Item | Value |
---|---|
geneid | 55914 |
ensemblid | ENSG00000112851.16 |
hgncid | 15842 |
symbol | ERBIN |
name | erbb2 interacting protein |
refseq_nuc | NM_001253697.2 |
refseq_prot | NP_001240626.1 |
ensembl_nuc | ENST00000284037.10 |
ensembl_prot | ENSP00000284037.4 |
mane_status | MANE Select |
chr | chr5 |
start | 65926575 |
end | 66082546 |
strand | + |
ver | v1.2 |
region | chr5:65926575-66082546 |
region5000 | chr5:65921575-66087546 |
regionname0 | ERBIN_chr5_65926575_66082546 |
regionname5000 | ERBIN_chr5_65921575_66087546 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1412 | 182 | 53 | 26 | 86 | 3 | 12 | 67 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0002 | 0/0 | 1412 | 46 | 1 | 9 | 32 | 1 | 3 | 30 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0003 | 0/0 | 1412 | 31 | 0 | 6 | 18 | 2 | 5 | 15 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0004 | 0/0 | 1412 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0005 | 0/0 | 1412 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0006 | 0/0 | 1412 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0007 | 0/0 | 1412 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0008 | 0/0 | 1412 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0009 | 0/0 | 1412 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0010 | 0/0 | 1412 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0011 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0012 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0013 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0014 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0015 | 0/0 | 1412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
a0016 | 0/0 | 1412 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | MTTKR others(1407): Show |
chr5 | 65921575 | 66087546 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4236 | 115 | 35 | 17 | 50 | 3 | 9 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0002 | 0/0 | 4236 | 53 | 9 | 8 | 33 | 0 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0007 | 1/0 | 4236 | 10 | 9 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0015 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0020 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0021 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0001c0022 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0002c0003 | 0/0 | 4236 | 46 | 1 | 9 | 32 | 1 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0003c0004 | 0/0 | 4236 | 30 | 0 | 6 | 17 | 2 | 5 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0003c0025 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0004c0005 | 0/0 | 4236 | 14 | 13 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0004c0014 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0004c0017 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0005c0006 | 0/0 | 4236 | 12 | 10 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0006c0008 | 0/0 | 4236 | 5 | 0 | 0 | 5 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0007c0011 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0008c0012 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0009c0009 | 0/0 | 4236 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0010c0010 | 0/0 | 4236 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0011c0016 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0012c0023 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0013c0024 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0014c0018 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0015c0013 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 | ||
a0016c0019 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | ATGAC others(4231): Show |
chr5 | 65921575 | 66087546 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8544 | 89 | 22 | 14 | 44 | 3 | 6 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0003 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0006 | 0/0 | 8544 | 11 | 10 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0009 | 0/0 | 8549 | 5 | 0 | 0 | 4 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8544): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0013 | 0/0 | 8544 | 3 | 0 | 1 | 0 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0014 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0020 | 0/1 | 8540 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8535): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0021 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0025 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0001t0029 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0002t0002 | 0/0 | 8544 | 52 | 9 | 8 | 32 | 0 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0002t0019 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0007t0001 | 1/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0007t0010 | 0/0 | 8544 | 6 | 6 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0007t0012 | 0/0 | 8545 | 3 | 3 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8540): Show |
chr5 | 65921575 | 66087546 |
a0001c0015t0030 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0020t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0021t0001 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0001c0022t0009 | 0/0 | 8549 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8544): Show |
chr5 | 65921575 | 66087546 |
a0002c0003t0002 | 0/0 | 8544 | 6 | 0 | 1 | 3 | 1 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0002c0003t0003 | 0/0 | 8544 | 19 | 1 | 3 | 13 | 0 | 2 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0002c0003t0005 | 0/0 | 8544 | 13 | 0 | 5 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0002c0003t0008 | 0/0 | 8544 | 8 | 0 | 0 | 8 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0001 | 0/0 | 8544 | 25 | 0 | 4 | 16 | 2 | 3 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0017 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0022 | 0/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0024 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0027 | 0/0 | 8544 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0004t0028 | 0/0 | 8544 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0003c0025t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0004c0005t0004 | 0/0 | 8544 | 13 | 12 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0004c0005t0026 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0004c0014t0004 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0004c0017t0004 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0005c0006t0002 | 0/0 | 8544 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0005c0006t0007 | 0/0 | 8544 | 8 | 6 | 2 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0005c0006t0015 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0005c0006t0016 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0006c0008t0003 | 0/0 | 8544 | 4 | 0 | 0 | 4 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0006c0008t0018 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0007c0011t0011 | 0/0 | 8540 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8535): Show |
chr5 | 65921575 | 66087546 |
a0008c0012t0011 | 0/0 | 8540 | 2 | 2 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8535): Show |
chr5 | 65921575 | 66087546 |
a0009c0009t0002 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0010c0010t0002 | 0/0 | 8544 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0011c0016t0007 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0012c0023t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0013c0024t0023 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0014c0018t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0015c0013t0001 | 0/0 | 8544 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
a0016c0019t0001 | 0/0 | 8544 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | GGCGG others(8539): Show |
chr5 | 65921575 | 66087546 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0013g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0020g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0025g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0001t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0002t0019g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0012g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0007t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0015t0030g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0020t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0021t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0001c0022t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0002c0003t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0017g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0022g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0024g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0027g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0004t0028g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0003c0025t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0005t0026g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0014t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0004c0017t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0005c0006t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0006c0008t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0006c0008t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0006c0008t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0006c0008t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0006c0008t0018g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0007c0011t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0007c0011t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0008c0012t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0008c0012t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0009c0009t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0009c0009t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0010c0010t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0010c0010t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0011c0016t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0012c0023t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0013c0024t0023g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0014c0018t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0015c0013t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
a0016c0019t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0001 | g0130 | EUR | GBR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00280 | hp2 | a0002 | c0003 | t0002 | g0215 | EUR | FIN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00408 | hp2 | a0002 | c0003 | t0008 | g0280 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00621 | hp1 | a0001 | c0001 | t0014 | g0070 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00621 | hp2 | a0003 | c0004 | t0001 | g0136 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0138 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0287 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | CHS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0286 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01081 | hp1 | a0002 | c0003 | t0005 | g0180 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01109 | hp1 | a0002 | c0003 | t0003 | g0299 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01109 | hp2 | a0005 | c0006 | t0007 | g0224 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01167 | hp1 | a0003 | c0004 | t0001 | g0304 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01167 | hp2 | a0004 | c0005 | t0004 | g0009 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01243 | hp1 | a0001 | c0001 | t0025 | g0157 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01243 | hp2 | a0005 | c0006 | t0007 | g0221 | AMR | PUR | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0236 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01257 | hp1 | a0002 | c0003 | t0005 | g0182 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01261 | hp2 | a0001 | c0001 | t0013 | g0123 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01433 | hp1 | a0002 | c0003 | t0003 | g0165 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01433 | hp2 | a0002 | c0003 | t0002 | g0201 | AMR | CLM | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01515 | hp2 | a0003 | c0004 | t0001 | g0137 | EUR | IBS | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01884 | hp1 | a0011 | c0016 | t0007 | g0228 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01934 | hp1 | a0002 | c0003 | t0005 | g0179 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01943 | hp1 | a0002 | c0003 | t0005 | g0171 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01943 | hp2 | a0003 | c0004 | t0028 | g0134 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01952 | hp2 | a0003 | c0004 | t0001 | g0305 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0261 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01981 | hp2 | a0001 | c0021 | t0001 | g0105 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01993 | hp1 | a0002 | c0003 | t0003 | g0199 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG01993 | hp2 | a0003 | c0004 | t0001 | g0131 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02055 | hp2 | a0001 | c0007 | t0010 | g0275 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02071 | hp1 | a0002 | c0003 | t0008 | g0257 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02132 | hp1 | a0003 | c0004 | t0001 | g0002 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02148 | hp1 | a0002 | c0003 | t0005 | g0185 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02165 | hp1 | a0001 | c0002 | t0019 | g0298 | EAS | CDX | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02257 | hp1 | a0005 | c0006 | t0002 | g0263 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02258 | hp1 | a0004 | c0005 | t0004 | g0016 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02258 | hp2 | a0005 | c0006 | t0007 | g0222 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02273 | hp1 | a0003 | c0004 | t0024 | g0303 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0250 | AMR | PEL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02451 | hp1 | a0005 | c0006 | t0015 | g0223 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02451 | hp2 | a0004 | c0005 | t0004 | g0020 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02572 | hp1 | a0004 | c0005 | t0004 | g0028 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02602 | hp2 | a0003 | c0004 | t0001 | g0139 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02615 | hp1 | a0001 | c0007 | t0012 | g0217 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0213 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02622 | hp1 | a0001 | c0007 | t0012 | g0219 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02647 | hp1 | a0005 | c0006 | t0002 | g0229 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0210 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02723 | hp1 | a0007 | c0011 | t0011 | g0026 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02723 | hp2 | a0004 | c0014 | t0004 | g0019 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02738 | hp1 | a0002 | c0003 | t0003 | g0197 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02738 | hp2 | a0003 | c0004 | t0001 | g0140 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02818 | hp1 | a0004 | c0017 | t0004 | g0012 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02886 | hp1 | a0001 | c0007 | t0010 | g0164 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02895 | hp1 | a0004 | c0005 | t0004 | g0021 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02896 | hp1 | a0005 | c0006 | t0007 | g0027 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02896 | hp2 | a0001 | c0007 | t0010 | g0163 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02897 | hp1 | a0004 | c0005 | t0004 | g0018 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02897 | hp2 | a0001 | c0007 | t0010 | g0162 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02922 | hp1 | a0008 | c0012 | t0011 | g0023 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02922 | hp2 | a0004 | c0005 | t0004 | g0014 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02965 | hp1 | a0005 | c0006 | t0016 | g0226 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02976 | hp1 | a0005 | c0006 | t0007 | g0227 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03017 | hp2 | a0003 | c0004 | t0027 | g0300 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03041 | hp1 | a0004 | c0005 | t0004 | g0008 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03098 | hp2 | a0013 | c0024 | t0023 | g0145 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03139 | hp2 | a0004 | c0005 | t0026 | g0013 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03195 | hp2 | a0008 | c0012 | t0011 | g0024 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03209 | hp2 | a0004 | c0005 | t0004 | g0015 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03225 | hp2 | a0005 | c0006 | t0007 | g0220 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0202 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03239 | hp2 | a0003 | c0004 | t0022 | g0301 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03486 | hp2 | a0004 | c0005 | t0004 | g0022 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03516 | hp1 | a0007 | c0011 | t0011 | g0025 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | ESN | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03540 | hp1 | a0014 | c0018 | t0001 | g0050 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03540 | hp2 | a0005 | c0006 | t0007 | g0225 | AFR | GWD | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03579 | hp2 | a0004 | c0005 | t0004 | g0010 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03704 | hp1 | a0002 | c0003 | t0003 | g0283 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03710 | hp1 | a0001 | c0001 | t0009 | g0037 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03710 | hp2 | a0003 | c0004 | t0001 | g0302 | SAS | PJL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG04115 | hp2 | a0001 | c0001 | t0013 | g0102 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG04228 | hp2 | a0001 | c0001 | t0013 | g0124 | SAS | STU | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18747 | hp1 | a0003 | c0004 | t0001 | g0114 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18747 | hp2 | a0001 | c0015 | t0030 | g0258 | EAS | CHB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18940 | hp1 | a0002 | c0003 | t0003 | g0192 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18942 | hp2 | a0003 | c0004 | t0001 | g0101 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18943 | hp1 | a0002 | c0003 | t0008 | g0173 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18944 | hp1 | a0002 | c0003 | t0005 | g0281 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18944 | hp2 | a0003 | c0025 | t0001 | g0142 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18946 | hp2 | a0002 | c0003 | t0003 | g0169 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18948 | hp1 | a0003 | c0004 | t0001 | g0127 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18948 | hp2 | a0002 | c0003 | t0003 | g0177 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18949 | hp1 | a0003 | c0004 | t0001 | g0126 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18950 | hp1 | a0002 | c0003 | t0008 | g0193 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18950 | hp2 | a0006 | c0008 | t0003 | g0072 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18951 | hp1 | a0009 | c0009 | t0002 | g0168 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18951 | hp2 | a0002 | c0003 | t0003 | g0204 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18954 | hp1 | a0002 | c0003 | t0003 | g0175 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18956 | hp2 | a0006 | c0008 | t0003 | g0194 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18957 | hp2 | a0002 | c0003 | t0003 | g0167 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18963 | hp1 | a0003 | c0004 | t0001 | g0269 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18968 | hp1 | a0002 | c0003 | t0008 | g0241 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18970 | hp1 | a0010 | c0010 | t0002 | g0290 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18970 | hp2 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18971 | hp2 | a0006 | c0008 | t0018 | g0195 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18972 | hp1 | a0002 | c0003 | t0008 | g0178 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18972 | hp2 | a0003 | c0004 | t0001 | g0129 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18977 | hp1 | a0003 | c0004 | t0001 | g0270 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18977 | hp2 | a0002 | c0003 | t0005 | g0183 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18978 | hp1 | a0002 | c0003 | t0003 | g0282 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18981 | hp1 | a0006 | c0008 | t0003 | g0190 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18982 | hp2 | a0003 | c0004 | t0001 | g0088 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18985 | hp1 | a0002 | c0003 | t0005 | g0200 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18985 | hp2 | a0001 | c0001 | t0009 | g0038 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18991 | hp2 | a0002 | c0003 | t0003 | g0277 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18992 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18992 | hp2 | a0009 | c0009 | t0002 | g0203 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18994 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18999 | hp1 | a0002 | c0003 | t0003 | g0189 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19001 | hp2 | a0002 | c0003 | t0002 | g0205 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19003 | hp1 | a0003 | c0004 | t0001 | g0100 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19004 | hp1 | a0003 | c0004 | t0001 | g0271 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0276 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19010 | hp1 | a0003 | c0004 | t0001 | g0093 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19012 | hp2 | a0002 | c0003 | t0005 | g0184 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19030 | hp1 | a0015 | c0013 | t0001 | g0083 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19030 | hp2 | a0001 | c0001 | t0021 | g0141 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | LWK | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19057 | hp2 | a0003 | c0004 | t0017 | g0120 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19060 | hp1 | a0002 | c0003 | t0003 | g0176 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19063 | hp2 | a0002 | c0003 | t0005 | g0198 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19064 | hp1 | a0001 | c0020 | t0001 | g0116 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19064 | hp2 | a0006 | c0008 | t0003 | g0196 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19066 | hp2 | a0010 | c0010 | t0002 | g0291 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19067 | hp2 | a0002 | c0003 | t0005 | g0187 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19068 | hp1 | a0002 | c0003 | t0005 | g0186 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19070 | hp1 | a0001 | c0001 | t0014 | g0069 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19070 | hp2 | a0002 | c0003 | t0008 | g0174 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19076 | hp1 | a0016 | c0019 | t0001 | g0087 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19076 | hp2 | a0002 | c0003 | t0002 | g0207 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19079 | hp2 | a0002 | c0003 | t0003 | g0191 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19080 | hp1 | a0002 | c0003 | t0002 | g0206 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19083 | hp1 | a0002 | c0003 | t0008 | g0278 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0041 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19087 | hp1 | a0001 | c0022 | t0009 | g0036 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19088 | hp1 | a0003 | c0004 | t0001 | g0113 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19088 | hp2 | a0002 | c0003 | t0003 | g0188 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19090 | hp2 | a0002 | c0003 | t0005 | g0181 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA20129 | hp1 | a0001 | c0007 | t0010 | g0160 | AFR | ASW | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA20129 | hp2 | a0002 | c0003 | t0003 | g0166 | AFR | ASW | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02109 | hp1 | a0004 | c0005 | t0004 | g0011 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02109 | hp2 | a0001 | c0007 | t0010 | g0161 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02559 | hp1 | a0012 | c0023 | t0001 | g0086 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG02559 | hp2 | a0001 | c0007 | t0012 | g0218 | AFR | ACB | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03471 | hp1 | a0004 | c0005 | t0004 | g0017 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG06807 | hp1 | a0005 | c0006 | t0007 | g0230 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0208 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
NA20300 | hp2 | a0001 | c0001 | t0029 | g0091 | AFR | USA | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
homoSapiens | chm13v2 | a0001 | c0001 | t0020 | g0098 | REF | REF | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
homoSapiens | grch38p0 | a0001 | c0007 | t0001 | g0245 | REF | REF | ERBIN_chr5_65921575_66087546 | ERBIN | chr5 | 65921575 | 66087546 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65992840 | T | C | 1 | a0015 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.122T>C | p.Ile41Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/26 | 411/8544 | 122/4239 | 41/1412 | chr5 | 65992840 | |||
chr5:66025483 | C | T | 1 | a0003 | 31 | HG00099.hp1 HG00621.hp2 HG00642.hp1 others(28): Show |
missense_variant | MODERATE | c.821C>T | p.Ser274Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1110/8544 | 821/4239 | 274/1412 | chr5 | 66025483 | |||
chr5:66025496 | A | G | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.834A>G | p.Ile278Met | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1123/8544 | 834/4239 | 278/1412 | chr5 | 66025496 | |||
chr5:66025867 | C | G | 1 | a0012 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.910C>G | p.Leu304Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/26 | 1199/8544 | 910/4239 | 304/1412 | chr5 | 66025867 | |||
chr5:66025922 | C | T | 2 | a0007 a0008 |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
missense_variant | MODERATE | c.965C>T | p.Thr322Ile | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/26 | 1254/8544 | 965/4239 | 322/1412 | chr5 | 66025922 | |||
chr5:66048704 | T | C | 1 | a0014 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1826T>C | p.Met609Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/26 | 2115/8544 | 1826/4239 | 609/1412 | chr5 | 66048704 | |||
chr5:66050951 | T | C | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2072T>C | p.Ile691Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/26 | 2361/8544 | 2072/4239 | 691/1412 | chr5 | 66050951 | |||
chr5:66053554 | A | G | 1 | a0004 | 16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
missense_variant | MODERATE | c.2236A>G | p.Lys746Glu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 2525/8544 | 2236/4239 | 746/1412 | chr5 | 66053554 | |||
chr5:66054059 | A | G | 1 | a0011 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2741A>G | p.Lys914Arg | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3030/8544 | 2741/4239 | 914/1412 | chr5 | 66054059 | |||
chr5:66054287 | C | G | 1 | a0008 | 2 | HG02922.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2969C>G | p.Thr990Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3258/8544 | 2969/4239 | 990/1412 | chr5 | 66054287 | |||
chr5:66054515 | T | C | 1 | a0009 | 2 | NA18951.hp1 NA18992.hp2 |
missense_variant | MODERATE | c.3197T>C | p.Ile1066Thr | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3486/8544 | 3197/4239 | 1066/1412 | chr5 | 66054515 | |||
chr5:66054578 | A | G | 1 | a0006 | 5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
missense_variant | MODERATE | c.3260A>G | p.Asn1087Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3549/8544 | 3260/4239 | 1087/1412 | chr5 | 66054578 | |||
chr5:66054584 | G | T | 1 | a0005 | 12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.3266G>T | p.Gly1089Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3555/8544 | 3266/4239 | 1089/1412 | chr5 | 66054584 | |||
chr5:66054613 | A | G | 1 | a0010 | 2 | NA18970.hp1 NA19066.hp2 |
missense_variant | MODERATE | c.3295A>G | p.Ile1099Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3584/8544 | 3295/4239 | 1099/1412 | chr5 | 66054613 | |||
chr5:66054653 | C | T | 3 | a0002 a0006 a0009 |
53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
missense_variant | MODERATE | c.3335C>T | p.Ser1112Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3624/8544 | 3335/4239 | 1112/1412 | chr5 | 66054653 | |||
chr5:66054707 | G | T | 1 | a0016 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.3389G>T | p.Arg1130Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3678/8544 | 3389/4239 | 1130/1412 | chr5 | 66054707 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:66021353 | C | T | 11 | a0001c0001 a0001c0020 a0001c0021 others(8): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
synonymous_variant | LOW | c.565C>T | p.Leu189Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/26 | 854/8544 | 565/4239 | 189/1412 | chr5 | 66021353 | |||
chr5:66025484 | G | A | 1 | a0004c0014 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.822G>A | p.Ser274Ser | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/26 | 1111/8544 | 822/4239 | 274/1412 | chr5 | 66025484 | |||
chr5:66046418 | C | T | 1 | a0001c0022 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.1668C>T | p.Asn556Asn | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/26 | 1957/8544 | 1668/4239 | 556/1412 | chr5 | 66046418 | |||
chr5:66054036 | T | C | 1 | a0003c0025 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.2718T>C | p.Asp906Asp | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3007/8544 | 2718/4239 | 906/1412 | chr5 | 66054036 | |||
chr5:66054051 | C | T | 1 | a0001c0021 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.2733C>T | p.Val911Val | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3022/8544 | 2733/4239 | 911/1412 | chr5 | 66054051 | |||
chr5:66054174 | C | T | 1 | a0004c0017 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.2856C>T | p.Pro952Pro | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3145/8544 | 2856/4239 | 952/1412 | chr5 | 66054174 | |||
chr5:66054345 | C | T | 1 | a0001c0020 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.3027C>T | p.Leu1009Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3316/8544 | 3027/4239 | 1009/1412 | chr5 | 66054345 | |||
chr5:66054546 | A | G | 6 | a0001c0002 a0001c0015 a0002c0003 others(3): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
synonymous_variant | LOW | c.3228A>G | p.Arg1076Arg | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3517/8544 | 3228/4239 | 1076/1412 | chr5 | 66054546 | |||
chr5:66054631 | T | C | 2 | a0007c0011 a0008c0012 |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.3313T>C | p.Leu1105Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/26 | 3602/8544 | 3313/4239 | 1105/1412 | chr5 | 66054631 | |||
chr5:66076920 | T | C | 1 | a0001c0015 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.4102T>C | p.Leu1368Leu | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/26 | 4391/8544 | 4102/4239 | 1368/1412 | chr5 | 66076920 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65926656 | G | C | 1 | a0002c0003t0005 | 13 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-208G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66063 | chr5 | 65926656 | ||||||
chr5:65926682 | C | T | 1 | a0001c0015t0030 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66037 | chr5 | 65926682 | ||||||
chr5:65926689 | A | C | 1 | a0001c0001t0029 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66030 | chr5 | 65926689 | ||||||
chr5:65926713 | T | G | 4 | a0005c0006t0007 a0005c0006t0015 a0005c0006t0016 others(1): Show |
11 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-151T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 66006 | chr5 | 65926713 | ||||||
chr5:65926728 | A | C | 1 | a0005c0006t0016 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-136A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65991 | chr5 | 65926728 | ||||||
chr5:65926791 | G | GAAAAA | 2 | a0001c0001t0009 a0001c0022t0009 |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-73_-72insAAAAA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65927 | chr5 | 65926791 | ||||||
chr5:65926792 | G | A | 1 | a0003c0004t0017 | 1 | NA19057.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | chr5 | 65926792 | |||||||
chr5:65926793 | T | C | 2 | a0001c0001t0009 a0001c0022t0009 |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-71T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65926 | chr5 | 65926793 | ||||||
chr5:65926794 | G | T | 2 | a0001c0001t0009 a0001c0022t0009 |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65925 | chr5 | 65926794 | ||||||
chr5:65926795 | T | G | 2 | a0001c0001t0009 a0001c0022t0009 |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65924 | chr5 | 65926795 | ||||||
chr5:65926798 | C | G | 1 | a0003c0004t0028 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | 65921 | chr5 | 65926798 | ||||||
chr5:65926801 | C | T | 1 | a0003c0004t0027 | 1 | HG03017.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/26 | chr5 | 65926801 | |||||||
chr5:66078665 | A | G | 5 | a0001c0007t0010 a0004c0005t0004 a0004c0005t0026 others(2): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 135 | chr5 | 66078665 | ||||||
chr5:66078691 | A | G | 2 | a0001c0001t0006 a0001c0001t0025 |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*161A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 161 | chr5 | 66078691 | ||||||
chr5:66078808 | T | C | 1 | a0006c0008t0018 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 278 | chr5 | 66078808 | ||||||
chr5:66078969 | C | A | 1 | a0001c0002t0019 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 439 | chr5 | 66078969 | ||||||
chr5:66079213 | A | G | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*683A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 683 | chr5 | 66079213 | ||||||
chr5:66079540 | CT | C | 5 | a0001c0007t0010 a0004c0005t0004 a0004c0005t0026 others(2): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1013delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1013 | INFO_REALIGN_3_PRIME | chr5 | 66079540 | |||||
chr5:66079585 | A | C | 1 | a0004c0005t0026 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1055A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1055 | chr5 | 66079585 | ||||||
chr5:66080359 | T | C | 1 | a0001c0007t0012 | 3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1829T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1829 | chr5 | 66080359 | ||||||
chr5:66080478 | T | TA | 6 | a0001c0007t0010 a0001c0007t0012 a0004c0005t0004 others(3): Show |
25 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1959dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 1960 | INFO_REALIGN_3_PRIME | chr5 | 66080478 | |||||
chr5:66080647 | T | C | 1 | a0001c0001t0021 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2117T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2117 | chr5 | 66080647 | ||||||
chr5:66080779 | T | C | 1 | a0003c0004t0022 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2249 | chr5 | 66080779 | ||||||
chr5:66080813 | A | G | 1 | a0003c0004t0024 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2283A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2283 | chr5 | 66080813 | ||||||
chr5:66080818 | C | T | 5 | a0001c0007t0010 a0004c0005t0004 a0004c0005t0026 others(2): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2288C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2288 | chr5 | 66080818 | ||||||
chr5:66080878 | G | A | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2348G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2348 | chr5 | 66080878 | ||||||
chr5:66080927 | T | C | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2397T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2397 | chr5 | 66080927 | ||||||
chr5:66081024 | A | C | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2494A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2494 | chr5 | 66081024 | ||||||
chr5:66081213 | C | T | 1 | a0001c0007t0010 | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2683C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2683 | chr5 | 66081213 | ||||||
chr5:66081364 | A | G | 6 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0005 others(3): Show |
46 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2834 | chr5 | 66081364 | ||||||
chr5:66081393 | C | G | 1 | a0002c0003t0008 | 8 | HG00408.hp2 HG02071.hp1 NA18943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2863C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2863 | chr5 | 66081393 | ||||||
chr5:66081430 | G | A | 6 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0005 others(3): Show |
46 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2900G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2900 | chr5 | 66081430 | ||||||
chr5:66081500 | G | T | 1 | a0001c0001t0014 | 2 | HG00621.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2970G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 2970 | chr5 | 66081500 | ||||||
chr5:66081604 | T | C | 2 | a0001c0001t0006 a0001c0001t0025 |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3074T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3074 | chr5 | 66081604 | ||||||
chr5:66081636 | ATATC | A | 2 | a0007c0011t0011 a0008c0012t0011 |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3109_*3112delTCTA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3109 | INFO_REALIGN_3_PRIME | chr5 | 66081636 | |||||
chr5:66081698 | G | C | 28 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0025 others(25): Show |
165 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3168 | chr5 | 66081698 | ||||||
chr5:66081713 | A | T | 1 | a0001c0001t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3183A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3183 | chr5 | 66081713 | ||||||
chr5:66081843 | A | G | 2 | a0007c0011t0011 a0008c0012t0011 |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3313 | chr5 | 66081843 | ||||||
chr5:66082042 | G | A | 1 | a0001c0001t0013 | 3 | HG01261.hp2 HG04115.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3512G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3512 | chr5 | 66082042 | ||||||
chr5:66082111 | G | A | 4 | a0004c0005t0004 a0004c0005t0026 a0004c0014t0004 others(1): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3581G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3581 | chr5 | 66082111 | ||||||
chr5:66082148 | C | T | 5 | a0001c0007t0010 a0004c0005t0004 a0004c0005t0026 others(2): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3618C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3618 | chr5 | 66082148 | ||||||
chr5:66082394 | C | T | 1 | a0005c0006t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3864C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3864 | chr5 | 66082394 | ||||||
chr5:66082425 | C | T | 1 | a0013c0024t0023 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3895C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 26/26 | 3895 | chr5 | 66082425 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:65926870 | G | T | 6 | a0003c0004t0001g0302 a0003c0004t0001g0304 a0003c0004t0001g0305 others(3): Show |
6 | HG01167.hp1 HG01952.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+64G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926870 | |||||||
chr5:65926876 | T | A | 1 | a0003c0004t0001g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-58+70T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926876 | |||||||
chr5:65926880 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-58+74T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926880 | |||||||
chr5:65926897 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 |
3 | HG02280.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-58+91C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926897 | |||||||
chr5:65926902 | A | T | 1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-58+96A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926902 | |||||||
chr5:65926917 | T | C | 21 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(18): Show |
21 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+111T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926917 | |||||||
chr5:65926990 | C | G | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-58+184C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65926990 | |||||||
chr5:65926997 | G | GC | 27 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(24): Show |
27 | HG00408.hp2 HG00438.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-58+199dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65926997 | ||||||
chr5:65927005 | C | G | 10 | a0001c0002t0002g0289 a0001c0002t0002g0292 a0001c0002t0002g0293 others(7): Show |
10 | HG00408.hp1 HG00438.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-58+199C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927005 | |||||||
chr5:65927070 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-58+264T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927070 | |||||||
chr5:65927104 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-58+298G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927104 | |||||||
chr5:65927201 | A | C | 1 | a0005c0006t0002g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-58+395A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927201 | |||||||
chr5:65927227 | G | A | 1 | a0003c0004t0027g0300 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-58+421G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927227 | |||||||
chr5:65927275 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-58+469T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927275 | |||||||
chr5:65927288 | A | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+482A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927288 | |||||||
chr5:65927359 | G | C | 6 | a0002c0003t0003g0165 a0002c0003t0003g0166 a0002c0003t0003g0167 others(3): Show |
6 | HG01433.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+553G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927359 | |||||||
chr5:65927392 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+586T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927392 | |||||||
chr5:65927429 | G | T | 1 | a0005c0006t0007g0230 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58+623G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927429 | |||||||
chr5:65927646 | A | G | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+840A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927646 | |||||||
chr5:65927679 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-58+873T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927679 | |||||||
chr5:65927693 | C | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+887C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927693 | |||||||
chr5:65927725 | G | T | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+919G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927725 | |||||||
chr5:65927873 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0231 others(3): Show |
6 | NA18954.hp2 NA18999.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+1067T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927873 | |||||||
chr5:65927902 | C | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-58+1096C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65927902 | |||||||
chr5:65928010 | T | C | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+1204T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928010 | |||||||
chr5:65928067 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-58+1261A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928067 | |||||||
chr5:65928068 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-58+1262G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928068 | |||||||
chr5:65928170 | C | G | 17 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+1364C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928170 | |||||||
chr5:65928246 | C | CT | 7 | a0001c0001t0001g0158 a0003c0004t0001g0302 a0003c0004t0001g0304 others(4): Show |
7 | HG01167.hp1 HG01952.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+1451dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65928246 | ||||||
chr5:65928311 | C | G | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+1505C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928311 | |||||||
chr5:65928384 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-58+1578G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928384 | |||||||
chr5:65928428 | T | C | 1 | a0001c0002t0002g0170 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-58+1622T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928428 | |||||||
chr5:65928648 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+1842G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928648 | |||||||
chr5:65928678 | T | C | 1 | a0001c0002t0002g0235 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-58+1872T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65928678 | |||||||
chr5:65929478 | C | T | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+2672C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929478 | |||||||
chr5:65929490 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+2684C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929490 | |||||||
chr5:65929557 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+2751T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929557 | |||||||
chr5:65929608 | A | C | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+2802A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929608 | |||||||
chr5:65929610 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+2804C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929610 | |||||||
chr5:65929637 | C | CT | 12 | a0001c0001t0001g0144 a0001c0002t0002g0261 a0001c0002t0002g0262 others(9): Show |
12 | HG01981.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+2851dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929637 | ||||||
chr5:65929637 | CT | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG01256.hp1 HG01515.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+2851delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929637 | ||||||
chr5:65929639 | T | TG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+2833_-58+2834i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929639 | |||||||
chr5:65929657 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(100): Show |
104 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-58+2851T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929657 | |||||||
chr5:65929657 | T | TC | 3 | a0001c0001t0001g0032 a0001c0001t0001g0125 a0003c0004t0001g0126 |
3 | NA18949.hp1 NA18954.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-58+2852dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65929657 | ||||||
chr5:65929741 | A | T | 3 | a0001c0001t0001g0272 a0001c0001t0013g0123 a0001c0001t0013g0124 |
3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-58+2935A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65929741 | |||||||
chr5:65930035 | C | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+3229C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930035 | |||||||
chr5:65930045 | C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-58+3239C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930045 | |||||||
chr5:65930171 | C | G | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+3365C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930171 | |||||||
chr5:65930213 | G | T | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+3407G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930213 | |||||||
chr5:65930227 | A | G | 2 | a0001c0007t0012g0217 a0001c0007t0012g0219 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+3421A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930227 | |||||||
chr5:65930460 | A | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+3654A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930460 | |||||||
chr5:65930470 | G | A | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+3664G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930470 | |||||||
chr5:65930485 | T | G | 1 | a0002c0003t0003g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-58+3679T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930485 | |||||||
chr5:65930621 | T | C | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-58+3815T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930621 | |||||||
chr5:65930689 | G | A | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+3883G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930689 | |||||||
chr5:65930705 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+3899A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930705 | |||||||
chr5:65930823 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+4017C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930823 | |||||||
chr5:65930849 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-58+4043A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930849 | |||||||
chr5:65930937 | A | C | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-58+4131A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65930937 | |||||||
chr5:65930989 | GTGTGGAA others(35): Show |
