Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 145173 |
| ensemblid | ENSG00000187676.8 |
| hgncid | 20207 |
| symbol | B3GLCT |
| name | beta 3-glucosyltransferase |
| refseq_nuc | NM_194318.4 |
| refseq_prot | NP_919299.3 |
| ensembl_nuc | ENST00000343307.5 |
| ensembl_prot | ENSP00000343002.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 31199975 |
| end | 31332276 |
| strand | + |
| ver | v1.2 |
| region | chr13:31199975-31332276 |
| region5000 | chr13:31194975-31337276 |
| regionname0 | B3GLCT_chr13_31199975_31332276 |
| regionname5000 | B3GLCT_chr13_31194975_31337276 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 498 | 140 | 22 | 33 | 65 | 5 | 15 | 44 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| a0002 | 1/1 | 498 | 118 | 56 | 15 | 32 | 3 | 10 | 27 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| a0003 | 0/0 | 498 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| a0004 | 0/0 | 498 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| a0005 | 0/0 | 338 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(333): Show |
chr13 | 31194975 | 31337276 |
| a0006 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| a0007 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | MRPPA others(493): Show |
chr13 | 31194975 | 31337276 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1494 | 139 | 21 | 33 | 65 | 5 | 15 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0001c0013 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0002 | 0/1 | 1494 | 106 | 47 | 14 | 32 | 2 | 10 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0003 | 1/0 | 1494 | 8 | 7 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0007 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0008 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0010 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0002c0011 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0003c0005 | 0/0 | 1494 | 3 | 1 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0004c0004 | 0/0 | 1494 | 3 | 0 | 3 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0005c0006 | 0/0 | 1494 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0006c0009 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 | ||
| a0007c0012 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | ATGCG others(1489): Show |
chr13 | 31194975 | 31337276 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4209 | 70 | 11 | 20 | 30 | 2 | 7 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0004 | 0/0 | 4215 | 21 | 7 | 1 | 12 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0005 | 0/0 | 4209 | 16 | 1 | 3 | 8 | 1 | 3 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0006 | 0/0 | 4215 | 12 | 0 | 2 | 9 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0007 | 0/0 | 4209 | 9 | 0 | 5 | 0 | 2 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0010 | 0/0 | 4209 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0014 | 0/0 | 4209 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0015 | 0/0 | 4210 | 2 | 1 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4205): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0022 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0024 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0001t0025 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0001c0013t0001 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0001 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0002 | 0/0 | 4209 | 40 | 17 | 1 | 18 | 0 | 4 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0003 | 0/1 | 4215 | 34 | 16 | 10 | 0 | 2 | 5 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0004 | 0/0 | 4215 | 7 | 4 | 2 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0006 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0008 | 0/0 | 4210 | 7 | 0 | 0 | 7 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4205): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0009 | 0/0 | 4216 | 4 | 0 | 0 | 4 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4211): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0011 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4201): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0012 | 0/0 | 4215 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0013 | 0/0 | 4216 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4211): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0016 | 0/0 | 4209 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0017 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0018 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0019 | 0/0 | 4215 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0002t0020 | 0/0 | 4215 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0003t0002 | 0/0 | 4209 | 2 | 2 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0003t0003 | 1/0 | 4215 | 5 | 4 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0003t0021 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0007t0023 | 0/0 | 4216 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4211): Show |
chr13 | 31194975 | 31337276 |
| a0002c0008t0002 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0002c0010t0003 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0002c0011t0004 | 0/0 | 4215 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0003c0005t0001 | 0/0 | 4209 | 3 | 1 | 1 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0004c0004t0004 | 0/0 | 4215 | 3 | 0 | 3 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0005c0006t0003 | 0/0 | 4215 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| a0006c0009t0002 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4204): Show |
chr13 | 31194975 | 31337276 |
| a0007c0012t0004 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | AGAGA others(4210): Show |
chr13 | 31194975 | 31337276 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0015g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0024g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0001t0025g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0001c0013t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0016g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0017g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0018g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0019g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0002t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0003t0021g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0007t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0008t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0010t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0002c0011t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0003c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0004t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0004t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0004c0004t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0005c0006t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0005c0006t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0006c0009t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| a0007c0012t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0010 | t0003 | g0012 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0198 | EUR | GBR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0005 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00621 | hp1 | a0002 | c0002 | t0008 | g0145 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0228 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00673 | hp2 | a0001 | c0001 | t0010 | g0111 | EAS | CHS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0092 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0075 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01071 | hp2 | a0004 | c0004 | t0004 | g0203 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0205 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01106 | hp2 | a0002 | c0011 | t0004 | g0179 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01167 | hp1 | a0004 | c0004 | t0004 | g0206 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0207 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0025 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0181 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0234 | AMR | PUR | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0241 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01255 | hp2 | a0001 | c0001 | t0014 | g0184 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01256 | hp2 | a0005 | c0006 | t0003 | g0224 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01258 | hp1 | a0005 | c0006 | t0003 | g0225 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0252 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0242 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0017 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01496 | hp2 | a0002 | c0002 | t0003 | g0238 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0244 | EUR | IBS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0019 | EUR | IBS | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01891 | hp1 | a0002 | c0008 | t0002 | g0065 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01943 | hp2 | a0002 | c0002 | t0019 | g0249 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0147 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0243 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0236 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02015 | hp1 | a0002 | c0002 | t0009 | g0209 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02055 | hp1 | a0001 | c0013 | t0001 | g0259 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02129 | hp2 | a0001 | c0001 | t0024 | g0120 | EAS | KHV | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0213 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0247 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02148 | hp2 | a0001 | c0001 | t0014 | g0038 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | CDX | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02280 | hp1 | a0002 | c0002 | t0011 | g0008 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0069 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0096 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02451 | hp2 | a0002 | c0003 | t0021 | g0070 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02572 | hp2 | a0002 | c0002 | t0011 | g0007 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02615 | hp1 | a0002 | c0003 | t0002 | g0169 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02615 | hp2 | a0002 | c0002 | t0013 | g0010 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0245 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02630 | hp2 | a0002 | c0002 | t0012 | g0174 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0253 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0139 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0255 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02717 | hp2 | a0002 | c0007 | t0023 | g0006 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0014 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0103 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02818 | hp2 | a0006 | c0009 | t0002 | g0262 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02886 | hp1 | a0002 | c0002 | t0011 | g0009 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02896 | hp2 | a0001 | c0001 | t0025 | g0258 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0263 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0034 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0233 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03098 | hp1 | a0002 | c0002 | t0004 | g0013 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03130 | hp1 | a0002 | c0002 | t0018 | g0251 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03139 | hp2 | a0002 | c0002 | t0012 | g0173 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0175 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03195 | hp2 | a0002 | c0002 | t0020 | g0237 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0261 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03239 | hp1 | a0002 | c0002 | t0017 | g0021 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0020 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0216 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0170 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0081 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0180 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0246 | AFR | ESN | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0248 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03710 | hp1 | a0002 | c0002 | t0003 | g0256 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03710 | hp2 | a0003 | c0005 | t0001 | g0074 | SAS | PJL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0080 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0211 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0195 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0068 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0079 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0232 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0023 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0118 | SAS | STU | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0036 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0101 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | CHB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0035 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | YRI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18963 | hp1 | a0002 | c0002 | t0009 | g0016 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18968 | hp1 | a0002 | c0002 | t0008 | g0125 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18975 | hp1 | a0002 | c0002 | t0016 | g0143 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18978 | hp1 | a0002 | c0002 | t0008 | g0062 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18984 | hp2 | a0007 | c0012 | t0004 | g0061 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18990 | hp2 | a0002 | c0002 | t0006 | g0140 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18997 | hp1 | a0002 | c0002 | t0009 | g0210 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18997 | hp2 | a0002 | c0002 | t0008 | g0085 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0218 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19030 | hp2 | a0002 | c0003 | t0002 | g0160 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0226 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19056 | hp1 | a0001 | c0001 | t0022 | g0056 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19058 | hp1 | a0002 | c0002 | t0008 | g0098 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19060 | hp2 | a0002 | c0002 | t0008 | g0099 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0113 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19072 | hp2 | a0002 | c0002 | t0008 | g0138 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19081 | hp1 | a0002 | c0002 | t0009 | g0208 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19082 | hp1 | a0001 | c0001 | t0010 | g0116 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | ASW | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ASW | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0027 | EUR | TSI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0029 | EUR | TSI | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02109 | hp2 | a0002 | c0003 | t0003 | g0186 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0076 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0220 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG02559 | hp2 | a0002 | c0002 | t0013 | g0189 | AFR | ACB | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0239 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | MSL | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG06807 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0257 | AFR | USA | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0217 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0227 | AFR | LWK | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0003 | g0260 | REF | REF | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0219 | REF | REF | B3GLCT_chr13_31194975_31337276 | B3GLCT | chr13 | 31194975 | 31337276 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31247957 | C | A | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.450C>A | p.Asp150Glu | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/15 | 560/4215 | 450/1497 | 150/498 | chr13 | 31247957 | |||
| chr13:31274581 | G | A | 1 | a0004 | 3 | HG01071.hp2 HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.733G>A | p.Val245Met | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/15 | 843/4215 | 733/1497 | 245/498 | chr13 | 31274581 | |||
| chr13:31284699 | A | T | 1 | a0007 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.902A>T | p.Tyr301Phe | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/15 | 1012/4215 | 902/1497 | 301/498 | chr13 | 31284699 | |||
| chr13:31286770 | C | T | 1 | a0005 | 2 | HG01256.hp2 HG01258.hp1 |
stop_gained | HIGH | c.1015C>T | p.Gln339* | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/15 | 1125/4215 | 1015/1497 | 339/498 | chr13 | 31286770 | |||
| chr13:31317606 | G | A | 1 | a0003 | 3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.1105G>A | p.Gly369Ser | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1215/4215 | 1105/1497 | 369/498 | chr13 | 31317606 | |||
| chr13:31317609 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
missense_variant | MODERATE | c.1108G>A | p.Glu370Lys | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1218/4215 | 1108/1497 | 370/498 | chr13 | 31317609 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200123 | G | C | 1 | a0002c0007 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.39G>C | p.Pro13Pro | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/15 | 149/4215 | 39/1497 | 13/498 | chr13 | 31200123 | |||
| chr13:31247049 | T | C | 1 | a0002c0008 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.297T>C | p.His99His | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/15 | 407/4215 | 297/1497 | 99/498 | chr13 | 31247049 | |||
| chr13:31247855 | T | C | 10 | a0001c0001 a0002c0002 a0002c0007 others(7): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
splice_region_variant&synonymous_variant | LOW | c.348T>C | p.His116His | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/15 | 458/4215 | 348/1497 | 116/498 | chr13 | 31247855 | |||
| chr13:31317635 | C | T | 1 | a0002c0011 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.1134C>T | p.Tyr378Tyr | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/15 | 1244/4215 | 1134/1497 | 378/498 | chr13 | 31317635 | |||
| chr13:31329542 | A | G | 1 | a0002c0010 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1371A>G | p.Gln457Gln | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1481/4215 | 1371/1497 | 457/498 | chr13 | 31329542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200049 | C | G | 1 | a0001c0001t0025 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/15 | 36 | chr13 | 31200049 | ||||||
| chr13:31329697 | G | T | 11 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(8): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*29G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 29 | chr13 | 31329697 | ||||||
| chr13:31329704 | A | G | 1 | a0001c0001t0007 | 9 | HG00738.hp1 HG01175.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*36A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 36 | chr13 | 31329704 | ||||||
| chr13:31330072 | G | A | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 404 | chr13 | 31330072 | ||||||
| chr13:31330079 | T | A | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 411 | chr13 | 31330079 | ||||||
| chr13:31330083 | A | G | 1 | a0002c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 415 | chr13 | 31330083 | ||||||
| chr13:31330190 | G | A | 1 | a0002c0002t0017 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 522 | chr13 | 31330190 | ||||||
| chr13:31330217 | ACAT | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*553_*555delCAT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 553 | INFO_REALIGN_3_PRIME | chr13 | 31330217 | |||||
| chr13:31330305 | A | G | 1 | a0002c0002t0013 | 2 | HG02559.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*637A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 637 | chr13 | 31330305 | ||||||
| chr13:31330324 | C | T | 1 | a0002c0007t0023 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 656 | chr13 | 31330324 | ||||||
| chr13:31330351 | G | A | 1 | a0002c0002t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 683 | chr13 | 31330351 | ||||||
| chr13:31330490 | T | A | 1 | a0001c0001t0024 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 822 | chr13 | 31330490 | ||||||
| chr13:31330540 | G | GT | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(18): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*888dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | INFO_REALIGN_3_PRIME | chr13 | 31330540 | |||||
| chr13:31330540 | G | GTT | 2 | a0001c0001t0015 a0002c0002t0008 |
9 | HG00621.hp1 HG02145.hp2 HG02735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*887_*888dupTT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | INFO_REALIGN_3_PRIME | chr13 | 31330540 | |||||
| chr13:31330557 | A | G | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(20): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*889A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | chr13 | 31330557 | ||||||
| chr13:31330557 | A | T | 2 | a0001c0001t0006 a0002c0002t0006 |
13 | HG00558.hp1 HG01943.hp1 HG01952.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*889A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 889 | chr13 | 31330557 | ||||||
| chr13:31330638 | G | C | 1 | a0002c0002t0009 | 4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*970G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 970 | chr13 | 31330638 | ||||||
| chr13:31330865 | A | T | 1 | a0002c0002t0013 | 2 | HG02559.hp2 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1197 | chr13 | 31330865 | ||||||
| chr13:31330874 | T | C | 1 | a0002c0003t0021 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1206 | chr13 | 31330874 | ||||||
| chr13:31330997 | T | A | 1 | a0002c0002t0012 | 2 | HG02630.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1329T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1329 | chr13 | 31330997 | ||||||
| chr13:31331008 | G | A | 1 | a0002c0002t0019 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1340 | chr13 | 31331008 | ||||||
| chr13:31331012 | C | T | 1 | a0002c0002t0020 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1344C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1344 | chr13 | 31331012 | ||||||
| chr13:31331184 | A | G | 1 | a0002c0002t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1516 | chr13 | 31331184 | ||||||
| chr13:31331312 | A | T | 8 | a0001c0001t0004 a0001c0001t0006 a0002c0002t0004 others(5): Show |
48 | HG00558.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1644A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1644 | chr13 | 31331312 | ||||||
| chr13:31331361 | G | C | 1 | a0001c0001t0005 | 16 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1693G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1693 | chr13 | 31331361 | ||||||
| chr13:31331412 | GCCTTCTA | G | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1746_*1752delCTTC others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1746 | INFO_REALIGN_3_PRIME | chr13 | 31331412 | |||||
| chr13:31331420 | C | T | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1752C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1752 | chr13 | 31331420 | ||||||
| chr13:31331469 | A | G | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(21): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1801A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1801 | chr13 | 31331469 | ||||||
| chr13:31331504 | G | A | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(21): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 1836 | chr13 | 31331504 | ||||||
| chr13:31331735 | A | G | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2067A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2067 | chr13 | 31331735 | ||||||
| chr13:31331750 | G | T | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(9): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2082G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2082 | chr13 | 31331750 | ||||||
| chr13:31331769 | T | C | 1 | a0001c0001t0010 | 4 | HG00558.hp2 HG00673.hp2 NA19070.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2101T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2101 | chr13 | 31331769 | ||||||
| chr13:31331805 | T | C | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(17): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2137T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2137 | chr13 | 31331805 | ||||||
| chr13:31331856 | T | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2188 | chr13 | 31331856 | ||||||
| chr13:31332004 | A | C | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(19): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*2336A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2336 | chr13 | 31332004 | ||||||
| chr13:31332114 | A | G | 1 | a0001c0001t0014 | 2 | HG01255.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2446A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2446 | chr13 | 31332114 | ||||||
| chr13:31332154 | T | C | 22 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(19): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*2486T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 15/15 | 2486 | chr13 | 31332154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:31200283 | C | G | 4 | a0002c0002t0002g0261 a0002c0002t0002g0264 a0002c0002t0003g0263 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+129C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200283 | |||||||
| chr13:31200594 | C | T | 25 | a0001c0001t0001g0240 a0001c0001t0001g0254 a0001c0001t0005g0252 others(22): Show |
26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.70+440C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200594 | |||||||
| chr13:31200681 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70+527C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200681 | |||||||
| chr13:31200938 | C | T | 1 | a0002c0002t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.70+784C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200938 | |||||||
| chr13:31200990 | T | A | 1 | a0001c0001t0010g0005 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.70+836T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31200990 | |||||||
| chr13:31201010 | T | TA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(162): Show |
167 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.70+871dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31201010 | ||||||
| chr13:31201237 | A | G | 1 | a0001c0001t0004g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+1083A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201237 | |||||||
| chr13:31201405 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70+1251A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201405 | |||||||
| chr13:31201637 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.70+1483T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201637 | |||||||
| chr13:31201641 | C | A | 5 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1487C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201641 | |||||||
| chr13:31201726 | A | G | 1 | a0002c0002t0002g0232 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70+1572A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201726 | |||||||
| chr13:31201842 | A | C | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.70+1688A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201842 | |||||||
| chr13:31201926 | C | A | 66 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0026 others(63): Show |
66 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.70+1772C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31201926 | |||||||
| chr13:31202068 | C | A | 1 | a0002c0002t0003g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+1914C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202068 | |||||||
| chr13:31202142 | A | G | 1 | a0002c0002t0003g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+1988A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202142 | |||||||
| chr13:31202161 | A | G | 20 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0194 others(17): Show |
21 | HG00140.hp2 HG00735.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+2007A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202161 | |||||||
| chr13:31202281 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(120): Show |
126 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.70+2127C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202281 | |||||||
| chr13:31202337 | G | A | 1 | a0001c0001t0005g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.70+2183G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202337 | |||||||
