | AT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1002+5740dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17321202 | ||||||
| chr11:17321240 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002+5765C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321240 | |||||||
| chr11:17321362 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1002+5887C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321362 | |||||||
| chr11:17321579 | C | G | 6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002+6104C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321579 | |||||||
| chr11:17321617 | G | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+6142G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321617 | |||||||
| chr11:17321894 | T | A | 8 | a0002c0002t0001g0299 a0002c0002t0001g0300 a0002c0002t0001g0305 others(5): Show |
8 | HG00408.hp1 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1002+6419T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321894 | |||||||
| chr11:17321897 | C | G | 1 | a0003c0003t0001g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1002+6422C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321897 | |||||||
| chr11:17321939 | T | C | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+6464T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321939 | |||||||
| chr11:17321972 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1002+6497C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17321972 | |||||||
| chr11:17322008 | C | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1002+6533C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322008 | |||||||
| chr11:17322009 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1002+6534G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322009 | |||||||
| chr11:17322395 | T | G | 1 | a0002c0002t0002g0156 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1002+6920T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322395 | |||||||
| chr11:17322473 | C | T | 1 | a0002c0002t0001g0299 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1002+6998C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322473 | |||||||
| chr11:17322733 | A | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0201 |
2 | HG02896.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1002+7258A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322733 | |||||||
| chr11:17322762 | ATC | A | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1002+7289_1002+729 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17322762 | ||||||
| chr11:17322956 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1003-7171G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322956 | |||||||
| chr11:17322975 | T | G | 1 | a0003c0003t0001g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1003-7152T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17322975 | |||||||
| chr11:17323008 | A | C | 3 | a0001c0001t0002g0146 a0001c0001t0002g0162 a0001c0001t0006g0163 |
3 | HG01433.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1003-7119A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323008 | |||||||
| chr11:17323033 | T | TA | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-7093dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17323033 | ||||||
| chr11:17323061 | A | G | 1 | a0003c0003t0001g0083 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1003-7066A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323061 | |||||||
| chr11:17323352 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1003-6775T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323352 | |||||||
| chr11:17323366 | TATATC | T | 5 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-6756_1003-675 others(9): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17323366 | ||||||
| chr11:17323469 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1003-6658T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323469 | |||||||
| chr11:17323484 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1003-6643G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323484 | |||||||
| chr11:17323584 | T | G | 3 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0002g0236 |
3 | HG02257.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1003-6543T>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323584 | |||||||
| chr11:17323692 | T | C | 1 | a0003c0003t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1003-6435T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323692 | |||||||
| chr11:17323703 | G | C | 1 | a0002c0002t0001g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6424G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323703 | |||||||
| chr11:17323704 | C | A | 1 | a0002c0002t0001g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6423C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323704 | |||||||
| chr11:17323705 | A | T | 1 | a0002c0002t0001g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-6422A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323705 | |||||||
| chr11:17323847 | T | C | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-6280T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323847 | |||||||
| chr11:17323908 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1003-6219G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17323908 | |||||||
| chr11:17324013 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1003-6114C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324013 | |||||||
| chr11:17324140 | T | C | 3 | a0001c0001t0002g0130 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-5987T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324140 | |||||||
| chr11:17324340 | C | T | 4 | a0001c0001t0002g0136 a0001c0001t0002g0150 a0001c0001t0002g0152 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-5787C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324340 | |||||||
| chr11:17324473 | G | T | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-5654G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324473 | |||||||
| chr11:17324498 | A | G | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1003-5629A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324498 | |||||||
| chr11:17324528 | G | C | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-5599G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324528 | |||||||
| chr11:17324531 | C | T | 100 | a0001c0001t0002g0239 a0001c0001t0007g0223 a0002c0002t0001g0004 others(97): Show |
102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1003-5596C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324531 | |||||||
| chr11:17324577 | G | T | 1 | a0002c0002t0002g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1003-5550G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324577 | |||||||
| chr11:17324587 | C | A | 1 | a0002c0002t0001g0249 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1003-5540C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324587 | |||||||
| chr11:17324608 | A | G | 1 | a0003c0003t0001g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1003-5519A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324608 | |||||||
| chr11:17324762 | A | G | 1 | a0003c0003t0001g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1003-5365A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324762 | |||||||