G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+4226_-58+4267d others(44): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65930989 | ||||||
chr5:65931275 | C | G | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+4469C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931275 | |||||||
chr5:65931640 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+4834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931640 | |||||||
chr5:65931692 | G | A | 1 | a0001c0022t0009g0036 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-58+4886G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931692 | |||||||
chr5:65931698 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-58+4892C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931698 | |||||||
chr5:65931819 | C | CT | 42 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0049 others(39): Show |
42 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-58+5030dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65931819 | ||||||
chr5:65931819 | CT | C | 14 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0158 others(11): Show |
14 | HG01256.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+5030delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65931819 | ||||||
chr5:65931823 | T | C | 43 | a0001c0002t0002g0170 a0001c0002t0002g0279 a0002c0003t0003g0165 others(40): Show |
43 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-58+5017T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931823 | |||||||
chr5:65931895 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+5089C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931895 | |||||||
chr5:65931922 | G | A | 1 | a0001c0001t0006g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-58+5116G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65931922 | |||||||
chr5:65932020 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-58+5214G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932020 | |||||||
chr5:65932033 | G | A | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-58+5227G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932033 | |||||||
chr5:65932055 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-58+5249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932055 | |||||||
chr5:65932108 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+5302G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932108 | |||||||
chr5:65932157 | A | G | 6 | a0001c0001t0001g0121 a0003c0004t0001g0088 a0003c0004t0001g0122 others(3): Show |
6 | NA18955.hp2 NA18977.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+5351A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932157 | |||||||
chr5:65932337 | C | CA | 7 | a0001c0001t0009g0037 a0003c0004t0001g0129 a0003c0004t0001g0302 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+5550dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65932337 | ||||||
chr5:65932337 | CA | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0118 others(17): Show |
20 | HG00438.hp1 HG01069.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58+5550delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65932337 | ||||||
chr5:65932423 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-58+5617G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932423 | |||||||
chr5:65932585 | A | G | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-58+5779A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932585 | |||||||
chr5:65932639 | A | G | 2 | a0001c0002t0002g0296 a0001c0002t0002g0297 |
2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-58+5833A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932639 | |||||||
chr5:65932712 | A | G | 2 | a0004c0005t0004g0020 a0004c0014t0004g0019 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-58+5906A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932712 | |||||||
chr5:65932866 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | NA18962.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-58+6060G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932866 | |||||||
chr5:65932963 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-58+6157T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65932963 | |||||||
chr5:65933067 | A | G | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-58+6261A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933067 | |||||||
chr5:65933072 | A | G | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+6266A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933072 | |||||||
chr5:65933491 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-58+6685A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933491 | |||||||
chr5:65933575 | C | T | 1 | a0002c0003t0002g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58+6769C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933575 | |||||||
chr5:65933616 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-58+6810C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933616 | |||||||
chr5:65933618 | C | T | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+6812C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933618 | |||||||
chr5:65933707 | A | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+6901A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933707 | |||||||
chr5:65933911 | T | A | 19 | a0001c0001t0001g0232 a0003c0004t0001g0130 a0005c0006t0002g0229 others(16): Show |
19 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-58+7105T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65933911 | |||||||
chr5:65934042 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-58+7236G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934042 | |||||||
chr5:65934175 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+7369C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934175 | |||||||
chr5:65934176 | G | A | 1 | a0001c0001t0029g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-58+7370G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934176 | |||||||
chr5:65934253 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-58+7447A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65934253 | |||||||
chr5:65934421 | T | TTCTCTTT others(195): Show |
1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+7616_-58+7817d others(204): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65934421 | ||||||
chr5:65934425 | CT | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+7627delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65934425 | ||||||
chr5:65935028 | C | A | 44 | a0001c0002t0002g0170 a0001c0002t0002g0279 a0002c0003t0003g0165 others(41): Show |
44 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-58+8222C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935028 | |||||||
chr5:65935140 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-58+8334T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935140 | |||||||
chr5:65935230 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-58+8424C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935230 | |||||||
chr5:65935233 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-58+8427G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935233 | |||||||
chr5:65935252 | T | G | 1 | a0003c0004t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-58+8446T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935252 | |||||||
chr5:65935336 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+8530A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935336 | |||||||
chr5:65935376 | G | GT | 17 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+8571dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65935376 | ||||||
chr5:65935399 | A | G | 6 | a0001c0002t0002g0172 a0001c0002t0002g0211 a0001c0002t0002g0212 others(3): Show |
6 | HG02280.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+8593A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935399 | |||||||
chr5:65935436 | T | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+8630T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935436 | |||||||
chr5:65935552 | C | T | 2 | a0001c0001t0001g0128 a0001c0020t0001g0116 |
2 | HG01891.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-58+8746C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935552 | |||||||
chr5:65935617 | A | G | 17 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+8811A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935617 | |||||||
chr5:65935816 | A | G | 17 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+9010A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935816 | |||||||
chr5:65935820 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58+9014C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935820 | |||||||
chr5:65935924 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0084 |
3 | NA18954.hp2 NA18955.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-58+9118C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935924 | |||||||
chr5:65935985 | C | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(87): Show |
91 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.-58+9179C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65935985 | |||||||
chr5:65936130 | C | G | 2 | a0001c0001t0009g0040 a0001c0001t0009g0041 |
2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+9324C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936130 | |||||||
chr5:65936175 | G | C | 1 | a0002c0003t0002g0202 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+9369G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936175 | |||||||
chr5:65936252 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+9446A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936252 | |||||||
chr5:65936672 | G | A | 1 | a0003c0004t0001g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-58+9866G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936672 | |||||||
chr5:65936724 | T | A | 2 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-58+9918T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936724 | |||||||
chr5:65936832 | G | A | 5 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(2): Show |
5 | HG03098.hp1 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+10026G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65936832 | |||||||
chr5:65937016 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-58+10210C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937016 | |||||||
chr5:65937055 | G | A | 26 | a0001c0002t0002g0170 a0001c0002t0002g0279 a0002c0003t0003g0175 others(23): Show |
26 | HG00408.hp2 HG01081.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-58+10249G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937055 | |||||||
chr5:65937111 | T | TA | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0016c0019t0001g0087 |
3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-58+10306dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65937111 | ||||||
chr5:65937343 | C | T | 21 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0274 others(18): Show |
21 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-58+10537C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937343 | |||||||
chr5:65937765 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-58+10959G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937765 | |||||||
chr5:65937863 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+11057C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937863 | |||||||
chr5:65937943 | T | G | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+11137T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937943 | |||||||
chr5:65937983 | C | T | 1 | a0002c0003t0003g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-58+11177C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937983 | |||||||
chr5:65937986 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+11180T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65937986 | |||||||
chr5:65938044 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0265 |
3 | NA18940.hp2 NA18978.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-58+11238G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938044 | |||||||
chr5:65938294 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+11488G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938294 | |||||||
chr5:65938371 | C | CT | 15 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-58+11583dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | ||||||
chr5:65938371 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-58+11583delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | ||||||
chr5:65938371 | CTT | C | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG00735.hp1 HG01069.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+11582_-58+1158 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938371 | ||||||
chr5:65938529 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+11723C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938529 | |||||||
chr5:65938552 | C | CTGTTT | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+11753_-58+1175 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65938552 | ||||||
chr5:65938585 | C | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+11779C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938585 | |||||||
chr5:65938773 | G | C | 1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-58+11967G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938773 | |||||||
chr5:65938796 | C | T | 5 | a0001c0002t0002g0289 a0001c0002t0002g0293 a0001c0002t0002g0294 others(2): Show |
5 | HG02165.hp1 NA18969.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+11990C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938796 | |||||||
chr5:65938802 | C | T | 2 | a0001c0002t0002g0259 a0002c0003t0008g0257 |
2 | HG02071.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-58+11996C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65938802 | |||||||
chr5:65939158 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+12352G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939158 | |||||||
chr5:65939383 | G | A | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-58+12577G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939383 | |||||||
chr5:65939394 | G | A | 1 | a0004c0005t0004g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-58+12588G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939394 | |||||||
chr5:65939482 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-58+12676T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939482 | |||||||
chr5:65939491 | A | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+12685A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939491 | |||||||
chr5:65939507 | TCCCTCTC others(20): Show |
T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+12717_-58+1274 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939507 | ||||||
chr5:65939524 | T | TTCCCTCT others(8): Show |
4 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0159 others(1): Show |
4 | HG00609.hp1 NA18950.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+12730_-58+1274 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939524 | ||||||
chr5:65939531 | TC | T | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+12731delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939531 | ||||||
chr5:65939536 | C | G | 1 | a0003c0004t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-58+12730C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939536 | |||||||
chr5:65939627 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-58+12821G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939627 | |||||||
chr5:65939664 | AGCCTGCC others(4): Show |
A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-58+12865_-58+1287 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65939664 | ||||||
chr5:65939706 | C | T | 1 | a0004c0005t0004g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-58+12900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939706 | |||||||
chr5:65939808 | C | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-58+13002C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939808 | |||||||
chr5:65939836 | G | C | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-58+13030G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939836 | |||||||
chr5:65939864 | G | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+13058G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939864 | |||||||
chr5:65939926 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+13120G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65939926 | |||||||
chr5:65940020 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13214G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940020 | |||||||
chr5:65940056 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+13250A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940056 | |||||||
chr5:65940080 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+13274G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940080 | |||||||
chr5:65940156 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13350G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940156 | |||||||
chr5:65940199 | G | A | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-58+13393G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940199 | |||||||
chr5:65940313 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+13507A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940313 | |||||||
chr5:65940341 | C | T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+13535C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940341 | |||||||
chr5:65940379 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13573A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940379 | |||||||
chr5:65940384 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13578C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940384 | |||||||
chr5:65940396 | A | ACCCCATC others(39): Show |
11 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13592_-58+1359 others(50): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940396 | ||||||
chr5:65940399 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13593T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940399 | |||||||
chr5:65940399 | TCGTCCGG others(42): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-58+13621_-58+1366 others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940399 | ||||||
chr5:65940401 | G | A | 5 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13595G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940401 | |||||||
chr5:65940426 | GC | G | 5 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13626delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940426 | ||||||
chr5:65940427 | C | A | 6 | a0002c0003t0003g0165 a0002c0003t0003g0166 a0002c0003t0003g0167 others(3): Show |
6 | HG01433.hp1 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+13621C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940427 | |||||||
chr5:65940427 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-58+13621C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940427 | |||||||
chr5:65940428 | CCCCCGCC others(41): Show |
C | 1 | a0001c0001t0001g0089 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-58+13627_-58+1367 others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940428 | ||||||
chr5:65940432 | C | A | 11 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13626C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940432 | |||||||
chr5:65940432 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13626C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940432 | |||||||
chr5:65940433 | G | A | 11 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13627G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940433 | |||||||
chr5:65940436 | C | A | 5 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13630C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940436 | |||||||
chr5:65940436 | C | T | 2 | a0010c0010t0002g0290 a0010c0010t0002g0291 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-58+13630C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940436 | |||||||
chr5:65940444 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-58+13638T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940444 | |||||||
chr5:65940447 | C | A | 11 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13641C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940447 | |||||||
chr5:65940449 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13643C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940449 | |||||||
chr5:65940450 | G | A | 11 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+13644G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940450 | |||||||
chr5:65940464 | T | TG | 17 | a0002c0003t0003g0197 a0003c0004t0001g0136 a0004c0005t0004g0014 others(14): Show |
17 | HG00621.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-58+13665dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940464 | ||||||
chr5:65940466 | GGGGGGTC others(171): Show |
G | 1 | a0001c0001t0001g0060 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-58+13666_-58+1384 others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940466 | ||||||
chr5:65940475 | G | GCCCCCAA others(49): Show |
3 | a0004c0005t0004g0008 a0004c0005t0004g0011 a0004c0005t0004g0028 |
3 | HG02109.hp1 HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-58+13669_-58+1367 others(60): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | |||||||
chr5:65940475 | G | GCCCCCAA others(50): Show |
1 | a0004c0005t0004g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-58+13669_-58+1367 others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | |||||||
chr5:65940475 | G | GCCCCCAA others(51): Show |
1 | a0004c0005t0004g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-58+13669_-58+1367 others(62): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940475 | |||||||
chr5:65940476 | T | C | 5 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13670T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940476 | |||||||
chr5:65940476 | T | TC | 85 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0049 others(82): Show |
85 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.-58+13682dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | ||||||
chr5:65940476 | T | TCC | 29 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0104 others(26): Show |
29 | HG00099.hp2 HG00408.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.-58+13681_-58+1368 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | ||||||
chr5:65940476 | T | TCCC | 19 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0149 others(16): Show |
19 | HG00408.hp2 HG01109.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58+13680_-58+1368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | ||||||
chr5:65940476 | T | TCCCCCCC others(3): Show |
1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-58+13673_-58+1368 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940476 | ||||||
chr5:65940488 | CG | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0132 others(2): Show |
5 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+13684delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940488 | ||||||
chr5:65940489 | G | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0143 a0001c0007t0010g0275 others(11): Show |
14 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+13683G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940489 | |||||||
chr5:65940516 | T | TG | 26 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0272 others(23): Show |
26 | HG00099.hp1 HG00738.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-58+13718dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940516 | ||||||
chr5:65940516 | TG | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13718delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940516 | ||||||
chr5:65940534 | T | TGCCCGGC others(168): Show |
1 | a0001c0002t0002g0256 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-58+13811_-58+1398 others(179): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940534 | ||||||
chr5:65940558 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13752G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940558 | |||||||
chr5:65940568 | GCGCCTCT others(12): Show |
G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+13764_-58+1378 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940568 | ||||||
chr5:65940590 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-58+13784A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940590 | |||||||
chr5:65940605 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13799G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940605 | |||||||
chr5:65940606 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+13800C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940606 | |||||||
chr5:65940617 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-58+13811G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940617 | |||||||
chr5:65940617 | GGCCA | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13815_-58+1381 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940617 | ||||||
chr5:65940624 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13818C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940624 | |||||||
chr5:65940644 | T | TG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13844dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | ||||||
chr5:65940644 | T | TGGGGGGT others(43): Show |
1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | ||||||
chr5:65940644 | T | TGGGGGGT others(43): Show |
143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | ||||||
chr5:65940644 | T | TGGGGGGT others(43): Show |
3 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 |
3 | HG02257.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | ||||||
chr5:65940644 | T | TGGGGGGT others(43): Show |
4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940644 | ||||||
chr5:65940645 | G | GGGGGGTC others(43): Show |
1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940645 | ||||||
chr5:65940655 | C | CCCCCGGC others(43): Show |
4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02970.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+13853_-58+1385 others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940655 | ||||||
chr5:65940660 | C | CGCCCGCC others(73): Show |
4 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13859_-58+1386 others(84): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940660 | ||||||
chr5:65940660 | C | CGCCCGGC others(73): Show |
12 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(9): Show |
12 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+13869_-58+1387 others(84): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65940660 | ||||||
chr5:65940660 | C | G | 13 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(10): Show |
13 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58+13854C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940660 | |||||||
chr5:65940676 | C | G | 2 | a0001c0001t0006g0149 a0001c0001t0006g0150 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-58+13870C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940676 | |||||||
chr5:65940677 | G | T | 1 | a0003c0004t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58+13871G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940677 | |||||||
chr5:65940726 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+13920C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940726 | |||||||
chr5:65940726 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+13920C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940726 | |||||||
chr5:65940730 | C | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+13924C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940730 | |||||||
chr5:65940830 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-58+14024T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940830 | |||||||
chr5:65940876 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+14070G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940876 | |||||||
chr5:65940906 | T | C | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+14100T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940906 | |||||||
chr5:65940992 | T | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+14186T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65940992 | |||||||
chr5:65941257 | A | G | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+14451A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941257 | |||||||
chr5:65941313 | TA | T | 103 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(100): Show |
103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-58+14526delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941313 | ||||||
chr5:65941313 | TAAA | T | 17 | a0001c0002t0002g0210 a0004c0005t0004g0008 a0004c0005t0004g0009 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+14524_-58+1452 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941313 | ||||||
chr5:65941314 | A | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0144 |
3 | HG02055.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-58+14508A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941314 | |||||||
chr5:65941329 | AAAAG | A | 13 | a0001c0015t0030g0258 a0003c0004t0001g0139 a0005c0006t0002g0229 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+14526_-58+1452 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941329 | ||||||
chr5:65941331 | AAG | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.-58+14527_-58+1452 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941331 | ||||||
chr5:65941332 | AG | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0231 a0001c0001t0001g0234 |
3 | NA19003.hp2 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-58+14527delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941332 | |||||||
chr5:65941333 | GAAC | G | 30 | a0001c0001t0001g0080 a0001c0001t0001g0133 a0001c0001t0001g0135 others(27): Show |
30 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-58+14530_-58+1453 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941333 | ||||||
chr5:65941336 | C | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-58+14530C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941336 | |||||||
chr5:65941345 | TAAC | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+14545_-58+1454 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941345 | ||||||
chr5:65941357 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+14551A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941357 | |||||||
chr5:65941432 | A | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+14626A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941432 | |||||||
chr5:65941524 | C | T | 1 | a0001c0002t0002g0292 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-58+14718C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941524 | |||||||
chr5:65941606 | TGTA | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+14805_-58+1480 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65941606 | ||||||
chr5:65941607 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-58+14801G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941607 | |||||||
chr5:65941680 | A | G | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+14874A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941680 | |||||||
chr5:65941689 | C | G | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+14883C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941689 | |||||||
chr5:65941694 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-58+14888G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941694 | |||||||
chr5:65941827 | G | A | 2 | a0001c0002t0002g0286 a0001c0002t0002g0287 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-58+15021G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941827 | |||||||
chr5:65941842 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15036T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941842 | |||||||
chr5:65941955 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+15149T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941955 | |||||||
chr5:65941982 | C | T | 18 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(15): Show |
18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-58+15176C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65941982 | |||||||
chr5:65942039 | C | CGAAA | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+15233_-58+1523 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942039 | |||||||
chr5:65942134 | C | T | 5 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG00673.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+15328C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942134 | |||||||
chr5:65942197 | T | C | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-58+15391T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942197 | |||||||
chr5:65942302 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15496G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942302 | |||||||
chr5:65942312 | C | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+15506C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942312 | |||||||
chr5:65942457 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-58+15651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942457 | |||||||
chr5:65942471 | G | A | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+15665G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942471 | |||||||
chr5:65942471 | G | T | 3 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 |
3 | HG01167.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-58+15665G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942471 | |||||||
chr5:65942529 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+15723T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942529 | |||||||
chr5:65942744 | G | A | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+15938G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942744 | |||||||
chr5:65942753 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-58+15947T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942753 | |||||||
chr5:65942757 | T | A | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+15951T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942757 | |||||||
chr5:65942838 | G | C | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-58+16032G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65942838 | |||||||
chr5:65942908 | CA | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0061 others(11): Show |
14 | HG00673.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58+16119delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942908 | ||||||
chr5:65942908 | CAA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-58+16118_-58+1611 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942908 | ||||||
chr5:65942930 | CTT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-58+16126_-58+1612 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65942930 | ||||||
chr5:65943001 | C | T | 2 | a0003c0004t0001g0137 a0003c0004t0001g0138 |
2 | HG00642.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-58+16195C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943001 | |||||||
chr5:65943521 | C | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+16715C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943521 | |||||||
chr5:65943579 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+16773T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943579 | |||||||
chr5:65943640 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-58+16834A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943640 | |||||||
chr5:65943641 | A | G | 4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+16835A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943641 | |||||||
chr5:65943861 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0268 |
2 | HG02056.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-58+17055C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943861 | |||||||
chr5:65943862 | T | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0016c0019t0001g0087 |
3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-58+17056T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943862 | |||||||
chr5:65943907 | T | C | 2 | a0001c0002t0002g0296 a0001c0002t0002g0297 |
2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-58+17101T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65943907 | |||||||
chr5:65944204 | A | AT | 42 | a0001c0002t0002g0235 a0001c0002t0002g0237 a0001c0002t0002g0259 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-58+17419dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65944204 | ||||||
chr5:65944204 | AT | A | 13 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0172 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58+17419delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65944204 | ||||||
chr5:65944222 | TTTTA | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0099 a0001c0001t0009g0038 others(5): Show |
8 | HG01257.hp2 HG01515.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58+17417_-58+1742 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944222 | |||||||
chr5:65944223 | TTTA | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-58+17418_-58+1742 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944223 | |||||||
chr5:65944224 | TTA | T | 17 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0112 others(14): Show |
17 | HG01109.hp2 HG02004.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+17419_-58+1742 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944224 | |||||||
chr5:65944278 | C | T | 2 | a0001c0007t0010g0160 a0001c0007t0010g0275 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-58+17472C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944278 | |||||||
chr5:65944393 | G | A | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+17587G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944393 | |||||||
chr5:65944416 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+17610G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944416 | |||||||
chr5:65944450 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+17644A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944450 | |||||||
chr5:65944503 | C | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+17697C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944503 | |||||||
chr5:65944635 | G | A | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-58+17829G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944635 | |||||||
chr5:65944850 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18044T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65944850 | |||||||
chr5:65945220 | A | T | 2 | a0001c0007t0012g0217 a0001c0007t0012g0219 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+18414A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945220 | |||||||
chr5:65945285 | A | G | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-58+18479A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945285 | |||||||
chr5:65945350 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18544T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945350 | |||||||
chr5:65945369 | C | T | 1 | a0001c0002t0002g0262 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-58+18563C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945369 | |||||||
chr5:65945486 | A | G | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+18680A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945486 | |||||||
chr5:65945537 | G | C | 2 | a0001c0007t0012g0217 a0001c0007t0012g0219 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-58+18731G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945537 | |||||||
chr5:65945618 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+18812A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945618 | |||||||
chr5:65945684 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+18878T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65945684 | |||||||
chr5:65946179 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19373A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946179 | |||||||
chr5:65946193 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19387C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946193 | |||||||
chr5:65946272 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-58+19466A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946272 | |||||||
chr5:65946366 | A | AAATG | 16 | a0003c0004t0001g0100 a0003c0004t0001g0101 a0004c0005t0004g0014 others(13): Show |
16 | HG02258.hp1 HG02451.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19585_-58+1958 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946366 | ||||||
chr5:65946422 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+19616T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946422 | |||||||
chr5:65946688 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+19882C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946688 | |||||||
chr5:65946739 | G | A | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+19933G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946739 | |||||||
chr5:65946787 | C | CT | 24 | a0001c0001t0001g0048 a0001c0001t0001g0074 a0001c0001t0006g0153 others(21): Show |
24 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-58+19998dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946787 | ||||||
chr5:65946787 | CT | C | 6 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 others(3): Show |
6 | HG01167.hp1 HG01943.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+19998delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946787 | ||||||
chr5:65946902 | C | T | 13 | a0003c0004t0001g0088 a0003c0004t0001g0093 a0003c0004t0001g0100 others(10): Show |
13 | NA18747.hp1 NA18942.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.-58+20096C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65946902 | |||||||
chr5:65946957 | A | AT | 18 | a0001c0001t0009g0041 a0001c0002t0002g0287 a0004c0005t0004g0008 others(15): Show |
18 | HG00642.hp2 HG01167.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-58+20161dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65946957 | ||||||
chr5:65947028 | G | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+20222G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947028 | |||||||
chr5:65947095 | A | G | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-58+20289A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947095 | |||||||
chr5:65947755 | C | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+20949C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947755 | |||||||
chr5:65947756 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+20950C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947756 | |||||||
chr5:65947956 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21150G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65947956 | |||||||
chr5:65948010 | C | CA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-58+21220dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948010 | ||||||
chr5:65948023 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21217A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948023 | |||||||
chr5:65948062 | A | G | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-58+21256A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948062 | |||||||
chr5:65948153 | TTTTG | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+21359_-58+2136 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948153 | ||||||
chr5:65948321 | C | T | 5 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG00673.hp1 NA18946.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58+21515C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948321 | |||||||
chr5:65948341 | A | AT | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0009g0041 others(4): Show |
7 | HG01256.hp1 HG01256.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+21549dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948341 | ||||||
chr5:65948429 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-58+21623A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948429 | |||||||
chr5:65948464 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-58+21658G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948464 | |||||||
chr5:65948479 | G | T | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+21673G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948479 | |||||||
chr5:65948762 | G | GT | 21 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(18): Show |
21 | HG00673.hp2 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-58+21975dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | ||||||
chr5:65948762 | G | GTT | 21 | a0001c0022t0009g0036 a0003c0004t0001g0127 a0004c0005t0004g0008 others(18): Show |
21 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+21974_-58+2197 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | ||||||
chr5:65948762 | G | GTTT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-58+21973_-58+2197 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | ||||||
chr5:65948762 | G | GTTTT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0032 others(28): Show |
31 | HG01071.hp2 HG01257.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.-58+21972_-58+2197 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948762 | ||||||
chr5:65948771 | T | TTTG | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+21967_-58+2196 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948771 | ||||||
chr5:65948782 | G | T | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21976G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948782 | |||||||
chr5:65948783 | A | T | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21977A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948783 | |||||||
chr5:65948786 | C | G | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21980C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948786 | |||||||
chr5:65948786 | CAG | C | 3 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0227 |
3 | HG02257.hp1 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-58+21983_-58+2198 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65948786 | ||||||
chr5:65948788 | G | C | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+21982G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948788 | |||||||
chr5:65948835 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-58+22029C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65948835 | |||||||
chr5:65949030 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-58+22224C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949030 | |||||||
chr5:65949305 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+22499C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949305 | |||||||
chr5:65949345 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-58+22539T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949345 | |||||||
chr5:65949363 | A | G | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-58+22557A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949363 | |||||||
chr5:65949579 | T | A | 1 | a0001c0001t0006g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-58+22773T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949579 | |||||||
chr5:65949594 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-58+22788A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949594 | |||||||
chr5:65949719 | A | G | 1 | a0001c0001t0013g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-58+22913A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949719 | |||||||
chr5:65949770 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-58+22964A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949770 | |||||||
chr5:65949794 | C | T | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-58+22988C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949794 | |||||||
chr5:65949977 | C | G | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-58+23171C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949977 | |||||||
chr5:65949993 | G | A | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+23187G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65949993 | |||||||
chr5:65950216 | A | G | 1 | a0001c0002t0002g0238 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-58+23410A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950216 | |||||||
chr5:65950219 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+23413A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950219 | |||||||
chr5:65950463 | C | T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58+23657C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950463 | |||||||
chr5:65950736 | C | T | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-58+23930C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950736 | |||||||
chr5:65950737 | T | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-58+23931T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65950737 | |||||||
chr5:65951155 | C | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+24349C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951155 | |||||||
chr5:65951168 | G | A | 1 | a0001c0002t0002g0246 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-58+24362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951168 | |||||||
chr5:65951290 | T | C | 5 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(2): Show |
5 | NA18951.hp2 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58+24484T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951290 | |||||||
chr5:65951354 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-58+24548G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951354 | |||||||
chr5:65951382 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+24576A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951382 | |||||||
chr5:65951654 | A | G | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-58+24848A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951654 | |||||||