| chr13:31202345 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70+2191C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202345 | |||||||
| chr13:31202418 | G | A | 1 | a0002c0002t0003g0236 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.70+2264G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202418 | |||||||
| chr13:31202601 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+2447G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202601 | |||||||
| chr13:31202698 | C | A | 29 | a0001c0001t0001g0071 a0001c0001t0001g0240 a0001c0001t0001g0254 others(26): Show |
30 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.70+2544C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202698 | |||||||
| chr13:31202861 | A | G | 71 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0026 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.70+2707A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202861 | |||||||
| chr13:31202875 | A | C | 1 | a0002c0002t0002g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.70+2721A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202875 | |||||||
| chr13:31202952 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70+2798A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202952 | |||||||
| chr13:31202983 | C | T | 1 | a0002c0002t0002g0232 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70+2829C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31202983 | |||||||
| chr13:31203357 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.70+3203T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203357 | |||||||
| chr13:31203400 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(97): Show |
102 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.70+3246A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203400 | |||||||
| chr13:31203428 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(97): Show |
102 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.70+3274A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203428 | |||||||
| chr13:31203429 | G | A | 4 | a0001c0001t0001g0071 a0002c0003t0002g0160 a0002c0003t0002g0169 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3275G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203429 | |||||||
| chr13:31203468 | C | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.70+3314C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203468 | |||||||
| chr13:31203583 | A | G | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+3429A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203583 | |||||||
| chr13:31203665 | T | A | 1 | a0002c0002t0002g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.70+3511T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203665 | |||||||
| chr13:31203675 | A | G | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.70+3521A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203675 | |||||||
| chr13:31203718 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(93): Show |
98 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.70+3564A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203718 | |||||||
| chr13:31203823 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.70+3669T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203823 | |||||||
| chr13:31203982 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.70+3828A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31203982 | |||||||
| chr13:31204026 | A | T | 32 | a0001c0001t0001g0071 a0001c0001t0001g0240 a0001c0001t0001g0254 others(29): Show |
33 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.70+3872A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204026 | |||||||
| chr13:31204069 | G | T | 3 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0008t0002g0065 |
3 | HG01891.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.70+3915G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204069 | |||||||
| chr13:31204161 | G | C | 1 | a0002c0002t0020g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70+4007G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204161 | |||||||
| chr13:31204391 | C | A | 1 | a0002c0010t0003g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.70+4237C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204391 | |||||||
| chr13:31204395 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+4241G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204395 | |||||||
| chr13:31204793 | T | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+4639T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204793 | |||||||
| chr13:31204859 | A | G | 5 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0004c0004t0004g0203 others(2): Show |
5 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+4705A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204859 | |||||||
| chr13:31204881 | A | T | 1 | a0002c0002t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.70+4727A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31204881 | |||||||
| chr13:31205136 | A | G | 1 | a0002c0002t0002g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.70+4982A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205136 | |||||||
| chr13:31205245 | T | G | 5 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+5091T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205245 | |||||||
| chr13:31205252 | T | G | 1 | a0002c0002t0004g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70+5098T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205252 | |||||||
| chr13:31205372 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+5218C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205372 | |||||||
| chr13:31205428 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0073 others(96): Show |
101 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.70+5274G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205428 | |||||||
| chr13:31205578 | C | T | 1 | a0002c0002t0002g0231 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70+5424C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205578 | |||||||
| chr13:31205745 | T | G | 4 | a0002c0002t0002g0261 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+5591T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205745 | |||||||
| chr13:31205882 | A | G | 1 | a0002c0002t0003g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+5728A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205882 | |||||||
| chr13:31205946 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70+5792T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31205946 | |||||||
| chr13:31206126 | G | C | 1 | a0002c0002t0004g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.70+5972G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206126 | |||||||
| chr13:31206523 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.70+6369G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206523 | |||||||
| chr13:31206584 | C | CA | 11 | a0001c0001t0001g0214 a0001c0001t0004g0161 a0001c0001t0004g0162 others(8): Show |
11 | HG02145.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+6449dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31206584 | ||||||
| chr13:31206584 | CA | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(182): Show |
187 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.70+6449delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31206584 | ||||||
| chr13:31206605 | G | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.70+6451G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206605 | |||||||
| chr13:31206611 | G | A | 2 | a0002c0002t0004g0013 a0004c0004t0004g0203 |
2 | HG01071.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.70+6457G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206611 | |||||||
| chr13:31206616 | T | C | 1 | a0002c0002t0003g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70+6462T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206616 | |||||||
| chr13:31206724 | G | A | 1 | a0002c0002t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70+6570G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206724 | |||||||
| chr13:31206826 | C | A | 4 | a0002c0002t0002g0261 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+6672C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206826 | |||||||
| chr13:31206851 | G | A | 38 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0240 others(35): Show |
39 | HG01106.hp2 HG01123.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.70+6697G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31206851 | |||||||
| chr13:31207048 | G | A | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+6894G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207048 | |||||||
| chr13:31207241 | T | C | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70+7087T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207241 | |||||||
| chr13:31207275 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0146 others(12): Show |
16 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.70+7121C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207275 | |||||||
| chr13:31207287 | A | AT | 66 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0026 others(63): Show |
66 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.70+7145dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31207287 | ||||||
| chr13:31207558 | T | C | 10 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(7): Show |
10 | HG01106.hp2 HG02630.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+7404T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207558 | |||||||
| chr13:31207625 | G | A | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-7426G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31207625 | |||||||
| chr13:31208096 | TGTACTCT others(14): Show |
T | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-6943_71-6923del others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208096 | ||||||
| chr13:31208145 | A | G | 3 | a0001c0001t0001g0071 a0001c0001t0004g0171 a0002c0002t0002g0233 |
3 | HG01891.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.71-6906A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208145 | |||||||
| chr13:31208148 | A | T | 2 | a0002c0002t0003g0081 a0002c0002t0003g0256 |
2 | HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.71-6903A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208148 | |||||||
| chr13:31208170 | C | CCGGGTCT others(3): Show |
1 | a0002c0002t0008g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.71-6879_71-6870dup others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208170 | ||||||
| chr13:31208172 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.71-6879G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208172 | |||||||
| chr13:31208243 | A | G | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-6808A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208243 | |||||||
| chr13:31208289 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-6762T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208289 | |||||||
| chr13:31208342 | G | A | 3 | a0002c0002t0003g0238 a0002c0002t0013g0010 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-6709G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208342 | |||||||
| chr13:31208407 | C | T | 2 | a0002c0002t0002g0264 a0002c0002t0003g0263 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.71-6644C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208407 | |||||||
| chr13:31208437 | A | G | 36 | a0001c0001t0001g0064 a0001c0001t0001g0119 a0001c0001t0001g0121 others(33): Show |
37 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-6614A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208437 | |||||||
| chr13:31208552 | T | G | 4 | a0002c0003t0002g0160 a0002c0003t0002g0169 a0002c0003t0021g0070 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6499T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208552 | |||||||
| chr13:31208561 | G | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(45): Show |
49 | HG00609.hp1 HG01192.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.71-6490G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208561 | |||||||
| chr13:31208594 | GC | G | 83 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0051 others(80): Show |
85 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.71-6455delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208594 | ||||||
| chr13:31208619 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-6432G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208619 | |||||||
| chr13:31208619 | G | GC | 50 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0072 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-6420dupC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | ||||||
| chr13:31208619 | G | GCC | 21 | a0001c0001t0001g0088 a0001c0001t0001g0190 a0001c0001t0001g0240 others(18): Show |
22 | HG00609.hp2 HG00735.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-6421_71-6420dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | ||||||
| chr13:31208619 | GC | G | 16 | a0001c0001t0004g0033 a0001c0001t0010g0005 a0001c0001t0010g0111 others(13): Show |
16 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-6420delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208619 | ||||||
| chr13:31208626 | C | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0001g0121 others(6): Show |
10 | HG02027.hp2 HG02129.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-6425C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208626 | |||||||
| chr13:31208626 | C | CCT | 86 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(83): Show |
86 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.71-6424_71-6423ins others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31208626 | ||||||
| chr13:31208626 | C | T | 1 | a0002c0002t0003g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-6425C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208626 | |||||||
| chr13:31208627 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71-6424C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208627 | |||||||
| chr13:31208631 | C | T | 97 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(94): Show |
97 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.71-6420C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208631 | |||||||
| chr13:31208730 | G | A | 4 | a0001c0001t0001g0172 a0002c0002t0003g0217 a0002c0002t0012g0173 others(1): Show |
4 | HG02630.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6321G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208730 | |||||||
| chr13:31208845 | A | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.71-6206A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208845 | |||||||
| chr13:31208879 | G | A | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-6172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31208879 | |||||||
| chr13:31209090 | C | T | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.71-5961C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209090 | |||||||
| chr13:31209094 | G | C | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-5957G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209094 | |||||||
| chr13:31209200 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5851A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209200 | |||||||
| chr13:31209227 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5824G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209227 | |||||||
| chr13:31209344 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-5707C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209344 | |||||||
| chr13:31209471 | A | G | 1 | a0001c0001t0005g0197 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.71-5580A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209471 | |||||||
| chr13:31209497 | C | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(17): Show |
21 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-5554C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209497 | |||||||
| chr13:31209571 | A | T | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-5480A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209571 | |||||||
| chr13:31209840 | C | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.71-5211C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31209840 | |||||||
| chr13:31210003 | T | G | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71-5048T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210003 | |||||||
| chr13:31210096 | T | C | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.71-4955T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210096 | |||||||
| chr13:31210219 | A | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.71-4832A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210219 | |||||||
| chr13:31210273 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.71-4778A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210273 | |||||||
| chr13:31210386 | G | A | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-4665G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210386 | |||||||
| chr13:31210553 | G | T | 5 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0004c0004t0004g0203 others(2): Show |
5 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-4498G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210553 | |||||||
| chr13:31210701 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-4350G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210701 | |||||||
| chr13:31210798 | G | A | 1 | a0002c0002t0003g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.71-4253G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210798 | |||||||
| chr13:31210812 | A | G | 3 | a0001c0001t0004g0046 a0001c0001t0004g0063 a0002c0002t0008g0062 |
3 | NA18953.hp1 NA18963.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.71-4239A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31210812 | |||||||
| chr13:31211026 | T | C | 2 | a0002c0002t0002g0089 a0002c0002t0002g0097 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-4025T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211026 | |||||||
| chr13:31211256 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71-3795A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211256 | |||||||
| chr13:31211267 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.71-3784T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211267 | |||||||
| chr13:31211282 | C | G | 2 | a0001c0013t0001g0259 a0002c0003t0003g0186 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.71-3769C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211282 | |||||||
| chr13:31211310 | C | T | 44 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(41): Show |
44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3741C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211310 | |||||||
| chr13:31211377 | C | T | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-3674C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211377 | |||||||
| chr13:31211411 | C | T | 44 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(41): Show |
44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3640C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211411 | |||||||
| chr13:31211425 | TC | T | 5 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3625delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211425 | |||||||
| chr13:31211463 | T | A | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-3588T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211463 | |||||||
| chr13:31211484 | T | C | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-3567T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211484 | |||||||
| chr13:31211589 | GT | G | 6 | a0001c0001t0001g0152 a0002c0002t0002g0126 a0002c0002t0003g0238 others(3): Show |
6 | HG01496.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3449delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31211589 | ||||||
| chr13:31211739 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(258): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.71-3312A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211739 | |||||||
| chr13:31211850 | C | G | 44 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(41): Show |
44 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3201C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211850 | |||||||
| chr13:31211923 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-3128G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31211923 | |||||||
| chr13:31212000 | G | A | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-3051G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212000 | |||||||
| chr13:31212109 | A | T | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71-2942A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212109 | |||||||
| chr13:31212109 | AT | A | 6 | a0001c0001t0001g0152 a0002c0002t0002g0127 a0002c0002t0003g0238 others(3): Show |
6 | HG01496.hp2 HG02451.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2928delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212109 | ||||||
| chr13:31212155 | A | G | 3 | a0002c0002t0003g0238 a0002c0003t0021g0070 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-2896A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212155 | |||||||
| chr13:31212267 | C | CT | 13 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0109 others(10): Show |
13 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-2759dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | ||||||
| chr13:31212267 | CT | C | 81 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0071 others(78): Show |
82 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.71-2759delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | ||||||
| chr13:31212267 | CTTTTTTT others(5): Show |
C | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-2770_71-2759del others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31212267 | ||||||
| chr13:31212309 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.71-2742C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212309 | |||||||
| chr13:31212516 | G | A | 6 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2535G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212516 | |||||||
| chr13:31212553 | G | C | 2 | a0002c0002t0002g0031 a0002c0002t0002g0032 |
2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.71-2498G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212553 | |||||||
| chr13:31212648 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-2403G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212648 | |||||||
| chr13:31212704 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-2347G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31212704 | |||||||
| chr13:31213018 | T | TTG | 6 | a0002c0002t0003g0238 a0002c0002t0003g0263 a0002c0002t0009g0208 others(3): Show |
6 | HG01496.hp2 HG02015.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-2016_71-2015dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213018 | ||||||
| chr13:31213019 | T | TGTGTGTG others(21): Show |
17 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0005g0003 others(14): Show |
18 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-2021_71-1994dup others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213019 | ||||||
| chr13:31213042 | G | A | 13 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(10): Show |
13 | HG01106.hp2 HG01243.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-2009G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213042 | |||||||
| chr13:31213045 | C | T | 1 | a0002c0008t0002g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.71-2006C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213045 | |||||||
| chr13:31213048 | G | A | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-2003G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213048 | |||||||
| chr13:31213090 | C | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-1961C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213090 | |||||||
| chr13:31213221 | C | G | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-1830C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213221 | |||||||
| chr13:31213416 | C | T | 3 | a0002c0002t0003g0238 a0002c0003t0021g0070 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1635C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213416 | |||||||
| chr13:31213461 | A | G | 3 | a0002c0002t0003g0238 a0002c0003t0021g0070 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1590A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213461 | |||||||
| chr13:31213608 | A | ACCCCCCC others(3): Show |
1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213608 | ||||||
| chr13:31213608 | A | ACCCCCCC others(13): Show |
1 | a0002c0002t0002g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213608 | ||||||
| chr13:31213610 | C | CCCCCCCA others(8): Show |
1 | a0001c0001t0001g0124 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.71-1436_71-1435ins others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213610 | ||||||
| chr13:31213616 | A | ACCCCCCA others(4): Show |
1 | a0001c0001t0001g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCA others(6): Show |
1 | a0002c0002t0002g0142 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(13): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(3): Show |
2 | a0001c0001t0001g0122 a0001c0001t0004g0001 |
3 | NA18944.hp1 NA18952.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.71-1431_71-1430ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(5): Show |
1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(8): Show |
1 | a0002c0002t0008g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(4): Show |
1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(3): Show |
1 | a0002c0002t0002g0141 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(5): Show |
1 | a0002c0002t0002g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(6): Show |
1 | a0002c0002t0008g0125 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(13): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | ACCCCCCC others(9): Show |
1 | a0002c0002t0002g0135 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.71-1431_71-1430ins others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213616 | ||||||
| chr13:31213616 | A | C | 7 | a0001c0001t0001g0124 a0002c0002t0002g0127 a0002c0002t0002g0128 others(4): Show |
7 | HG02698.hp2 HG03225.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1435A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213616 | |||||||
| chr13:31213617 | C | A | 1 | a0002c0002t0002g0164 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.71-1434C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213617 | |||||||
| chr13:31213620 | C | A | 9 | a0001c0001t0001g0176 a0002c0002t0002g0177 a0002c0002t0002g0178 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-1431C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213620 | |||||||
| chr13:31213621 | A | AC | 29 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0077 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-1418dupC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | ||||||
| chr13:31213621 | A | ACC | 79 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(76): Show |
79 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.71-1419_71-1418dup others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | ||||||
| chr13:31213621 | A | ACCC | 32 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0090 others(29): Show |
32 | HG00738.hp1 HG00738.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-1420_71-1418dup others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | ||||||
| chr13:31213621 | A | ACCCCACC others(3): Show |
1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-1426_71-1425ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | ||||||
| chr13:31213621 | A | C | 34 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0121 others(31): Show |
35 | HG00609.hp1 HG02027.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.71-1430A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213621 | |||||||
| chr13:31213621 | ACC | A | 18 | a0001c0001t0001g0240 a0001c0001t0005g0252 a0002c0002t0001g0250 others(15): Show |
19 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-1419_71-1418del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213621 | ||||||
| chr13:31213622 | C | A | 2 | a0001c0001t0001g0172 a0002c0002t0012g0173 |
2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.71-1429C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213622 | |||||||
| chr13:31213623 | C | CCCCCCCC others(3): Show |
1 | a0001c0001t0005g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71-1419_71-1418ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213623 | ||||||
| chr13:31213623 | C | CCCCCCCC others(4): Show |
3 | a0001c0001t0005g0198 a0001c0001t0005g0204 a0001c0001t0006g0195 |
3 | HG00140.hp2 HG00735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213623 | ||||||
| chr13:31213624 | C | CCCCCCCC others(3): Show |
10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(7): Show |
10 | HG01071.hp2 HG01074.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213624 | ||||||
| chr13:31213624 | C | CCCCCCCC others(4): Show |
2 | a0001c0001t0005g0047 a0004c0004t0004g0207 |