| chr11:17324778 | G | GTTTATTT others(1): Show |
3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01243.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1003-5348_1003-534 others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324778 | ||||||
| chr11:17324780 | C | CTATT | 54 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0111 others(51): Show |
54 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1003-5313_1003-531 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | ||||||
| chr11:17324780 | C | CTATTTAT others(1): Show |
23 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0259 others(20): Show |
23 | HG00735.hp1 HG02055.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1003-5317_1003-531 others(12): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | ||||||
| chr11:17324780 | C | CTATTTAT others(5): Show |
1 | a0001c0001t0002g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1003-5321_1003-531 others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | ||||||
| chr11:17324780 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01243.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1003-5347C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324780 | |||||||
| chr11:17324780 | CTATT | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1003-5313_1003-531 others(8): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | ||||||
| chr11:17324780 | CTATTTAT others(5): Show |
C | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-5321_1003-531 others(16): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324780 | ||||||
| chr11:17324797 | T | TA | 7 | a0001c0001t0001g0096 a0001c0001t0002g0116 a0001c0001t0002g0172 others(4): Show |
7 | HG01175.hp2 HG03710.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1003-5329dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17324797 | ||||||
| chr11:17324832 | C | T | 94 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(91): Show |
96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1003-5295C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324832 | |||||||
| chr11:17324863 | G | A | 4 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0002g0147 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-5264G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324863 | |||||||
| chr11:17324887 | C | T | 5 | a0002c0002t0001g0099 a0002c0002t0001g0249 a0002c0002t0001g0278 others(2): Show |
5 | NA18940.hp1 NA18942.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-5240C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324887 | |||||||
| chr11:17324892 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-5235C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17324892 | |||||||
| chr11:17325264 | C | A | 1 | a0002c0002t0002g0160 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1003-4863C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325264 | |||||||
| chr11:17325444 | C | T | 2 | a0001c0001t0001g0351 a0001c0001t0002g0127 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1003-4683C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325444 | |||||||
| chr11:17325514 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0002g0180 |
2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1003-4613C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325514 | |||||||
| chr11:17325812 | C | CT | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-4308dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17325812 | ||||||
| chr11:17325833 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1003-4294T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325833 | |||||||
| chr11:17325908 | C | T | 94 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(91): Show |
96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1003-4219C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325908 | |||||||
| chr11:17325933 | G | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0349 |
2 | NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1003-4194G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17325933 | |||||||
| chr11:17326013 | T | C | 25 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(22): Show |
25 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1003-4114T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326013 | |||||||
| chr11:17326257 | C | G | 1 | a0002c0002t0002g0208 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1003-3870C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326257 | |||||||
| chr11:17326297 | G | A | 3 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0002g0236 |
3 | HG02257.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1003-3830G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326297 | |||||||
| chr11:17326311 | G | GT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1003-3793dupT | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326311 | ||||||
| chr11:17326311 | G | GTT | 23 | a0001c0001t0001g0016 a0001c0001t0001g0243 a0003c0003t0001g0006 others(20): Show |
23 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1003-3794_1003-379 others(6): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326311 | ||||||
| chr11:17326417 | A | T | 2 | a0002c0002t0001g0296 a0002c0002t0001g0303 |
2 | NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1003-3710A>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326417 | |||||||
| chr11:17326421 | G | A | 1 | a0003c0003t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1003-3706G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326421 | |||||||
| chr11:17326566 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1003-3561A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326566 | |||||||
| chr11:17326608 | C | T | 1 | a0002c0004t0002g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1003-3519C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326608 | |||||||
| chr11:17326628 | A | G | 1 | a0001c0009t0002g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1003-3499A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326628 | |||||||
| chr11:17326705 | C | T | 4 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0323 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-3422C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326705 | |||||||
| chr11:17326726 | CAAGAGAA others(17): Show |
C | 1 | a0003c0003t0001g0097 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1003-3399_1003-337 others(28): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17326726 | ||||||
| chr11:17326729 | G | C | 92 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0029 others(89): Show |
94 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1003-3398G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326729 | |||||||
| chr11:17326760 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0180 |
2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1003-3367T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326760 | |||||||
| chr11:17326841 | C | A | 1 | a0002c0002t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1003-3286C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326841 | |||||||
| chr11:17326990 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-3137G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326990 | |||||||