chr5:65951802 | A | G | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-58+24996A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951802 | |||||||
chr5:65951848 | T | C | 1 | a0002c0003t0002g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58+25042T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65951848 | |||||||
chr5:65952065 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-58+25259C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952065 | |||||||
chr5:65952202 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25396C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952202 | |||||||
chr5:65952221 | G | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25415G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952221 | |||||||
chr5:65952282 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+25476A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952282 | |||||||
chr5:65952338 | T | G | 1 | a0002c0003t0008g0174 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-58+25532T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952338 | |||||||
chr5:65952380 | A | G | 1 | a0005c0006t0007g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-58+25574A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952380 | |||||||
chr5:65952435 | T | TGAGGCC | 7 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(4): Show |
7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25629_-58+2563 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952435 | |||||||
chr5:65952436 | T | A | 7 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(4): Show |
7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25630T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952436 | |||||||
chr5:65952437 | G | T | 7 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(4): Show |
7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+25631G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952437 | |||||||
chr5:65952474 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+25668C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952474 | |||||||
chr5:65952549 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-58+25743T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952549 | |||||||
chr5:65952551 | CT | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0084 others(4): Show |
7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+25756delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65952551 | ||||||
chr5:65952663 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-58+25857T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952663 | |||||||
chr5:65952737 | T | G | 1 | a0003c0004t0001g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-58+25931T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952737 | |||||||
chr5:65952925 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+26119A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952925 | |||||||
chr5:65952969 | T | G | 2 | a0003c0004t0001g0305 a0003c0004t0024g0303 |
2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-58+26163T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952969 | |||||||
chr5:65952978 | T | A | 1 | a0001c0001t0013g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-58+26172T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65952978 | |||||||
chr5:65953081 | T | A | 1 | a0003c0004t0001g0304 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-58+26275T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953081 | |||||||
chr5:65953142 | A | G | 4 | a0002c0003t0005g0183 a0002c0003t0005g0184 a0002c0003t0005g0186 others(1): Show |
4 | NA18977.hp2 NA18985.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+26336A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953142 | |||||||
chr5:65953152 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+26346G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953152 | |||||||
chr5:65953576 | G | C | 1 | a0003c0004t0001g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-58+26770G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953576 | |||||||
chr5:65953872 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+27066A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953872 | |||||||
chr5:65953882 | C | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+27076C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953882 | |||||||
chr5:65953922 | C | T | 1 | a0001c0015t0030g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-58+27116C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953922 | |||||||
chr5:65953982 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27176G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65953982 | |||||||
chr5:65954002 | T | A | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+27196T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954002 | |||||||
chr5:65954026 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0013g0102 |
2 | HG00438.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-58+27220C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954026 | |||||||
chr5:65954031 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-58+27225C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954031 | |||||||
chr5:65954135 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-58+27329T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954135 | |||||||
chr5:65954160 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+27354C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954160 | |||||||
chr5:65954238 | A | C | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-58+27432A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954238 | |||||||
chr5:65954280 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27474A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954280 | |||||||
chr5:65954284 | C | T | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-58+27478C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954284 | |||||||
chr5:65954304 | T | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+27498T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954304 | |||||||
chr5:65954357 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0084 others(4): Show |
7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58+27551A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954357 | |||||||
chr5:65954485 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27679G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954485 | |||||||
chr5:65954646 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27840A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954646 | |||||||
chr5:65954687 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+27881C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954687 | |||||||
chr5:65954724 | G | A | 2 | a0004c0005t0004g0018 a0004c0005t0004g0021 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-58+27918G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954724 | |||||||
chr5:65954762 | GA | G | 21 | a0001c0001t0013g0102 a0004c0005t0004g0008 a0004c0005t0004g0009 others(18): Show |
21 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-58+27968delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65954762 | ||||||
chr5:65954805 | C | T | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-58+27999C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954805 | |||||||
chr5:65954825 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-58+28019G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954825 | |||||||
chr5:65954882 | T | A | 1 | a0002c0003t0003g0204 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-58+28076T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954882 | |||||||
chr5:65954894 | G | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+28088G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65954894 | |||||||
chr5:65955030 | C | T | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-58+28224C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955030 | |||||||
chr5:65955082 | A | C | 2 | a0002c0003t0003g0276 a0009c0009t0002g0168 |
2 | NA18951.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-58+28276A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955082 | |||||||
chr5:65955173 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28367A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955173 | |||||||
chr5:65955310 | C | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28504C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955310 | |||||||
chr5:65955405 | G | A | 7 | a0001c0001t0001g0044 a0001c0007t0010g0160 a0001c0007t0010g0161 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+28599G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955405 | |||||||
chr5:65955431 | A | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+28625A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955431 | |||||||
chr5:65955544 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+28738C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955544 | |||||||
chr5:65955602 | C | G | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-58+28796C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955602 | |||||||
chr5:65955717 | A | G | 1 | a0001c0002t0002g0287 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-58+28911A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955717 | |||||||
chr5:65955913 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29107G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955913 | |||||||
chr5:65955918 | A | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+29112A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65955918 | |||||||
chr5:65956006 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-58+29200A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956006 | |||||||
chr5:65956047 | A | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+29241A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956047 | |||||||
chr5:65956217 | T | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-58+29411T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956217 | |||||||
chr5:65956372 | A | AT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0232 others(3): Show |
6 | HG06807.hp2 NA18949.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+29585dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | ||||||
chr5:65956372 | AT | A | 9 | a0001c0001t0001g0059 a0001c0001t0001g0089 a0001c0001t0021g0141 others(6): Show |
9 | NA18949.hp2 NA18954.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+29585delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | ||||||
chr5:65956372 | ATT | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29584_-58+2958 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956372 | ||||||
chr5:65956406 | CT | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-58+29602delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956406 | ||||||
chr5:65956444 | T | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-58+29638T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956444 | |||||||
chr5:65956450 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-58+29644C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956450 | |||||||
chr5:65956457 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956457 | |||||||
chr5:65956505 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+29699G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956505 | |||||||
chr5:65956526 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0013g0102 |
2 | HG01952.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-58+29720C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956526 | |||||||
chr5:65956545 | C | CT | 12 | a0001c0007t0010g0160 a0001c0007t0010g0275 a0004c0005t0004g0014 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+29754dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956545 | ||||||
chr5:65956545 | CT | C | 9 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(6): Show |
9 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58+29754delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956545 | ||||||
chr5:65956625 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-58+29819C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956625 | |||||||
chr5:65956626 | T | G | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58+29820T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956626 | |||||||
chr5:65956673 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-58+29867C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956673 | |||||||
chr5:65956821 | T | C | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-58+30015T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65956821 | |||||||
chr5:65956986 | TG | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+30182delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65956986 | ||||||
chr5:65957017 | A | G | 2 | a0001c0001t0009g0040 a0001c0001t0009g0041 |
2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-58+30211A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957017 | |||||||
chr5:65957205 | T | A | 4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+30399T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957205 | |||||||
chr5:65957206 | A | T | 17 | a0001c0001t0006g0155 a0004c0005t0004g0008 a0004c0005t0004g0009 others(14): Show |
17 | HG01167.hp2 HG01884.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+30400A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957206 | |||||||
chr5:65957209 | TTTTTA | T | 7 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(4): Show |
7 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-58+30423_-58+3042 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65957209 | ||||||
chr5:65957223 | TATTTTA | T | 8 | a0004c0005t0004g0015 a0004c0005t0004g0016 a0004c0005t0004g0017 others(5): Show |
8 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58+30418_-58+3042 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957223 | |||||||
chr5:65957229 | A | T | 2 | a0001c0001t0001g0064 a0004c0005t0004g0014 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-58+30423A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957229 | |||||||
chr5:65957243 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-58+30437T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957243 | |||||||
chr5:65957280 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-58+30474G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957280 | |||||||
chr5:65957397 | G | C | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-58+30591G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957397 | |||||||
chr5:65957472 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58+30666C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957472 | |||||||
chr5:65957636 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-58+30830A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957636 | |||||||
chr5:65957737 | C | G | 1 | a0003c0004t0024g0303 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-57-30898C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957737 | |||||||
chr5:65957739 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30896A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957739 | |||||||
chr5:65957815 | C | G | 1 | a0002c0003t0003g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-57-30820C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957815 | |||||||
chr5:65957860 | C | T | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57-30775C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957860 | |||||||
chr5:65957883 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30752A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957883 | |||||||
chr5:65957912 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30723C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957912 | |||||||
chr5:65957913 | G | A | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-30722G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957913 | |||||||
chr5:65957954 | G | A | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-30681G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957954 | |||||||
chr5:65957978 | G | C | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-30657G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957978 | |||||||
chr5:65957986 | C | T | 1 | a0001c0007t0010g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57-30649C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65957986 | |||||||
chr5:65958090 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-30545C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958090 | |||||||
chr5:65958194 | C | T | 1 | a0002c0003t0003g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57-30441C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958194 | |||||||
chr5:65958212 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-57-30423T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958212 | |||||||
chr5:65958212 | T | G | 2 | a0001c0001t0021g0141 a0004c0005t0004g0011 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-57-30423T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958212 | |||||||
chr5:65958243 | C | T | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-30392C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958243 | |||||||
chr5:65958291 | C | T | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-30344C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958291 | |||||||
chr5:65958292 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-30343A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958292 | |||||||
chr5:65958383 | C | T | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57-30252C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958383 | |||||||
chr5:65958410 | G | A | 1 | a0003c0004t0022g0301 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-57-30225G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958410 | |||||||
chr5:65958445 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30190C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958445 | |||||||
chr5:65958466 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30169C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958466 | |||||||
chr5:65958487 | G | A | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-30148G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958487 | |||||||
chr5:65958501 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57-30134A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958501 | |||||||
chr5:65958596 | C | CAGAGGGA others(12): Show |
1 | a0002c0003t0008g0278 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-57-30023_-57-3000 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65958596 | ||||||
chr5:65958596 | CAGAGGGA others(12): Show |
C | 1 | a0001c0001t0029g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-57-30023_-57-3000 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65958596 | ||||||
chr5:65958613 | A | AAGAGAG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-30022_-57-3002 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958613 | |||||||
chr5:65958636 | G | C | 8 | a0002c0003t0002g0201 a0002c0003t0002g0202 a0002c0003t0002g0205 others(5): Show |
8 | HG00280.hp2 HG01433.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-29999G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958636 | |||||||
chr5:65958639 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-29996G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958639 | |||||||
chr5:65958836 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-29799G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65958836 | |||||||
chr5:65959029 | A | T | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-29606A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959029 | |||||||
chr5:65959663 | C | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-28972C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959663 | |||||||
chr5:65959669 | C | T | 1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57-28966C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959669 | |||||||
chr5:65959727 | A | G | 1 | a0003c0004t0027g0300 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57-28908A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959727 | |||||||
chr5:65959809 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-28826G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959809 | |||||||
chr5:65959842 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-28793C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959842 | |||||||
chr5:65959844 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0106 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-28791C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959844 | |||||||
chr5:65959859 | T | C | 1 | a0001c0002t0002g0247 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-57-28776T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959859 | |||||||
chr5:65959909 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-28726C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959909 | |||||||
chr5:65959988 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-57-28647C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65959988 | |||||||
chr5:65960207 | G | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-28428G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960207 | |||||||
chr5:65960427 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-28208C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960427 | |||||||
chr5:65960455 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-57-28180G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960455 | |||||||
chr5:65960491 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-28144C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960491 | |||||||
chr5:65960678 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-27957A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960678 | |||||||
chr5:65960709 | AT | A | 6 | a0001c0002t0002g0246 a0002c0003t0003g0175 a0002c0003t0003g0176 others(3): Show |
6 | NA18948.hp2 NA18954.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-27920delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65960709 | ||||||
chr5:65960963 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-27672T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65960963 | |||||||
chr5:65961095 | A | G | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-27540A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961095 | |||||||
chr5:65961265 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-27370T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961265 | |||||||
chr5:65961600 | G | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-27035G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961600 | |||||||
chr5:65961810 | C | CT | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-26820dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65961810 | ||||||
chr5:65961912 | A | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-26723A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65961912 | |||||||
chr5:65962086 | A | G | 1 | a0003c0004t0028g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-57-26549A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962086 | |||||||
chr5:65962188 | A | G | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-26447A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962188 | |||||||
chr5:65962416 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26219G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962416 | |||||||
chr5:65962469 | C | CAG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26166_-57-2616 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962469 | |||||||
chr5:65962499 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-26136T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962499 | |||||||
chr5:65962639 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0118 |
3 | HG00735.hp1 HG01069.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-57-25996C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962639 | |||||||
chr5:65962787 | C | A | 1 | a0001c0002t0002g0292 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-57-25848C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962787 | |||||||
chr5:65962845 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-57-25790G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65962845 | |||||||
chr5:65963160 | TAAC | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-57-25472_-57-2547 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963160 | ||||||
chr5:65963197 | A | T | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-25438A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963197 | |||||||
chr5:65963257 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-57-25378G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963257 | |||||||
chr5:65963322 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-57-25313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963322 | |||||||
chr5:65963344 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25291T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963344 | |||||||
chr5:65963414 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25221C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963414 | |||||||
chr5:65963443 | A | C | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-25192A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963443 | |||||||
chr5:65963463 | T | G | 1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57-25172T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963463 | |||||||
chr5:65963499 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-25136G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963499 | |||||||
chr5:65963792 | C | CT | 10 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-24828dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963792 | ||||||
chr5:65963792 | CT | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-57-24828delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963792 | ||||||
chr5:65963829 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24806G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963829 | |||||||
chr5:65963839 | G | GAGTGC | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-24791_-57-2478 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65963839 | ||||||
chr5:65963939 | A | G | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-24696A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963939 | |||||||
chr5:65963990 | G | A | 17 | a0001c0001t0001g0097 a0004c0005t0004g0008 a0004c0005t0004g0009 others(14): Show |
17 | HG00738.hp1 HG01167.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-24645G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65963990 | |||||||
chr5:65964056 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-24579C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964056 | |||||||
chr5:65964270 | G | A | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-57-24365G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964270 | |||||||
chr5:65964270 | G | T | 1 | a0001c0002t0002g0004 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-57-24365G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964270 | |||||||
chr5:65964531 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-24104A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964531 | |||||||
chr5:65964741 | C | CT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57-23875dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | ||||||
chr5:65964741 | C | CTT | 8 | a0001c0001t0001g0073 a0001c0001t0001g0089 a0001c0001t0001g0133 others(5): Show |
8 | HG01109.hp2 HG02451.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23876_-57-2387 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | ||||||
chr5:65964741 | CT | C | 18 | a0001c0002t0002g0293 a0004c0005t0004g0008 a0004c0005t0004g0009 others(15): Show |
18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-57-23875delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964741 | ||||||
chr5:65964894 | C | A | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23741C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964894 | |||||||
chr5:65964908 | T | TTG | 19 | a0001c0002t0002g0035 a0001c0002t0002g0237 a0001c0002t0002g0244 others(16): Show |
19 | HG00438.hp2 HG00609.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57-23691_-57-2369 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | T | TTGTG | 12 | a0001c0002t0002g0243 a0001c0007t0012g0219 a0002c0003t0002g0215 others(9): Show |
12 | HG00280.hp2 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-23693_-57-2369 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | T | TTGTGTGT others(3): Show |
3 | a0008c0012t0011g0023 a0008c0012t0011g0024 a0011c0016t0007g0228 |
3 | HG01884.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-23699_-57-2369 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | T | TTGTGTGT others(5): Show |
2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-57-23701_-57-2369 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | T | TTGTGTGT others(7): Show |
1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57-23703_-57-2369 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTG | T | 3 | a0001c0002t0002g0033 a0001c0002t0002g0286 a0001c0002t0002g0292 |
3 | HG00408.hp1 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-57-23691_-57-2369 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTG | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG02280.hp1 HG03209.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23693_-57-2369 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTG | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0042 others(19): Show |
22 | HG01071.hp2 HG01256.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57-23695_-57-2369 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTGT others(1): Show |
T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-57-23697_-57-2369 others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTGT others(3): Show |
T | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-23699_-57-2369 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTGT others(5): Show |
T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-23701_-57-2369 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-23705_-57-2369 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964908 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57-23709_-57-2369 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964908 | ||||||
chr5:65964937 | TGTGTGTG | T | 8 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0073 others(5): Show |
8 | HG00642.hp1 HG02970.hp2 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-23697_-57-2369 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964937 | |||||||
chr5:65964941 | T | TGTGTGTG others(5): Show |
2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964941 | ||||||
chr5:65964944 | GTAAT | G | 9 | a0004c0005t0004g0008 a0004c0005t0004g0014 a0004c0005t0004g0015 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57-23689_-57-2368 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964944 | ||||||
chr5:65964945 | T | A | 10 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0073 others(7): Show |
10 | HG00642.hp1 HG02970.hp2 HG04228.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-23690T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | |||||||
chr5:65964945 | T | TGTA | 7 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | |||||||
chr5:65964945 | T | TGTGTGTG others(4): Show |
2 | a0001c0007t0010g0162 a0001c0007t0010g0163 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-57-23690_-57-2368 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | |||||||
chr5:65964945 | T | TGTGTGTG others(8): Show |
1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-57-23690_-57-2368 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | |||||||
chr5:65964945 | TAA | T | 4 | a0004c0005t0004g0009 a0004c0005t0004g0011 a0004c0005t0004g0020 others(1): Show |
4 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23689_-57-2368 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964945 | |||||||
chr5:65964946 | A | G | 3 | a0004c0005t0004g0010 a0004c0005t0004g0017 a0004c0017t0004g0012 |
3 | HG02818.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57-23689A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964946 | |||||||
chr5:65964946 | A | T | 7 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-23689A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964946 | |||||||
chr5:65964947 | A | T | 23 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0073 others(20): Show |
23 | HG00642.hp1 HG01109.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.-57-23688A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964947 | |||||||
chr5:65964948 | T | A | 7 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-23687T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964948 | |||||||
chr5:65964948 | T | G | 7 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 others(4): Show |
7 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-23687T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964948 | |||||||
chr5:65964950 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23685T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964950 | |||||||
chr5:65964952 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23683T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964952 | |||||||
chr5:65964954 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23681T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964954 | |||||||
chr5:65964956 | T | A | 15 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0011 others(12): Show |
15 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-23679T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964956 | |||||||
chr5:65964956 | T | G | 1 | a0004c0005t0004g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57-23679T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964956 | |||||||
chr5:65964957 | T | A | 15 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0011 others(12): Show |
15 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-23678T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964957 | |||||||
chr5:65964969 | TA | T | 3 | a0001c0001t0001g0032 a0003c0004t0001g0131 a0003c0004t0001g0137 |
3 | HG01515.hp2 HG01993.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-57-23664delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65964969 | ||||||
chr5:65964970 | A | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.-57-23665A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65964970 | |||||||
chr5:65965095 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23540C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965095 | |||||||
chr5:65965170 | A | ATAAAATG others(9): Show |
170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-57-23462_-57-2344 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965170 | ||||||
chr5:65965372 | GTTTTTTG others(19): Show |
G | 3 | a0004c0005t0004g0008 a0004c0005t0004g0028 a0004c0005t0026g0013 |
3 | HG02572.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-23256_-57-2323 others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965372 | ||||||
chr5:65965372 | GTTTTTTG others(20): Show |
G | 13 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 others(10): Show |
13 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23256_-57-2323 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965372 | ||||||
chr5:65965379 | G | GTTTTTTT others(5): Show |
1 | a0009c0009t0002g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-57-23254_-57-2325 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | ||||||
chr5:65965379 | G | GTTTTTTT others(10): Show |
1 | a0002c0003t0003g0204 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-57-23254_-57-2325 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | ||||||
chr5:65965379 | G | T | 1 | a0002c0003t0008g0257 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-57-23256G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965379 | |||||||
chr5:65965379 | GTTGTTTT others(12): Show |
G | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-23253_-57-2323 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965379 | ||||||
chr5:65965382 | G | GT | 9 | a0001c0002t0002g0003 a0001c0002t0002g0209 a0001c0002t0002g0240 others(6): Show |
9 | HG00408.hp1 HG02071.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-23212dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTGTTTT others(7): Show |
1 | a0001c0002t0002g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57-23251_-57-2325 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(4): Show |
2 | a0002c0003t0008g0178 a0002c0003t0008g0280 |
2 | HG00408.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-57-23222_-57-2321 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(5): Show |
1 | a0002c0003t0005g0182 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-57-23223_-57-2321 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(6): Show |
2 | a0002c0003t0005g0179 a0002c0003t0005g0180 |
2 | HG01081.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-57-23224_-57-2321 others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(9): Show |
1 | a0002c0003t0002g0207 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-57-23227_-57-2321 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(11): Show |
1 | a0002c0003t0002g0205 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57-23229_-57-2321 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(12): Show |
1 | a0002c0003t0005g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-57-23230_-57-2321 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(13): Show |
1 | a0002c0003t0005g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-57-23231_-57-2321 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(17): Show |
1 | a0002c0003t0008g0173 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-57-23235_-57-2321 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | GTTTTTTT others(47): Show |
1 | a0002c0003t0005g0185 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-57-23212_-57-2321 others(58): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | G | T | 4 | a0002c0003t0003g0165 a0002c0003t0003g0166 a0002c0003t0003g0204 others(1): Show |
4 | HG01433.hp1 NA18951.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23253G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965382 | |||||||
chr5:65965382 | GT | G | 14 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 others(11): Show |
14 | HG02004.hp2 HG02056.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-23212delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTT | G | 11 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0214 others(8): Show |
11 | HG00438.hp2 HG00609.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-23213_-57-2321 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(3): Show |
G | 5 | a0001c0007t0012g0219 a0002c0003t0003g0175 a0002c0003t0003g0177 others(2): Show |
5 | HG02622.hp1 NA18940.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57-23221_-57-2321 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(5): Show |
G | 3 | a0002c0003t0002g0202 a0002c0003t0005g0181 a0002c0003t0005g0281 |
3 | HG03239.hp1 NA18944.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-57-23223_-57-2321 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(8): Show |
G | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57-23226_-57-2321 others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(9): Show |
G | 3 | a0001c0002t0002g0255 a0001c0002t0002g0260 a0002c0003t0003g0197 |
3 | HG01069.hp1 HG01071.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-57-23227_-57-2321 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(10): Show |
G | 1 | a0002c0003t0003g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-57-23228_-57-2321 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(11): Show |
G | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57-23229_-57-2321 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(12): Show |
G | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-23230_-57-2321 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(15): Show |
G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23233_-57-2321 others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(16): Show |
G | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(11): Show |
14 | HG00673.hp1 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-23234_-57-2321 others(27): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(17): Show |
G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-57-23235_-57-2321 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965382 | GTTTTTTT others(20): Show |
G | 2 | a0006c0008t0003g0190 a0006c0008t0018g0195 |
2 | NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-57-23238_-57-2321 others(31): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965382 | ||||||
chr5:65965384 | T | TG | 4 | a0001c0002t0002g0235 a0001c0002t0002g0251 a0001c0002t0002g0256 others(1): Show |
4 | NA18949.hp2 NA18975.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-23251_-57-2325 others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965384 | |||||||
chr5:65965385 | T | G | 2 | a0001c0002t0002g0252 a0006c0008t0003g0194 |
2 | NA18612.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-57-23250T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965385 | |||||||
chr5:65965386 | T | G | 2 | a0001c0002t0002g0246 a0002c0003t0003g0176 |
2 | NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-57-23249T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965386 | |||||||
chr5:65965389 | T | G | 1 | a0001c0002t0002g0288 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-57-23246T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965389 | |||||||
chr5:65965399 | T | G | 3 | a0004c0005t0004g0008 a0004c0005t0004g0028 a0004c0005t0026g0013 |
3 | HG02572.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-23236T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965399 | |||||||
chr5:65965400 | T | G | 13 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 others(10): Show |
13 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57-23235T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965400 | |||||||
chr5:65965429 | G | A | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-23206G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965429 | |||||||
chr5:65965545 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-23090C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965545 | |||||||
chr5:65965559 | C | CATGCCTG others(4): Show |
186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-23074_-57-2307 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65965559 | ||||||
chr5:65965569 | T | G | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57-23066T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965569 | |||||||
chr5:65965607 | A | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-23028A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965607 | |||||||
chr5:65965631 | G | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-23004G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965631 | |||||||
chr5:65965732 | G | A | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-22903G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965732 | |||||||
chr5:65965841 | T | C | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57-22794T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965841 | |||||||
chr5:65965895 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57-22740A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965895 | |||||||
chr5:65965998 | G | T | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-22637G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65965998 | |||||||
chr5:65966020 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-22615A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966020 | |||||||
chr5:65966107 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-57-22528A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966107 | |||||||
chr5:65966112 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-57-22523A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966112 | |||||||
chr5:65966115 | CTG | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-22518_-57-2251 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966115 | ||||||
chr5:65966183 | G | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-22452G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966183 | |||||||
chr5:65966245 | A | G | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-22390A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966245 | |||||||
chr5:65966311 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-22324A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966311 | |||||||
chr5:65966349 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-22286A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966349 | |||||||
chr5:65966378 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-22257G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966378 | |||||||
chr5:65966461 | A | T | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-22174A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966461 | |||||||
chr5:65966468 | G | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-22167G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966468 | |||||||
chr5:65966680 | C | CA | 33 | a0001c0001t0001g0047 a0001c0002t0002g0034 a0001c0002t0002g0208 others(30): Show |
33 | HG00609.hp2 HG00735.hp2 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.-57-21926dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966680 | CA | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0272 others(4): Show |
7 | HG01257.hp1 HG02280.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57-21926delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966680 | CAA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(38): Show |
42 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.-57-21927_-57-2192 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966680 | CAAA | C | 112 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(109): Show |
112 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.-57-21928_-57-2192 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966680 | CAAAA | C | 10 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0119 others(7): Show |
10 | HG01243.hp2 HG02165.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-21929_-57-2192 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966680 | CAAAAAAA | C | 15 | a0004c0005t0004g0008 a0004c0005t0004g0010 a0004c0005t0004g0011 others(12): Show |
15 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57-21932_-57-2192 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65966680 | ||||||
chr5:65966790 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-57-21845C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966790 | |||||||
chr5:65966792 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-21843G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65966792 | |||||||
chr5:65967014 | G | C | 1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57-21621G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967014 | |||||||
chr5:65967036 | C | T | 1 | a0003c0004t0001g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-57-21599C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967036 | |||||||
chr5:65967140 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-21495A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967140 | |||||||
chr5:65967161 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-21474A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967161 | |||||||
chr5:65967170 | C | A | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-21465C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967170 | |||||||
chr5:65967262 | C | T | 1 | a0001c0001t0013g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-21373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967262 | |||||||
chr5:65967290 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-21345G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967290 | |||||||
chr5:65967313 | C | T | 1 | a0003c0004t0001g0122 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-57-21322C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967313 | |||||||
chr5:65967403 | T | A | 1 | a0003c0004t0001g0129 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-57-21232T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967403 | |||||||
chr5:65967566 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57-21069T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967566 | |||||||
chr5:65967598 | G | A | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-21037G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967598 | |||||||
chr5:65967802 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-20833T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967802 | |||||||
chr5:65967846 | A | C | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-20789A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967846 | |||||||
chr5:65967988 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-20647C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65967988 | |||||||
chr5:65968072 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20563G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968072 | |||||||
chr5:65968262 | A | G | 41 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0049 others(38): Show |
41 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-57-20373A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968262 | |||||||
chr5:65968380 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20255G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968380 | |||||||
chr5:65968386 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-20249A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968386 | |||||||