2 | HG00609.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.71-1418_71-1417ins others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31213624 | ||||||
| chr13:31213642 | T | C | 3 | a0002c0002t0003g0238 a0002c0003t0021g0070 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.71-1409T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213642 | |||||||
| chr13:31213789 | G | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1262G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213789 | |||||||
| chr13:31213867 | G | T | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.71-1184G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213867 | |||||||
| chr13:31213966 | A | C | 1 | a0002c0002t0003g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.71-1085A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31213966 | |||||||
| chr13:31214111 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-940C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214111 | |||||||
| chr13:31214198 | T | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.71-853T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214198 | |||||||
| chr13:31214235 | A | C | 1 | a0002c0002t0003g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-816A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214235 | |||||||
| chr13:31214388 | A | G | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-663A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214388 | |||||||
| chr13:31214423 | C | T | 2 | a0001c0001t0001g0108 a0002c0002t0008g0099 |
2 | HG02074.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.71-628C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214423 | |||||||
| chr13:31214488 | C | T | 1 | a0002c0002t0003g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-563C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214488 | |||||||
| chr13:31214516 | G | C | 5 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-535G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214516 | |||||||
| chr13:31214665 | G | T | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.71-386G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214665 | |||||||
| chr13:31214754 | T | A | 1 | a0001c0001t0004g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.71-297T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214754 | |||||||
| chr13:31214811 | T | G | 1 | a0002c0002t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71-240T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214811 | |||||||
| chr13:31214957 | A | C | 1 | a0001c0001t0005g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71-94A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | chr13 | 31214957 | |||||||
| chr13:31215032 | CT | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
splice_region_variant&intron_variant | LOW | c.71-5delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr13 | 31215032 | ||||||
| chr13:31215259 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.120+159A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215259 | |||||||
| chr13:31215339 | G | A | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.120+239G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215339 | |||||||
| chr13:31215433 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.120+333C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215433 | |||||||
| chr13:31215600 | G | T | 2 | a0001c0001t0001g0045 a0007c0012t0004g0061 |
2 | NA18984.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.120+500G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215600 | |||||||
| chr13:31215603 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.120+503G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215603 | |||||||
| chr13:31215639 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+539C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215639 | |||||||
| chr13:31215699 | C | T | 25 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(22): Show |
26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.120+599C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215699 | |||||||
| chr13:31215756 | T | C | 4 | a0002c0002t0003g0263 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 HG02922.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+656T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215756 | |||||||
| chr13:31215794 | A | G | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.120+694A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215794 | |||||||
| chr13:31215796 | C | T | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120+696C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215796 | |||||||
| chr13:31215856 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.120+756G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215856 | |||||||
| chr13:31215916 | C | T | 28 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(25): Show |
29 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+816C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31215916 | |||||||
| chr13:31216147 | C | CT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.120+1050dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216147 | ||||||
| chr13:31216237 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.120+1137G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216237 | |||||||
| chr13:31216384 | TTTTTTCT others(51): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+1337_120+1394d others(60): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216384 | ||||||
| chr13:31216483 | T | TG | 6 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0003g0263 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+1384dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31216483 | ||||||
| chr13:31216605 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.120+1505C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216605 | |||||||
| chr13:31216639 | C | G | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120+1539C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216639 | |||||||
| chr13:31216786 | C | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.120+1686C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216786 | |||||||
| chr13:31216875 | A | T | 7 | a0002c0002t0003g0011 a0002c0002t0003g0034 a0002c0002t0003g0035 others(4): Show |
7 | HG01175.hp1 HG01243.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+1775A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31216875 | |||||||
| chr13:31217221 | T | C | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.120+2121T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217221 | |||||||
| chr13:31217279 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.120+2179A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217279 | |||||||
| chr13:31217389 | G | C | 50 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(47): Show |
51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.120+2289G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217389 | |||||||
| chr13:31217518 | A | G | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2418A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217518 | |||||||
| chr13:31217519 | C | A | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2419C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217519 | |||||||
| chr13:31217548 | T | C | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2448T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217548 | |||||||
| chr13:31217626 | A | G | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2526A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217626 | |||||||
| chr13:31217664 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+2564C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217664 | |||||||
| chr13:31217806 | A | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.120+2706A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217806 | |||||||
| chr13:31217822 | G | T | 2 | a0001c0001t0004g0039 a0001c0001t0004g0060 |
2 | HG00673.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.120+2722G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217822 | |||||||
| chr13:31217830 | T | C | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.120+2730T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217830 | |||||||
| chr13:31217972 | T | A | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.120+2872T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217972 | |||||||
| chr13:31217978 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+2878G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31217978 | |||||||
| chr13:31218186 | A | G | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.120+3086A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218186 | |||||||
| chr13:31218187 | C | CT | 6 | a0001c0001t0001g0088 a0002c0002t0003g0096 a0002c0002t0003g0245 others(3): Show |
6 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+3106dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218187 | ||||||
| chr13:31218187 | CT | C | 71 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(68): Show |
73 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.120+3106delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218187 | ||||||
| chr13:31218238 | A | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(254): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.120+3138A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218238 | |||||||
| chr13:31218239 | G | T | 1 | a0002c0002t0009g0016 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.120+3139G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218239 | |||||||
| chr13:31218617 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.120+3517A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218617 | |||||||
| chr13:31218751 | G | A | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.120+3651G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218751 | |||||||
| chr13:31218811 | G | A | 1 | a0002c0002t0004g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120+3711G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218811 | |||||||
| chr13:31218930 | C | CT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.120+3843dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31218930 | ||||||
| chr13:31218990 | A | G | 1 | a0002c0002t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.120+3890A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31218990 | |||||||
| chr13:31219154 | G | A | 1 | a0002c0002t0003g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.121-3798G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219154 | |||||||
| chr13:31219155 | T | C | 3 | a0001c0001t0001g0172 a0002c0002t0012g0173 a0002c0002t0012g0174 |
3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.121-3797T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219155 | |||||||
| chr13:31219229 | C | G | 2 | a0002c0002t0003g0079 a0002c0002t0003g0080 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.121-3723C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219229 | |||||||
| chr13:31219324 | A | C | 1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121-3628A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219324 | |||||||
| chr13:31219434 | T | C | 25 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(22): Show |
26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-3518T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219434 | |||||||
| chr13:31219435 | T | A | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-3517T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219435 | |||||||
| chr13:31219621 | T | C | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.121-3331T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219621 | |||||||
| chr13:31219752 | A | G | 5 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-3200A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219752 | |||||||
| chr13:31219813 | A | C | 52 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(49): Show |
53 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.121-3139A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219813 | |||||||
| chr13:31219885 | G | C | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-3067G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31219885 | |||||||
| chr13:31220465 | T | G | 1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121-2487T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220465 | |||||||
| chr13:31220488 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.121-2464T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220488 | |||||||
| chr13:31220594 | T | G | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.121-2358T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220594 | |||||||
| chr13:31220658 | A | G | 1 | a0001c0001t0007g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.121-2294A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220658 | |||||||
| chr13:31220843 | T | C | 3 | a0002c0002t0002g0127 a0002c0002t0002g0135 a0002c0002t0002g0137 |
3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.121-2109T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220843 | |||||||
| chr13:31220899 | A | T | 1 | a0002c0002t0002g0164 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.121-2053A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220899 | |||||||
| chr13:31220940 | T | C | 1 | a0001c0001t0004g0063 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.121-2012T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220940 | |||||||
| chr13:31220967 | A | G | 9 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0003g0263 others(6): Show |
9 | HG02015.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-1985A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31220967 | |||||||
| chr13:31221053 | T | C | 2 | a0001c0001t0006g0050 a0001c0001t0006g0167 |
2 | NA18947.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.121-1899T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221053 | |||||||
| chr13:31221291 | T | C | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.121-1661T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221291 | |||||||
| chr13:31221409 | G | A | 50 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(47): Show |
51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-1543G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221409 | |||||||
| chr13:31221570 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.121-1382C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221570 | |||||||
| chr13:31221640 | C | T | 1 | a0001c0001t0007g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.121-1312C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221640 | |||||||
| chr13:31221641 | C | T | 1 | a0001c0001t0005g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121-1311C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221641 | |||||||
| chr13:31221818 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.121-1134A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221818 | |||||||
| chr13:31221823 | G | A | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.121-1129G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221823 | |||||||
| chr13:31221921 | T | C | 1 | a0002c0002t0003g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.121-1031T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221921 | |||||||
| chr13:31221973 | C | T | 1 | a0001c0001t0010g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.121-979C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31221973 | |||||||
| chr13:31222043 | C | A | 20 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(17): Show |
21 | HG01123.hp1 HG01192.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121-909C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222043 | |||||||
| chr13:31222043 | C | G | 5 | a0002c0002t0003g0014 a0002c0002t0003g0081 a0002c0002t0003g0241 others(2): Show |
5 | HG01255.hp1 HG01358.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-909C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222043 | |||||||
| chr13:31222074 | A | AT | 8 | a0001c0001t0001g0071 a0002c0002t0003g0014 a0002c0002t0003g0081 others(5): Show |
8 | HG01255.hp1 HG01358.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.121-856dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | ||||||
| chr13:31222074 | AT | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0026 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.121-856delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | ||||||
| chr13:31222074 | ATT | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0110 others(2): Show |
5 | HG00140.hp1 HG01169.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-857_121-856del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr13 | 31222074 | ||||||
| chr13:31222169 | C | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.121-783C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222169 | |||||||
| chr13:31222266 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(254): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.121-686G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222266 | |||||||
| chr13:31222341 | G | T | 50 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(47): Show |
51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-611G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222341 | |||||||
| chr13:31222426 | T | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.121-526T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222426 | |||||||
| chr13:31222503 | A | C | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.121-449A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222503 | |||||||
| chr13:31222605 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.121-347A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222605 | |||||||
| chr13:31222832 | G | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.121-120G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222832 | |||||||
| chr13:31222869 | A | G | 77 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(74): Show |
79 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.121-83A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222869 | |||||||
| chr13:31222871 | G | A | 1 | a0002c0002t0002g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.121-81G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 2/14 | chr13 | 31222871 | |||||||
| chr13:31223294 | G | A | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.160+303G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223294 | |||||||
| chr13:31223318 | C | T | 50 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(47): Show |
51 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.160+327C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223318 | |||||||
| chr13:31223504 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.160+513T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223504 | |||||||
| chr13:31223758 | G | T | 5 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+767G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223758 | |||||||
| chr13:31223842 | G | A | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+851G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223842 | |||||||
| chr13:31223938 | T | C | 48 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0240 others(45): Show |
50 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.160+947T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223938 | |||||||
| chr13:31223939 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+948C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31223939 | |||||||
| chr13:31224071 | A | G | 1 | a0001c0001t0007g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+1080A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224071 | |||||||
| chr13:31224083 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+1092C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224083 | |||||||
| chr13:31224084 | G | A | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.160+1093G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224084 | |||||||
| chr13:31224089 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+1098C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224089 | |||||||
| chr13:31224274 | A | G | 1 | a0002c0002t0002g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+1283A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224274 | |||||||
| chr13:31224290 | C | T | 1 | a0002c0002t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.160+1299C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224290 | |||||||
| chr13:31224313 | C | T | 1 | a0002c0002t0013g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160+1322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224313 | |||||||
| chr13:31224355 | T | G | 3 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0008t0002g0065 |
3 | HG01891.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.160+1364T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224355 | |||||||
| chr13:31224713 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+1722G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224713 | |||||||
| chr13:31224720 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160+1729G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224720 | |||||||
| chr13:31224770 | T | G | 1 | a0002c0002t0003g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+1779T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224770 | |||||||
| chr13:31224816 | G | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+1825G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224816 | |||||||
| chr13:31224928 | T | C | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.160+1937T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31224928 | |||||||
| chr13:31225091 | C | T | 2 | a0001c0001t0001g0045 a0007c0012t0004g0061 |
2 | NA18984.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+2100C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225091 | |||||||
| chr13:31225161 | G | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+2170G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225161 | |||||||
| chr13:31225509 | G | A | 29 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(26): Show |
30 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.160+2518G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225509 | |||||||
| chr13:31225582 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+2591C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225582 | |||||||
| chr13:31225595 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+2604G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225595 | |||||||
| chr13:31225653 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160+2662C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225653 | |||||||
| chr13:31225694 | G | A | 2 | a0001c0001t0005g0100 a0001c0001t0005g0101 |
2 | NA18612.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.160+2703G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225694 | |||||||
| chr13:31225804 | A | G | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.160+2813A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225804 | |||||||
| chr13:31225842 | C | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.160+2851C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31225842 | |||||||
| chr13:31226032 | A | G | 2 | a0002c0002t0011g0007 a0002c0002t0011g0008 |
2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.160+3041A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226032 | |||||||
| chr13:31226072 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.160+3081C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226072 | |||||||
| chr13:31226101 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.161-3084A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226101 | |||||||
| chr13:31226115 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.161-3070A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226115 | |||||||
| chr13:31226120 | C | A | 25 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(22): Show |
26 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-3065C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226120 | |||||||
| chr13:31226147 | G | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-3038G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226147 | |||||||
| chr13:31226202 | T | C | 2 | a0002c0002t0003g0079 a0002c0002t0003g0080 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.161-2983T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226202 | |||||||
| chr13:31226205 | C | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-2980C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226205 | |||||||
| chr13:31226237 | G | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-2948G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226237 | |||||||
| chr13:31226348 | A | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.161-2837A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226348 | |||||||
| chr13:31226488 | A | G | 14 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0157 others(11): Show |
14 | HG00558.hp1 HG01943.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-2697A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226488 | |||||||
| chr13:31226580 | C | T | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.161-2605C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226580 | |||||||
| chr13:31226596 | T | A | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.161-2589T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226596 | |||||||
| chr13:31226608 | A | AT | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-2568dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31226608 | ||||||
| chr13:31226878 | A | C | 2 | a0002c0002t0012g0173 a0002c0002t0012g0174 |
2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.161-2307A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226878 | |||||||
| chr13:31226947 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.161-2238A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226947 | |||||||
| chr13:31226954 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.161-2231T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31226954 | |||||||
| chr13:31227329 | TA | T | 7 | a0001c0001t0001g0071 a0001c0001t0004g0043 a0002c0002t0003g0238 others(4): Show |
7 | HG01071.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-1846delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31227329 | ||||||
| chr13:31227405 | G | A | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.161-1780G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227405 | |||||||
| chr13:31227431 | T | C | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-1754T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227431 | |||||||
| chr13:31227771 | T | C | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-1414T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227771 | |||||||
| chr13:31227811 | G | A | 4 | a0002c0002t0003g0236 a0002c0002t0003g0243 a0002c0002t0003g0244 others(1): Show |
4 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-1374G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227811 | |||||||
| chr13:31227872 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161-1313G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227872 | |||||||
| chr13:31227894 | G | C | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.161-1291G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227894 | |||||||
| chr13:31227911 | C | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-1274C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227911 | |||||||
| chr13:31227990 | C | T | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-1195C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31227990 | |||||||
| chr13:31228090 | G | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.161-1095G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228090 | |||||||
| chr13:31228156 | G | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-1029G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228156 | |||||||
| chr13:31228219 | C | CG | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.161-965dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31228219 | ||||||
| chr13:31228265 | T | G | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.161-920T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228265 | |||||||
| chr13:31228275 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-910A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228275 | |||||||
| chr13:31228402 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(181): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.161-783A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228402 | |||||||
| chr13:31228494 | A | G | 48 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0240 others(45): Show |
50 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-691A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228494 | |||||||
| chr13:31228563 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-622G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228563 | |||||||
| chr13:31228707 | A | G | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-478A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228707 | |||||||