| chr11:17326998 | T | A | 1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-3129T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17326998 | |||||||
| chr11:17327045 | G | A | 4 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0002g0147 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-3082G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327045 | |||||||
| chr11:17327049 | A | G | 1 | a0003c0003t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1003-3078A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327049 | |||||||
| chr11:17327138 | G | A | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-2989G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327138 | |||||||
| chr11:17327262 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1003-2865C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327262 | |||||||
| chr11:17327331 | G | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1003-2796G>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327331 | |||||||
| chr11:17327638 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-2489C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327638 | |||||||
| chr11:17327704 | T | TAAGAGAC others(322): Show |
1 | a0001c0001t0007g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-2412_1003-241 others(333): Show |
NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr11 | 17327704 | ||||||
| chr11:17327729 | C | T | 2 | a0003c0003t0003g0043 a0003c0003t0003g0098 |
2 | HG02080.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1003-2398C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327729 | |||||||
| chr11:17327735 | C | T | 6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-2392C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17327735 | |||||||
| chr11:17328000 | G | A | 1 | a0003c0003t0001g0112 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1003-2127G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328000 | |||||||
| chr11:17328094 | C | T | 4 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0002g0147 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1003-2033C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328094 | |||||||
| chr11:17328097 | G | A | 20 | a0002c0002t0001g0007 a0002c0002t0001g0031 a0002c0002t0001g0099 others(17): Show |
21 | HG00423.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1003-2030G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328097 | |||||||
| chr11:17328645 | G | A | 1 | a0003c0003t0001g0112 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1003-1482G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328645 | |||||||
| chr11:17328723 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1003-1404G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328723 | |||||||
| chr11:17328828 | C | A | 6 | a0003c0003t0001g0033 a0003c0003t0001g0037 a0003c0003t0001g0040 others(3): Show |
6 | HG02129.hp2 HG02523.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-1299C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328828 | |||||||
| chr11:17328836 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0238 |
2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1003-1291G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328836 | |||||||
| chr11:17328847 | C | T | 95 | a0001c0001t0002g0170 a0003c0003t0001g0003 a0003c0003t0001g0006 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1003-1280C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328847 | |||||||
| chr11:17328874 | C | G | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-1253C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328874 | |||||||
| chr11:17328877 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1003-1250G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328877 | |||||||
| chr11:17328910 | C | A | 3 | a0001c0001t0002g0130 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01070.hp2 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1003-1217C>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17328910 | |||||||
| chr11:17329031 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1003-1096C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329031 | |||||||
| chr11:17329093 | A | G | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-1034A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329093 | |||||||
| chr11:17329623 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1003-504C>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329623 | |||||||
| chr11:17329656 | A | G | 114 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0325 others(111): Show |
116 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1003-471A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329656 | |||||||
| chr11:17329739 | C | T | 98 | a0002c0002t0001g0004 a0002c0002t0001g0007 a0002c0002t0001g0023 others(95): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1003-388C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329739 | |||||||
| chr11:17329828 | G | C | 1 | a0002c0002t0001g0029 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-299G>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 11/13 | chr11 | 17329828 | |||||||
| chr11:17330326 | T | TA | 100 | a0001c0001t0002g0239 a0001c0001t0007g0223 a0002c0002t0001g0004 others(97): Show |
102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1173+34dupA | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr11 | 17330326 | ||||||
| chr11:17330604 | G | A | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0325 others(11): Show |
14 | HG01081.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1174-298G>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330604 | |||||||
| chr11:17330670 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1174-232T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330670 | |||||||
| chr11:17330748 | C | T | 5 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-154C>T | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330748 | |||||||
| chr11:17330791 | A | C | 26 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(23): Show |
26 | HG00735.hp1 HG01243.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1174-111A>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330791 | |||||||
| chr11:17330877 | T | C | 4 | a0002c0002t0002g0144 a0002c0002t0002g0145 a0002c0002t0002g0167 others(1): Show |
4 | HG00597.hp1 HG02071.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1174-25T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 12/13 | chr11 | 17330877 | |||||||
| chr11:17331051 | T | A | 1 | a0002c0002t0001g0299 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1255+68T>A | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331051 | |||||||
| chr11:17331340 | T | C | 2 | a0002c0002t0001g0285 a0002c0002t0001g0288 |
2 | HG00423.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1256-72T>C | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331340 | |||||||
| chr11:17331354 | A | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0168 a0001c0001t0002g0203 |
3 | HG01167.hp2 HG01516.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1256-58A>G | NUCB2 | ENSG00000070081.18 | transcript | ENST00000529010.6 | protein_coding | 13/13 | chr11 | 17331354 |