chr5:65968587 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-20048G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968587 | |||||||
chr5:65968616 | A | G | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57-20019A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968616 | |||||||
chr5:65968660 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-19975A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968660 | |||||||
chr5:65968751 | G | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0273 |
2 | HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-57-19884G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968751 | |||||||
chr5:65968853 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57-19782G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968853 | |||||||
chr5:65968925 | A | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-19710A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968925 | |||||||
chr5:65968990 | T | A | 1 | a0001c0001t0013g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57-19645T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65968990 | |||||||
chr5:65969020 | A | G | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-57-19615A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969020 | |||||||
chr5:65969027 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-19608C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969027 | |||||||
chr5:65969041 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57-19594T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969041 | |||||||
chr5:65969143 | A | G | 1 | a0002c0003t0003g0192 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-57-19492A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969143 | |||||||
chr5:65969372 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-19263C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65969372 | |||||||
chr5:65970007 | G | A | 1 | a0001c0001t0029g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-57-18628G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970007 | |||||||
chr5:65970093 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18542G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970093 | |||||||
chr5:65970126 | TA | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-18508delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970126 | |||||||
chr5:65970130 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-57-18505C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970130 | |||||||
chr5:65970142 | T | C | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-18493T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970142 | |||||||
chr5:65970150 | T | A | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-18485T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970150 | |||||||
chr5:65970297 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-18338A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970297 | |||||||
chr5:65970463 | CACTA | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18167_-57-1816 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65970463 | ||||||
chr5:65970474 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-18161A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970474 | |||||||
chr5:65970489 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-18146G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970489 | |||||||
chr5:65970649 | G | C | 34 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0274 others(31): Show |
34 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.-57-17986G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970649 | |||||||
chr5:65970694 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-17941T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970694 | |||||||
chr5:65970744 | A | G | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-17891A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65970744 | |||||||
chr5:65971008 | A | G | 2 | a0002c0003t0008g0174 a0002c0003t0008g0178 |
2 | NA18972.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-57-17627A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971008 | |||||||
chr5:65971102 | G | A | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-17533G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971102 | |||||||
chr5:65971217 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0273 |
3 | HG01071.hp2 HG01934.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-57-17418T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971217 | |||||||
chr5:65971270 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-57-17365G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971270 | |||||||
chr5:65971396 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-17239A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971396 | |||||||
chr5:65971512 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-17123A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971512 | |||||||
chr5:65971778 | A | G | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-16857A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971778 | |||||||
chr5:65971780 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57-16855C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65971780 | |||||||
chr5:65971821 | TTGAC | T | 4 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-16811_-57-1680 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65971821 | ||||||
chr5:65972066 | C | A | 8 | a0002c0003t0002g0201 a0002c0003t0002g0202 a0002c0003t0002g0205 others(5): Show |
8 | HG00280.hp2 HG01433.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-16569C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972066 | |||||||
chr5:65972112 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-16523G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972112 | |||||||
chr5:65972197 | CACCCTTG others(1934): Show |
C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-16347_-57-1440 others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65972197 | ||||||
chr5:65972364 | A | G | 6 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(3): Show |
6 | HG00280.hp2 NA18951.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-16271A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972364 | |||||||
chr5:65972684 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57-15951G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972684 | |||||||
chr5:65972762 | T | C | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-15873T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972762 | |||||||
chr5:65972842 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(41): Show |
45 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-57-15793T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972842 | |||||||
chr5:65972857 | T | C | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-15778T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972857 | |||||||
chr5:65972936 | A | G | 1 | a0001c0002t0002g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-57-15699A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65972936 | |||||||
chr5:65973028 | C | T | 2 | a0001c0002t0002g0255 a0001c0002t0002g0260 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-57-15607C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973028 | |||||||
chr5:65973039 | T | G | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-15596T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973039 | |||||||
chr5:65973046 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
15 | HG01071.hp2 HG01934.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57-15589T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973046 | |||||||
chr5:65973073 | T | C | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-15562T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973073 | |||||||
chr5:65973094 | A | C | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57-15541A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973094 | |||||||
chr5:65973393 | A | G | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-15242A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973393 | |||||||
chr5:65973485 | G | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-15150G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973485 | |||||||
chr5:65973636 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-14999A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973636 | |||||||
chr5:65973732 | G | T | 1 | a0001c0001t0009g0040 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-57-14903G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973732 | |||||||
chr5:65973750 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-57-14885G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973750 | |||||||
chr5:65973790 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-14845A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973790 | |||||||
chr5:65973822 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14813T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973822 | |||||||
chr5:65973918 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14717A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973918 | |||||||
chr5:65973925 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-14710A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973925 | |||||||
chr5:65973928 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-57-14707G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65973928 | |||||||
chr5:65974084 | A | T | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-57-14551A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974084 | |||||||
chr5:65974173 | C | G | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-14462C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974173 | |||||||
chr5:65974184 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-57-14451A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974184 | |||||||
chr5:65974519 | G | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-14116G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974519 | |||||||
chr5:65974524 | CCTGTTAT | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-14108_-57-1410 others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65974524 | ||||||
chr5:65974956 | G | T | 2 | a0001c0007t0010g0160 a0001c0007t0010g0275 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-57-13679G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974956 | |||||||
chr5:65974981 | G | A | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-57-13654G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65974981 | |||||||
chr5:65975128 | C | G | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-57-13507C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975128 | |||||||
chr5:65975160 | A | AC | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-13474dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65975160 | ||||||
chr5:65975278 | G | T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57-13357G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975278 | |||||||
chr5:65975602 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-13033G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975602 | |||||||
chr5:65975634 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-13001A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975634 | |||||||
chr5:65975839 | C | G | 1 | a0001c0001t0013g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-57-12796C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65975839 | |||||||
chr5:65976150 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-12485C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976150 | |||||||
chr5:65976203 | G | A | 1 | a0002c0003t0003g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-57-12432G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976203 | |||||||
chr5:65976262 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-12373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976262 | |||||||
chr5:65976263 | C | T | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-12372C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976263 | |||||||
chr5:65976397 | C | T | 10 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0235 others(7): Show |
10 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-12238C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976397 | |||||||
chr5:65976520 | CT | C | 19 | a0003c0004t0001g0088 a0003c0004t0017g0120 a0004c0005t0004g0008 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57-12100delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65976520 | ||||||
chr5:65976542 | C | T | 2 | a0002c0003t0003g0204 a0009c0009t0002g0203 |
2 | NA18951.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-57-12093C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976542 | |||||||
chr5:65976597 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-12038A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976597 | |||||||
chr5:65976631 | G | T | 2 | a0002c0003t0003g0204 a0009c0009t0002g0203 |
2 | NA18951.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-57-12004G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976631 | |||||||
chr5:65976711 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11924G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976711 | |||||||
chr5:65976718 | C | CTTA | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-11916_-57-1191 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65976718 | ||||||
chr5:65976722 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11913C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976722 | |||||||
chr5:65976723 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11912G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976723 | |||||||
chr5:65976771 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11864G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976771 | |||||||
chr5:65976774 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11861C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976774 | |||||||
chr5:65976785 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11850C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976785 | |||||||
chr5:65976799 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11836T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976799 | |||||||
chr5:65976818 | A | G | 1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-57-11817A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976818 | |||||||
chr5:65976836 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11799A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976836 | |||||||
chr5:65976843 | A | C | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-57-11792A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976843 | |||||||
chr5:65976880 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-57-11755A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976880 | |||||||
chr5:65976944 | A | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-11691A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65976944 | |||||||
chr5:65977039 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-57-11596C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977039 | |||||||
chr5:65977118 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-11517C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977118 | |||||||
chr5:65977127 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11508C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977127 | |||||||
chr5:65977144 | G | A | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-11491G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977144 | |||||||
chr5:65977161 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-11474C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977161 | |||||||
chr5:65977198 | AC | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11428delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977198 | ||||||
chr5:65977200 | CCCCCCCC others(42): Show |
C | 8 | a0003c0004t0001g0136 a0005c0006t0007g0220 a0005c0006t0007g0221 others(5): Show |
8 | HG00621.hp2 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57-11364_-57-1131 others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977200 | ||||||
chr5:65977201 | CCCCCCCA others(41): Show |
C | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57-11427_-57-1138 others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977201 | ||||||
chr5:65977205 | C | T | 2 | a0002c0003t0003g0165 a0002c0003t0003g0166 |
2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-57-11430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977205 | |||||||
chr5:65977240 | G | A | 11 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(8): Show |
11 | HG00738.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-11395G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977240 | |||||||
chr5:65977245 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57-11390G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977245 | |||||||
chr5:65977271 | T | C | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11364T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977271 | |||||||
chr5:65977273 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977273 | |||||||
chr5:65977276 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11359C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977276 | |||||||
chr5:65977280 | TG | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11353delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977280 | ||||||
chr5:65977293 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977293 | |||||||
chr5:65977295 | C | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11340C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977295 | |||||||
chr5:65977297 | GAC | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11337_-57-1133 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977297 | |||||||
chr5:65977301 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11334C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977301 | |||||||
chr5:65977304 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11331C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977304 | |||||||
chr5:65977308 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11327C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977308 | |||||||
chr5:65977312 | C | CAGACGGG others(29): Show |
4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11323_-57-1132 others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977312 | |||||||
chr5:65977315 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11320C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977315 | |||||||
chr5:65977317 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11318G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977317 | |||||||
chr5:65977322 | A | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977322 | |||||||
chr5:65977325 | T | C | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-11310T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977325 | |||||||
chr5:65977368 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-11267C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977368 | |||||||
chr5:65977376 | C | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-11259C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977376 | |||||||
chr5:65977416 | C | G | 2 | a0004c0005t0004g0020 a0004c0014t0004g0019 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-57-11219C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977416 | |||||||
chr5:65977439 | A | G | 38 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0121 others(35): Show |
38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-57-11196A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977439 | |||||||
chr5:65977445 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11190T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977445 | |||||||
chr5:65977481 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57-11154G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977481 | |||||||
chr5:65977490 | G | A | 1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57-11145G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977490 | |||||||
chr5:65977500 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57-11135G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977500 | |||||||
chr5:65977553 | A | G | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57-11082A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977553 | |||||||
chr5:65977579 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-11056C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977579 | |||||||
chr5:65977749 | C | CG | 7 | a0001c0001t0001g0047 a0001c0001t0001g0135 a0001c0001t0001g0273 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57-10882dupG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977749 | ||||||
chr5:65977762 | G | C | 1 | a0003c0004t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-57-10873G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977762 | |||||||
chr5:65977788 | C | T | 2 | a0004c0005t0004g0008 a0004c0005t0004g0028 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57-10847C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977788 | |||||||
chr5:65977794 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-10841G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977794 | |||||||
chr5:65977892 | C | T | 2 | a0002c0003t0003g0188 a0002c0003t0003g0189 |
2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57-10743C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977892 | |||||||
chr5:65977904 | C | T | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-57-10731C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977904 | |||||||
chr5:65977913 | A | G | 1 | a0003c0004t0027g0300 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57-10722A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65977913 | |||||||
chr5:65977919 | C | CCGAGGCT others(7): Show |
1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-10714_-57-1070 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977919 | ||||||
chr5:65977958 | G | GGGGAGA | 80 | a0001c0001t0001g0092 a0001c0001t0003g0110 a0001c0001t0006g0146 others(77): Show |
80 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-57-10653_-57-1064 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65977958 | G | GGGGAGAG others(5): Show |
194 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(191): Show |
195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.-57-10659_-57-1064 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65977958 | G | GGGGAGAG others(11): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(10): Show |
13 | HG01071.hp2 HG01261.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57-10665_-57-1064 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65977958 | G | GGGGAGAG others(17): Show |
6 | a0005c0006t0007g0220 a0005c0006t0007g0221 a0005c0006t0007g0224 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-10671_-57-1064 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65977958 | G | GGGGAGAG others(23): Show |
1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-10648_-57-1064 others(34): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65977958 | G | GGGGAGAG others(35): Show |
1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57-10648_-57-1064 others(46): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65977958 | ||||||
chr5:65978093 | A | G | 1 | a0002c0003t0003g0189 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-57-10542A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978093 | |||||||
chr5:65978472 | A | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57-10163A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978472 | |||||||
chr5:65978483 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-10152G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978483 | |||||||
chr5:65978585 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-57-10050G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978585 | |||||||
chr5:65978927 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-9708C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65978927 | |||||||
chr5:65979135 | A | T | 38 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0121 others(35): Show |
38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-57-9500A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979135 | |||||||
chr5:65979195 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-57-9440G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979195 | |||||||
chr5:65979285 | TGTG | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-57-9340_-57-9338d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65979285 | ||||||
chr5:65979666 | A | G | 2 | a0001c0002t0002g0255 a0001c0002t0002g0260 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-57-8969A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979666 | |||||||
chr5:65979812 | T | A | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-57-8823T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979812 | |||||||
chr5:65979817 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8818C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979817 | |||||||
chr5:65979818 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-57-8817G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65979818 | |||||||
chr5:65980030 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8605T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980030 | |||||||
chr5:65980241 | C | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-57-8394C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980241 | |||||||
chr5:65980274 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8361G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980274 | |||||||
chr5:65980583 | A | G | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-8052A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980583 | |||||||
chr5:65980587 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-8048G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980587 | |||||||
chr5:65980644 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-7991A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980644 | |||||||
chr5:65980650 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-7985A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980650 | |||||||
chr5:65980722 | G | GA | 14 | a0002c0003t0002g0207 a0002c0003t0005g0198 a0005c0006t0002g0229 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57-7903dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65980722 | ||||||
chr5:65980779 | A | G | 2 | a0001c0001t0014g0069 a0001c0001t0014g0070 |
2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-57-7856A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980779 | |||||||
chr5:65980797 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-57-7838T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980797 | |||||||
chr5:65980842 | A | G | 2 | a0001c0001t0029g0091 a0004c0005t0004g0017 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-57-7793A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980842 | |||||||
chr5:65980929 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7706T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65980929 | |||||||
chr5:65981011 | G | A | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-7624G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981011 | |||||||
chr5:65981034 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7601C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981034 | |||||||
chr5:65981150 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-7485A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981150 | |||||||
chr5:65981458 | A | G | 1 | a0003c0004t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-57-7177A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981458 | |||||||
chr5:65981651 | C | CA | 18 | a0001c0001t0001g0095 a0001c0001t0009g0037 a0001c0001t0009g0038 others(15): Show |
18 | HG01109.hp2 HG01243.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57-6974dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65981651 | ||||||
chr5:65981652 | A | AAC | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-6982_-57-6981i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65981652 | ||||||
chr5:65981654 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-57-6981A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981654 | |||||||
chr5:65981986 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
42 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57-6649C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65981986 | |||||||
chr5:65982170 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-57-6465C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982170 | |||||||
chr5:65982282 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-6353G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982282 | |||||||
chr5:65982307 | G | A | 3 | a0003c0004t0001g0131 a0003c0004t0001g0140 a0003c0004t0028g0134 |
3 | HG01943.hp2 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-57-6328G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982307 | |||||||
chr5:65982379 | A | T | 5 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(2): Show |
5 | HG03098.hp1 HG03486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-6256A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982379 | |||||||
chr5:65982385 | A | G | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-6250A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982385 | |||||||
chr5:65982590 | G | C | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-57-6045G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982590 | |||||||
chr5:65982653 | T | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57-5982T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982653 | |||||||
chr5:65982680 | A | AGACTG | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-5955_-57-5954i others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982680 | |||||||
chr5:65982791 | G | A | 1 | a0003c0004t0001g0270 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-57-5844G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982791 | |||||||
chr5:65982872 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-5763G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982872 | |||||||
chr5:65982909 | T | G | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57-5726T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65982909 | |||||||
chr5:65983159 | T | C | 1 | a0002c0003t0005g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57-5476T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983159 | |||||||
chr5:65983176 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-57-5459A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983176 | |||||||
chr5:65983284 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-5351A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983284 | |||||||
chr5:65983602 | CAACCACT others(13): Show |
C | 3 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-57-5032_-57-5013d others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983602 | |||||||
chr5:65983613 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57-5022T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983613 | |||||||
chr5:65983709 | C | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-4926C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983709 | |||||||
chr5:65983795 | C | A | 1 | a0001c0007t0012g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-57-4840C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983795 | |||||||
chr5:65983795 | C | T | 1 | a0003c0004t0001g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-57-4840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983795 | |||||||
chr5:65983817 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4818A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983817 | |||||||
chr5:65983927 | A | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-57-4708A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983927 | |||||||
chr5:65983974 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG00735.hp1 HG01069.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-4661C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983974 | |||||||
chr5:65983977 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4658G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65983977 | |||||||
chr5:65984091 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-57-4544A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984091 | |||||||
chr5:65984094 | G | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0067 |
3 | HG02145.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-57-4541G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984094 | |||||||
chr5:65984140 | A | ACTGACGT others(24): Show |
16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-4490_-57-4489i others(33): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984140 | ||||||
chr5:65984293 | G | A | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57-4342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984293 | |||||||
chr5:65984320 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-4315A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984320 | |||||||
chr5:65984377 | C | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-4258C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984377 | |||||||
chr5:65984495 | C | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-4140C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984495 | |||||||
chr5:65984574 | C | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-57-4061C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984574 | |||||||
chr5:65984657 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57-3978A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984657 | |||||||
chr5:65984737 | A | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3898A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984737 | |||||||
chr5:65984869 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3766C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984869 | |||||||
chr5:65984900 | T | TA | 20 | a0001c0001t0001g0066 a0001c0001t0001g0075 a0001c0001t0001g0267 others(17): Show |
20 | HG01167.hp2 HG02056.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57-3722dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984900 | ||||||
chr5:65984900 | TA | T | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3722delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65984900 | ||||||
chr5:65984901 | A | T | 1 | a0001c0022t0009g0036 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-57-3734A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984901 | |||||||
chr5:65984912 | A | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-3723A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984912 | |||||||
chr5:65984913 | A | C | 1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-57-3722A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984913 | |||||||
chr5:65984915 | C | T | 1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-57-3720C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984915 | |||||||
chr5:65984984 | A | G | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-57-3651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65984984 | |||||||
chr5:65985077 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-57-3558A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985077 | |||||||
chr5:65985093 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57-3542A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985093 | |||||||
chr5:65985098 | T | G | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-3537T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985098 | |||||||
chr5:65985124 | C | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-3511C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985124 | |||||||
chr5:65985178 | G | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3457G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985178 | |||||||
chr5:65985206 | G | A | 1 | a0001c0002t0002g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-57-3429G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985206 | |||||||
chr5:65985241 | C | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-57-3394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985241 | |||||||
chr5:65985422 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3213T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985422 | |||||||
chr5:65985620 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-3015C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985620 | |||||||
chr5:65985670 | A | G | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57-2965A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985670 | |||||||
chr5:65985810 | T | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-2825T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985810 | |||||||
chr5:65985839 | T | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-2796T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985839 | |||||||
chr5:65985958 | A | G | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-2677A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65985958 | |||||||
chr5:65986231 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57-2404A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986231 | |||||||
chr5:65986512 | A | T | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57-2123A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986512 | |||||||
chr5:65986608 | G | T | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57-2027G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65986608 | |||||||
chr5:65987105 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-1530C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987105 | |||||||
chr5:65987195 | A | G | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-1440A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987195 | |||||||
chr5:65987367 | T | TAC | 3 | a0001c0002t0002g0170 a0001c0002t0002g0246 a0001c0002t0002g0297 |
3 | NA18962.hp1 NA18968.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-57-1241_-57-1240d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACAC | 50 | a0001c0001t0025g0157 a0002c0003t0002g0201 a0002c0003t0002g0202 others(47): Show |
50 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.-57-1245_-57-1240d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(1): Show |
8 | a0001c0002t0002g0296 a0002c0003t0003g0192 a0002c0003t0003g0282 others(5): Show |
8 | HG00438.hp2 HG01884.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-1247_-57-1240d others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(3): Show |
14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(11): Show |
14 | HG00738.hp2 HG01081.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-1249_-57-1240d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(5): Show |
10 | a0001c0001t0006g0150 a0001c0001t0006g0152 a0001c0001t0013g0124 others(7): Show |
10 | HG01167.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1251_-57-1240d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(7): Show |
59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
59 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-57-1253_-57-1240d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(9): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
35 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57-1255_-57-1240d others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(11): Show |
31 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0043 others(28): Show |
31 | HG00280.hp1 HG00735.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57-1257_-57-1240d others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(13): Show |
30 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0062 others(27): Show |
30 | HG00438.hp1 HG01069.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-57-1259_-57-1240d others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(15): Show |
5 | a0001c0001t0001g0089 a0001c0007t0010g0275 a0003c0004t0001g0115 others(2): Show |
5 | HG00621.hp2 HG02055.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57-1261_-57-1240d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(17): Show |
4 | a0001c0001t0001g0084 a0001c0001t0001g0117 a0001c0001t0009g0037 others(1): Show |
4 | HG03710.hp1 HG03834.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-1263_-57-1240d others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987367 | T | TACACACA others(19): Show |
2 | a0001c0001t0001g0111 a0003c0004t0001g0269 |
2 | HG01256.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-57-1265_-57-1240d others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987367 | ||||||
chr5:65987394 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57-1240_-57-1239i others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987394 | ||||||
chr5:65987439 | A | G | 45 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0054 others(42): Show |
45 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-57-1196A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987439 | |||||||
chr5:65987487 | A | G | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-57-1148A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987487 | |||||||
chr5:65987590 | G | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57-1045G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987590 | |||||||
chr5:65987610 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-57-1025C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987610 | |||||||
chr5:65987722 | G | A | 1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57-913G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65987722 | |||||||
chr5:65987842 | C | CA | 14 | a0001c0001t0003g0110 a0001c0001t0006g0146 a0001c0001t0006g0147 others(11): Show |
14 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57-776dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987842 | ||||||
chr5:65987842 | CAAAA | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-779_-57-776del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65987842 | ||||||
chr5:65988183 | C | T | 9 | a0001c0002t0002g0289 a0001c0002t0002g0292 a0001c0002t0002g0293 others(6): Show |
9 | HG00408.hp1 HG02165.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57-452C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988183 | |||||||
chr5:65988211 | AG | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-423delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988211 | |||||||
chr5:65988290 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0125 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-57-345T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988290 | |||||||
chr5:65988334 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-57-301T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988334 | |||||||
chr5:65988374 | T | TA | 17 | a0002c0003t0003g0282 a0004c0005t0004g0008 a0004c0005t0004g0009 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-248dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65988374 | ||||||
chr5:65988417 | A | ATG | 10 | a0002c0003t0003g0191 a0002c0003t0003g0192 a0004c0005t0004g0014 others(7): Show |
10 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-201_-57-200dup others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr5 | 65988417 | ||||||
chr5:65988451 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57-184A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988451 | |||||||
chr5:65988465 | CT | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-169delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988465 | |||||||
chr5:65988557 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57-78G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988557 | |||||||
chr5:65988605 | T | G | 1 | a0003c0004t0001g0302 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57-30T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 1/25 | chr5 | 65988605 | |||||||
chr5:65988696 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0108 |
2 | HG00738.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-10+14A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65988696 | |||||||
chr5:65988931 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-10+249C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65988931 | |||||||
chr5:65988983 | C | CA | 27 | a0001c0002t0002g0209 a0001c0002t0002g0244 a0001c0007t0010g0160 others(24): Show |
27 | HG01167.hp2 HG01243.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10+323dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65988983 | ||||||
chr5:65988983 | CA | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-10+323delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65988983 | ||||||
chr5:65989016 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+334G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989016 | |||||||
chr5:65989033 | C | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+351C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989033 | |||||||
chr5:65989040 | TTCTTCTT others(19): Show |
T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-10+360_-10+385del others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65989040 | ||||||
chr5:65989471 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10+789C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989471 | |||||||
chr5:65989539 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-10+857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989539 | |||||||
chr5:65989648 | T | C | 3 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-10+966T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65989648 | |||||||
chr5:65989862 | CCTAA | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(37): Show |
41 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-10+1183_-10+1186d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65989862 | ||||||
chr5:65990019 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+1337T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990019 | |||||||
chr5:65990440 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-10+1758A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990440 | |||||||
chr5:65990533 | G | C | 1 | a0001c0002t0002g0287 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-10+1851G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990533 | |||||||
chr5:65990540 | G | GGCACCTG others(5): Show |
16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10+1861_-10+1862i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990540 | ||||||
chr5:65990582 | C | T | 3 | a0001c0002t0002g0236 a0001c0002t0002g0249 a0001c0002t0002g0250 |
3 | HG01256.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-10+1900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990582 | |||||||
chr5:65990627 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10+1945C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990627 | |||||||
chr5:65990765 | A | AT | 9 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0014g0070 others(6): Show |
9 | HG00621.hp1 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-1932dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990765 | ||||||
chr5:65990765 | AT | A | 17 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(14): Show |
17 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-1932delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65990765 | ||||||
chr5:65990868 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1842A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990868 | |||||||
chr5:65990912 | C | A | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-1798C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990912 | |||||||
chr5:65990927 | A | G | 2 | a0001c0002t0002g0286 a0001c0002t0002g0287 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-9-1783A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990927 | |||||||
chr5:65990978 | A | T | 1 | a0003c0004t0001g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-9-1732A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990978 | |||||||
chr5:65990998 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1712T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65990998 | |||||||
chr5:65991066 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-9-1644A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991066 | |||||||
chr5:65991114 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1596C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991114 | |||||||
chr5:65991432 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1278T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991432 | |||||||
chr5:65991509 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-9-1201A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991509 | |||||||
chr5:65991670 | ATAATCTT others(32): Show |
A | 1 | a0003c0004t0028g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-9-1038_-9-1000del others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr5 | 65991670 | ||||||
chr5:65991852 | C | G | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-858C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991852 | |||||||
chr5:65991947 | G | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-763G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65991947 | |||||||
chr5:65992001 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-709C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992001 | |||||||
chr5:65992028 | C | T | 1 | a0003c0004t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-9-682C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992028 | |||||||
chr5:65992180 | C | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-530C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992180 | |||||||