| chr13:31228733 | T | C | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.161-452T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228733 | |||||||
| chr13:31228786 | A | G | 1 | a0002c0003t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.161-399A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228786 | |||||||
| chr13:31228856 | C | G | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.161-329C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228856 | |||||||
| chr13:31228879 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161-306C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | chr13 | 31228879 | |||||||
| chr13:31229021 | AAG | A | 3 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0007t0023g0006 |
3 | HG01496.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.161-158_161-157del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr13 | 31229021 | ||||||
| chr13:31229472 | G | A | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.270+178G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229472 | |||||||
| chr13:31229521 | G | A | 1 | a0002c0002t0003g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+227G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229521 | |||||||
| chr13:31229635 | A | T | 1 | a0002c0002t0004g0025 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.270+341A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229635 | |||||||
| chr13:31229762 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.270+468G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229762 | |||||||
| chr13:31229815 | T | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.270+521T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229815 | |||||||
| chr13:31229817 | T | G | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.270+523T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229817 | |||||||
| chr13:31229819 | T | G | 5 | a0001c0001t0001g0071 a0002c0002t0003g0238 a0002c0002t0008g0062 others(2): Show |
5 | HG01496.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+525T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229819 | |||||||
| chr13:31229820 | TG | T | 4 | a0001c0001t0004g0171 a0002c0002t0002g0233 a0003c0005t0001g0075 others(1): Show |
4 | HG00741.hp2 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+527delG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229820 | |||||||
| chr13:31229821 | G | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.270+527G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229821 | |||||||
| chr13:31229823 | G | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.270+529G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229823 | |||||||
| chr13:31229839 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.270+545A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229839 | |||||||
| chr13:31229844 | A | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0002c0002t0003g0238 others(1): Show |
4 | HG01496.hp2 HG02148.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+550A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229844 | |||||||
| chr13:31229904 | G | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.270+610G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229904 | |||||||
| chr13:31229953 | T | C | 2 | a0001c0001t0004g0215 a0002c0002t0003g0239 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.270+659T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31229953 | |||||||
| chr13:31230039 | C | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+745C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230039 | |||||||
| chr13:31230156 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+862G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230156 | |||||||
| chr13:31230303 | A | G | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.270+1009A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230303 | |||||||
| chr13:31230348 | G | A | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.270+1054G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230348 | |||||||
| chr13:31230428 | T | C | 2 | a0001c0001t0010g0005 a0001c0001t0010g0111 |
2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.270+1134T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230428 | |||||||
| chr13:31230537 | T | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(258): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.270+1243T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230537 | |||||||
| chr13:31230613 | GCTCTGCT others(65): Show |
G | 1 | a0002c0002t0009g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.270+1320_270+1391d others(74): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230613 | |||||||
| chr13:31230721 | C | T | 1 | a0002c0002t0009g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.270+1427C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230721 | |||||||
| chr13:31230786 | G | A | 1 | a0002c0002t0003g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.270+1492G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230786 | |||||||
| chr13:31230855 | A | G | 48 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0240 others(45): Show |
50 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.270+1561A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31230855 | |||||||
| chr13:31231008 | A | G | 1 | a0002c0002t0003g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.270+1714A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231008 | |||||||
| chr13:31231482 | C | T | 5 | a0001c0001t0001g0176 a0002c0002t0002g0177 a0002c0002t0004g0170 others(2): Show |
5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+2188C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231482 | |||||||
| chr13:31231679 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+2385C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231679 | |||||||
| chr13:31231710 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.270+2416A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231710 | |||||||
| chr13:31231984 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+2690T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31231984 | |||||||
| chr13:31232158 | T | C | 5 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+2864T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232158 | |||||||
| chr13:31232279 | A | C | 5 | a0001c0001t0001g0176 a0002c0002t0002g0177 a0002c0002t0004g0170 others(2): Show |
5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+2985A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232279 | |||||||
| chr13:31232420 | TAGAG | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3133_270+3136d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31232420 | ||||||
| chr13:31232430 | G | C | 1 | a0002c0002t0003g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.270+3136G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232430 | |||||||
| chr13:31232439 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3145C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232439 | |||||||
| chr13:31232486 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.270+3192C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232486 | |||||||
| chr13:31232501 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+3207G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232501 | |||||||
| chr13:31232537 | C | G | 1 | a0002c0002t0002g0135 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.270+3243C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232537 | |||||||
| chr13:31232621 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.270+3327G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232621 | |||||||
| chr13:31232747 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+3453G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232747 | |||||||
| chr13:31232835 | C | T | 52 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(49): Show |
53 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.270+3541C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232835 | |||||||
| chr13:31232986 | C | T | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.270+3692C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232986 | |||||||
| chr13:31232994 | C | T | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+3700C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31232994 | |||||||
| chr13:31233146 | T | A | 2 | a0002c0002t0003g0238 a0002c0007t0023g0006 |
2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.270+3852T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233146 | |||||||
| chr13:31233246 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.270+3952G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233246 | |||||||
| chr13:31233594 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4300G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233594 | |||||||
| chr13:31233659 | C | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4365C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233659 | |||||||
| chr13:31233900 | A | G | 48 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0240 others(45): Show |
50 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.270+4606A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233900 | |||||||
| chr13:31233906 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4612C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31233906 | |||||||
| chr13:31234007 | C | CT | 134 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.270+4725dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31234007 | ||||||
| chr13:31234007 | CT | C | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+4725delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31234007 | ||||||
| chr13:31234103 | C | T | 4 | a0001c0001t0010g0005 a0001c0001t0010g0111 a0001c0001t0010g0113 others(1): Show |
4 | HG00558.hp2 HG00673.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+4809C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234103 | |||||||
| chr13:31234143 | G | A | 1 | a0001c0001t0004g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.270+4849G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234143 | |||||||
| chr13:31234163 | A | G | 1 | a0001c0001t0006g0058 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.270+4869A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234163 | |||||||
| chr13:31234166 | C | T | 3 | a0002c0002t0009g0208 a0002c0002t0009g0209 a0002c0002t0009g0210 |
3 | HG02015.hp1 NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.270+4872C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234166 | |||||||
| chr13:31234176 | C | T | 1 | a0002c0002t0003g0257 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270+4882C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234176 | |||||||
| chr13:31234248 | C | T | 50 | a0001c0001t0001g0071 a0001c0001t0001g0190 a0001c0001t0001g0191 others(47): Show |
52 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.270+4954C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234248 | |||||||
| chr13:31234277 | C | T | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+4983C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234277 | |||||||
| chr13:31234457 | T | C | 1 | a0002c0002t0003g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.270+5163T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234457 | |||||||
| chr13:31234489 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.270+5195C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234489 | |||||||
| chr13:31234672 | G | A | 1 | a0002c0002t0011g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.270+5378G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234672 | |||||||
| chr13:31234748 | A | T | 2 | a0001c0001t0004g0215 a0002c0002t0003g0239 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.270+5454A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234748 | |||||||
| chr13:31234914 | G | A | 5 | a0002c0002t0002g0264 a0002c0002t0003g0227 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+5620G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31234914 | |||||||
| chr13:31235038 | C | T | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+5744C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235038 | |||||||
| chr13:31235202 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.270+5908A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235202 | |||||||
| chr13:31235236 | A | G | 1 | a0002c0002t0020g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.270+5942A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235236 | |||||||
| chr13:31235300 | G | A | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+6006G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235300 | |||||||
| chr13:31235444 | G | A | 57 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(54): Show |
58 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.270+6150G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235444 | |||||||
| chr13:31235564 | CAG | C | 39 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(36): Show |
39 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+6276_270+6277d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31235564 | ||||||
| chr13:31235587 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.270+6293C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235587 | |||||||
| chr13:31235602 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.270+6308T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235602 | |||||||
| chr13:31235612 | G | A | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+6318G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235612 | |||||||
| chr13:31235723 | A | G | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+6429A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235723 | |||||||
| chr13:31235751 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.270+6457G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235751 | |||||||
| chr13:31235773 | C | T | 1 | a0001c0001t0005g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.270+6479C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235773 | |||||||
| chr13:31235803 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.270+6509T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235803 | |||||||
| chr13:31235831 | A | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.270+6537A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235831 | |||||||
| chr13:31235962 | G | T | 1 | a0002c0002t0003g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.270+6668G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31235962 | |||||||
| chr13:31236844 | G | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18950.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.270+7550G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236844 | |||||||
| chr13:31236937 | G | A | 10 | a0001c0001t0007g0022 a0002c0002t0003g0011 a0002c0002t0003g0027 others(7): Show |
10 | HG00738.hp1 HG01175.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.270+7643G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236937 | |||||||
| chr13:31236982 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.270+7688C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31236982 | |||||||
| chr13:31237042 | C | T | 1 | a0002c0002t0012g0173 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.270+7748C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237042 | |||||||
| chr13:31237125 | C | CA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.270+7844dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237125 | ||||||
| chr13:31237350 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.270+8056G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237350 | |||||||
| chr13:31237353 | G | GT | 183 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.270+8077dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237353 | ||||||
| chr13:31237353 | G | GTT | 65 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0106 others(62): Show |
67 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.270+8076_270+8077d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31237353 | ||||||
| chr13:31237551 | C | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+8257C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237551 | |||||||
| chr13:31237613 | C | T | 1 | a0003c0005t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+8319C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237613 | |||||||
| chr13:31237652 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+8358G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237652 | |||||||
| chr13:31237678 | G | A | 62 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(59): Show |
63 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.270+8384G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237678 | |||||||
| chr13:31237682 | A | G | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+8388A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237682 | |||||||
| chr13:31237717 | G | A | 1 | a0002c0002t0003g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+8423G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237717 | |||||||
| chr13:31237828 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0006g0058 others(2): Show |
5 | HG00558.hp1 NA18968.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+8534A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237828 | |||||||
| chr13:31237902 | G | C | 3 | a0001c0001t0001g0172 a0002c0002t0012g0173 a0002c0002t0012g0174 |
3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.270+8608G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237902 | |||||||
| chr13:31237961 | G | A | 1 | a0002c0002t0003g0244 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.270+8667G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31237961 | |||||||
| chr13:31238110 | T | A | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+8816T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238110 | |||||||
| chr13:31238237 | G | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-8786G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238237 | |||||||
| chr13:31238441 | T | C | 1 | a0002c0002t0004g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.271-8582T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238441 | |||||||
| chr13:31238523 | C | G | 1 | a0001c0001t0001g0015 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.271-8500C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238523 | |||||||
| chr13:31238575 | T | G | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-8448T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238575 | |||||||
| chr13:31238677 | C | T | 17 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0005g0003 others(14): Show |
18 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-8346C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238677 | |||||||
| chr13:31238752 | G | C | 9 | a0001c0001t0001g0064 a0001c0001t0001g0093 a0001c0001t0001g0102 others(6): Show |
9 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-8271G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238752 | |||||||
| chr13:31238888 | C | T | 1 | a0002c0002t0002g0142 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271-8135C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238888 | |||||||
| chr13:31238895 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-8128G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238895 | |||||||
| chr13:31238977 | C | T | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-8046C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238977 | |||||||
| chr13:31238978 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0144 |
2 | NA18978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.271-8045G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31238978 | |||||||
| chr13:31239085 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.271-7938G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239085 | |||||||
| chr13:31239396 | GAGAC | G | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-7619_271-7616d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239396 | ||||||
| chr13:31239636 | A | G | 1 | a0001c0013t0001g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-7387A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239636 | |||||||
| chr13:31239684 | C | CT | 14 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(11): Show |
14 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-7324dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | ||||||
| chr13:31239684 | C | CTT | 20 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(17): Show |
21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-7325_271-7324d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | ||||||
| chr13:31239684 | CT | C | 54 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(51): Show |
55 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.271-7324delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31239684 | ||||||
| chr13:31239730 | C | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(254): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.271-7293C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239730 | |||||||
| chr13:31239734 | T | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.271-7289T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239734 | |||||||
| chr13:31239853 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.271-7170G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31239853 | |||||||
| chr13:31240181 | T | C | 24 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(21): Show |
25 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-6842T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240181 | |||||||
| chr13:31240234 | C | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.271-6789C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240234 | |||||||
| chr13:31240285 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-6738A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240285 | |||||||
| chr13:31240327 | G | A | 24 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(21): Show |
25 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-6696G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240327 | |||||||
| chr13:31240463 | T | G | 115 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(112): Show |
118 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.271-6560T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240463 | |||||||
| chr13:31240467 | G | GT | 26 | a0001c0001t0001g0107 a0001c0001t0001g0187 a0001c0001t0001g0240 others(23): Show |
27 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.271-6546dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240467 | ||||||
| chr13:31240477 | T | TTC | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0064 others(58): Show |
62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.271-6546_271-6545i others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240477 | |||||||
| chr13:31240478 | C | CT | 94 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0119 others(91): Show |
95 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-6532dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240478 | ||||||
| chr13:31240478 | C | CTT | 14 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0172 others(11): Show |
14 | HG00099.hp1 HG00741.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-6533_271-6532d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31240478 | ||||||
| chr13:31240478 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0064 others(58): Show |
62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.271-6545C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240478 | |||||||
| chr13:31240494 | A | G | 51 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(48): Show |
52 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.271-6529A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240494 | |||||||
| chr13:31240522 | A | G | 1 | a0001c0013t0001g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-6501A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240522 | |||||||
| chr13:31240586 | C | T | 24 | a0001c0001t0001g0240 a0001c0001t0004g0215 a0001c0001t0005g0252 others(21): Show |
25 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-6437C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240586 | |||||||
| chr13:31240780 | T | C | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-6243T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31240780 | |||||||
| chr13:31241194 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-5829C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241194 | |||||||
| chr13:31241224 | C | G | 1 | a0002c0002t0003g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271-5799C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241224 | |||||||
| chr13:31241252 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-5771G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241252 | |||||||
| chr13:31241281 | C | T | 1 | a0002c0002t0002g0177 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.271-5742C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241281 | |||||||
| chr13:31241296 | G | T | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271-5727G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241296 | |||||||
| chr13:31241532 | A | G | 11 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(8): Show |
11 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-5491A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241532 | |||||||
| chr13:31241580 | T | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0144 |
2 | NA18978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.271-5443T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241580 | |||||||
| chr13:31241665 | A | C | 15 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0002g0177 others(12): Show |
15 | HG01106.hp2 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-5358A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241665 | |||||||
| chr13:31241741 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.271-5282T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241741 | |||||||
| chr13:31241743 | G | A | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.271-5280G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241743 | |||||||
| chr13:31241770 | C | T | 2 | a0002c0002t0013g0010 a0002c0002t0013g0189 |
2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.271-5253C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241770 | |||||||
| chr13:31241820 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-5203G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241820 | |||||||
| chr13:31241879 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.271-5144G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241879 | |||||||
| chr13:31241998 | A | C | 2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.271-5025A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31241998 | |||||||
| chr13:31242164 | TTC | T | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4853_271-4852d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31242164 | ||||||
| chr13:31242192 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4831G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242192 | |||||||
| chr13:31242285 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4738T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242285 | |||||||
| chr13:31242371 | G | T | 1 | a0001c0001t0004g0052 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.271-4652G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242371 | |||||||
| chr13:31242387 | A | G | 53 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0240 others(50): Show |
55 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.271-4636A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242387 | |||||||
| chr13:31242423 | G | A | 1 | a0001c0001t0015g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.271-4600G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242423 | |||||||
| chr13:31242429 | T | G | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4594T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242429 | |||||||
| chr13:31242473 | C | T | 54 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(51): Show |
55 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.271-4550C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242473 | |||||||
| chr13:31242632 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-4391A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242632 | |||||||
| chr13:31242754 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-4269C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242754 | |||||||
| chr13:31242787 | A | G | 1 | a0002c0002t0004g0025 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.271-4236A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242787 | |||||||
| chr13:31242811 | T | C | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(16): Show |
20 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.271-4212T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31242811 | |||||||
| chr13:31243026 | C | T | 3 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0042 |