chr5:65992218 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-492C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992218 | |||||||
chr5:65992243 | G | A | 1 | a0001c0002t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-9-467G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992243 | |||||||
chr5:65992274 | C | T | 1 | a0001c0021t0001g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-9-436C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992274 | |||||||
chr5:65992416 | G | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9-294G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 2/25 | chr5 | 65992416 | |||||||
chr5:65992963 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.189+56A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65992963 | |||||||
chr5:65992999 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189+92A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65992999 | |||||||
chr5:65993005 | G | A | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0084 others(4): Show |
7 | NA18954.hp2 NA18955.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+98G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993005 | |||||||
chr5:65993232 | A | T | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+325A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993232 | |||||||
chr5:65993285 | G | C | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+378G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993285 | |||||||
chr5:65993377 | T | C | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+470T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993377 | |||||||
chr5:65993589 | ATATTTAA others(16): Show |
A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.189+683_189+705del others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993589 | |||||||
chr5:65993851 | A | C | 5 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(2): Show |
5 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-896A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993851 | |||||||
chr5:65993945 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-802T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65993945 | |||||||
chr5:65994239 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.190-508T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994239 | |||||||
chr5:65994297 | G | T | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.190-450G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994297 | |||||||
chr5:65994404 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-343T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994404 | |||||||
chr5:65994602 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-145G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994602 | |||||||
chr5:65994715 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-32A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994715 | |||||||
chr5:65994716 | A | G | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.190-31A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 3/25 | chr5 | 65994716 | |||||||
chr5:65994885 | A | G | 6 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(3): Show |
6 | HG00280.hp2 NA18951.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.307+21A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65994885 | |||||||
chr5:65994949 | TA | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+86delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65994949 | |||||||
chr5:65995253 | C | A | 3 | a0001c0001t0001g0272 a0001c0001t0013g0123 a0001c0001t0013g0124 |
3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.307+389C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995253 | |||||||
chr5:65995267 | T | A | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+403T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995267 | |||||||
chr5:65995373 | AT | A | 20 | a0001c0001t0001g0092 a0002c0003t0003g0191 a0002c0003t0008g0173 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.307+525delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | ||||||
chr5:65995373 | ATT | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.307+524_307+525del others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | ||||||
chr5:65995373 | ATTTT | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+522_307+525del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65995373 | ||||||
chr5:65995517 | C | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+653C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995517 | |||||||
chr5:65995581 | T | C | 2 | a0010c0010t0002g0290 a0010c0010t0002g0291 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.307+717T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995581 | |||||||
chr5:65995974 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1110T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65995974 | |||||||
chr5:65996011 | A | T | 19 | a0002c0003t0003g0175 a0002c0003t0003g0176 a0002c0003t0003g0177 others(16): Show |
19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.307+1147A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996011 | |||||||
chr5:65996226 | A | AT | 45 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0054 others(42): Show |
45 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.307+1372dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996226 | ||||||
chr5:65996244 | G | GT | 12 | a0001c0002t0002g0210 a0001c0002t0002g0235 a0001c0002t0002g0288 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+1401dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | ||||||
chr5:65996244 | GT | G | 40 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0043 others(37): Show |
40 | HG00280.hp1 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.307+1401delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | ||||||
chr5:65996244 | GTT | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.307+1400_307+1401d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | ||||||
chr5:65996244 | GTTT | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(4): Show |
7 | HG02080.hp2 NA18940.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+1399_307+1401d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996244 | ||||||
chr5:65996255 | T | TTTG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1393_307+1394i others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65996255 | ||||||
chr5:65996260 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+1396T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996260 | |||||||
chr5:65996473 | G | C | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.307+1609G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996473 | |||||||
chr5:65996519 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.307+1655A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996519 | |||||||
chr5:65996797 | T | C | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.307+1933T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996797 | |||||||
chr5:65996840 | A | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+1976A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65996840 | |||||||
chr5:65997013 | A | AT | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2153dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997013 | ||||||
chr5:65997050 | G | A | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+2186G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997050 | |||||||
chr5:65997295 | G | A | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.307+2431G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997295 | |||||||
chr5:65997426 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2562G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997426 | |||||||
chr5:65997477 | C | T | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.307+2613C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997477 | |||||||
chr5:65997598 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+2734T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997598 | |||||||
chr5:65997633 | C | T | 2 | a0001c0002t0002g0034 a0013c0024t0023g0145 |
2 | HG03098.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.307+2769C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997633 | |||||||
chr5:65997634 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.307+2770G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997634 | |||||||
chr5:65997717 | G | A | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.307+2853G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997717 | |||||||
chr5:65997721 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+2857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997721 | |||||||
chr5:65997779 | A | G | 1 | a0004c0005t0004g0020 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307+2915A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997779 | |||||||
chr5:65997841 | A | G | 1 | a0005c0006t0007g0221 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.307+2977A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997841 | |||||||
chr5:65997927 | T | TAC | 7 | a0001c0001t0001g0055 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
7 | HG00735.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+3083_307+3084d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | ||||||
chr5:65997927 | T | TACAC | 3 | a0005c0006t0007g0220 a0005c0006t0007g0221 a0011c0016t0007g0228 |
3 | HG01243.hp2 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.307+3081_307+3084d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | ||||||
chr5:65997927 | TACACAC | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3079_307+3084d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65997927 | ||||||
chr5:65997965 | C | T | 1 | a0001c0007t0012g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.307+3101C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997965 | |||||||
chr5:65997966 | G | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3102G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65997966 | |||||||
chr5:65998086 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+3222G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998086 | |||||||
chr5:65998214 | C | G | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+3350C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998214 | |||||||
chr5:65998223 | C | CA | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3368dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998223 | ||||||
chr5:65998231 | A | T | 27 | a0001c0001t0001g0109 a0001c0001t0006g0146 a0001c0001t0006g0147 others(24): Show |
27 | HG01884.hp1 HG01952.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.307+3367A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998231 | |||||||
chr5:65998232 | A | T | 1 | a0001c0002t0002g0296 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.307+3368A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998232 | |||||||
chr5:65998233 | T | A | 16 | a0001c0001t0001g0135 a0002c0003t0008g0173 a0002c0003t0008g0174 others(13): Show |
16 | HG00408.hp2 HG01109.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3369T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998233 | |||||||
chr5:65998411 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3547T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998411 | |||||||
chr5:65998522 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3658A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998522 | |||||||
chr5:65998698 | A | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3834A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998698 | |||||||
chr5:65998710 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+3846G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998710 | |||||||
chr5:65998781 | C | T | 20 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(17): Show |
20 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.307+3917C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65998781 | |||||||
chr5:65998894 | C | CA | 12 | a0001c0002t0002g0242 a0001c0002t0002g0249 a0001c0002t0002g0254 others(9): Show |
12 | HG00673.hp2 HG02004.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+4055dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | ||||||
chr5:65998894 | CA | C | 128 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0043 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.307+4055delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | ||||||
chr5:65998894 | CAA | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0079 others(12): Show |
15 | HG01943.hp2 HG02273.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.307+4054_307+4055d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | ||||||
chr5:65998894 | CAAAA | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4052_307+4055d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 65998894 | ||||||
chr5:65999188 | G | GTGAA | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4324_307+4325i others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999188 | |||||||
chr5:65999258 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.307+4394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999258 | |||||||
chr5:65999456 | G | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.307+4592G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999456 | |||||||
chr5:65999508 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4644T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999508 | |||||||
chr5:65999527 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.307+4663A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999527 | |||||||
chr5:65999726 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+4862A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999726 | |||||||
chr5:65999830 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.307+4966T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999830 | |||||||
chr5:65999934 | T | C | 3 | a0001c0001t0001g0272 a0001c0001t0013g0123 a0001c0001t0013g0124 |
3 | HG01261.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.307+5070T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999934 | |||||||
chr5:65999966 | T | C | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.307+5102T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 65999966 | |||||||
chr5:66000487 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+5623T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000487 | |||||||
chr5:66000789 | C | G | 5 | a0001c0002t0002g0289 a0001c0002t0002g0293 a0001c0002t0002g0294 others(2): Show |
5 | HG02165.hp1 NA18969.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.307+5925C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000789 | |||||||
chr5:66000930 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6066C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000930 | |||||||
chr5:66000933 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6069A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66000933 | |||||||
chr5:66001000 | A | G | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.307+6136A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001000 | |||||||
chr5:66001052 | C | G | 1 | a0003c0004t0028g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.307+6188C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001052 | |||||||
chr5:66001122 | A | G | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.307+6258A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001122 | |||||||
chr5:66001148 | T | A | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.307+6284T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001148 | |||||||
chr5:66001185 | T | A | 1 | a0002c0003t0002g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.307+6321T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001185 | |||||||
chr5:66001217 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6353C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001217 | |||||||
chr5:66001229 | A | C | 1 | a0005c0006t0007g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.307+6365A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001229 | |||||||
chr5:66001515 | A | G | 8 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(5): Show |
8 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.307+6651A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001515 | |||||||
chr5:66001642 | A | T | 1 | a0005c0006t0007g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.307+6778A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001642 | |||||||
chr5:66001855 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+6991A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66001855 | |||||||
chr5:66002012 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+7148C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002012 | |||||||
chr5:66002205 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307+7341C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002205 | |||||||
chr5:66002429 | TTC | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+7567_307+7568d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66002429 | ||||||
chr5:66002501 | C | A | 1 | a0001c0002t0002g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.307+7637C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002501 | |||||||
chr5:66002698 | G | GA | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+7838dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66002698 | ||||||
chr5:66002932 | T | C | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.307+8068T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66002932 | |||||||
chr5:66003027 | C | T | 2 | a0004c0005t0004g0020 a0004c0014t0004g0019 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.307+8163C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003027 | |||||||
chr5:66003136 | C | T | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.307+8272C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003136 | |||||||
chr5:66003356 | T | TA | 16 | a0001c0001t0001g0274 a0004c0005t0004g0008 a0004c0005t0004g0009 others(13): Show |
16 | HG00438.hp1 HG01167.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.307+8502dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003356 | ||||||
chr5:66003662 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.308-8387G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003662 | |||||||
chr5:66003798 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-8251G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003798 | |||||||
chr5:66003887 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.308-8162C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003887 | |||||||
chr5:66003923 | C | CT | 22 | a0001c0001t0001g0108 a0001c0002t0002g0033 a0001c0002t0002g0034 others(19): Show |
22 | HG01167.hp2 HG01433.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.308-8101dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003923 | C | CTT | 7 | a0002c0003t0002g0205 a0002c0003t0002g0215 a0004c0005t0004g0008 others(4): Show |
7 | HG00280.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.308-8102_308-8101d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003923 | CT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0030 others(88): Show |
92 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.308-8101delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003923 | CTT | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0068 others(19): Show |
22 | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.308-8102_308-8101d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003923 | CTTT | C | 8 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(5): Show |
8 | HG01243.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-8103_308-8101d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003923 | CTTTTTTT others(4): Show |
C | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308-8111_308-8101d others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66003923 | ||||||
chr5:66003948 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.308-8101T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003948 | |||||||
chr5:66003978 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-8071T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66003978 | |||||||
chr5:66004070 | T | C | 1 | a0002c0003t0005g0182 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.308-7979T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004070 | |||||||
chr5:66004103 | A | AT | 52 | a0001c0001t0001g0068 a0001c0001t0013g0123 a0001c0007t0010g0160 others(49): Show |
52 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.308-7926dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | ||||||
chr5:66004103 | AT | A | 20 | a0001c0001t0001g0118 a0001c0002t0002g0285 a0001c0002t0002g0293 others(17): Show |
20 | HG01069.hp2 HG01109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.308-7926delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | ||||||
chr5:66004103 | ATTTTTTT others(5): Show |
A | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.308-7937_308-7926d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004103 | ||||||
chr5:66004139 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-7910G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004139 | |||||||
chr5:66004189 | G | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.308-7860G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004189 | |||||||
chr5:66004225 | C | T | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-7824C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004225 | |||||||
chr5:66004379 | CGT | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-7660_308-7659d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66004379 | ||||||
chr5:66004389 | T | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-7660T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004389 | |||||||
chr5:66004391 | C | T | 1 | a0001c0002t0002g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.308-7658C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004391 | |||||||
chr5:66004395 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-7654C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004395 | |||||||
chr5:66004399 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.308-7650T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004399 | |||||||
chr5:66004401 | C | T | 2 | a0001c0001t0001g0085 a0001c0007t0012g0218 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.308-7648C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004401 | |||||||
chr5:66004402 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.308-7647G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004402 | |||||||
chr5:66004434 | C | T | 2 | a0001c0001t0006g0149 a0001c0001t0006g0150 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.308-7615C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004434 | |||||||
chr5:66004639 | A | G | 3 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.308-7410A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004639 | |||||||
chr5:66004680 | T | C | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.308-7369T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004680 | |||||||
chr5:66004689 | C | T | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-7360C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004689 | |||||||
chr5:66004716 | T | G | 1 | a0001c0002t0002g0254 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.308-7333T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004716 | |||||||
chr5:66004790 | T | A | 8 | a0001c0002t0002g0235 a0001c0002t0002g0246 a0001c0002t0002g0247 others(5): Show |
8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.308-7259T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66004790 | |||||||
chr5:66005049 | G | A | 2 | a0001c0007t0010g0161 a0001c0007t0010g0164 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.308-7000G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005049 | |||||||
chr5:66005078 | CTGT | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6970_308-6968d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005078 | |||||||
chr5:66005084 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6965A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005084 | |||||||
chr5:66005085 | TA | T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.308-6963delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005085 | |||||||
chr5:66005240 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6809C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005240 | |||||||
chr5:66005500 | C | T | 1 | a0001c0002t0002g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.308-6549C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005500 | |||||||
chr5:66005643 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-6406G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005643 | |||||||
chr5:66005734 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6315A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005734 | |||||||
chr5:66005795 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.308-6254A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005795 | |||||||
chr5:66005835 | C | A | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-6214C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005835 | |||||||
chr5:66005935 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6114A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005935 | |||||||
chr5:66005951 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-6098G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005951 | |||||||
chr5:66005993 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-6056A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66005993 | |||||||
chr5:66006124 | G | A | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.308-5925G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006124 | |||||||
chr5:66006259 | C | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5790C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006259 | |||||||
chr5:66006343 | T | G | 1 | a0001c0002t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.308-5706T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006343 | |||||||
chr5:66006381 | C | T | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.308-5668C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006381 | |||||||
chr5:66006518 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5531A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006518 | |||||||
chr5:66006534 | T | C | 1 | a0001c0002t0002g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.308-5515T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006534 | |||||||
chr5:66006617 | T | C | 1 | a0001c0001t0006g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.308-5432T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006617 | |||||||
chr5:66006636 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308-5413T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006636 | |||||||
chr5:66006642 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308-5407T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006642 | |||||||
chr5:66006868 | G | A | 23 | a0003c0004t0001g0131 a0003c0004t0028g0134 a0004c0005t0004g0008 others(20): Show |
23 | HG01167.hp2 HG01884.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.308-5181G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006868 | |||||||
chr5:66006903 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.308-5146A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006903 | |||||||
chr5:66006917 | T | C | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-5132T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006917 | |||||||
chr5:66006990 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5059T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006990 | |||||||
chr5:66006991 | A | T | 53 | a0002c0003t0002g0201 a0002c0003t0002g0202 a0002c0003t0002g0205 others(50): Show |
53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.308-5058A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66006991 | |||||||
chr5:66007000 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | NA18946.hp1 NA18969.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.308-5049G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007000 | |||||||
chr5:66007002 | A | AC | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.308-5047_308-5046i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007002 | |||||||
chr5:66007009 | T | TA | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-5039dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007009 | ||||||
chr5:66007012 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.308-5037C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007012 | |||||||
chr5:66007056 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.308-4993G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007056 | |||||||
chr5:66007262 | C | G | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308-4787C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007262 | |||||||
chr5:66007334 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-4715A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007334 | |||||||
chr5:66007361 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.308-4688G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007361 | |||||||
chr5:66007403 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-4646C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007403 | |||||||
chr5:66007412 | G | T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308-4637G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007412 | |||||||
chr5:66007426 | ATATACC | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.308-4614_308-4609d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007426 | ||||||
chr5:66007540 | G | A | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-4509G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007540 | |||||||
chr5:66007546 | T | TA | 11 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(8): Show |
11 | HG01109.hp2 HG02451.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.308-4489dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007546 | ||||||
chr5:66007546 | TA | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(87): Show |
91 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.308-4489delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66007546 | ||||||
chr5:66007547 | A | T | 1 | a0005c0006t0002g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.308-4502A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007547 | |||||||
chr5:66007549 | A | T | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308-4500A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66007549 | |||||||
chr5:66008185 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-3864G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008185 | |||||||
chr5:66008264 | A | G | 1 | a0001c0001t0013g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.308-3785A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008264 | |||||||
chr5:66008280 | G | A | 1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.308-3769G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008280 | |||||||
chr5:66008403 | T | C | 2 | a0001c0002t0002g0255 a0001c0002t0002g0260 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.308-3646T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008403 | |||||||
chr5:66008416 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.308-3633C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008416 | |||||||
chr5:66008488 | AAAT | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG01256.hp2 HG02004.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.308-3556_308-3554d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66008488 | ||||||
chr5:66008562 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.308-3487G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008562 | |||||||
chr5:66008833 | G | A | 2 | a0002c0003t0003g0165 a0002c0003t0003g0166 |
2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.308-3216G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008833 | |||||||
chr5:66008869 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-3180A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008869 | |||||||
chr5:66008915 | A | T | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.308-3134A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66008915 | |||||||
chr5:66009178 | C | T | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.308-2871C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66009178 | |||||||
chr5:66009741 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-2308T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66009741 | |||||||
chr5:66010068 | A | G | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.308-1981A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010068 | |||||||
chr5:66010283 | G | A | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.308-1766G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010283 | |||||||
chr5:66010318 | T | C | 18 | a0001c0007t0010g0162 a0001c0007t0010g0163 a0004c0005t0004g0008 others(15): Show |
18 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.308-1731T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010318 | |||||||
chr5:66010350 | C | CATG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1692_308-1690d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010350 | ||||||
chr5:66010627 | T | TATATG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1417_308-1413d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010627 | ||||||
chr5:66010652 | T | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.308-1397T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010652 | |||||||
chr5:66010777 | T | C | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.308-1272T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66010777 | |||||||
chr5:66010981 | AT | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-1065delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66010981 | ||||||
chr5:66011172 | A | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.308-877A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011172 | |||||||
chr5:66011309 | CTG | C | 4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-738_308-737del others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66011309 | ||||||
chr5:66011371 | T | A | 19 | a0002c0003t0003g0175 a0002c0003t0003g0176 a0002c0003t0003g0177 others(16): Show |
19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.308-678T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011371 | |||||||
chr5:66011517 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.308-532G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011517 | |||||||
chr5:66011521 | C | G | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.308-528C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011521 | |||||||
chr5:66011522 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.308-527T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011522 | |||||||
chr5:66011660 | G | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.308-389G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011660 | |||||||
chr5:66011717 | CT | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-323delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr5 | 66011717 | ||||||
chr5:66011726 | T | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0092 a0001c0001t0001g0111 others(2): Show |
5 | HG01256.hp2 HG02004.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-323T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011726 | |||||||
chr5:66011760 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.308-289C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 4/25 | chr5 | 66011760 | |||||||
chr5:66012148 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.386+21T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012148 | |||||||
chr5:66012227 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(77): Show |
81 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.386+100C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012227 | |||||||
chr5:66012239 | C | T | 7 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+112C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012239 | |||||||
chr5:66012481 | T | TAAAG | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.386+354_386+355ins others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012481 | |||||||
chr5:66012639 | C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386+512C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012639 | |||||||
chr5:66012699 | A | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386+572A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012699 | |||||||
chr5:66012776 | A | T | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+649A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012776 | |||||||
chr5:66012856 | C | T | 1 | a0001c0015t0030g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.387-693C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012856 | |||||||
chr5:66012972 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.387-577A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66012972 | |||||||
chr5:66013080 | T | G | 1 | a0001c0001t0006g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.387-469T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013080 | |||||||
chr5:66013112 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.387-437T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013112 | |||||||
chr5:66013120 | A | G | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-429A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013120 | |||||||
chr5:66013311 | T | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.387-238T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013311 | |||||||
chr5:66013433 | A | T | 1 | a0001c0002t0002g0247 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.387-116A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 5/25 | chr5 | 66013433 | |||||||
chr5:66013723 | A | G | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.476+85A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66013723 | |||||||
chr5:66013781 | G | C | 193 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.476+143G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66013781 | |||||||
chr5:66014005 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.476+367T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014005 | |||||||
chr5:66014014 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.476+376G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014014 | |||||||
chr5:66014176 | A | G | 7 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.477-493A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014176 | |||||||
chr5:66014258 | A | G | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.477-411A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014258 | |||||||
chr5:66014541 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-128T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014541 | |||||||
chr5:66014563 | G | A | 1 | a0001c0001t0006g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.477-106G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014563 | |||||||
chr5:66014577 | A | T | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.477-92A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | chr5 | 66014577 | |||||||
chr5:66014649 | AT | A | 28 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(25): Show |
28 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.477-10delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr5 | 66014649 | ||||||
chr5:66014886 | G | T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.533+161G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66014886 | |||||||
chr5:66015026 | A | G | 1 | a0001c0002t0002g0279 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.533+301A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015026 | |||||||
chr5:66015114 | C | G | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.533+389C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015114 | |||||||
chr5:66015143 | A | G | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.533+418A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015143 | |||||||
chr5:66015389 | C | CAA | 285 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(282): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.533+665_533+666dup others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66015389 | ||||||
chr5:66015714 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+989A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015714 | |||||||
chr5:66015902 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1177T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66015902 | |||||||
chr5:66016157 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+1432T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016157 | |||||||
chr5:66016254 | A | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+1529A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016254 | |||||||
chr5:66016300 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.533+1575G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016300 | |||||||
chr5:66016322 | A | G | 1 | a0001c0001t0013g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.533+1597A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016322 | |||||||
chr5:66016353 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1628C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016353 | |||||||
chr5:66016359 | T | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.533+1634T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016359 | |||||||
chr5:66016449 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1724C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016449 | |||||||
chr5:66016582 | C | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+1857C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016582 | |||||||
chr5:66016615 | C | CT | 12 | a0001c0002t0002g0214 a0004c0005t0004g0014 a0004c0005t0004g0015 others(9): Show |
12 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+1906dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | ||||||
chr5:66016615 | C | CTT | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+1905_533+1906d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | ||||||
chr5:66016615 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.533+1906delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66016615 | ||||||
chr5:66016637 | G | A | 1 | a0001c0002t0002g0293 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.533+1912G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016637 | |||||||
chr5:66016750 | A | G | 1 | a0015c0013t0001g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.533+2025A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016750 | |||||||
chr5:66016821 | G | A | 2 | a0001c0007t0010g0160 a0001c0007t0010g0275 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.533+2096G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016821 | |||||||
chr5:66016835 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.533+2110G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016835 | |||||||
chr5:66016845 | C | T | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.533+2120C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016845 | |||||||
chr5:66016857 | C | T | 1 | a0003c0004t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.533+2132C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016857 | |||||||
chr5:66016866 | C | T | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533+2141C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016866 | |||||||
chr5:66016916 | G | A | 1 | a0003c0004t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.533+2191G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66016916 | |||||||
chr5:66017098 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+2373C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017098 | |||||||
chr5:66017339 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+2614C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017339 | |||||||
chr5:66017436 | A | AT | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+2717dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017436 | ||||||
chr5:66017518 | AT | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.533+2810delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017518 | ||||||
chr5:66017518 | ATTT | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+2808_533+2810d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017518 | ||||||
chr5:66017562 | A | G | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.533+2837A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017562 | |||||||
chr5:66017654 | G | GT | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+2935dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66017654 | ||||||
chr5:66017685 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+2960A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017685 | |||||||
chr5:66017779 | A | G | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.533+3054A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017779 | |||||||
chr5:66017888 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+3163T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66017888 | |||||||
chr5:66018061 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.534-3261G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018061 | |||||||
chr5:66018073 | A | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.534-3249A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018073 | |||||||
chr5:66018404 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2918G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018404 | |||||||
chr5:66018441 | A | AATATAAT others(26): Show |
1 | a0001c0002t0002g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.534-2875_534-2843d others(35): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018441 | ||||||
chr5:66018443 | TATAATAT others(109): Show |
T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.534-2875_534-2760d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018443 | ||||||
chr5:66018447 | A | T | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2875A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018447 | |||||||
chr5:66018447 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0002g0295 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.534-2835_534-2803d others(35): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018447 | ||||||
chr5:66018447 | ATATATAT others(146): Show |
A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2867_534-2715d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018447 | ||||||
chr5:66018448 | T | A | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2874T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018448 | |||||||
chr5:66018449 | A | T | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.534-2873A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018449 | |||||||
chr5:66018452 | TATTATAT others(40): Show |
T | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.534-2869_534-2823d others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018452 | |||||||
chr5:66018454 | T | TTATATTA others(80): Show |
1 | a0001c0001t0001g0103 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(89): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018454 | ||||||
chr5:66018459 | T | TAATATAA others(116): Show |
1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534-2863_534-2862i others(125): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018459 | |||||||
chr5:66018460 | TATATA | T | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | NA18999.hp2 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2856_534-2852d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018460 | ||||||
chr5:66018466 | A | ATATATAT | 69 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(66): Show |
69 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.534-2836_534-2830d others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018466 | A | ATATATAT others(7): Show |
6 | a0001c0002t0002g0292 a0001c0002t0002g0293 a0001c0002t0002g0294 others(3): Show |
6 | HG00408.hp1 HG03704.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-2843_534-2830d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018466 | A | ATATATAT others(14): Show |
2 | a0001c0002t0002g0296 a0001c0002t0002g0297 |
2 | HG00438.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.534-2850_534-2830d others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018466 | A | ATATATAT others(40): Show |
1 | a0001c0002t0002g0288 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018466 | A | ATATATAT others(19): Show |
1 | a0002c0003t0003g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.534-2844_534-2843i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018466 | A | T | 3 | a0001c0002t0002g0248 a0002c0003t0003g0167 a0005c0006t0007g0222 |
3 | HG02258.hp2 NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.534-2856A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018466 | |||||||
chr5:66018466 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0117 |
2 | HG03834.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.534-2843_534-2830d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018466 | ||||||
chr5:66018468 | ATATATTA others(12): Show |
A | 1 | a0005c0006t0015g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.534-2842_534-2824d others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018468 | ||||||
chr5:66018468 | ATATATTA others(52): Show |
A | 5 | a0005c0006t0007g0220 a0005c0006t0007g0221 a0005c0006t0007g0224 others(2): Show |
5 | HG01109.hp2 HG01243.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2842_534-2784d others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018468 | ||||||