3 | NA18953.hp2 NA18954.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.271-3997C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243026 | |||||||
| chr13:31243031 | G | A | 2 | a0001c0001t0007g0030 a0001c0001t0007g0114 |
2 | HG01175.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.271-3992G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243031 | |||||||
| chr13:31243108 | A | T | 56 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0057 others(53): Show |
57 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.271-3915A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243108 | |||||||
| chr13:31243320 | C | A | 2 | a0001c0013t0001g0259 a0002c0003t0021g0070 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-3703C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243320 | |||||||
| chr13:31243560 | A | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3463A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243560 | |||||||
| chr13:31243765 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3258G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31243765 | |||||||
| chr13:31244053 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2970C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244053 | |||||||
| chr13:31244219 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2804C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244219 | |||||||
| chr13:31244616 | G | A | 1 | a0001c0001t0005g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.271-2407G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244616 | |||||||
| chr13:31244747 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.271-2276A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244747 | |||||||
| chr13:31244847 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.271-2176G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244847 | |||||||
| chr13:31244904 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271-2119T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31244904 | |||||||
| chr13:31244963 | ATGT | A | 78 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(75): Show |
80 | HG00140.hp2 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-2055_271-2053d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31244963 | ||||||
| chr13:31245049 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.271-1974A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245049 | |||||||
| chr13:31245188 | T | C | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.271-1835T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245188 | |||||||
| chr13:31245230 | T | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-1793T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245230 | |||||||
| chr13:31245247 | A | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.271-1776A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245247 | |||||||
| chr13:31245254 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.271-1769C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245254 | |||||||
| chr13:31245306 | T | TTA | 5 | a0001c0001t0005g0252 a0002c0002t0003g0236 a0002c0002t0003g0243 others(2): Show |
5 | HG01358.hp1 HG01516.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1707_271-1706d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31245306 | ||||||
| chr13:31245403 | T | A | 1 | a0002c0002t0009g0209 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.271-1620T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245403 | |||||||
| chr13:31245486 | G | A | 2 | a0001c0013t0001g0259 a0002c0003t0021g0070 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-1537G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245486 | |||||||
| chr13:31245721 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.271-1302A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245721 | |||||||
| chr13:31245814 | C | A | 62 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(59): Show |
63 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.271-1209C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245814 | |||||||
| chr13:31245859 | A | G | 58 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(55): Show |
59 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.271-1164A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31245859 | |||||||
| chr13:31246015 | T | G | 20 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(17): Show |
21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-1008T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246015 | |||||||
| chr13:31246234 | A | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-789A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246234 | |||||||
| chr13:31246306 | A | G | 6 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0261 others(3): Show |
6 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-717A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246306 | |||||||
| chr13:31246533 | AAAAGT | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.271-482_271-478del others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246533 | ||||||
| chr13:31246667 | C | CT | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-355dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246667 | ||||||
| chr13:31246726 | G | A | 4 | a0001c0001t0001g0176 a0002c0002t0004g0170 a0002c0002t0004g0180 others(1): Show |
4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-297G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246726 | |||||||
| chr13:31246792 | A | G | 1 | a0001c0001t0004g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.271-231A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246792 | |||||||
| chr13:31246814 | A | G | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0004g0170 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-209A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246814 | |||||||
| chr13:31246881 | C | G | 2 | a0001c0013t0001g0259 a0002c0003t0021g0070 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-142C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246881 | |||||||
| chr13:31246937 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-86T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246937 | |||||||
| chr13:31246946 | C | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-77C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246946 | |||||||
| chr13:31246951 | C | CT | 127 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.271-57dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | ||||||
| chr13:31246951 | C | CTT | 5 | a0001c0001t0001g0176 a0001c0001t0001g0223 a0002c0002t0004g0170 others(2): Show |
5 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-58_271-57dupTT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | ||||||
| chr13:31246951 | C | G | 2 | a0002c0002t0009g0208 a0002c0002t0009g0210 |
2 | NA18997.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.271-72C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246951 | |||||||
| chr13:31246951 | CT | C | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.271-57delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr13 | 31246951 | ||||||
| chr13:31246956 | T | C | 60 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(57): Show |
61 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.271-67T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246956 | |||||||
| chr13:31246985 | C | T | 2 | a0001c0013t0001g0259 a0002c0003t0021g0070 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.271-38C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31246985 | |||||||
| chr13:31247011 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.271-12T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31247011 | |||||||
| chr13:31247015 | T | C | 1 | a0002c0010t0003g0012 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.271-8T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 4/14 | chr13 | 31247015 | |||||||
| chr13:31247103 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
splice_region_variant&intron_variant | LOW | c.347+4C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247103 | |||||||
| chr13:31247119 | C | G | 54 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.347+20C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247119 | |||||||
| chr13:31247194 | A | G | 20 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(17): Show |
21 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.347+95A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247194 | |||||||
| chr13:31247289 | C | CT | 18 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0005g0003 others(15): Show |
19 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.347+199dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr13 | 31247289 | ||||||
| chr13:31247313 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.347+214G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247313 | |||||||
| chr13:31247332 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.347+233A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247332 | |||||||
| chr13:31247368 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.347+269A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247368 | |||||||
| chr13:31247442 | T | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.347+343T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 5/14 | chr13 | 31247442 | |||||||
| chr13:31248100 | A | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+134A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248100 | |||||||
| chr13:31248170 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.459+204C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248170 | |||||||
| chr13:31248326 | A | T | 62 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(59): Show |
63 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.459+360A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248326 | |||||||
| chr13:31248404 | T | C | 1 | a0002c0002t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+438T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248404 | |||||||
| chr13:31248464 | G | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.459+498G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248464 | |||||||
| chr13:31248500 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.459+534A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248500 | |||||||
| chr13:31248530 | C | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.459+564C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248530 | |||||||
| chr13:31248645 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+679G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248645 | |||||||
| chr13:31248647 | G | A | 2 | a0001c0001t0004g0171 a0002c0002t0002g0233 |
2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.459+681G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248647 | |||||||
| chr13:31248886 | G | A | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+920G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31248886 | |||||||
| chr13:31249063 | G | T | 6 | a0002c0002t0001g0250 a0002c0002t0003g0096 a0002c0002t0003g0245 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+1097G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249063 | |||||||
| chr13:31249100 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+1134T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249100 | |||||||
| chr13:31249102 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0064 others(58): Show |
62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.459+1136A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249102 | |||||||
| chr13:31249418 | CTT | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+1454_459+1455d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31249418 | ||||||
| chr13:31249452 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+1486G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249452 | |||||||
| chr13:31249798 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+1832G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249798 | |||||||
| chr13:31249855 | A | G | 24 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(21): Show |
25 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+1889A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249855 | |||||||
| chr13:31249918 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0006g0059 a0001c0001t0022g0056 |
3 | NA18968.hp2 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.459+1952T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249918 | |||||||
| chr13:31249919 | G | A | 1 | a0001c0001t0004g0046 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.459+1953G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249919 | |||||||
| chr13:31249933 | G | A | 38 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(35): Show |
38 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+1967G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31249933 | |||||||
| chr13:31250237 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.459+2271A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250237 | |||||||
| chr13:31250247 | C | T | 1 | a0002c0002t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.459+2281C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250247 | |||||||
| chr13:31250278 | A | G | 1 | a0001c0001t0004g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.459+2312A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250278 | |||||||
| chr13:31250294 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+2328C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250294 | |||||||
| chr13:31250391 | C | T | 1 | a0002c0002t0002g0231 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.459+2425C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250391 | |||||||
| chr13:31250444 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+2478G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250444 | |||||||
| chr13:31250470 | T | C | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.459+2504T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250470 | |||||||
| chr13:31250513 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+2547C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250513 | |||||||
| chr13:31250581 | A | G | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.459+2615A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250581 | |||||||
| chr13:31250669 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.459+2703C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250669 | |||||||
| chr13:31250685 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.459+2719G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250685 | |||||||
| chr13:31250711 | G | A | 25 | a0001c0001t0001g0190 a0001c0001t0004g0171 a0001c0001t0005g0003 others(22): Show |
26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+2745G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250711 | |||||||
| chr13:31250847 | A | G | 24 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(21): Show |
25 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+2881A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250847 | |||||||
| chr13:31250950 | C | G | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+2984C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31250950 | |||||||
| chr13:31251020 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.459+3054A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251020 | |||||||
| chr13:31251033 | T | G | 71 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(68): Show |
72 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.459+3067T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251033 | |||||||
| chr13:31251049 | C | G | 2 | a0002c0002t0002g0139 a0002c0002t0002g0232 |
2 | HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.459+3083C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251049 | |||||||
| chr13:31251085 | G | T | 2 | a0001c0013t0001g0259 a0002c0003t0021g0070 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.459+3119G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251085 | |||||||
| chr13:31251146 | TAAAC | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3182_459+3185d others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31251146 | ||||||
| chr13:31251214 | C | G | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459+3248C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251214 | |||||||
| chr13:31251264 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+3298T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251264 | |||||||
| chr13:31251446 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.459+3480G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251446 | |||||||
| chr13:31251447 | T | C | 1 | a0002c0002t0002g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.459+3481T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251447 | |||||||
| chr13:31251670 | GAA | G | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.459+3705_459+3706d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251670 | |||||||
| chr13:31251807 | C | T | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.459+3841C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251807 | |||||||
| chr13:31251964 | GA | G | 25 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(22): Show |
26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+3999delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31251964 | |||||||
| chr13:31252257 | C | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+4291C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252257 | |||||||
| chr13:31252286 | G | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+4320G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252286 | |||||||
| chr13:31252287 | A | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.459+4321A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252287 | |||||||
| chr13:31252362 | A | G | 1 | a0002c0002t0002g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.459+4396A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252362 | |||||||
| chr13:31252400 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.459+4434T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252400 | |||||||
| chr13:31252404 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+4438G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252404 | |||||||
| chr13:31252423 | C | A | 1 | a0001c0001t0005g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.459+4457C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252423 | |||||||
| chr13:31252494 | C | G | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.459+4528C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252494 | |||||||
| chr13:31252543 | CA | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+4586delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31252543 | ||||||
| chr13:31252555 | G | A | 1 | a0002c0002t0008g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.459+4589G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252555 | |||||||
| chr13:31252594 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459+4628A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252594 | |||||||
| chr13:31252698 | G | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4732G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252698 | |||||||
| chr13:31252701 | C | A | 1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4735C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252701 | |||||||
| chr13:31252702 | C | G | 1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4736C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252702 | |||||||
| chr13:31252703 | C | A | 1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4737C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252703 | |||||||
| chr13:31252704 | A | C | 1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4738A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252704 | |||||||
| chr13:31252705 | G | C | 1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4739G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252705 | |||||||
| chr13:31252797 | G | C | 7 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0261 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+4831G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31252797 | |||||||
| chr13:31253070 | G | A | 1 | a0002c0002t0006g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.459+5104G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253070 | |||||||
| chr13:31253130 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459+5164C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253130 | |||||||
| chr13:31253131 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+5165G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253131 | |||||||
| chr13:31253373 | C | T | 25 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(22): Show |
26 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.459+5407C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253373 | |||||||
| chr13:31253434 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.459+5468G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253434 | |||||||
| chr13:31253466 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459+5500G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253466 | |||||||
| chr13:31253467 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.459+5501C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253467 | |||||||
| chr13:31253485 | C | T | 1 | a0002c0002t0003g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.459+5519C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253485 | |||||||
| chr13:31253512 | G | T | 4 | a0001c0001t0001g0176 a0002c0002t0004g0170 a0002c0002t0004g0180 others(1): Show |
4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+5546G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253512 | |||||||
| chr13:31253542 | T | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.459+5576T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253542 | |||||||
| chr13:31253544 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.459+5578T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253544 | |||||||
| chr13:31253595 | C | CA | 34 | a0001c0001t0001g0024 a0001c0001t0001g0190 a0001c0001t0001g0191 others(31): Show |
35 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.459+5655dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAA | 17 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0005g0196 others(14): Show |
17 | HG00741.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+5654_459+5655d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(8): Show |
1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.459+5641_459+5655d others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(9): Show |
1 | a0002c0002t0012g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.459+5640_459+5655d others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0176 |
2 | HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.459+5639_459+5655d others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(11): Show |
1 | a0002c0002t0004g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.459+5638_459+5655d others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(14): Show |
1 | a0002c0002t0004g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+5635_459+5655d others(23): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | C | CAAAAAAA others(16): Show |
2 | a0002c0002t0012g0173 a0002c0011t0004g0179 |
2 | HG01106.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.459+5633_459+5655d others(25): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | CAA | C | 54 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(51): Show |
55 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.459+5654_459+5655d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253595 | CAAA | C | 6 | a0002c0002t0002g0264 a0002c0002t0003g0080 a0002c0002t0003g0239 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+5653_459+5655d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253595 | ||||||
| chr13:31253613 | A | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+5647A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253613 | |||||||
| chr13:31253618 | A | AAAAAACA others(3): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0235 |
2 | HG02300.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+5655_459+5656i others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | ||||||
| chr13:31253618 | A | AAAAACAA others(2): Show |
28 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0090 others(25): Show |
28 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+5655_459+5656i others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | ||||||
| chr13:31253618 | A | AAAACAAA others(1): Show |
86 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0057 others(83): Show |
88 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.459+5656_459+5657i others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31253618 | ||||||
| chr13:31253618 | A | C | 5 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+5652A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253618 | |||||||
| chr13:31253640 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.459+5674G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253640 | |||||||
| chr13:31253911 | A | G | 1 | a0001c0001t0015g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.459+5945A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253911 | |||||||
| chr13:31253986 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6020G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31253986 | |||||||
| chr13:31254059 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6093C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254059 | |||||||
| chr13:31254142 | A | G | 6 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0261 others(3): Show |
6 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+6176A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254142 | |||||||
| chr13:31254230 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.459+6264G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254230 | |||||||
| chr13:31254292 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.459+6326T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254292 | |||||||
| chr13:31254327 | A | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6361A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254327 | |||||||
| chr13:31254364 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+6398G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254364 | |||||||
| chr13:31254372 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.459+6406T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254372 | |||||||
| chr13:31254617 | T | C | 1 | a0004c0004t0004g0203 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.460-6329T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254617 | |||||||
| chr13:31254837 | G | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-6109G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254837 | |||||||
| chr13:31254847 | T | G | 1 | a0002c0002t0003g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.460-6099T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254847 | |||||||
| chr13:31254910 | G | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-6036G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254910 | |||||||
| chr13:31254968 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0105 |
3 | NA18950.hp2 NA18952.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.460-5978C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254968 | |||||||
| chr13:31254989 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-5957A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31254989 | |||||||
| chr13:31255023 | CA | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.460-5920delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255023 | ||||||
| chr13:31255029 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.460-5917C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255029 | |||||||
| chr13:31255037 | C | CA | 26 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(23): Show |
26 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-5892dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255037 | ||||||
| chr13:31255037 | CA | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.460-5892delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31255037 | ||||||
| chr13:31255051 | A | G | 1 | a0001c0001t0004g0060 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.460-5895A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255051 | |||||||
| chr13:31255054 | A | G | 1 | a0002c0002t0003g0004 | 2 | HG01123.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.460-5892A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255054 | |||||||
| chr13:31255450 | A | G | 2 | a0001c0001t0014g0184 a0002c0002t0003g0092 |
2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.460-5496A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255450 | |||||||
| chr13:31255505 | G | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-5441G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255505 | |||||||