chr5:66018473 | T | TTATATAT others(45): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG02572.hp2 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(5): Show |
9 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0078 others(6): Show |
9 | HG01978.hp1 HG03098.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(31): Show |
1 | a0001c0001t0014g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.534-2844_534-2843i others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(40): Show |
1 | a0001c0001t0001g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(31): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0051 others(23): Show |
27 | HG00099.hp2 HG00609.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(40): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(45): Show |
9 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(45): Show |
3 | a0001c0001t0001g0064 a0001c0001t0013g0123 a0001c0020t0001g0116 |
3 | HG01261.hp2 HG02145.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.534-2844_534-2843i others(54): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(57): Show |
1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(66): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(59): Show |
9 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0001g0082 others(6): Show |
9 | HG01256.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2844_534-2843i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(66): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0075 a0001c0001t0001g0268 |
3 | HG02056.hp1 NA18954.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.534-2844_534-2843i others(75): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | T | TTATATTA others(94): Show |
1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.534-2844_534-2843i others(103): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018473 | TTATATAT others(19): Show |
T | 1 | a0001c0002t0019g0298 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.534-2829_534-2804d others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018473 | ||||||
chr5:66018475 | ATATATTA others(5): Show |
A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2835_534-2824d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018475 | ||||||
chr5:66018475 | ATATATTA others(85): Show |
A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2835_534-2744d others(94): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018475 | ||||||
chr5:66018480 | T | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0144 others(9): Show |
12 | HG01515.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-2842T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018480 | |||||||
chr5:66018480 | T | TAATATAA | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.534-2842_534-2841i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018480 | |||||||
chr5:66018480 | T | TTATAATA others(33): Show |
1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.534-2838_534-2837i others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAA | 45 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0121 others(42): Show |
45 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.534-2836_534-2835i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAA others(15): Show |
1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAA others(19): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0043 |
3 | HG02818.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAA others(38): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0055 |
2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.534-2836_534-2835i others(47): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAA others(19): Show |
1 | a0003c0004t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.534-2836_534-2835i others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAT others(40): Show |
1 | a0001c0002t0002g0247 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(49): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATAT others(33): Show |
1 | a0001c0002t0002g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.534-2769_534-2730d others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | T | TTATATTA others(17): Show |
1 | a0001c0001t0001g0007 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.534-2837_534-2836i others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018480 | TTATATAT others(7): Show |
T | 4 | a0001c0001t0006g0152 a0001c0001t0006g0155 a0001c0001t0006g0156 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2837_534-2824d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018480 | ||||||
chr5:66018481 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0119 |
2 | HG00280.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.534-2841T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018481 | |||||||
chr5:66018482 | A | ATAATATA others(10): Show |
3 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 |
3 | HG03486.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-2838_534-2837i others(19): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018482 | ||||||
chr5:66018482 | ATATAT | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | NA18999.hp2 NA19003.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2829_534-2825d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018482 | ||||||
chr5:66018485 | T | A | 2 | a0001c0001t0006g0151 a0001c0001t0006g0153 |
2 | HG00738.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534-2837T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018485 | |||||||
chr5:66018486 | A | AAT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(49): Show |
53 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.534-2836_534-2835i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018486 | A | AATATATA others(85): Show |
1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(94): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018486 | A | AATATATA others(132): Show |
1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(141): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018486 | A | AATATATA others(146): Show |
1 | a0001c0001t0001g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(155): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018486 | A | AATATATA others(59): Show |
1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.534-2836_534-2835i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018486 | A | T | 2 | a0001c0001t0006g0151 a0001c0001t0006g0153 |
2 | HG00738.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.534-2836A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018486 | |||||||
chr5:66018487 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(58): Show |
62 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.534-2835T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TAATA | 3 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 |
3 | HG03486.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.534-2835_534-2834i others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TATAATAT others(27): Show |
1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.534-2835_534-2834i others(36): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TATAATAT others(41): Show |
1 | a0001c0001t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.534-2835_534-2834i others(50): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TATTATAT others(30): Show |
1 | a0001c0001t0001g0029 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.534-2835_534-2834i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TATTATAT others(49): Show |
1 | a0001c0001t0001g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.534-2835_534-2834i others(58): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018487 | |||||||
chr5:66018487 | T | TTA | 3 | a0001c0001t0001g0103 a0001c0001t0001g0264 a0001c0001t0006g0154 |
3 | HG01978.hp2 HG02145.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.534-2831_534-2830d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | ||||||
chr5:66018487 | T | TTATAATA others(7): Show |
2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.534-2831_534-2830i others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | ||||||
chr5:66018487 | T | TTATATAT others(21): Show |
1 | a0002c0003t0003g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.534-2830_534-2829i others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | ||||||
chr5:66018487 | TTATATTA others(5): Show |
T | 2 | a0002c0003t0005g0187 a0002c0003t0005g0198 |
2 | NA19063.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.534-2829_534-2818d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018487 | ||||||
chr5:66018492 | T | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG01978.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2830T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | |||||||
chr5:66018492 | T | TAA | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0013g0123 |
3 | HG01261.hp2 HG03139.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.534-2830_534-2829i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | |||||||
chr5:66018492 | T | TATTATAT others(52): Show |
1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.534-2830_534-2829i others(61): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | |||||||
chr5:66018492 | T | TATTATAT others(94): Show |
1 | a0003c0004t0001g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.534-2830_534-2829i others(103): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018492 | |||||||
chr5:66018493 | T | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0055 others(9): Show |
12 | HG01515.hp1 HG02055.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.534-2829T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018493 | |||||||
chr5:66018494 | A | T | 9 | a0001c0001t0001g0049 a0001c0001t0001g0272 a0001c0001t0003g0110 others(6): Show |
9 | HG01515.hp1 HG04115.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-2828A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018494 | |||||||
chr5:66018498 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.534-2824A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018498 | |||||||
chr5:66018499 | A | T | 13 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0264 others(10): Show |
13 | HG00738.hp2 HG01978.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.534-2823A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018499 | |||||||
chr5:66018506 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
55 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.534-2816T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018506 | |||||||
chr5:66018506 | T | TTATATAA | 4 | a0001c0001t0006g0154 a0001c0001t0013g0102 a0001c0001t0029g0091 others(1): Show |
4 | HG02145.hp2 HG03540.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2810_534-2809i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATAT others(61): Show |
1 | a0003c0004t0001g0304 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.534-2805_534-2804i others(70): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATTA others(59): Show |
1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534-2811_534-2810i others(68): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATTA others(87): Show |
1 | a0001c0001t0001g0054 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.534-2811_534-2810i others(96): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATTA others(101): Show |
1 | a0001c0001t0001g0053 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.534-2811_534-2810i others(110): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATTA others(38): Show |
2 | a0003c0004t0001g0137 a0003c0004t0001g0138 |
2 | HG00642.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.534-2811_534-2810i others(47): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | T | TTATATTA others(57): Show |
1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.534-2811_534-2810i others(66): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018506 | TTA | T | 37 | a0001c0001t0001g0121 a0001c0001t0001g0135 a0001c0001t0001g0274 others(34): Show |
37 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.534-2810_534-2809d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018506 | ||||||
chr5:66018507 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2815T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018507 | |||||||
chr5:66018508 | A | ATATAT | 3 | a0001c0001t0001g0128 a0001c0002t0002g0261 a0002c0003t0003g0197 |
3 | HG01891.hp2 HG01981.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.534-2808_534-2804d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018508 | ||||||
chr5:66018508 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2814A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018508 | |||||||
chr5:66018512 | ATT | A | 5 | a0001c0001t0001g0267 a0007c0011t0011g0025 a0007c0011t0011g0026 others(2): Show |
5 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2809_534-2808d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018512 | |||||||
chr5:66018513 | T | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0044 others(32): Show |
35 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.534-2809T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018513 | |||||||
chr5:66018513 | T | TTATAA | 3 | a0001c0001t0001g0043 a0001c0001t0006g0151 a0003c0004t0001g0127 |
3 | HG02976.hp2 HG03516.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.534-2805_534-2804i others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018513 | ||||||
chr5:66018518 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2804T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018518 | |||||||
chr5:66018519 | A | T | 2 | a0001c0001t0001g0084 a0002c0003t0008g0278 |
2 | NA18955.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.534-2803A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018519 | |||||||
chr5:66018519 | AATATATA others(56): Show |
A | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.534-2798_534-2736d others(65): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018519 | ||||||
chr5:66018520 | A | T | 42 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0044 others(39): Show |
42 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.534-2802A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018520 | |||||||
chr5:66018522 | ATATAT | A | 9 | a0001c0001t0001g0117 a0001c0001t0006g0155 a0001c0001t0025g0157 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2789_534-2785d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018522 | ||||||
chr5:66018525 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2797T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018525 | |||||||
chr5:66018526 | A | AAT | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2796_534-2795i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018526 | |||||||
chr5:66018526 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.534-2796A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018526 | |||||||
chr5:66018527 | T | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0045 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.534-2795T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018527 | |||||||
chr5:66018527 | T | TTA | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0067 others(10): Show |
13 | HG00642.hp1 HG01167.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.534-2791_534-2790d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | ||||||
chr5:66018527 | T | TTATATAA others(2): Show |
7 | a0001c0001t0001g0043 a0001c0001t0006g0146 a0001c0001t0006g0147 others(4): Show |
7 | HG02976.hp2 HG03098.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.534-2790_534-2789i others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | ||||||
chr5:66018527 | T | TTATATAA others(30): Show |
1 | a0001c0001t0013g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | ||||||
chr5:66018527 | T | TTATATAT others(56): Show |
1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(65): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018527 | ||||||
chr5:66018532 | T | A | 5 | a0006c0008t0003g0072 a0006c0008t0003g0190 a0006c0008t0003g0194 others(2): Show |
5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.534-2790T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.534-2790_534-2789i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(9): Show |
1 | a0001c0001t0001g0078 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(44): Show |
1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(53): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(100): Show |
1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(86): Show |
1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(95): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(30): Show |
1 | a0001c0001t0001g0095 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(39): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(194): Show |
1 | a0001c0001t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(203): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(131): Show |
1 | a0001c0001t0001g0007 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.534-2790_534-2789i others(140): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TAATATAT others(299): Show |
1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.534-2790_534-2789i others(308): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TATTATAT others(2): Show |
3 | a0001c0001t0001g0132 a0001c0001t0006g0154 a0014c0018t0001g0050 |
3 | HG01071.hp2 HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.534-2790_534-2789i others(11): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018532 | |||||||
chr5:66018532 | T | TTATATAA others(120): Show |
2 | a0001c0001t0009g0039 a0001c0022t0009g0036 |
2 | NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.534-2771_534-2770i others(129): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018532 | ||||||
chr5:66018532 | T | TTATATAA others(106): Show |
1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(115): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018532 | ||||||
chr5:66018533 | T | A | 38 | a0001c0001t0001g0048 a0001c0001t0001g0121 a0001c0001t0001g0135 others(35): Show |
38 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.534-2789T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018533 | |||||||
chr5:66018534 | A | T | 29 | a0001c0001t0001g0121 a0001c0001t0001g0135 a0001c0001t0001g0274 others(26): Show |
29 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.534-2788A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018534 | |||||||
chr5:66018539 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
90 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-2783A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018539 | |||||||
chr5:66018540 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2782T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018540 | |||||||
chr5:66018541 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2781A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018541 | |||||||
chr5:66018546 | T | A | 40 | a0001c0001t0001g0055 a0001c0001t0001g0106 a0001c0001t0001g0121 others(37): Show |
40 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.534-2776T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018546 | |||||||
chr5:66018546 | T | TTATATTA others(5): Show |
1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018546 | ||||||
chr5:66018546 | TTA | T | 8 | a0001c0001t0009g0038 a0001c0001t0009g0041 a0006c0008t0003g0072 others(5): Show |
8 | HG01884.hp1 NA18950.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-2770_534-2769d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018546 | ||||||
chr5:66018547 | T | TATATTAT others(71): Show |
1 | a0001c0001t0009g0040 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.534-2771_534-2770i others(80): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018547 | ||||||
chr5:66018548 | A | ATATAT | 10 | a0002c0003t0002g0202 a0002c0003t0002g0205 a0002c0003t0002g0206 others(7): Show |
10 | HG00280.hp2 HG02738.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.534-2768_534-2764d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | ||||||
chr5:66018548 | A | ATATATTA others(83): Show |
1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(92): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | ||||||
chr5:66018548 | A | ATATATTA others(36): Show |
1 | a0002c0003t0003g0192 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.534-2764_534-2763i others(45): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | ||||||
chr5:66018548 | A | ATATATTA others(43): Show |
30 | a0002c0003t0003g0165 a0002c0003t0003g0166 a0002c0003t0003g0167 others(27): Show |
30 | HG00408.hp2 HG01081.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.534-2764_534-2763i others(52): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018548 | ||||||
chr5:66018553 | T | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG01891.hp2 HG02055.hp1 HG02273.hp1 others(23): Show |
intron_variant | MODIFIER | c.534-2769T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018553 | |||||||
chr5:66018553 | T | TTATATTA others(24): Show |
4 | a0002c0003t0003g0175 a0002c0003t0003g0176 a0002c0003t0003g0277 others(1): Show |
4 | NA18954.hp1 NA18978.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2764_534-2763i others(33): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018553 | ||||||
chr5:66018560 | A | T | 7 | a0001c0001t0006g0155 a0002c0003t0003g0175 a0002c0003t0003g0176 others(4): Show |
7 | HG01884.hp2 HG02965.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.534-2762A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018560 | |||||||
chr5:66018566 | A | AAT | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.534-2756_534-2755i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | |||||||
chr5:66018566 | A | AATATATA others(9): Show |
4 | a0003c0004t0001g0137 a0003c0004t0001g0138 a0003c0004t0001g0304 others(1): Show |
4 | HG00642.hp1 HG01167.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-2756_534-2755i others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | |||||||
chr5:66018566 | A | T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.534-2756A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018566 | |||||||
chr5:66018567 | T | A | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
16 | HG00642.hp1 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-2755T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018567 | |||||||
chr5:66018567 | T | TTA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
100 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.534-2751_534-2750d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(107): Show |
6 | a0001c0001t0001g0135 a0001c0001t0001g0274 a0003c0004t0001g0302 others(3): Show |
6 | HG00438.hp1 HG02273.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(116): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(107): Show |
1 | a0016c0019t0001g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.534-2750_534-2749i others(116): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(93): Show |
1 | a0003c0004t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534-2750_534-2749i others(102): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(93): Show |
3 | a0003c0004t0001g0131 a0003c0004t0001g0140 a0003c0004t0028g0134 |
3 | HG01943.hp2 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.534-2750_534-2749i others(102): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(58): Show |
4 | a0003c0004t0001g0093 a0003c0004t0001g0113 a0003c0004t0001g0115 others(1): Show |
4 | NA18963.hp1 NA18970.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(67): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(100): Show |
1 | a0003c0004t0017g0120 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAA others(100): Show |
9 | a0001c0001t0001g0121 a0003c0004t0001g0088 a0003c0004t0001g0100 others(6): Show |
9 | NA18942.hp2 NA18944.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(109): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | T | TTATATAT others(147): Show |
1 | a0003c0004t0001g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(156): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | TTATATTA others(5): Show |
T | 1 | a0007c0011t0011g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.534-2749_534-2738d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018567 | TTATATTA others(9): Show |
T | 1 | a0005c0006t0016g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.534-2751_534-2736d others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018567 | ||||||
chr5:66018569 | A | ATATATTA others(3): Show |
1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.534-2750_534-2749i others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018569 | ||||||
chr5:66018572 | T | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2750T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018572 | |||||||
chr5:66018572 | T | TAA | 12 | a0001c0001t0001g0084 a0001c0001t0001g0106 a0001c0001t0001g0266 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-2750_534-2749i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018572 | |||||||
chr5:66018572 | T | TTATATAA others(66): Show |
1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.534-2737_534-2736i others(75): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018572 | ||||||
chr5:66018573 | T | A | 4 | a0001c0001t0001g0048 a0001c0007t0012g0217 a0001c0007t0012g0218 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2749T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018573 | |||||||
chr5:66018574 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.534-2748A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018574 | |||||||
chr5:66018579 | A | T | 18 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
18 | HG00738.hp2 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.534-2743A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018579 | |||||||
chr5:66018583 | A | T | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.534-2739A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018583 | |||||||
chr5:66018586 | T | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.534-2736T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018586 | |||||||
chr5:66018586 | T | TTATATAT others(138): Show |
1 | a0003c0004t0001g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(147): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | ||||||
chr5:66018586 | T | TTATATAT others(143): Show |
1 | a0001c0001t0009g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.534-2730_534-2729i others(152): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | ||||||
chr5:66018586 | T | TTATATAT others(187): Show |
1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.534-2730_534-2729i others(196): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | ||||||
chr5:66018586 | T | TTATATAT others(14): Show |
1 | a0001c0001t0029g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.534-2730_534-2729i others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | ||||||
chr5:66018586 | T | TTATATTA others(223): Show |
1 | a0001c0001t0009g0041 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.534-2731_534-2730i others(232): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018586 | ||||||
chr5:66018591 | T | C | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.534-2731T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018591 | |||||||
chr5:66018592 | A | T | 5 | a0002c0003t0003g0175 a0002c0003t0003g0176 a0002c0003t0003g0177 others(2): Show |
5 | NA18948.hp2 NA18954.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-2730A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018592 | |||||||
chr5:66018593 | A | ATATATAT others(98): Show |
1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.534-2716_534-2715i others(107): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018593 | ||||||
chr5:66018593 | A | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.534-2729A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018593 | |||||||
chr5:66018600 | T | A | 1 | a0003c0004t0001g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.534-2722T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018600 | |||||||
chr5:66018621 | CAT | C | 5 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0040 others(2): Show |
5 | NA18961.hp1 NA18985.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.534-2697_534-2696d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018621 | ||||||
chr5:66018634 | T | A | 16 | a0001c0001t0029g0091 a0004c0005t0004g0014 a0004c0005t0004g0015 others(13): Show |
16 | HG01884.hp1 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.534-2688T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018634 | |||||||
chr5:66018637 | T | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-2685T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018637 | |||||||
chr5:66018647 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.534-2675T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018647 | |||||||
chr5:66018649 | G | T | 8 | a0001c0002t0002g0235 a0001c0002t0002g0246 a0001c0002t0002g0247 others(5): Show |
8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.534-2673G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018649 | |||||||
chr5:66018698 | A | G | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.534-2624A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018698 | |||||||
chr5:66018838 | T | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2484T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018838 | |||||||
chr5:66018857 | G | A | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.534-2465G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018857 | |||||||
chr5:66018892 | C | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-2430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66018892 | |||||||
chr5:66018945 | AT | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2371delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66018945 | ||||||
chr5:66019066 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.534-2256C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019066 | |||||||
chr5:66019095 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-2227A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019095 | |||||||
chr5:66019165 | T | C | 1 | a0001c0015t0030g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.534-2157T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019165 | |||||||
chr5:66019470 | C | G | 3 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | HG03017.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.534-1852C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019470 | |||||||
chr5:66019791 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-1531T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019791 | |||||||
chr5:66019814 | A | G | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.534-1508A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019814 | |||||||
chr5:66019897 | C | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-1425C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019897 | |||||||
chr5:66019903 | C | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(3): Show |
6 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-1419C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019903 | |||||||
chr5:66019960 | G | A | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-1362G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66019960 | |||||||
chr5:66020123 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(36): Show |
40 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.534-1199A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020123 | |||||||
chr5:66020131 | G | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.534-1191G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020131 | |||||||
chr5:66020214 | G | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(12): Show |
15 | HG01071.hp2 HG01934.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.534-1108G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020214 | |||||||
chr5:66020360 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-962T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020360 | |||||||
chr5:66020377 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.534-945G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020377 | |||||||
chr5:66020466 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.534-856A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020466 | |||||||
chr5:66020474 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-848C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020474 | |||||||
chr5:66020536 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.534-786A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020536 | |||||||
chr5:66020861 | G | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.534-461G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020861 | |||||||
chr5:66020891 | G | A | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.534-431G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66020891 | |||||||
chr5:66021113 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-209T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021113 | |||||||
chr5:66021169 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.534-153T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021169 | |||||||
chr5:66021169 | TA | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.534-149delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr5 | 66021169 | ||||||
chr5:66021277 | A | G | 2 | a0001c0002t0002g0239 a0001c0002t0002g0240 |
2 | HG02056.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.534-45A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 7/25 | chr5 | 66021277 | |||||||
chr5:66021504 | A | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.597+119A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021504 | |||||||
chr5:66021510 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.597+125T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021510 | |||||||
chr5:66021618 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.597+233A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021618 | |||||||
chr5:66021624 | A | AC | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.597+240dupC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr5 | 66021624 | ||||||
chr5:66021646 | A | G | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597+261A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66021646 | |||||||
chr5:66022082 | A | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+697A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022082 | |||||||
chr5:66022085 | C | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.597+700C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022085 | |||||||
chr5:66022416 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-874A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022416 | |||||||
chr5:66022447 | T | G | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.598-843T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022447 | |||||||
chr5:66022493 | A | G | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-797A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022493 | |||||||
chr5:66022519 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-771A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022519 | |||||||
chr5:66022720 | A | G | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-570A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66022720 | |||||||
chr5:66023041 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.598-249C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023041 | |||||||
chr5:66023075 | T | G | 4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-215T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023075 | |||||||
chr5:66023272 | C | G | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.598-18C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 8/25 | chr5 | 66023272 | |||||||
chr5:66023469 | T | C | 1 | a0005c0006t0007g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.672+105T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023469 | |||||||
chr5:66023673 | A | AT | 34 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0089 others(31): Show |
34 | HG00621.hp2 HG01109.hp2 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.672+329dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 66023673 | ||||||
chr5:66023673 | AT | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0111 a0001c0007t0010g0160 others(6): Show |
9 | HG01256.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.672+329delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr5 | 66023673 | ||||||
chr5:66023868 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.673-438G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023868 | |||||||
chr5:66023879 | G | A | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.673-427G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023879 | |||||||
chr5:66023934 | A | C | 1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.673-372A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66023934 | |||||||
chr5:66024013 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-293C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66024013 | |||||||
chr5:66024025 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.673-281A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 9/25 | chr5 | 66024025 | |||||||
chr5:66024497 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.817+47G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024497 | |||||||
chr5:66024542 | T | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817+92T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024542 | |||||||
chr5:66024618 | A | G | 1 | a0002c0003t0008g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.817+168A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024618 | |||||||
chr5:66024642 | A | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.817+192A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024642 | |||||||
chr5:66024699 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.817+249T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024699 | |||||||
chr5:66024778 | A | G | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.817+328A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024778 | |||||||
chr5:66024825 | A | G | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.817+375A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024825 | |||||||
chr5:66024973 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.818-507T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024973 | |||||||
chr5:66024988 | A | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-492A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66024988 | |||||||
chr5:66025112 | A | G | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.818-368A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66025112 | |||||||
chr5:66025133 | A | G | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.818-347A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 10/25 | chr5 | 66025133 | |||||||
chr5:66025651 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.890+99T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/25 | chr5 | 66025651 | |||||||
chr5:66025687 | T | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.890+135T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 11/25 | chr5 | 66025687 | |||||||
chr5:66026025 | T | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+48T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026025 | |||||||
chr5:66026050 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+73G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026050 | |||||||
chr5:66026169 | A | T | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1021-133A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 12/25 | chr5 | 66026169 | |||||||
chr5:66026600 | T | G | 6 | a0005c0006t0007g0222 a0005c0006t0007g0224 a0005c0006t0007g0225 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1136+183T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026600 | |||||||
chr5:66026611 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1136+194G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026611 | |||||||
chr5:66026650 | C | T | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1136+233C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66026650 | |||||||
chr5:66027210 | C | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136+793C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027210 | |||||||
chr5:66027312 | C | CT | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1136+895_1136+896i others(3): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027312 | |||||||
chr5:66027328 | T | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1136+911T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027328 | |||||||
chr5:66027344 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1136+927G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027344 | |||||||
chr5:66027422 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1137-852A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027422 | |||||||
chr5:66027665 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1137-609G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66027665 | |||||||
chr5:66028006 | A | C | 1 | a0001c0007t0010g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1137-268A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66028006 | |||||||
chr5:66028169 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-105G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 13/25 | chr5 | 66028169 | |||||||
chr5:66029122 | A | C | 1 | a0001c0001t0001g0233 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1206+779A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029122 | |||||||
chr5:66029289 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+946G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029289 | |||||||
chr5:66029512 | G | A | 2 | a0001c0021t0001g0105 a0004c0005t0004g0008 |
2 | HG01981.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1206+1169G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029512 | |||||||
chr5:66029539 | G | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+1196G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029539 | |||||||
chr5:66029547 | TTTCTG | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+1226_1206+123 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66029547 | ||||||
chr5:66029569 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1226T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029569 | |||||||
chr5:66029569 | T | TCTGTC | 15 | a0002c0003t0005g0183 a0002c0003t0005g0186 a0002c0003t0005g0200 others(12): Show |
15 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1206+1252_1206+125 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66029569 | ||||||
chr5:66029574 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1206+1231C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029574 | |||||||
chr5:66029591 | TG | T | 5 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(2): Show |
5 | NA18951.hp1 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+1249delG | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029591 | |||||||
chr5:66029645 | G | A | 1 | a0005c0006t0015g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1206+1302G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029645 | |||||||
chr5:66029689 | C | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+1346C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029689 | |||||||
chr5:66029707 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+1364C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029707 | |||||||
chr5:66029728 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+1385C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029728 | |||||||
chr5:66029824 | C | T | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+1481C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66029824 | |||||||
chr5:66030200 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1206+1857G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030200 | |||||||
chr5:66030204 | A | G | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1206+1861A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030204 | |||||||
chr5:66030438 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+2095T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030438 | |||||||
chr5:66030470 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+2127C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030470 | |||||||
chr5:66030523 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2180C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030523 | |||||||
chr5:66030562 | C | CT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0002t0002g0296 others(12): Show |
15 | HG00438.hp2 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1206+2237dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66030562 | ||||||
chr5:66030588 | G | A | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+2245G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030588 | |||||||
chr5:66030782 | G | C | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1206+2439G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030782 | |||||||
chr5:66030784 | T | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+2441T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030784 | |||||||
chr5:66030838 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2495C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66030838 | |||||||
chr5:66031043 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+2700C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031043 | |||||||
chr5:66031050 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+2707G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031050 | |||||||
chr5:66031141 | A | T | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1206+2798A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031141 | |||||||
chr5:66031184 | T | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1206+2841T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031184 | |||||||
chr5:66031198 | G | C | 1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1206+2855G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031198 | |||||||
chr5:66031361 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+3018T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031361 | |||||||
chr5:66031390 | A | C | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+3047A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031390 | |||||||
chr5:66031452 | G | C | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+3109G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031452 | |||||||
chr5:66031608 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1206+3265G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031608 | |||||||
chr5:66031643 | A | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+3300A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031643 | |||||||
chr5:66031696 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1206+3353G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031696 | |||||||
chr5:66031701 | A | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1206+3358A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031701 | |||||||
chr5:66031717 | G | T | 3 | a0003c0004t0001g0302 a0003c0004t0022g0301 a0003c0004t0027g0300 |
3 | HG03017.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1206+3374G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66031717 | |||||||
chr5:66032064 | T | C | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+3721T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032064 | |||||||
chr5:66032282 | T | C | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1206+3939T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032282 | |||||||
chr5:66032330 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1206+3987T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032330 | |||||||
chr5:66032538 | G | A | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1206+4195G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032538 | |||||||
chr5:66032619 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
44 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1206+4276A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032619 | |||||||
chr5:66032820 | A | G | 1 | a0001c0021t0001g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1206+4477A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66032820 | |||||||
chr5:66033029 | G | A | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1206+4686G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033029 | |||||||
chr5:66033120 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+4777C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033120 | |||||||
chr5:66033166 | A | G | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1206+4823A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033166 | |||||||
chr5:66033506 | A | G | 1 | a0001c0002t0002g0249 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1207-4877A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033506 | |||||||
chr5:66033677 | T | A | 1 | a0001c0002t0002g0240 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1207-4706T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033677 | |||||||
chr5:66033678 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1207-4705C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033678 | |||||||
chr5:66033749 | G | A | 8 | a0003c0004t0001g0093 a0003c0004t0001g0100 a0003c0004t0001g0101 others(5): Show |
8 | NA18747.hp1 NA18942.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-4634G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033749 | |||||||