| chr13:31255579 | G | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-5367G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255579 | |||||||
| chr13:31255620 | A | G | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460-5326A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255620 | |||||||
| chr13:31255669 | C | G | 2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.460-5277C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255669 | |||||||
| chr13:31255841 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.460-5105T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255841 | |||||||
| chr13:31255874 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.460-5072A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255874 | |||||||
| chr13:31255899 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-5047C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31255899 | |||||||
| chr13:31256096 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0107 others(1): Show |
4 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-4850G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256096 | |||||||
| chr13:31256173 | T | C | 1 | a0001c0013t0001g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.460-4773T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256173 | |||||||
| chr13:31256227 | A | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0238 |
2 | HG01496.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.460-4719A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256227 | |||||||
| chr13:31256278 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-4668A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256278 | |||||||
| chr13:31256497 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-4449C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256497 | |||||||
| chr13:31256544 | T | C | 1 | a0002c0002t0003g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-4402T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256544 | |||||||
| chr13:31256728 | C | T | 3 | a0001c0001t0004g0171 a0001c0001t0004g0215 a0002c0002t0002g0233 |
3 | HG01891.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.460-4218C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256728 | |||||||
| chr13:31256755 | C | G | 3 | a0001c0001t0001g0172 a0002c0002t0012g0173 a0002c0002t0012g0174 |
3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.460-4191C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256755 | |||||||
| chr13:31256911 | TA | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.460-4023delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31256911 | ||||||
| chr13:31256955 | A | G | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-3991A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31256955 | |||||||
| chr13:31257112 | A | G | 1 | a0002c0002t0002g0142 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.460-3834A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257112 | |||||||
| chr13:31257302 | A | C | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-3644A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257302 | |||||||
| chr13:31257380 | G | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.460-3566G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257380 | |||||||
| chr13:31257410 | A | G | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.460-3536A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257410 | |||||||
| chr13:31257503 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3443C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257503 | |||||||
| chr13:31257917 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-3029A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257917 | |||||||
| chr13:31257940 | A | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.460-3006A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257940 | |||||||
| chr13:31257994 | T | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2952T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31257994 | |||||||
| chr13:31258000 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2946G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258000 | |||||||
| chr13:31258016 | C | G | 1 | a0001c0001t0007g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.460-2930C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258016 | |||||||
| chr13:31258056 | A | G | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2890A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258056 | |||||||
| chr13:31258282 | C | G | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.460-2664C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258282 | |||||||
| chr13:31258292 | T | C | 35 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(32): Show |
35 | HG00609.hp1 HG00621.hp1 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.460-2654T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258292 | |||||||
| chr13:31258388 | G | A | 27 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(24): Show |
28 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.460-2558G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258388 | |||||||
| chr13:31258445 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2501C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258445 | |||||||
| chr13:31258446 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.460-2500G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258446 | |||||||
| chr13:31258594 | A | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-2352A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31258594 | |||||||
| chr13:31259133 | G | A | 3 | a0001c0001t0001g0172 a0002c0002t0012g0173 a0002c0002t0012g0174 |
3 | HG02630.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.460-1813G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259133 | |||||||
| chr13:31259136 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-1810C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259136 | |||||||
| chr13:31259284 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-1662G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259284 | |||||||
| chr13:31259335 | G | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.460-1611G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259335 | |||||||
| chr13:31259352 | TTCC | T | 5 | a0002c0002t0003g0011 a0002c0002t0003g0034 a0002c0002t0003g0035 others(2): Show |
5 | HG01243.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1592_460-1590d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31259352 | ||||||
| chr13:31259396 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.460-1550G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259396 | |||||||
| chr13:31259441 | C | G | 57 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(54): Show |
58 | HG00609.hp1 HG00621.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.460-1505C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259441 | |||||||
| chr13:31259498 | G | T | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.460-1448G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259498 | |||||||
| chr13:31259540 | CT | C | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.460-1399delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr13 | 31259540 | ||||||
| chr13:31259587 | A | G | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1359A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259587 | |||||||
| chr13:31259835 | T | A | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1111T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259835 | |||||||
| chr13:31259850 | T | C | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.460-1096T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31259850 | |||||||
| chr13:31260150 | A | C | 1 | a0002c0002t0009g0016 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.460-796A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260150 | |||||||
| chr13:31260291 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.460-655T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260291 | |||||||
| chr13:31260358 | T | C | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-588T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260358 | |||||||
| chr13:31260445 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.460-501G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260445 | |||||||
| chr13:31260634 | G | T | 1 | a0002c0002t0002g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-312G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260634 | |||||||
| chr13:31260874 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0235 |
3 | HG03834.hp1 HG03927.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.460-72T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 6/14 | chr13 | 31260874 | |||||||
| chr13:31261125 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.596+43G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261125 | |||||||
| chr13:31261127 | A | G | 1 | a0002c0002t0002g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.596+45A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261127 | |||||||
| chr13:31261131 | AC | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+50delC | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261131 | |||||||
| chr13:31261163 | A | C | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.596+81A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261163 | |||||||
| chr13:31261214 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.596+132C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261214 | |||||||
| chr13:31261238 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.596+156G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261238 | |||||||
| chr13:31261254 | G | A | 1 | a0001c0001t0004g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.596+172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261254 | |||||||
| chr13:31261449 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.596+367A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261449 | |||||||
| chr13:31261471 | A | G | 27 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(24): Show |
28 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.596+389A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261471 | |||||||
| chr13:31261647 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.596+565A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31261647 | |||||||
| chr13:31262096 | C | T | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.596+1014C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262096 | |||||||
| chr13:31262130 | G | A | 1 | a0002c0002t0002g0018 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.596+1048G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262130 | |||||||
| chr13:31262165 | G | A | 56 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(53): Show |
57 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.596+1083G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262165 | |||||||
| chr13:31262230 | G | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.596+1148G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262230 | |||||||
| chr13:31262341 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1259C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262341 | |||||||
| chr13:31262424 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.596+1342C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262424 | |||||||
| chr13:31262526 | C | T | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1444C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262526 | |||||||
| chr13:31262599 | CTT | C | 29 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(26): Show |
29 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.596+1519_596+1520d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31262599 | ||||||
| chr13:31262631 | T | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.596+1549T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262631 | |||||||
| chr13:31262633 | C | G | 72 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(69): Show |
73 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.596+1551C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262633 | |||||||
| chr13:31262644 | A | T | 57 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+1562A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31262644 | |||||||
| chr13:31263064 | C | T | 3 | a0001c0001t0004g0171 a0001c0001t0004g0215 a0002c0002t0002g0233 |
3 | HG01891.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.596+1982C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263064 | |||||||
| chr13:31263101 | G | A | 5 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0003g0257 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.596+2019G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263101 | |||||||
| chr13:31263229 | C | T | 3 | a0002c0002t0002g0089 a0002c0002t0002g0097 a0002c0002t0002g0213 |
3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.596+2147C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263229 | |||||||
| chr13:31263283 | C | T | 1 | a0001c0001t0004g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.596+2201C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263283 | |||||||
| chr13:31263411 | A | G | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+2329A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263411 | |||||||
| chr13:31263419 | G | A | 57 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.596+2337G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263419 | |||||||
| chr13:31263436 | T | C | 3 | a0002c0002t0002g0127 a0002c0002t0002g0135 a0002c0002t0002g0137 |
3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.596+2354T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263436 | |||||||
| chr13:31263832 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+2750G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31263832 | |||||||
| chr13:31264030 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0048 others(19): Show |
22 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.596+2948G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264030 | |||||||
| chr13:31264162 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.596+3080C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264162 | |||||||
| chr13:31264319 | C | T | 1 | a0001c0013t0001g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.596+3237C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264319 | |||||||
| chr13:31264350 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.596+3268C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264350 | |||||||
| chr13:31264365 | C | T | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+3283C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264365 | |||||||
| chr13:31264379 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.596+3297T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264379 | |||||||
| chr13:31264423 | G | A | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.596+3341G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264423 | |||||||
| chr13:31264505 | A | G | 6 | a0002c0002t0001g0250 a0002c0002t0003g0096 a0002c0002t0003g0245 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.596+3423A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264505 | |||||||
| chr13:31264551 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.596+3469A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264551 | |||||||
| chr13:31264590 | A | G | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.596+3508A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264590 | |||||||
| chr13:31264691 | T | C | 1 | a0003c0005t0001g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.596+3609T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264691 | |||||||
| chr13:31264731 | C | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.596+3649C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264731 | |||||||
| chr13:31264755 | C | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0004g0170 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+3673C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264755 | |||||||
| chr13:31264827 | A | T | 1 | a0002c0010t0003g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.596+3745A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264827 | |||||||
| chr13:31264836 | C | A | 4 | a0001c0001t0001g0176 a0002c0002t0004g0170 a0002c0002t0004g0180 others(1): Show |
4 | HG01106.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+3754C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264836 | |||||||
| chr13:31264928 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.596+3846C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31264928 | |||||||
| chr13:31265137 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.596+4055G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265137 | |||||||
| chr13:31265151 | A | C | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0002c0002t0004g0170 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.597-4063A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265151 | |||||||
| chr13:31265165 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0166 a0001c0001t0025g0258 |
3 | HG02056.hp2 HG02896.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.597-4049C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265165 | |||||||
| chr13:31265293 | C | A | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0004g0171 others(18): Show |
22 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.597-3921C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265293 | |||||||
| chr13:31265556 | C | T | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.597-3658C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31265556 | |||||||
| chr13:31265832 | TGGAAGTG others(19): Show |
T | 1 | a0001c0001t0004g0052 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.597-3361_597-3336d others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31265832 | ||||||
| chr13:31266053 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.597-3161A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266053 | |||||||
| chr13:31266091 | G | A | 2 | a0002c0002t0003g0238 a0002c0003t0021g0070 |
2 | HG01496.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.597-3123G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266091 | |||||||
| chr13:31266123 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0048 |
2 | HG00741.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.597-3091G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266123 | |||||||
| chr13:31266127 | A | C | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.597-3087A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266127 | |||||||
| chr13:31266155 | A | G | 1 | a0002c0002t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.597-3059A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266155 | |||||||
| chr13:31266172 | G | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.597-3042G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266172 | |||||||
| chr13:31266182 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18950.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.597-3032T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266182 | |||||||
| chr13:31266199 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.597-3015C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266199 | |||||||
| chr13:31266216 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0149 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.597-2998C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266216 | |||||||
| chr13:31266219 | C | A | 1 | a0001c0001t0007g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.597-2995C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266219 | |||||||
| chr13:31266249 | T | C | 4 | a0002c0003t0003g0028 a0002c0003t0003g0226 a0005c0006t0003g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-2965T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266249 | |||||||
| chr13:31266264 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-2950G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266264 | |||||||
| chr13:31266270 | C | T | 1 | a0001c0001t0010g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.597-2944C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266270 | |||||||
| chr13:31266324 | G | A | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.597-2890G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266324 | |||||||
| chr13:31266325 | G | A | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.597-2889G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266325 | |||||||
| chr13:31266436 | A | G | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.597-2778A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266436 | |||||||
| chr13:31266568 | A | T | 2 | a0001c0001t0004g0215 a0002c0002t0002g0233 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.597-2646A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266568 | |||||||
| chr13:31266569 | C | G | 1 | a0001c0013t0001g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.597-2645C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266569 | |||||||
| chr13:31266719 | A | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.597-2495A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266719 | |||||||
| chr13:31266792 | A | G | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.597-2422A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31266792 | |||||||
| chr13:31267190 | C | T | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597-2024C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267190 | |||||||
| chr13:31267217 | T | C | 2 | a0002c0002t0003g0227 a0002c0002t0018g0251 |
2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.597-1997T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267217 | |||||||
| chr13:31267252 | G | C | 1 | a0007c0012t0004g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.597-1962G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267252 | |||||||
| chr13:31267315 | G | A | 22 | a0001c0013t0001g0259 a0002c0002t0002g0031 a0002c0002t0002g0032 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.597-1899G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267315 | |||||||
| chr13:31267340 | C | A | 3 | a0002c0002t0002g0127 a0002c0002t0002g0135 a0002c0002t0002g0137 |
3 | NA18998.hp1 NA19082.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.597-1874C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267340 | |||||||
| chr13:31267757 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.597-1457C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267757 | |||||||
| chr13:31267768 | C | T | 15 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(12): Show |
15 | HG00639.hp1 HG01243.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-1446C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31267768 | |||||||
| chr13:31267851 | C | CT | 5 | a0002c0002t0002g0264 a0002c0002t0003g0248 a0002c0002t0011g0007 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.597-1350dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31267851 | ||||||
| chr13:31268009 | A | T | 71 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(68): Show |
73 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.597-1205A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268009 | |||||||
| chr13:31268046 | A | G | 1 | a0002c0002t0002g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.597-1168A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268046 | |||||||
| chr13:31268354 | T | C | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.597-860T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268354 | |||||||
| chr13:31268533 | T | C | 1 | a0001c0001t0007g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.597-681T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268533 | |||||||
| chr13:31268633 | C | T | 4 | a0002c0003t0003g0028 a0002c0003t0003g0226 a0005c0006t0003g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-581C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268633 | |||||||
| chr13:31268683 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.597-531T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268683 | |||||||
| chr13:31268966 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.597-248T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31268966 | |||||||
| chr13:31269050 | C | T | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.597-164C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | chr13 | 31269050 | |||||||
| chr13:31269183 | TA | T | 67 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(64): Show |
68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.597-23delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr13 | 31269183 | ||||||
| chr13:31269360 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+83A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269360 | |||||||
| chr13:31269461 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(148): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.660+184A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269461 | |||||||
| chr13:31269489 | A | G | 21 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.660+212A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269489 | |||||||
| chr13:31269527 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.660+250A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269527 | |||||||
| chr13:31269601 | C | T | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.660+324C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269601 | |||||||
| chr13:31269602 | G | A | 67 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(64): Show |
68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.660+325G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269602 | |||||||
| chr13:31269642 | CG | C | 89 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(86): Show |
90 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.660+366delG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269642 | |||||||
| chr13:31269643 | G | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(154): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.660+366G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269643 | |||||||
| chr13:31269643 | G | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+366G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269643 | |||||||
| chr13:31269645 | C | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(147): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.660+368C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269645 | |||||||
| chr13:31269650 | T | A | 13 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(10): Show |
13 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.660+373T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269650 | |||||||
| chr13:31269650 | T | C | 19 | a0002c0002t0003g0257 a0002c0002t0004g0170 a0002c0002t0004g0175 others(16): Show |
19 | HG01106.hp2 HG01243.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.660+373T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269650 | |||||||
| chr13:31269755 | C | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.660+478C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269755 | |||||||
| chr13:31269772 | G | T | 2 | a0002c0002t0003g0227 a0002c0002t0018g0251 |
2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.660+495G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269772 | |||||||
| chr13:31269810 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.660+533C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269810 | |||||||
| chr13:31269934 | C | G | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.660+657C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269934 | |||||||
| chr13:31269951 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.660+674C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269951 | |||||||
| chr13:31269983 | C | T | 67 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(64): Show |
68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.660+706C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31269983 | |||||||
| chr13:31270283 | A | T | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.660+1006A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270283 | |||||||
| chr13:31270346 | T | C | 1 | a0002c0002t0004g0025 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.660+1069T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270346 | |||||||
| chr13:31270444 | A | G | 2 | a0002c0002t0012g0173 a0002c0002t0012g0174 |
2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.660+1167A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270444 | |||||||
| chr13:31270618 | G | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(223): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.660+1341G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270618 | |||||||
| chr13:31270663 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.660+1386G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31270663 | |||||||
| chr13:31270934 | AAG | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+1662_660+1663d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31270934 | ||||||
| chr13:31271237 | T | C | 4 | a0002c0003t0003g0028 a0002c0003t0003g0226 a0005c0006t0003g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1960T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271237 | |||||||
| chr13:31271265 | A | T | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+1988A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271265 | |||||||
| chr13:31271331 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.660+2054C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271331 | |||||||
| chr13:31271669 | C | A | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.660+2392C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271669 | |||||||
| chr13:31271751 | T | G | 1 | a0002c0002t0002g0135 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.660+2474T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271751 | |||||||
| chr13:31271879 | A | G | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+2602A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271879 | |||||||
| chr13:31271983 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.661-2526T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271983 | |||||||
| chr13:31271992 | T | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-2517T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31271992 | |||||||
| chr13:31272218 | C | CT | 159 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(156): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.661-2276dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31272218 | ||||||
| chr13:31272316 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.661-2193A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272316 | |||||||
| chr13:31272363 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.661-2146C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272363 | |||||||
| chr13:31272744 | CTTG | C | 2 | a0001c0001t0004g0040 a0001c0001t0004g0063 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.661-1759_661-1757d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31272744 | ||||||
| chr13:31272836 | T | A | 1 | a0002c0002t0003g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.661-1673T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272836 | |||||||
| chr13:31272903 | T | C | 6 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(3): Show |
6 | HG01106.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-1606T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31272903 | |||||||
| chr13:31273027 | A | G | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.661-1482A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273027 | |||||||
| chr13:31273089 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.661-1420T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273089 | |||||||
| chr13:31273094 | CTTTGTTT others(7): Show |
C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-1414_661-1401d others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273094 | |||||||
| chr13:31273176 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1333C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273176 | |||||||
| chr13:31273187 | C | T | 74 | a0001c0001t0001g0071 a0001c0001t0001g0119 a0001c0001t0001g0121 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.661-1322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273187 | |||||||
| chr13:31273205 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.661-1304C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273205 | |||||||
| chr13:31273240 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.661-1269G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273240 | |||||||
| chr13:31273273 | T | C | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.661-1236T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273273 | |||||||
| chr13:31273374 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.661-1135G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273374 | |||||||
| chr13:31273431 | A | T | 1 | a0002c0002t0002g0165 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.661-1078A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273431 | |||||||
| chr13:31273502 | AATTTT | A | 75 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(72): Show |
76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.661-1004_661-1000d others(7): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr13 | 31273502 | ||||||
| chr13:31273610 | A | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-899A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273610 | |||||||
| chr13:31273612 | T | A | 2 | a0002c0002t0003g0027 a0002c0002t0017g0021 |
2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.661-897T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273612 | |||||||
| chr13:31273751 | T | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0124 |
2 | NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.661-758T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273751 | |||||||
| chr13:31273774 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.661-735T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273774 | |||||||
| chr13:31273831 | T | A | 1 | a0001c0001t0007g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.661-678T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273831 | |||||||
| chr13:31273959 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.661-550A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31273959 | |||||||
| chr13:31274246 | A | G | 19 | a0002c0002t0003g0004 a0002c0002t0003g0014 a0002c0002t0003g0069 others(16): Show |
20 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.661-263A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274246 | |||||||
| chr13:31274318 | G | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.661-191G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274318 | |||||||
| chr13:31274398 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.661-111G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 8/14 | chr13 | 31274398 | |||||||
| chr13:31274686 | A | G | 72 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(69): Show |
73 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.780+58A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31274686 | |||||||
| chr13:31275216 | A | G | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.780+588A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275216 | |||||||
| chr13:31275250 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+622T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275250 | |||||||
| chr13:31275268 | A | G | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.780+640A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275268 | |||||||
| chr13:31275313 | C | T | 1 | a0002c0002t0003g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.780+685C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275313 | |||||||
| chr13:31275394 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.780+766C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275394 | |||||||
| chr13:31275403 | G | T | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.780+775G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275403 | |||||||
| chr13:31275434 | A | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.780+806A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275434 | |||||||
| chr13:31275675 | A | G | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.781-1027A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275675 | |||||||
| chr13:31275713 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(135): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.781-989C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275713 | |||||||
| chr13:31275852 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781-850G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31275852 | |||||||
| chr13:31276148 | C | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.781-554C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276148 | |||||||
| chr13:31276197 | G | T | 20 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(17): Show |
20 | HG00639.hp1 HG01243.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.781-505G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276197 | |||||||
| chr13:31276203 | C | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.781-499C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276203 | |||||||
| chr13:31276225 | G | A | 1 | a0002c0002t0004g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.781-477G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276225 | |||||||
| chr13:31276577 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.781-125G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276577 | |||||||
| chr13:31276580 | G | A | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.781-122G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | chr13 | 31276580 | |||||||
| chr13:31276666 | C | CACAT | 13 | a0002c0002t0003g0004 a0002c0002t0003g0014 a0002c0002t0003g0069 others(10): Show |
14 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.781-34_781-31dupCA others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr13 | 31276666 | ||||||
| chr13:31276852 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.850+81G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31276852 | |||||||
| chr13:31276922 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.850+151A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31276922 | |||||||
| chr13:31277062 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.850+291G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277062 | |||||||
| chr13:31277171 | G | T | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.850+400G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277171 | |||||||
| chr13:31277190 | A | G | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850+419A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277190 | |||||||
| chr13:31277218 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.850+447T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277218 | |||||||
| chr13:31277389 | TA | T | 19 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(16): Show |
19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+629delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31277389 | ||||||
| chr13:31277751 | C | A | 4 | a0001c0001t0006g0058 a0001c0001t0006g0059 a0001c0001t0006g0156 others(1): Show |
4 | HG00558.hp1 NA18983.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.850+980C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277751 | |||||||
| chr13:31277824 | G | T | 1 | a0002c0002t0020g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850+1053G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277824 | |||||||
| chr13:31277997 | T | G | 1 | a0002c0002t0003g0255 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.850+1226T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31277997 | |||||||
| chr13:31278056 | C | T | 7 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(4): Show |
7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1285C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278056 | |||||||
| chr13:31278088 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.850+1317G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278088 | |||||||
| chr13:31278139 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(135): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.850+1368A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278139 | |||||||
| chr13:31278248 | T | C | 75 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(72): Show |
76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.850+1477T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278248 | |||||||
| chr13:31278422 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.850+1651A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278422 | |||||||
| chr13:31278426 | C | T | 1 | a0002c0002t0003g0257 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.850+1655C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278426 | |||||||
| chr13:31278760 | A | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(146): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.850+1989A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31278760 | |||||||
| chr13:31279117 | T | C | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.850+2346T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279117 | |||||||
| chr13:31279146 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0107 others(2): Show |
5 | HG01256.hp1 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+2375C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279146 | |||||||
| chr13:31279244 | A | G | 1 | a0002c0002t0003g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850+2473A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279244 | |||||||
| chr13:31279264 | C | G | 1 | a0002c0002t0003g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850+2493C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279264 | |||||||
| chr13:31279493 | G | A | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+2722G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279493 | |||||||
| chr13:31279504 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.850+2733A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279504 | |||||||
| chr13:31279543 | C | T | 1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.850+2772C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279543 | |||||||
| chr13:31279582 | G | A | 4 | a0002c0002t0002g0264 a0002c0002t0011g0007 a0002c0002t0011g0008 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.850+2811G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279582 | |||||||
| chr13:31279620 | G | A | 7 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(4): Show |
7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+2849G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279620 | |||||||
| chr13:31279697 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.850+2926G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279697 | |||||||
| chr13:31279811 | C | G | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.850+3040C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279811 | |||||||
| chr13:31279811 | C | T | 2 | a0002c0002t0002g0084 a0002c0002t0002g0112 |
2 | HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.850+3040C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279811 | |||||||
| chr13:31279845 | C | T | 1 | a0002c0002t0002g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.850+3074C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279845 | |||||||
| chr13:31279858 | C | T | 1 | a0002c0002t0002g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850+3087C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279858 | |||||||
| chr13:31279985 | A | G | 2 | a0001c0001t0014g0184 a0002c0002t0002g0233 |
2 | HG01255.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.850+3214A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31279985 | |||||||
| chr13:31280051 | C | T | 1 | a0001c0001t0004g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.850+3280C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280051 | |||||||
| chr13:31280183 | A | G | 1 | a0002c0002t0011g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850+3412A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280183 | |||||||
| chr13:31280357 | T | G | 19 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(16): Show |
19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+3586T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280357 | |||||||
| chr13:31280360 | G | A | 1 | a0002c0003t0002g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.850+3589G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280360 | |||||||
| chr13:31280380 | C | T | 1 | a0002c0002t0002g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850+3609C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280380 | |||||||
| chr13:31280480 | G | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.850+3709G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280480 | |||||||
| chr13:31280556 | G | A | 69 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(66): Show |
70 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.850+3785G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280556 | |||||||
| chr13:31280607 | G | A | 19 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(16): Show |
19 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850+3836G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280607 | |||||||
| chr13:31280922 | C | T | 1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.851-3726C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31280922 | |||||||
| chr13:31281119 | G | A | 2 | a0002c0002t0003g0241 a0002c0002t0003g0242 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.851-3529G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281119 | |||||||
| chr13:31281126 | C | A | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.851-3522C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281126 | |||||||
| chr13:31281209 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.851-3439G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281209 | |||||||
| chr13:31281755 | C | A | 1 | a0002c0002t0020g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.851-2893C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31281755 | |||||||
| chr13:31282019 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.851-2629C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282019 | |||||||
| chr13:31282378 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-2270G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282378 | |||||||
| chr13:31282406 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.851-2242G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282406 | |||||||
| chr13:31282411 | G | A | 69 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(66): Show |
70 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.851-2237G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282411 | |||||||
| chr13:31282415 | G | A | 1 | a0001c0001t0006g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.851-2233G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282415 | |||||||
| chr13:31282456 | G | A | 2 | a0001c0001t0004g0046 a0001c0001t0004g0052 |
2 | NA18963.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.851-2192G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282456 | |||||||
| chr13:31282503 | G | A | 1 | a0001c0001t0007g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.851-2145G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282503 | |||||||
| chr13:31282511 | G | A | 7 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(4): Show |
7 | HG02015.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-2137G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282511 | |||||||
| chr13:31282515 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.851-2133G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282515 | |||||||
| chr13:31282617 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-2031G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282617 | |||||||
| chr13:31282629 | G | A | 1 | a0002c0002t0008g0099 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.851-2019G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282629 | |||||||
| chr13:31282649 | C | CA | 146 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.851-1982dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | ||||||
| chr13:31282649 | C | CAA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0166 others(3): Show |
6 | HG02055.hp2 HG02056.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-1983_851-1982d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | ||||||
| chr13:31282649 | C | CAAA | 7 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0218 others(4): Show |
7 | HG00639.hp1 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.851-1984_851-1982d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | ||||||
| chr13:31282649 | CA | C | 74 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.851-1982delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31282649 | ||||||
| chr13:31282941 | G | A | 7 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(4): Show |
7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-1707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31282941 | |||||||
| chr13:31283138 | G | C | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.851-1510G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283138 | |||||||
| chr13:31283282 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-1366C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283282 | |||||||
| chr13:31283288 | G | A | 75 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(72): Show |
76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.851-1360G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283288 | |||||||
| chr13:31283293 | G | A | 1 | a0001c0001t0014g0038 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.851-1355G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283293 | |||||||
| chr13:31283597 | G | GT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(161): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.851-1044dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr13 | 31283597 | ||||||
| chr13:31283604 | T | TTA | 73 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(70): Show |
74 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.851-1044_851-1043i others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283604 | |||||||
| chr13:31283657 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.851-991A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283657 | |||||||
| chr13:31283723 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.851-925T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283723 | |||||||
| chr13:31283747 | T | A | 1 | a0002c0002t0003g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.851-901T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283747 | |||||||
| chr13:31283786 | T | C | 1 | a0003c0005t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.851-862T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283786 | |||||||
| chr13:31283837 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.851-811C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31283837 | |||||||
| chr13:31284099 | A | G | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.851-549A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284099 | |||||||
| chr13:31284205 | G | A | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.851-443G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284205 | |||||||
| chr13:31284290 | C | T | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.851-358C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284290 | |||||||
| chr13:31284320 | G | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0057 others(13): Show |
17 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.851-328G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284320 | |||||||
| chr13:31284348 | C | T | 1 | a0002c0002t0003g0092 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.851-300C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 10/14 | chr13 | 31284348 | |||||||
| chr13:31284902 | T | A | 75 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(72): Show |
76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.964+141T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31284902 | |||||||
| chr13:31285241 | G | C | 3 | a0001c0001t0007g0022 a0002c0002t0003g0027 a0002c0002t0017g0021 |
3 | HG00738.hp1 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.964+480G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285241 | |||||||
| chr13:31285358 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+597G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285358 | |||||||
| chr13:31285604 | T | TA | 11 | a0002c0002t0002g0089 a0002c0002t0002g0097 a0002c0002t0002g0112 others(8): Show |
11 | HG01106.hp2 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+869dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | ||||||
| chr13:31285604 | TA | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(134): Show |
140 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.964+869delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | ||||||
| chr13:31285604 | TAAA | T | 6 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(3): Show |
6 | HG02015.hp1 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+867_964+869del others(3): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | ||||||
| chr13:31285604 | TAAAAA | T | 61 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(58): Show |
62 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.964+865_964+869del others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | ||||||
| chr13:31285604 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.964+860_964+869del others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31285604 | ||||||
| chr13:31285625 | A | G | 1 | a0002c0002t0002g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.964+864A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285625 | |||||||
| chr13:31285695 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.964+934C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285695 | |||||||
| chr13:31285695 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.964+934C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285695 | |||||||
| chr13:31285799 | A | G | 1 | a0002c0002t0003g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.965-921A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285799 | |||||||
| chr13:31285810 | C | T | 1 | a0002c0002t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.965-910C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285810 | |||||||
| chr13:31285847 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.965-873A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285847 | |||||||
| chr13:31285850 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.965-870C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31285850 | |||||||
| chr13:31286121 | A | G | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.965-599A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286121 | |||||||
| chr13:31286144 | A | G | 1 | a0002c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.965-576A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286144 | |||||||
| chr13:31286262 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-458C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286262 | |||||||
| chr13:31286287 | C | T | 1 | a0001c0001t0006g0037 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.965-433C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286287 | |||||||
| chr13:31286330 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.965-390G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286330 | |||||||
| chr13:31286541 | TCC | T | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-177_965-176del others(2): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr13 | 31286541 | ||||||
| chr13:31286546 | C | T | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-174C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286546 | |||||||
| chr13:31286548 | G | A | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-172G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286548 | |||||||
| chr13:31286549 | G | T | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-171G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286549 | |||||||
| chr13:31286550 | T | C | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-170T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286550 | |||||||
| chr13:31286632 | G | C | 75 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(72): Show |
76 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.965-88G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 11/14 | chr13 | 31286632 | |||||||
| chr13:31286829 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+10C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286829 | |||||||
| chr13:31286922 | G | A | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1064+103G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286922 | |||||||
| chr13:31286993 | T | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+174T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31286993 | |||||||
| chr13:31287141 | C | T | 2 | a0001c0001t0005g0199 a0002c0002t0003g0239 |
2 | HG02165.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1064+322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287141 | |||||||
| chr13:31287142 | G | A | 1 | a0002c0002t0002g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1064+323G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287142 | |||||||
| chr13:31287270 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+451A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287270 | |||||||
| chr13:31287338 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1064+519G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287338 | |||||||