chr5:66033874 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-4509C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033874 | |||||||
chr5:66033938 | G | A | 2 | a0001c0001t0009g0040 a0001c0001t0009g0041 |
2 | NA18961.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1207-4445G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033938 | |||||||
chr5:66033970 | G | A | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1207-4413G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033970 | |||||||
chr5:66033978 | G | A | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1207-4405G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66033978 | |||||||
chr5:66034115 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1207-4253dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | ||||||
chr5:66034115 | C | CAA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0009g0038 others(5): Show |
8 | HG02647.hp2 HG03098.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-4254_1207-425 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | ||||||
chr5:66034115 | CA | C | 15 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(12): Show |
15 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1207-4253delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | ||||||
chr5:66034115 | CAA | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-4254_1207-425 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034115 | ||||||
chr5:66034181 | A | G | 12 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0001t0006g0148 others(9): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207-4202A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034181 | |||||||
chr5:66034291 | T | C | 1 | a0001c0002t0002g0236 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1207-4092T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034291 | |||||||
chr5:66034301 | T | A | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1207-4082T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034301 | |||||||
chr5:66034305 | T | G | 1 | a0002c0003t0008g0173 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1207-4078T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034305 | |||||||
chr5:66034569 | G | A | 1 | a0004c0017t0004g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1207-3814G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034569 | |||||||
chr5:66034606 | C | CT | 23 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(20): Show |
23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1207-3763dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034606 | ||||||
chr5:66034694 | GTAT | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-3683_1207-368 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66034694 | ||||||
chr5:66034980 | C | A | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1207-3403C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034980 | |||||||
chr5:66034994 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1207-3389C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034994 | |||||||
chr5:66034997 | G | A | 45 | a0002c0003t0003g0165 a0002c0003t0003g0166 a0002c0003t0003g0167 others(42): Show |
45 | HG00408.hp2 HG01081.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1207-3386G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66034997 | |||||||
chr5:66035014 | G | A | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1207-3369G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035014 | |||||||
chr5:66035169 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-3214C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035169 | |||||||
chr5:66035328 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-3055C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035328 | |||||||
chr5:66035349 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-3034C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035349 | |||||||
chr5:66035465 | G | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-2918G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035465 | |||||||
chr5:66035483 | C | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1207-2900C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035483 | |||||||
chr5:66035543 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1207-2840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035543 | |||||||
chr5:66035565 | G | T | 1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1207-2818G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035565 | |||||||
chr5:66035648 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2735T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035648 | |||||||
chr5:66035702 | G | T | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1207-2681G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035702 | |||||||
chr5:66035778 | T | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2605T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035778 | |||||||
chr5:66035888 | G | T | 1 | a0001c0001t0021g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1207-2495G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035888 | |||||||
chr5:66035978 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-2405C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66035978 | |||||||
chr5:66036021 | C | G | 1 | a0001c0002t0002g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1207-2362C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036021 | |||||||
chr5:66036035 | G | T | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1207-2348G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036035 | |||||||
chr5:66036144 | TCTTAC | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-2233_1207-222 others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr5 | 66036144 | ||||||
chr5:66036550 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-1833A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036550 | |||||||
chr5:66036607 | A | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1776A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036607 | |||||||
chr5:66036740 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1643G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036740 | |||||||
chr5:66036791 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1592G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036791 | |||||||
chr5:66036857 | C | G | 1 | a0004c0005t0004g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1207-1526C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036857 | |||||||
chr5:66036870 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1207-1513G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036870 | |||||||
chr5:66036876 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207-1507A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036876 | |||||||
chr5:66036976 | G | T | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1207-1407G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66036976 | |||||||
chr5:66037068 | G | A | 1 | a0002c0003t0008g0257 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1207-1315G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037068 | |||||||
chr5:66037126 | T | C | 5 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(2): Show |
5 | NA18951.hp1 NA18992.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-1257T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037126 | |||||||
chr5:66037227 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1207-1156G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037227 | |||||||
chr5:66037629 | A | T | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-754A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037629 | |||||||
chr5:66037659 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1207-724T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037659 | |||||||
chr5:66037856 | C | G | 1 | a0001c0002t0002g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1207-527C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037856 | |||||||
chr5:66037921 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-462A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037921 | |||||||
chr5:66037928 | T | G | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-455T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037928 | |||||||
chr5:66037929 | T | A | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-454T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037929 | |||||||
chr5:66037931 | C | A | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-452C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037931 | |||||||
chr5:66037933 | G | A | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-450G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037933 | |||||||
chr5:66037936 | G | T | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1207-447G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037936 | |||||||
chr5:66037979 | C | A | 23 | a0001c0001t0006g0146 a0001c0007t0010g0160 a0001c0007t0010g0161 others(20): Show |
23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1207-404C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66037979 | |||||||
chr5:66038093 | G | A | 2 | a0005c0006t0007g0224 a0005c0006t0007g0230 |
2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207-290G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038093 | |||||||
chr5:66038113 | A | G | 1 | a0003c0004t0001g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1207-270A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038113 | |||||||
chr5:66038144 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-239G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 14/25 | chr5 | 66038144 | |||||||
chr5:66038488 | A | G | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
splice_region_variant&intron_variant | LOW | c.1306+6A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038488 | |||||||
chr5:66038636 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306+154C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038636 | |||||||
chr5:66038801 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1306+319T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038801 | |||||||
chr5:66038807 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+325T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038807 | |||||||
chr5:66038951 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+469G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038951 | |||||||
chr5:66038990 | G | A | 1 | a0004c0005t0004g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+508G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66038990 | |||||||
chr5:66039025 | C | CGT | 19 | a0001c0001t0001g0084 a0001c0001t0001g0103 a0001c0001t0001g0107 others(16): Show |
19 | HG01081.hp2 HG02165.hp1 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.1306+562_1306+563d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66039025 | ||||||
chr5:66039025 | C | CGTGTGTG others(3): Show |
14 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 others(11): Show |
14 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1306+554_1306+563d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66039025 | ||||||
chr5:66039044 | G | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+562G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039044 | |||||||
chr5:66039087 | C | A | 1 | a0001c0002t0002g0004 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1306+605C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039087 | |||||||
chr5:66039224 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1306+742G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039224 | |||||||
chr5:66039932 | A | G | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1450A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66039932 | |||||||
chr5:66040036 | G | C | 1 | a0003c0004t0001g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1306+1554G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040036 | |||||||
chr5:66040124 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1642G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040124 | |||||||
chr5:66040169 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+1687C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040169 | |||||||
chr5:66040180 | A | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+1698A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040180 | |||||||
chr5:66040185 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1703C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040185 | |||||||
chr5:66040210 | T | C | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1306+1728T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040210 | |||||||
chr5:66040227 | A | G | 1 | a0003c0004t0001g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1306+1745A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040227 | |||||||
chr5:66040241 | C | T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1759C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040241 | |||||||
chr5:66040254 | G | C | 1 | a0008c0012t0011g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1306+1772G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040254 | |||||||
chr5:66040258 | G | A | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306+1776G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040258 | |||||||
chr5:66040295 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+1813G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040295 | |||||||
chr5:66040297 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+1815T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040297 | |||||||
chr5:66040374 | T | C | 1 | a0004c0005t0004g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1306+1892T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040374 | |||||||
chr5:66040391 | A | G | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1306+1909A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040391 | |||||||
chr5:66040455 | A | G | 4 | a0001c0002t0002g0292 a0001c0015t0030g0258 a0010c0010t0002g0290 others(1): Show |
4 | HG00408.hp1 NA18747.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+1973A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040455 | |||||||
chr5:66040571 | TC | T | 9 | a0001c0002t0002g0289 a0001c0002t0002g0292 a0001c0002t0002g0293 others(6): Show |
9 | HG00408.hp1 HG02165.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1306+2092delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040571 | ||||||
chr5:66040573 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1306+2091C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040573 | |||||||
chr5:66040579 | G | A | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1306+2097G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040579 | |||||||
chr5:66040627 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1306+2145A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040627 | |||||||
chr5:66040689 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+2207T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040689 | |||||||
chr5:66040704 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1306+2222G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040704 | |||||||
chr5:66040844 | T | TA | 23 | a0001c0002t0002g0235 a0001c0007t0010g0160 a0001c0007t0010g0161 others(20): Show |
23 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-2222dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040844 | ||||||
chr5:66040859 | GA | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1307-2211delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr5 | 66040859 | ||||||
chr5:66040877 | A | G | 1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1307-2200A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66040877 | |||||||
chr5:66041026 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1307-2051T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041026 | |||||||
chr5:66041044 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1307-2033T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041044 | |||||||
chr5:66041224 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1307-1853A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041224 | |||||||
chr5:66041593 | G | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1307-1484G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041593 | |||||||
chr5:66041620 | G | A | 1 | a0003c0004t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1307-1457G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041620 | |||||||
chr5:66041756 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-1321T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041756 | |||||||
chr5:66041913 | A | T | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1307-1164A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66041913 | |||||||
chr5:66042347 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1307-730C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042347 | |||||||
chr5:66042654 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1307-423A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042654 | |||||||
chr5:66042745 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1307-332T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042745 | |||||||
chr5:66042752 | A | G | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1307-325A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042752 | |||||||
chr5:66042850 | C | T | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-227C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042850 | |||||||
chr5:66042918 | C | T | 3 | a0003c0004t0001g0302 a0003c0004t0022g0301 a0003c0004t0027g0300 |
3 | HG03017.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1307-159C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042918 | |||||||
chr5:66042977 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1307-100T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 15/25 | chr5 | 66042977 | |||||||
chr5:66043320 | C | G | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1428+122C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043320 | |||||||
chr5:66043513 | C | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1428+315C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043513 | |||||||
chr5:66043792 | A | T | 1 | a0003c0004t0001g0002 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1429-345A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66043792 | |||||||
chr5:66044072 | A | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1429-65A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 16/25 | chr5 | 66044072 | |||||||
chr5:66044339 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1602+29G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044339 | |||||||
chr5:66044342 | T | C | 1 | a0001c0002t0002g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1602+32T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044342 | |||||||
chr5:66044456 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1602+146T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044456 | |||||||
chr5:66044480 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1602+170A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044480 | |||||||
chr5:66044621 | T | C | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1602+311T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044621 | |||||||
chr5:66044626 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+316G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044626 | |||||||
chr5:66044719 | C | T | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+409C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044719 | |||||||
chr5:66044721 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1602+411T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044721 | |||||||
chr5:66044727 | T | A | 1 | a0003c0004t0001g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1602+417T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044727 | |||||||
chr5:66044759 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1602+449T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044759 | |||||||
chr5:66044782 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+472G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044782 | |||||||
chr5:66044887 | T | C | 2 | a0002c0003t0005g0187 a0002c0003t0005g0198 |
2 | NA19063.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1602+577T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66044887 | |||||||
chr5:66045206 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1602+896G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045206 | |||||||
chr5:66045235 | T | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+925T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045235 | |||||||
chr5:66045293 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602+983G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045293 | |||||||
chr5:66045398 | TATATTAC others(71): Show |
T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-936_1603-859d others(80): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66045398 | ||||||
chr5:66045406 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1603-947A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045406 | |||||||
chr5:66045407 | T | G | 1 | a0003c0004t0001g0127 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1603-946T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045407 | |||||||
chr5:66045481 | T | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-872T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045481 | |||||||
chr5:66045491 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-862C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045491 | |||||||
chr5:66045537 | CTG | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-813_1603-812d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66045537 | ||||||
chr5:66045608 | G | A | 1 | a0001c0001t0013g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1603-745G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045608 | |||||||
chr5:66045631 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1603-722G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045631 | |||||||
chr5:66045689 | A | G | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-664A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045689 | |||||||
chr5:66045754 | A | C | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603-599A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045754 | |||||||
chr5:66045911 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1603-442C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045911 | |||||||
chr5:66045959 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18999.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1603-394C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045959 | |||||||
chr5:66045962 | A | G | 1 | a0003c0004t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1603-391A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045962 | |||||||
chr5:66045996 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-357T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66045996 | |||||||
chr5:66046073 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-280G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66046073 | |||||||
chr5:66046091 | T | TACAA | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-261_1603-258d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr5 | 66046091 | ||||||
chr5:66046224 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1603-129T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 17/25 | chr5 | 66046224 | |||||||
chr5:66046946 | C | CT | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1788+415dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr5 | 66046946 | ||||||
chr5:66046961 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1788+423A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66046961 | |||||||
chr5:66047062 | C | T | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1788+524C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047062 | |||||||
chr5:66047207 | A | C | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1788+669A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047207 | |||||||
chr5:66047227 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1788+689T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047227 | |||||||
chr5:66047498 | A | G | 2 | a0006c0008t0003g0190 a0006c0008t0018g0195 |
2 | NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1788+960A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047498 | |||||||
chr5:66047585 | C | A | 1 | a0003c0004t0001g0304 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1788+1047C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047585 | |||||||
chr5:66047645 | A | G | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1789-1022A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047645 | |||||||
chr5:66047825 | G | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1789-842G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047825 | |||||||
chr5:66047862 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | HG02970.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-805G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66047862 | |||||||
chr5:66048038 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-629G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048038 | |||||||
chr5:66048127 | T | C | 2 | a0001c0007t0010g0160 a0001c0007t0010g0275 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1789-540T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048127 | |||||||
chr5:66048194 | A | G | 3 | a0001c0001t0013g0102 a0001c0001t0013g0123 a0001c0001t0013g0124 |
3 | HG01261.hp2 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1789-473A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048194 | |||||||
chr5:66048267 | C | T | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-400C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048267 | |||||||
chr5:66048281 | T | G | 1 | a0004c0005t0004g0011 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1789-386T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048281 | |||||||
chr5:66048354 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1789-313A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048354 | |||||||
chr5:66048541 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1789-126G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048541 | |||||||
chr5:66048541 | G | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1789-126G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048541 | |||||||
chr5:66048559 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1789-108A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048559 | |||||||
chr5:66048578 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-89G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 18/25 | chr5 | 66048578 | |||||||
chr5:66048795 | G | A | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1903+14G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048795 | |||||||
chr5:66048834 | A | G | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1903+53A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048834 | |||||||
chr5:66048836 | A | G | 7 | a0003c0004t0001g0100 a0003c0004t0001g0101 a0006c0008t0003g0072 others(4): Show |
7 | NA18942.hp2 NA18950.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1903+55A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66048836 | |||||||
chr5:66049023 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1903+242T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049023 | |||||||
chr5:66049164 | A | G | 1 | a0009c0009t0002g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1903+383A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049164 | |||||||
chr5:66049188 | C | T | 1 | a0002c0003t0005g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1903+407C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049188 | |||||||
chr5:66049194 | T | G | 1 | a0001c0007t0012g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1903+413T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049194 | |||||||
chr5:66049397 | T | C | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1903+616T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049397 | |||||||
chr5:66049479 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1903+698C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049479 | |||||||
chr5:66049497 | G | A | 2 | a0001c0007t0012g0217 a0001c0007t0012g0219 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1903+716G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049497 | |||||||
chr5:66049776 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1903+995A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049776 | |||||||
chr5:66049788 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1904-995A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049788 | |||||||
chr5:66049830 | T | C | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1904-953T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66049830 | |||||||
chr5:66050002 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1904-781A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050002 | |||||||
chr5:66050213 | ACTAAATC others(323): Show |
A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1904-554_1904-225d others(2): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050213 | ||||||
chr5:66050226 | C | CT | 15 | a0001c0001t0001g0159 a0001c0002t0002g0003 a0001c0002t0002g0240 others(12): Show |
15 | HG00609.hp1 HG02080.hp1 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1904-521dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | C | CTT | 9 | a0001c0002t0002g0004 a0001c0002t0002g0248 a0002c0003t0002g0202 others(6): Show |
9 | HG01257.hp1 HG01433.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1904-522_1904-521d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | C | CTTT | 8 | a0001c0002t0002g0210 a0002c0003t0002g0201 a0002c0003t0003g0199 others(5): Show |
8 | HG01081.hp1 HG01433.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1904-523_1904-521d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | C | CTTTT | 6 | a0002c0003t0003g0176 a0002c0003t0003g0177 a0002c0003t0003g0188 others(3): Show |
6 | HG01934.hp1 NA18948.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1904-524_1904-521d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | C | CTTTTT | 6 | a0001c0002t0002g0254 a0002c0003t0003g0175 a0002c0003t0003g0277 others(3): Show |
6 | HG00673.hp2 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1904-525_1904-521d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CT | C | 17 | a0001c0002t0002g0033 a0001c0002t0002g0235 a0001c0002t0002g0236 others(14): Show |
17 | HG00408.hp1 HG01069.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1904-521delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTT | C | 7 | a0001c0002t0002g0034 a0001c0002t0002g0035 a0001c0002t0002g0239 others(4): Show |
7 | HG00642.hp2 HG02056.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1904-522_1904-521d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTTTTTTT others(3): Show |
C | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1904-530_1904-521d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTTTTTTT others(4): Show |
C | 1 | a0002c0003t0002g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1904-531_1904-521d others(13): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTTTTTTT others(6): Show |
C | 2 | a0001c0002t0002g0289 a0001c0002t0002g0295 |
2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1904-533_1904-521d others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTTTTTTT others(8): Show |
C | 2 | a0001c0002t0002g0261 a0002c0003t0003g0299 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1904-535_1904-521d others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050226 | CTTTTTTT others(12): Show |
C | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1904-539_1904-521d others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr5 | 66050226 | ||||||
chr5:66050467 | G | A | 8 | a0001c0002t0002g0235 a0001c0002t0002g0246 a0001c0002t0002g0247 others(5): Show |
8 | NA18612.hp1 NA18949.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1904-316G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050467 | |||||||
chr5:66050662 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1904-121A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050662 | |||||||
chr5:66050697 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1904-86G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050697 | |||||||
chr5:66050771 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1904-12G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 19/25 | chr5 | 66050771 | |||||||
chr5:66051061 | T | C | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2087+95T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051061 | |||||||
chr5:66051147 | T | C | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2087+181T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051147 | |||||||
chr5:66051529 | G | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2087+563G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051529 | |||||||
chr5:66051852 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2087+886C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051852 | |||||||
chr5:66051894 | C | CA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.2087+942dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051894 | ||||||
chr5:66051907 | A | AAAAAAAA others(14): Show |
1 | a0001c0007t0010g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2087+942_2087+943i others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | ||||||
chr5:66051907 | A | AAAAAAAA others(12): Show |
1 | a0001c0007t0010g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2087+942_2087+943i others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | ||||||
chr5:66051907 | A | AAAAAAAA others(11): Show |
4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2087+942_2087+943i others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr5 | 66051907 | ||||||
chr5:66051983 | T | G | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2087+1017T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66051983 | |||||||
chr5:66052177 | A | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2087+1211A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052177 | |||||||
chr5:66052292 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2088-1114G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052292 | |||||||
chr5:66052325 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2088-1081C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052325 | |||||||
chr5:66052326 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088-1080G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052326 | |||||||
chr5:66052495 | A | C | 1 | a0001c0007t0012g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2088-911A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052495 | |||||||
chr5:66052544 | A | G | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2088-862A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052544 | |||||||
chr5:66052600 | T | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2088-806T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66052600 | |||||||
chr5:66053103 | A | AATTCCAC | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2088-303_2088-302i others(9): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053103 | |||||||
chr5:66053112 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2088-294A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053112 | |||||||
chr5:66053233 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2088-173T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053233 | |||||||
chr5:66053328 | CAATT | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2088-77_2088-74del others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 20/25 | chr5 | 66053328 | |||||||
chr5:66055124 | A | G | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3633+173A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055124 | |||||||
chr5:66055137 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3633+186A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055137 | |||||||
chr5:66055312 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3633+361A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055312 | |||||||
chr5:66055369 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+418T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055369 | |||||||
chr5:66055543 | C | T | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3633+592C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055543 | |||||||
chr5:66055572 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+621T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055572 | |||||||
chr5:66055780 | C | A | 1 | a0001c0001t0013g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3633+829C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055780 | |||||||
chr5:66055800 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+849T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055800 | |||||||
chr5:66055825 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+874A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055825 | |||||||
chr5:66055946 | A | G | 3 | a0004c0005t0004g0009 a0004c0005t0004g0010 a0004c0005t0004g0011 |
3 | HG01167.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3633+995A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66055946 | |||||||
chr5:66056169 | G | T | 1 | a0001c0001t0006g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3633+1218G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056169 | |||||||
chr5:66056384 | G | C | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3633+1433G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056384 | |||||||
chr5:66056477 | T | C | 1 | a0005c0006t0015g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3633+1526T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056477 | |||||||
chr5:66056495 | TAAG | T | 112 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+1548_3633+155 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66056495 | ||||||
chr5:66056585 | C | T | 2 | a0005c0006t0007g0222 a0005c0006t0016g0226 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3633+1634C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056585 | |||||||
chr5:66056719 | A | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+1768A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056719 | |||||||
chr5:66056772 | C | T | 8 | a0001c0002t0002g0172 a0001c0002t0002g0208 a0001c0002t0002g0209 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3633+1821C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056772 | |||||||
chr5:66056842 | TGTA | T | 112 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+1895_3633+189 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66056842 | ||||||
chr5:66056893 | G | C | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.3633+1942G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056893 | |||||||
chr5:66056895 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+1944A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056895 | |||||||
chr5:66056919 | C | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0118 |
3 | HG00735.hp1 HG01069.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3633+1968C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66056919 | |||||||
chr5:66057072 | A | C | 2 | a0005c0006t0002g0229 a0005c0006t0002g0263 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3633+2121A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057072 | |||||||
chr5:66057123 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3633+2172T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057123 | |||||||
chr5:66057205 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2254A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057205 | |||||||
chr5:66057331 | A | G | 1 | a0001c0002t0002g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3633+2380A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057331 | |||||||
chr5:66057341 | C | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2390C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057341 | |||||||
chr5:66057553 | CT | C | 4 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3633+2609delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66057553 | ||||||
chr5:66057593 | C | T | 1 | a0002c0003t0003g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3633+2642C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057593 | |||||||
chr5:66057657 | C | T | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(106): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3633+2706C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057657 | |||||||
chr5:66057668 | A | G | 1 | a0004c0017t0004g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3633+2717A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057668 | |||||||
chr5:66057813 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+2862G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057813 | |||||||
chr5:66057843 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+2892T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057843 | |||||||
chr5:66057884 | T | C | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3633+2933T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057884 | |||||||
chr5:66057908 | T | TCCATGAT others(10): Show |
22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+2958_3633+295 others(21): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66057908 | ||||||
chr5:66057948 | C | G | 1 | a0002c0003t0003g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3633+2997C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057948 | |||||||
chr5:66057977 | G | T | 5 | a0003c0004t0001g0088 a0003c0004t0001g0122 a0003c0004t0001g0270 others(2): Show |
5 | NA18977.hp1 NA18982.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.3633+3026G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66057977 | |||||||
chr5:66058047 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3633+3096C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058047 | |||||||
chr5:66058198 | T | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3633+3247T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058198 | |||||||
chr5:66058244 | GTATC | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+3299_3633+330 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66058244 | ||||||
chr5:66058272 | T | C | 7 | a0001c0001t0014g0070 a0001c0007t0010g0160 a0001c0007t0010g0161 others(4): Show |
7 | HG00621.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.3633+3321T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058272 | |||||||
chr5:66058371 | C | T | 1 | a0015c0013t0001g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3633+3420C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058371 | |||||||
chr5:66058397 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3633+3446G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058397 | |||||||
chr5:66058417 | T | C | 2 | a0002c0003t0003g0188 a0002c0003t0003g0189 |
2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3633+3466T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058417 | |||||||
chr5:66058445 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3633+3494A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058445 | |||||||
chr5:66058474 | G | A | 23 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.3633+3523G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058474 | |||||||
chr5:66058532 | T | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+3581T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058532 | |||||||
chr5:66058573 | C | T | 112 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+3622C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058573 | |||||||
chr5:66058636 | C | T | 1 | a0002c0003t0002g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3633+3685C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058636 | |||||||
chr5:66058691 | G | C | 152 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(149): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3633+3740G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058691 | |||||||
chr5:66058709 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.3633+3758A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058709 | |||||||
chr5:66058717 | G | C | 1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3633+3766G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058717 | |||||||
chr5:66058748 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+3797C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058748 | |||||||
chr5:66058768 | C | T | 2 | a0001c0002t0002g0255 a0001c0002t0002g0260 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3633+3817C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058768 | |||||||
chr5:66058849 | T | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+3898T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058849 | |||||||
chr5:66058948 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+3997G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058948 | |||||||
chr5:66058968 | G | A | 2 | a0007c0011t0011g0025 a0007c0011t0011g0026 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3633+4017G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66058968 | |||||||
chr5:66059006 | T | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4055T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059006 | |||||||
chr5:66059010 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4059G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059010 | |||||||
chr5:66059014 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+4063A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059014 | |||||||
chr5:66059060 | C | A | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(106): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3633+4109C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059060 | |||||||
chr5:66059063 | A | G | 2 | a0010c0010t0002g0290 a0010c0010t0002g0291 |
2 | NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3633+4112A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059063 | |||||||
chr5:66059159 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+4208C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059159 | |||||||
chr5:66059168 | A | T | 5 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(2): Show |
5 | HG01884.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3633+4217A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059168 | |||||||
chr5:66059337 | TTGTC | T | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+4390_3633+439 others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66059337 | ||||||
chr5:66059383 | A | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0016c0019t0001g0087 |
3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3633+4432A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059383 | |||||||
chr5:66059403 | G | A | 1 | a0002c0003t0002g0207 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3633+4452G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059403 | |||||||
chr5:66059539 | T | A | 6 | a0001c0001t0009g0037 a0001c0001t0009g0038 a0001c0001t0009g0039 others(3): Show |
6 | HG03710.hp1 NA18961.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.3633+4588T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059539 | |||||||
chr5:66059716 | G | A | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3633+4765G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059716 | |||||||
chr5:66059741 | C | G | 1 | a0005c0006t0007g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3633+4790C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059741 | |||||||
chr5:66059790 | G | C | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3633+4839G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059790 | |||||||
chr5:66059893 | T | C | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+4942T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059893 | |||||||
chr5:66059926 | T | C | 1 | a0001c0001t0025g0157 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3633+4975T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66059926 | |||||||
chr5:66060028 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3633+5077C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060028 | |||||||
chr5:66060037 | A | T | 1 | a0001c0002t0002g0251 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3633+5086A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060037 | |||||||
chr5:66060060 | G | A | 1 | a0001c0020t0001g0116 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3633+5109G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060060 | |||||||
chr5:66060136 | T | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+5185T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060136 | |||||||
chr5:66060159 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3633+5208A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060159 | |||||||
chr5:66060215 | A | C | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+5264A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060215 | |||||||
chr5:66060216 | G | T | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+5265G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060216 | |||||||
chr5:66060337 | T | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+5386T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060337 | |||||||
chr5:66060409 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+5458G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060409 | |||||||
chr5:66060582 | T | C | 26 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(23): Show |
26 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.3633+5631T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060582 | |||||||
chr5:66060614 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+5663G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060614 | |||||||
chr5:66060722 | A | C | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+5771A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060722 | |||||||
chr5:66060769 | C | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
44 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3633+5818C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060769 | |||||||
chr5:66060769 | CT | C | 134 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(131): Show |
134 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3633+5826delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66060769 | ||||||
chr5:66060791 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3633+5840G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060791 | |||||||
chr5:66060793 | T | G | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+5842T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060793 | |||||||
chr5:66060795 | G | T | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3633+5844G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66060795 | |||||||
chr5:66061083 | G | C | 152 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(149): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3633+6132G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061083 | |||||||
chr5:66061120 | G | A | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3633+6169G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061120 | |||||||
chr5:66061218 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3633+6267T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061218 | |||||||
chr5:66061236 | G | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+6285G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061236 | |||||||
chr5:66061260 | TA | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6310delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061260 | |||||||
chr5:66061262 | G | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6311G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061262 | |||||||
chr5:66061262 | G | GTTC | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+6314_3633+631 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66061262 | ||||||
chr5:66061347 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+6396G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061347 | |||||||
chr5:66061414 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+6463G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061414 | |||||||
chr5:66061498 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+6547A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061498 | |||||||
chr5:66061682 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3633+6731C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061682 | |||||||
chr5:66061779 | A | G | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3633+6828A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66061779 | |||||||
chr5:66062123 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7172A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062123 | |||||||
chr5:66062131 | C | CAG | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7181_3633+718 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66062131 | ||||||
chr5:66062158 | C | T | 1 | a0001c0001t0009g0037 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3633+7207C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062158 | |||||||
chr5:66062181 | G | A | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3633+7230G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062181 | |||||||
chr5:66062183 | G | C | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3633+7232G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062183 | |||||||
chr5:66062237 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+7286G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062237 | |||||||
chr5:66062247 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7296A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062247 | |||||||
chr5:66062275 | G | A | 2 | a0001c0007t0010g0160 a0001c0007t0010g0275 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3633+7324G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062275 | |||||||
chr5:66062280 | A | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7329A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062280 | |||||||
chr5:66062293 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3633+7342C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062293 | |||||||
chr5:66062304 | G | A | 1 | a0002c0003t0005g0182 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3633+7353G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062304 | |||||||
chr5:66062329 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3633+7378C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062329 | |||||||
chr5:66062415 | G | A | 53 | a0002c0003t0002g0201 a0002c0003t0002g0202 a0002c0003t0002g0205 others(50): Show |
53 | HG00280.hp2 HG00408.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.3633+7464G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062415 | |||||||
chr5:66062530 | CCT | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7585_3633+758 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66062530 | ||||||
chr5:66062625 | G | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+7674G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062625 | |||||||
chr5:66062695 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3633+7744T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062695 | |||||||
chr5:66062763 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3633+7812C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062763 | |||||||
chr5:66062765 | A | G | 112 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3633+7814A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062765 | |||||||
chr5:66062779 | G | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3633+7828G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062779 | |||||||
chr5:66062979 | T | A | 1 | a0009c0009t0002g0168 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3633+8028T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062979 | |||||||
chr5:66062998 | T | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8047T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66062998 | |||||||
chr5:66063056 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3633+8105C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063056 | |||||||
chr5:66063184 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3633+8233T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063184 | |||||||
chr5:66063339 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8388C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063339 | |||||||
chr5:66063381 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3633+8430C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063381 | |||||||
chr5:66063395 | A | G | 8 | a0002c0003t0008g0173 a0002c0003t0008g0174 a0002c0003t0008g0178 others(5): Show |
8 | HG00408.hp2 HG02071.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.3633+8444A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063395 | |||||||
chr5:66063416 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0015c0013t0001g0083 |
3 | NA19030.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3633+8465C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063416 | |||||||
chr5:66063538 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3633+8587C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063538 | |||||||
chr5:66063586 | G | A | 112 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(109): Show |
112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3634-8583G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063586 | |||||||
chr5:66063622 | C | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3634-8547C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063622 | |||||||
chr5:66063625 | C | T | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3634-8544C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063625 | |||||||
chr5:66063653 | G | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0057 others(16): Show |
20 | HG00609.hp1 HG00673.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.3634-8516G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063653 | |||||||
chr5:66063702 | A | G | 152 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(149): Show |
152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.3634-8467A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063702 | |||||||
chr5:66063766 | A | G | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3634-8403A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063766 | |||||||
chr5:66063917 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.3634-8252G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063917 | |||||||
chr5:66063993 | A | G | 1 | a0001c0001t0006g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3634-8176A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66063993 | |||||||
chr5:66064484 | G | T | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-7685G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064484 | |||||||
chr5:66064595 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3634-7574G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064595 | |||||||
chr5:66064743 | G | C | 1 | a0005c0006t0002g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3634-7426G>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064743 | |||||||
chr5:66064898 | C | G | 3 | a0006c0008t0003g0072 a0006c0008t0003g0190 a0006c0008t0018g0195 |
3 | NA18950.hp2 NA18971.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3634-7271C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66064898 | |||||||
chr5:66065039 | G | A | 2 | a0003c0004t0001g0302 a0003c0004t0022g0301 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3634-7130G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065039 | |||||||
chr5:66065236 | A | C | 1 | a0001c0001t0013g0102 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3634-6933A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065236 | |||||||
chr5:66065330 | G | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-6839G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065330 | |||||||
chr5:66065337 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3634-6832A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065337 | |||||||
chr5:66065359 | AC | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(83): Show |
87 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.3634-6807delC | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065359 | ||||||
chr5:66065425 | T | C | 1 | a0001c0015t0030g0258 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3634-6744T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065425 | |||||||
chr5:66065556 | C | T | 1 | a0004c0005t0004g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3634-6613C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065556 | |||||||
chr5:66065559 | G | A | 21 | a0001c0001t0001g0133 a0001c0001t0001g0267 a0001c0001t0001g0274 others(18): Show |
21 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.3634-6610G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065559 | |||||||
chr5:66065590 | CCTGTGTG others(12): Show |
C | 6 | a0001c0002t0002g0172 a0001c0002t0002g0209 a0001c0002t0002g0211 others(3): Show |
6 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-6578_3634-656 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | |||||||
chr5:66065590 | CCTGTGTG others(14): Show |
C | 1 | a0001c0002t0002g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3634-6578_3634-655 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | |||||||
chr5:66065590 | CCTGTGTG others(16): Show |
C | 1 | a0001c0002t0002g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3634-6578_3634-655 others(27): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065590 | |||||||
chr5:66065591 | CTGTGTG | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0009g0040 others(3): Show |
6 | HG03041.hp2 NA18961.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6514_3634-650 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(1): Show |
C | 16 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0097 others(13): Show |
16 | HG00738.hp1 HG01261.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-6516_3634-650 others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(3): Show |
C | 20 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0062 others(17): Show |
20 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3634-6518_3634-650 others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(5): Show |
C | 21 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0057 others(18): Show |
21 | HG00673.hp1 HG01069.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.3634-6520_3634-650 others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(7): Show |
C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(21): Show |
25 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.3634-6522_3634-650 others(18): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(9): Show |
C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0059 a0001c0001t0001g0067 others(11): Show |
14 | HG00099.hp1 HG00438.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.3634-6524_3634-650 others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(11): Show |
C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(28): Show |
31 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3634-6526_3634-650 others(22): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(13): Show |
C | 42 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0068 others(39): Show |
42 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.3634-6528_3634-650 others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(15): Show |
C | 55 | a0001c0002t0002g0034 a0001c0002t0002g0246 a0001c0002t0002g0248 others(52): Show |
55 | HG00280.hp2 HG00408.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.3634-6530_3634-650 others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(17): Show |
C | 29 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0158 others(26): Show |
29 | HG01167.hp2 HG02071.hp1 HG02165.hp1 others(26): Show |
intron_variant | MODIFIER | c.3634-6532_3634-650 others(28): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(19): Show |
C | 10 | a0001c0001t0006g0146 a0001c0001t0006g0147 a0001c0007t0012g0217 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3634-6534_3634-650 others(30): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(21): Show |
C | 6 | a0001c0001t0006g0148 a0001c0001t0006g0149 a0001c0001t0006g0150 others(3): Show |
6 | HG02717.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6536_3634-650 others(32): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065591 | CTGTGTGT others(31): Show |
C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6546_3634-650 others(42): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065591 | ||||||
chr5:66065637 | G | A | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3634-6532G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065637 | |||||||
chr5:66065639 | G | A | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6530G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065639 | |||||||
chr5:66065639 | GTGTGTGT others(14): Show |
G | 1 | a0002c0003t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3634-6528_3634-650 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065639 | ||||||
chr5:66065641 | GTGTGTGT others(12): Show |
G | 1 | a0001c0002t0002g0261 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3634-6526_3634-650 others(23): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065641 | ||||||
chr5:66065641 | GTGTGTGT others(14): Show |
G | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3634-6525_3634-650 others(25): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065641 | ||||||
chr5:66065647 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3634-6520_3634-650 others(17): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065647 | ||||||
chr5:66065649 | GTGTGTGT others(4): Show |
G | 1 | a0003c0004t0001g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3634-6518_3634-650 others(15): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66065649 | ||||||
chr5:66065655 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3634-6514G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065655 | |||||||
chr5:66065753 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3634-6416G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065753 | |||||||
chr5:66065803 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-6366T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065803 | |||||||
chr5:66065942 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-6227C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065942 | |||||||
chr5:66065949 | A | G | 1 | a0001c0002t0002g0239 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3634-6220A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065949 | |||||||
chr5:66065959 | T | A | 1 | a0001c0002t0002g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3634-6210T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66065959 | |||||||
chr5:66066038 | T | G | 1 | a0001c0002t0002g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3634-6131T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066038 | |||||||
chr5:66066269 | C | G | 1 | a0002c0003t0003g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3634-5900C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066269 | |||||||
chr5:66066275 | G | A | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.3634-5894G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066275 | |||||||
chr5:66066359 | A | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5810A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066359 | |||||||
chr5:66066367 | G | A | 1 | a0014c0018t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3634-5802G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066367 | |||||||
chr5:66066493 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5676C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066493 | |||||||
chr5:66066502 | TA | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5665delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066502 | ||||||
chr5:66066522 | T | TA | 6 | a0002c0003t0003g0197 a0003c0004t0001g0137 a0003c0004t0001g0138 others(3): Show |
6 | HG00642.hp1 HG01515.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5634dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066522 | ||||||
chr5:66066526 | A | AAAAAAT | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5638_3634-563 others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066526 | ||||||
chr5:66066530 | A | AAT | 10 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(7): Show |
10 | HG02258.hp1 HG02451.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3634-5638_3634-563 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66066530 | ||||||
chr5:66066534 | A | T | 1 | a0001c0007t0010g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3634-5635A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066534 | |||||||
chr5:66066535 | A | T | 4 | a0001c0007t0010g0161 a0001c0007t0010g0162 a0001c0007t0010g0163 others(1): Show |
4 | HG02109.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-5634A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066535 | |||||||
chr5:66066536 | C | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5633C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066536 | |||||||
chr5:66066568 | A | G | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-5601A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066568 | |||||||
chr5:66066714 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3634-5455C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066714 | |||||||
chr5:66066773 | C | T | 6 | a0002c0003t0002g0205 a0002c0003t0002g0206 a0002c0003t0002g0207 others(3): Show |
6 | HG00280.hp2 NA18951.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-5396C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066773 | |||||||
chr5:66066834 | C | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5335C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066834 | |||||||
chr5:66066835 | T | C | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-5334T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066835 | |||||||
chr5:66066841 | G | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-5328G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066841 | |||||||
chr5:66066857 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-5312C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66066857 | |||||||
chr5:66067204 | C | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-4965C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067204 | |||||||
chr5:66067215 | G | A | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-4954G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067215 | |||||||
chr5:66067480 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-4689G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067480 | |||||||
chr5:66067595 | A | G | 2 | a0001c0002t0002g0289 a0001c0002t0002g0295 |
2 | NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3634-4574A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067595 | |||||||
chr5:66067724 | TTTC | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-4436_3634-443 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66067724 | ||||||
chr5:66067913 | C | A | 1 | a0002c0003t0008g0241 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3634-4256C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067913 | |||||||
chr5:66067938 | C | A | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0156 |
3 | HG01891.hp1 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3634-4231C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067938 | |||||||
chr5:66067989 | T | C | 4 | a0005c0006t0007g0224 a0005c0006t0007g0225 a0005c0006t0007g0230 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-4180T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66067989 | |||||||
chr5:66068051 | G | A | 12 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.3634-4118G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068051 | |||||||
chr5:66068168 | A | AAAT | 8 | a0001c0001t0001g0045 a0001c0001t0006g0148 a0001c0002t0002g0238 others(5): Show |
8 | NA18522.hp1 NA18522.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.3634-3980_3634-397 others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068168 | ||||||
chr5:66068189 | T | C | 7 | a0001c0002t0002g0246 a0001c0007t0010g0160 a0001c0007t0010g0161 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3634-3980T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068189 | |||||||
chr5:66068306 | C | T | 1 | a0002c0003t0003g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3634-3863C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068306 | |||||||
chr5:66068326 | T | TAAAAAAA others(324): Show |
1 | a0004c0005t0004g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3634-3831_3634-383 others(335): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068326 | ||||||
chr5:66068326 | T | TAAAAAAA others(325): Show |
1 | a0004c0005t0004g0021 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3634-3831_3634-383 others(336): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068326 | ||||||
chr5:66068338 | A | T | 1 | a0001c0007t0010g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3634-3831A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068338 | |||||||
chr5:66068339 | A | T | 20 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(17): Show |
20 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3634-3830A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068339 | |||||||
chr5:66068340 | A | T | 31 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0006g0146 others(28): Show |
31 | HG01167.hp2 HG01261.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.3634-3829A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068340 | |||||||
chr5:66068346 | G | A | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-3823G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068346 | |||||||
chr5:66068352 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3634-3817G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068352 | |||||||
chr5:66068381 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3634-3788G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068381 | |||||||
chr5:66068423 | A | G | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3634-3746A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068423 | |||||||
chr5:66068679 | G | A | 2 | a0002c0003t0003g0188 a0002c0003t0003g0189 |
2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3634-3490G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068679 | |||||||
chr5:66068707 | C | A | 19 | a0002c0003t0003g0175 a0002c0003t0003g0176 a0002c0003t0003g0177 others(16): Show |
19 | HG01081.hp1 HG01257.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.3634-3462C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068707 | |||||||
chr5:66068726 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-3443T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068726 | |||||||
chr5:66068823 | G | A | 1 | a0003c0025t0001g0142 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3634-3346G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66068823 | |||||||
chr5:66068864 | CCT | C | 25 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0049 others(22): Show |
25 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.3634-3302_3634-330 others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66068864 | ||||||
chr5:66069113 | A | T | 1 | a0004c0014t0004g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3634-3056A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069113 | |||||||
chr5:66069237 | C | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-2932C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069237 | |||||||
chr5:66069264 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2905T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069264 | |||||||
chr5:66069296 | C | T | 1 | a0002c0003t0002g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3634-2873C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069296 | |||||||
chr5:66069302 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2867A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069302 | |||||||
chr5:66069560 | T | C | 1 | a0002c0003t0005g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3634-2609T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069560 | |||||||
chr5:66069604 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-2565C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069604 | |||||||
chr5:66069675 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-2494C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069675 | |||||||
chr5:66069740 | G | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-2429G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069740 | |||||||
chr5:66069776 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3634-2393C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069776 | |||||||
chr5:66069811 | A | G | 2 | a0008c0012t0011g0023 a0008c0012t0011g0024 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3634-2358A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069811 | |||||||
chr5:66069840 | G | A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-2329G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66069840 | |||||||
chr5:66070067 | G | A | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-2102G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070067 | |||||||
chr5:66070084 | G | A | 109 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(106): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3634-2085G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070084 | |||||||
chr5:66070289 | C | T | 1 | a0001c0002t0002g0296 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3634-1880C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070289 | |||||||
chr5:66070329 | C | T | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3634-1840C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070329 | |||||||
chr5:66070482 | G | GT | 3 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0067 |
3 | HG02145.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3634-1686dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66070482 | ||||||
chr5:66070520 | GT | G | 12 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(9): Show |
12 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3634-1640delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66070520 | ||||||
chr5:66070817 | C | T | 113 | a0001c0001t0003g0110 a0001c0002t0002g0003 a0001c0002t0002g0004 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3634-1352C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070817 | |||||||
chr5:66070910 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-1259A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070910 | |||||||
chr5:66070920 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-1249C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070920 | |||||||
chr5:66070978 | A | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-1191A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66070978 | |||||||
chr5:66071223 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3634-946C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071223 | |||||||
chr5:66071351 | AAAGT | A | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-817_3634-814d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071351 | |||||||
chr5:66071369 | AAAAG | A | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3634-780_3634-777d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071369 | ||||||
chr5:66071410 | AT | A | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-757delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071410 | ||||||
chr5:66071438 | T | G | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3634-731T>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071438 | |||||||
chr5:66071580 | A | G | 1 | a0001c0001t0001g0005 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3634-589A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071580 | |||||||
chr5:66071676 | GA | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.3634-486delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071676 | ||||||
chr5:66071722 | A | AT | 31 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0064 others(28): Show |
31 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.3634-428dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr5 | 66071722 | ||||||
chr5:66071722 | A | T | 1 | a0002c0003t0005g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3634-447A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071722 | |||||||
chr5:66071813 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3634-356T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071813 | |||||||
chr5:66071973 | A | C | 1 | a0003c0004t0001g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3634-196A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66071973 | |||||||
chr5:66072006 | G | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-163G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072006 | |||||||
chr5:66072089 | A | G | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3634-80A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072089 | |||||||
chr5:66072104 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3634-65G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072104 | |||||||
chr5:66072146 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3634-23A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 21/25 | chr5 | 66072146 | |||||||
chr5:66072511 | T | C | 1 | a0005c0006t0007g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3756+220T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072511 | |||||||
chr5:66072659 | A | G | 7 | a0004c0005t0004g0014 a0004c0005t0004g0015 a0004c0005t0004g0016 others(4): Show |
7 | HG02258.hp1 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3756+368A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072659 | |||||||
chr5:66072824 | A | G | 1 | a0001c0007t0012g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3756+533A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66072824 | |||||||
chr5:66073062 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3756+771T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073062 | |||||||
chr5:66073117 | C | G | 1 | a0002c0003t0002g0202 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3756+826C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073117 | |||||||
chr5:66073318 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3756+1027G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073318 | |||||||
chr5:66073352 | A | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3756+1061A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073352 | |||||||
chr5:66073400 | G | GT | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3756+1116dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66073400 | ||||||
chr5:66073607 | A | C | 1 | a0001c0002t0002g0213 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3756+1316A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073607 | |||||||
chr5:66073616 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3756+1325A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073616 | |||||||
chr5:66073791 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3757-1233A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073791 | |||||||
chr5:66073841 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3757-1183C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073841 | |||||||
chr5:66073867 | T | C | 1 | a0001c0002t0002g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3757-1157T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66073867 | |||||||
chr5:66074045 | A | AT | 138 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0051 others(135): Show |
138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3757-952dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | A | ATT | 28 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0053 others(25): Show |
28 | HG00408.hp1 HG00642.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.3757-953_3757-952d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | AT | A | 8 | a0001c0001t0001g0099 a0001c0001t0006g0146 a0001c0001t0006g0147 others(5): Show |
8 | HG00738.hp2 HG01257.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3757-952delT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | ATTT | A | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3757-954_3757-952d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | ATTTT | A | 15 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3757-955_3757-952d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0014g0069 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3757-963_3757-952d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074045 | ATTTTTTT others(7): Show |
A | 1 | a0001c0002t0002g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3757-965_3757-952d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074045 | ||||||
chr5:66074072 | T | TA | 3 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0022t0009g0036 |
3 | NA18985.hp2 NA18994.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3757-951dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074072 | ||||||
chr5:66074135 | C | T | 1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3757-889C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074135 | |||||||
chr5:66074147 | C | T | 1 | a0001c0002t0002g0246 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3757-877C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074147 | |||||||
chr5:66074314 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3757-710A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074314 | |||||||
chr5:66074352 | T | TACTTTAT others(7): Show |
1 | a0011c0016t0007g0228 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3757-671_3757-658d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074352 | ||||||
chr5:66074417 | A | ATAT | 149 | a0001c0001t0003g0110 a0001c0002t0002g0003 a0001c0002t0002g0004 others(146): Show |
149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.3757-605_3757-604i others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr5 | 66074417 | ||||||
chr5:66074551 | C | T | 113 | a0001c0001t0003g0110 a0001c0002t0002g0003 a0001c0002t0002g0004 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3757-473C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074551 | |||||||
chr5:66074745 | AAAG | A | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3757-278_3757-276d others(5): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074745 | |||||||
chr5:66074832 | T | C | 1 | a0001c0007t0012g0218 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3757-192T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 22/25 | chr5 | 66074832 | |||||||
chr5:66075312 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3963+82A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075312 | |||||||
chr5:66075326 | C | T | 4 | a0007c0011t0011g0025 a0007c0011t0011g0026 a0008c0012t0011g0023 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3963+96C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075326 | |||||||
chr5:66075327 | G | A | 2 | a0005c0006t0007g0220 a0005c0006t0007g0221 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3963+97G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075327 | |||||||
chr5:66075929 | T | C | 1 | a0013c0024t0023g0145 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3964-387T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075929 | |||||||
chr5:66075974 | G | A | 1 | a0004c0005t0004g0009 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3964-342G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075974 | |||||||
chr5:66075983 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0016c0019t0001g0087 |
3 | NA18957.hp1 NA18990.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.3964-333A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66075983 | |||||||
chr5:66076059 | T | C | 6 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(3): Show |
6 | HG01167.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3964-257T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66076059 | |||||||
chr5:66076069 | T | C | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3964-247T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 23/25 | chr5 | 66076069 | |||||||
chr5:66076458 | G | A | 2 | a0003c0004t0001g0305 a0003c0004t0024g0303 |
2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.4056+50G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076458 | |||||||
chr5:66076623 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4056+215A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076623 | |||||||
chr5:66076638 | C | T | 1 | a0003c0004t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4056+230C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076638 | |||||||
chr5:66076708 | A | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4057-167A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 24/25 | chr5 | 66076708 | |||||||
chr5:66076964 | T | C | 3 | a0001c0002t0002g0235 a0001c0002t0002g0247 a0001c0002t0002g0256 |
3 | NA18949.hp2 NA18990.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.4131+15T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66076964 | |||||||
chr5:66076965 | C | CT | 146 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0033 others(143): Show |
146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.4131+27dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66076965 | ||||||
chr5:66076977 | C | T | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4131+28C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66076977 | |||||||
chr5:66077076 | G | A | 1 | a0004c0005t0004g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4131+127G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077076 | |||||||
chr5:66077082 | C | T | 3 | a0001c0001t0006g0153 a0001c0001t0006g0154 a0001c0001t0006g0155 |
3 | HG00738.hp2 HG01884.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.4131+133C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077082 | |||||||
chr5:66077085 | C | A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+136C>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077085 | |||||||
chr5:66077086 | A | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+137A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077086 | |||||||
chr5:66077150 | C | CA | 29 | a0001c0001t0001g0231 a0001c0001t0001g0272 a0001c0001t0006g0146 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.4131+220dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077150 | ||||||
chr5:66077150 | CA | C | 20 | a0001c0001t0001g0049 a0001c0001t0001g0075 a0001c0002t0002g0252 others(17): Show |
20 | HG01167.hp2 HG01515.hp1 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+220delA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077150 | ||||||
chr5:66077166 | A | C | 2 | a0001c0007t0012g0217 a0001c0007t0012g0219 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4131+217A>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077166 | |||||||
chr5:66077191 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4131+242T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077191 | |||||||
chr5:66077391 | A | G | 22 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(19): Show |
22 | HG01167.hp2 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.4131+442A>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077391 | |||||||
chr5:66077395 | A | T | 5 | a0006c0008t0003g0072 a0006c0008t0003g0190 a0006c0008t0003g0194 others(2): Show |
5 | NA18950.hp2 NA18956.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4131+446A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077395 | |||||||
chr5:66077423 | C | T | 1 | a0002c0003t0003g0169 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4131+474C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077423 | |||||||
chr5:66077481 | C | CA | 113 | a0001c0001t0003g0110 a0001c0002t0002g0003 a0001c0002t0002g0004 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.4131+541dupA | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077481 | ||||||
chr5:66077591 | C | T | 165 | a0001c0001t0003g0110 a0001c0001t0006g0146 a0001c0001t0006g0147 others(162): Show |
165 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.4131+642C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077591 | |||||||
chr5:66077604 | A | T | 13 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(10): Show |
13 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.4131+655A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077604 | |||||||
chr5:66077605 | T | A | 1 | a0002c0003t0002g0202 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4131+656T>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077605 | |||||||
chr5:66077759 | T | TAC | 53 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(50): Show |
53 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.4132-630_4132-629d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACAC | 13 | a0001c0001t0001g0071 a0001c0001t0001g0231 a0001c0002t0002g0213 others(10): Show |
13 | HG00408.hp1 HG02148.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.4132-632_4132-629d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACACAC | 8 | a0001c0002t0002g0251 a0002c0003t0002g0202 a0002c0003t0002g0205 others(5): Show |
8 | HG00280.hp2 HG03239.hp1 NA19001.hp2 others(5): Show |
intron_variant | MODIFIER | c.4132-634_4132-629d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACACACA others(1): Show |
30 | a0002c0003t0002g0201 a0002c0003t0003g0165 a0002c0003t0003g0175 others(27): Show |
30 | HG00408.hp2 HG01257.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.4132-636_4132-629d others(10): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACACACA others(3): Show |
8 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0002c0003t0003g0197 others(5): Show |
8 | HG01081.hp1 HG01934.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4132-638_4132-629d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACACACA others(5): Show |
2 | a0002c0003t0003g0167 a0002c0003t0003g0169 |
2 | NA18946.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.4132-640_4132-629d others(14): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | T | TACACACA others(7): Show |
1 | a0002c0003t0003g0299 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4132-642_4132-629d others(16): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | TAC | T | 12 | a0001c0001t0001g0048 a0001c0001t0001g0158 a0001c0001t0006g0147 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.4132-630_4132-629d others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | TACAC | T | 4 | a0001c0001t0006g0149 a0003c0004t0001g0136 a0005c0006t0016g0226 others(1): Show |
4 | HG00621.hp2 HG01884.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4132-632_4132-629d others(6): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | TACACAC | T | 4 | a0005c0006t0002g0229 a0005c0006t0002g0263 a0005c0006t0007g0027 others(1): Show |
4 | HG02257.hp1 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4132-634_4132-629d others(8): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | TACACACA others(3): Show |
T | 1 | a0005c0006t0007g0220 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4132-638_4132-629d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077759 | TACACACA others(11): Show |
T | 1 | a0012c0023t0001g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4132-646_4132-629d others(20): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077759 | ||||||
chr5:66077771 | CACACACA others(17): Show |
C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
5 | HG01071.hp2 HG01934.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.4132-636_4132-613d others(26): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077771 | ||||||
chr5:66077773 | CACACACA others(15): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4132-634_4132-613d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077773 | ||||||
chr5:66077782 | A | AGT | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-641_4132-640i others(4): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077782 | |||||||
chr5:66077785 | CACACACA others(3): Show |
C | 3 | a0003c0004t0001g0122 a0003c0004t0001g0270 a0003c0004t0017g0120 |
3 | NA18977.hp1 NA18992.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4132-628_4132-619d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077785 | ||||||
chr5:66077788 | A | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-635A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077788 | |||||||
chr5:66077792 | A | T | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-631A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077792 | |||||||
chr5:66077793 | C | G | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-630C>G | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077793 | |||||||
chr5:66077794 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-629A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077794 | |||||||
chr5:66077795 | T | C | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-628T>C | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077795 | |||||||
chr5:66077796 | ACACACAC others(15): Show |
A | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-623_4132-602d others(24): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077796 | ||||||
chr5:66077797 | C | T | 1 | a0005c0006t0007g0222 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4132-626C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077797 | |||||||
chr5:66077800 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-623A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077800 | |||||||
chr5:66077804 | A | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-619A>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077804 | |||||||
chr5:66077807 | C | T | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-616C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077807 | |||||||
chr5:66077808 | ACAGTCAC others(3): Show |
A | 16 | a0004c0005t0004g0008 a0004c0005t0004g0009 a0004c0005t0004g0010 others(13): Show |
16 | HG01167.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4132-612_4132-603d others(12): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077808 | ||||||
chr5:66077877 | G | A | 1 | a0002c0003t0003g0277 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4132-546G>A | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66077877 | |||||||
chr5:66077883 | G | GT | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-538dupT | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66077883 | ||||||
chr5:66078096 | G | T | 3 | a0001c0007t0012g0217 a0001c0007t0012g0218 a0001c0007t0012g0219 |
3 | HG02559.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.4132-327G>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66078096 | |||||||
chr5:66078307 | GTTATT | G | 6 | a0001c0007t0010g0160 a0001c0007t0010g0161 a0001c0007t0010g0162 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-112_4132-108d others(7): Show |
ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr5 | 66078307 | ||||||
chr5:66078414 | C | T | 1 | a0001c0001t0006g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4132-9C>T | ERBIN | ENSG00000112851.16 | transcript | ENST00000284037.10 | protein_coding | 25/25 | chr5 | 66078414 |