| chr13:31287349 | G | A | 1 | a0001c0001t0006g0055 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1064+530G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287349 | |||||||
| chr13:31287386 | G | A | 3 | a0002c0002t0002g0089 a0002c0002t0002g0097 a0002c0002t0002g0213 |
3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+567G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287386 | |||||||
| chr13:31287467 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+648C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287467 | |||||||
| chr13:31287634 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+815G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287634 | |||||||
| chr13:31287663 | A | G | 2 | a0002c0002t0003g0241 a0002c0002t0003g0242 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1064+844A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287663 | |||||||
| chr13:31287669 | G | GA | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1064+858dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31287669 | ||||||
| chr13:31287677 | AT | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
5 | HG02027.hp2 HG02129.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+860delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31287677 | ||||||
| chr13:31287727 | T | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+908T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287727 | |||||||
| chr13:31287730 | T | C | 1 | a0002c0002t0002g0112 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1064+911T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287730 | |||||||
| chr13:31287773 | T | C | 1 | a0002c0002t0008g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1064+954T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287773 | |||||||
| chr13:31287833 | A | G | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1064+1014A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287833 | |||||||
| chr13:31287932 | A | G | 11 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(8): Show |
11 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1064+1113A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287932 | |||||||
| chr13:31287935 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1064+1116A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31287935 | |||||||
| chr13:31288015 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1064+1196G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288015 | |||||||
| chr13:31288038 | G | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0057 others(13): Show |
17 | HG00735.hp1 HG01074.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1064+1219G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288038 | |||||||
| chr13:31288197 | C | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+1378C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288197 | |||||||
| chr13:31288335 | A | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+1516A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288335 | |||||||
| chr13:31288369 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+1550A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288369 | |||||||
| chr13:31288380 | C | T | 1 | a0002c0011t0004g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1064+1561C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288380 | |||||||
| chr13:31288405 | A | G | 1 | a0001c0001t0005g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1064+1586A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288405 | |||||||
| chr13:31288754 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+1935C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288754 | |||||||
| chr13:31288806 | A | C | 1 | a0001c0001t0024g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1064+1987A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288806 | |||||||
| chr13:31288872 | A | G | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1064+2053A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288872 | |||||||
| chr13:31288893 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+2074A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31288893 | |||||||
| chr13:31289104 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+2285T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289104 | |||||||
| chr13:31289183 | A | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(159): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1064+2364A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289183 | |||||||
| chr13:31289321 | C | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+2502C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289321 | |||||||
| chr13:31289458 | A | T | 1 | a0002c0002t0002g0132 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1064+2639A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289458 | |||||||
| chr13:31289466 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1064+2647T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289466 | |||||||
| chr13:31289536 | T | C | 1 | a0002c0002t0002g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1064+2717T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289536 | |||||||
| chr13:31289593 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+2774A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289593 | |||||||
| chr13:31289619 | GA | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+2811delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31289619 | ||||||
| chr13:31289866 | GT | G | 5 | a0002c0002t0003g0011 a0002c0002t0009g0016 a0002c0002t0009g0208 others(2): Show |
5 | HG02015.hp1 HG03209.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+3059delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31289866 | ||||||
| chr13:31289870 | T | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3051T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31289870 | |||||||
| chr13:31290011 | C | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3192C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290011 | |||||||
| chr13:31290116 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3297C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290116 | |||||||
| chr13:31290140 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1064+3321A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290140 | |||||||
| chr13:31290199 | G | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1064+3380G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290199 | |||||||
| chr13:31290470 | A | G | 2 | a0002c0002t0002g0218 a0002c0003t0021g0070 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1064+3651A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290470 | |||||||
| chr13:31290485 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+3666G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290485 | |||||||
| chr13:31290589 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+3770T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290589 | |||||||
| chr13:31290672 | C | T | 1 | a0002c0002t0004g0025 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1064+3853C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290672 | |||||||
| chr13:31290682 | C | A | 5 | a0001c0001t0006g0050 a0001c0001t0006g0053 a0001c0001t0006g0054 others(2): Show |
5 | NA18942.hp1 NA18947.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+3863C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290682 | |||||||
| chr13:31290800 | T | C | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+3981T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290800 | |||||||
| chr13:31290835 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1064+4016C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290835 | |||||||
| chr13:31290867 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+4048G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290867 | |||||||
| chr13:31290923 | G | A | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1064+4104G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290923 | |||||||
| chr13:31290949 | G | T | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1064+4130G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31290949 | |||||||
| chr13:31291201 | T | C | 1 | a0001c0001t0007g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1064+4382T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291201 | |||||||
| chr13:31291346 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1064+4527T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291346 | |||||||
| chr13:31291681 | T | C | 3 | a0003c0005t0001g0074 a0003c0005t0001g0075 a0003c0005t0001g0076 |
3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1064+4862T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291681 | |||||||
| chr13:31291693 | T | C | 3 | a0003c0005t0001g0074 a0003c0005t0001g0075 a0003c0005t0001g0076 |
3 | HG00741.hp2 HG02486.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1064+4874T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291693 | |||||||
| chr13:31291859 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1064+5040G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291859 | |||||||
| chr13:31291877 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+5058A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31291877 | |||||||
| chr13:31292041 | T | C | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1064+5222T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292041 | |||||||
| chr13:31292141 | G | A | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1064+5322G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292141 | |||||||
| chr13:31292182 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+5363C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292182 | |||||||
| chr13:31292208 | T | G | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+5389T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292208 | |||||||
| chr13:31292246 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1064+5427G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292246 | |||||||
| chr13:31292449 | T | C | 1 | a0001c0001t0005g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1064+5630T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292449 | |||||||
| chr13:31292699 | C | CT | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1064+5890dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31292699 | ||||||
| chr13:31292804 | C | G | 1 | a0002c0002t0003g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1064+5985C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292804 | |||||||
| chr13:31292816 | T | TG | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+5998dupG | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31292816 | ||||||
| chr13:31292883 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0229 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1064+6064T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292883 | |||||||
| chr13:31292893 | G | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+6074G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31292893 | |||||||
| chr13:31293034 | A | C | 8 | a0002c0002t0003g0004 a0002c0002t0003g0069 a0002c0002t0003g0092 others(5): Show |
9 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1064+6215A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293034 | |||||||
| chr13:31293055 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+6236A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293055 | |||||||
| chr13:31293110 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+6291G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293110 | |||||||
| chr13:31293171 | T | C | 2 | a0001c0001t0004g0033 a0001c0001t0004g0171 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1064+6352T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293171 | |||||||
| chr13:31293441 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+6622T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293441 | |||||||
| chr13:31293487 | G | A | 1 | a0002c0003t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1064+6668G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293487 | |||||||
| chr13:31293557 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0214 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1064+6738G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293557 | |||||||
| chr13:31293693 | G | GGGTGTCT others(39): Show |
1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+6877_1064+692 others(50): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31293693 | ||||||
| chr13:31293902 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+7083C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31293902 | |||||||
| chr13:31294273 | T | G | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1064+7454T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294273 | |||||||
| chr13:31294307 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1064+7488T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294307 | |||||||
| chr13:31294457 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1064+7638T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294457 | |||||||
| chr13:31294769 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064+7950G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294769 | |||||||
| chr13:31294987 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+8168T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31294987 | |||||||
| chr13:31295007 | C | CT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+8197dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31295007 | ||||||
| chr13:31295017 | G | T | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+8198G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295017 | |||||||
| chr13:31295089 | C | T | 6 | a0002c0002t0003g0014 a0002c0002t0003g0081 a0002c0002t0003g0241 others(3): Show |
6 | HG01255.hp1 HG01358.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064+8270C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295089 | |||||||
| chr13:31295090 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+8271G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295090 | |||||||
| chr13:31295139 | T | C | 1 | a0002c0002t0003g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1064+8320T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295139 | |||||||
| chr13:31295209 | G | A | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1064+8390G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295209 | |||||||
| chr13:31295301 | C | G | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1064+8482C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295301 | |||||||
| chr13:31295337 | A | C | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1064+8518A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295337 | |||||||
| chr13:31295442 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+8623C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295442 | |||||||
| chr13:31295485 | T | G | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1064+8666T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295485 | |||||||
| chr13:31295571 | G | T | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1064+8752G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295571 | |||||||
| chr13:31295654 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+8835T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295654 | |||||||
| chr13:31295675 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1064+8856C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295675 | |||||||
| chr13:31295886 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1064+9067A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295886 | |||||||
| chr13:31295988 | G | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+9169G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31295988 | |||||||
| chr13:31296075 | C | T | 5 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0002t0002g0177 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064+9256C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296075 | |||||||
| chr13:31296092 | C | G | 1 | a0002c0003t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1064+9273C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296092 | |||||||
| chr13:31296135 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+9316G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296135 | |||||||
| chr13:31296257 | G | A | 66 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(63): Show |
67 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1064+9438G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296257 | |||||||
| chr13:31296377 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+9558C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296377 | |||||||
| chr13:31296493 | G | A | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1064+9674G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296493 | |||||||
| chr13:31296702 | CA | C | 5 | a0002c0002t0003g0034 a0002c0002t0003g0035 a0002c0002t0003g0217 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+9884delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296702 | |||||||
| chr13:31296703 | AT | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1064+9894delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31296703 | ||||||
| chr13:31296750 | C | A | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+9931C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296750 | |||||||
| chr13:31296785 | T | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+9966T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296785 | |||||||
| chr13:31296812 | A | G | 3 | a0002c0002t0002g0089 a0002c0002t0002g0097 a0002c0002t0002g0213 |
3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+9993A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296812 | |||||||
| chr13:31296956 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+10137A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31296956 | |||||||
| chr13:31297025 | G | GT | 70 | a0001c0001t0001g0090 a0001c0001t0001g0185 a0001c0001t0006g0044 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1064+10218dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297025 | ||||||
| chr13:31297085 | G | A | 3 | a0002c0002t0002g0089 a0002c0002t0002g0097 a0002c0002t0002g0213 |
3 | HG02145.hp1 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1064+10266G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297085 | |||||||
| chr13:31297375 | G | GT | 29 | a0001c0001t0001g0088 a0001c0001t0001g0108 a0001c0001t0001g0110 others(26): Show |
29 | HG01074.hp2 HG01106.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.1064+10575dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | ||||||
| chr13:31297375 | GT | G | 38 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0064 others(35): Show |
38 | HG00639.hp1 HG01071.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1064+10575delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | ||||||
| chr13:31297375 | GTT | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0119 a0001c0001t0001g0229 others(3): Show |
6 | HG03098.hp2 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064+10574_1064+10 others(8): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | ||||||
| chr13:31297375 | GTTTT | G | 5 | a0002c0002t0002g0233 a0002c0002t0002g0264 a0002c0002t0009g0016 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+10572_1064+10 others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31297375 | ||||||
| chr13:31297382 | T | G | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1064+10563T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297382 | |||||||
| chr13:31297465 | C | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+10646C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297465 | |||||||
| chr13:31297526 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1064+10707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297526 | |||||||
| chr13:31297576 | A | G | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+10757A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297576 | |||||||
| chr13:31297664 | A | C | 8 | a0002c0002t0003g0004 a0002c0002t0003g0069 a0002c0002t0003g0092 others(5): Show |
9 | HG00099.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1064+10845A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297664 | |||||||
| chr13:31297832 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11013T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297832 | |||||||
| chr13:31297894 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064+11075G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31297894 | |||||||
| chr13:31298044 | A | C | 48 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0133 others(45): Show |
49 | HG00558.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1064+11225A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298044 | |||||||
| chr13:31298068 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+11249C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298068 | |||||||
| chr13:31298069 | C | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1064+11250C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298069 | |||||||
| chr13:31298127 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1064+11308C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298127 | |||||||
| chr13:31298198 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11379G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298198 | |||||||
| chr13:31298267 | C | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1064+11448C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298267 | |||||||
| chr13:31298282 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+11463T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298282 | |||||||
| chr13:31298377 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(161): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1064+11558T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298377 | |||||||
| chr13:31298456 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0229 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1064+11637G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298456 | |||||||
| chr13:31298508 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11689G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298508 | |||||||
| chr13:31298621 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0240 a0001c0001t0007g0030 |
3 | HG00140.hp1 HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1064+11802C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298621 | |||||||
| chr13:31298682 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+11863C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298682 | |||||||
| chr13:31298688 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+11869G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298688 | |||||||
| chr13:31298689 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1064+11870G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298689 | |||||||
| chr13:31298728 | T | C | 5 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(2): Show |
5 | HG02015.hp1 HG03130.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+11909T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298728 | |||||||
| chr13:31298793 | T | G | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+11974T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298793 | |||||||
| chr13:31298834 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+12015G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298834 | |||||||
| chr13:31298984 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1064+12165C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31298984 | |||||||
| chr13:31299249 | G | A | 2 | a0002c0002t0003g0079 a0002c0002t0003g0080 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1064+12430G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299249 | |||||||
| chr13:31299367 | C | T | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+12548C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299367 | |||||||
| chr13:31299410 | G | A | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1064+12591G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299410 | |||||||
| chr13:31299492 | T | C | 1 | a0002c0002t0003g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1064+12673T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299492 | |||||||
| chr13:31299679 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+12860C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31299679 | |||||||
| chr13:31300086 | C | G | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1064+13267C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300086 | |||||||
| chr13:31300158 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+13339G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300158 | |||||||
| chr13:31300166 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(164): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1064+13347C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300166 | |||||||
| chr13:31300168 | G | T | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+13349G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300168 | |||||||
| chr13:31300307 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1064+13488C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300307 | |||||||
| chr13:31300370 | C | T | 7 | a0001c0001t0001g0057 a0001c0001t0001g0150 a0001c0001t0001g0152 others(4): Show |
7 | HG01074.hp1 HG01952.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.1064+13551C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300370 | |||||||
| chr13:31300380 | T | C | 1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1064+13561T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300380 | |||||||
| chr13:31300718 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+13899C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300718 | |||||||
| chr13:31300779 | T | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1064+13960T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300779 | |||||||
| chr13:31300856 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1064+14037G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300856 | |||||||
| chr13:31300917 | G | A | 1 | a0002c0002t0008g0125 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1064+14098G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300917 | |||||||
| chr13:31300953 | C | T | 1 | a0002c0002t0006g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1064+14134C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31300953 | |||||||
| chr13:31301003 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14184C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301003 | |||||||
| chr13:31301465 | C | T | 1 | a0001c0001t0025g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1064+14646C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301465 | |||||||
| chr13:31301509 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14690G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301509 | |||||||
| chr13:31301624 | G | A | 4 | a0002c0003t0003g0028 a0002c0003t0003g0226 a0005c0006t0003g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+14805G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301624 | |||||||
| chr13:31301633 | C | T | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+14814C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301633 | |||||||
| chr13:31301668 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+14849C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31301668 | |||||||
| chr13:31302006 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1064+15187G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302006 | |||||||
| chr13:31302015 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064+15196T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302015 | |||||||
| chr13:31302018 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064+15199T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302018 | |||||||
| chr13:31302049 | C | T | 1 | a0002c0002t0008g0138 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1064+15230C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302049 | |||||||
| chr13:31302075 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1064+15256C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302075 | |||||||
| chr13:31302234 | C | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15332C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302234 | |||||||
| chr13:31302350 | C | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-15216C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302350 | |||||||
| chr13:31302351 | G | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15215G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302351 | |||||||
| chr13:31302374 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15192G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302374 | |||||||
| chr13:31302385 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-15181C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302385 | |||||||
| chr13:31302386 | G | A | 5 | a0002c0002t0004g0083 a0002c0002t0009g0016 a0002c0002t0009g0208 others(2): Show |
5 | HG02015.hp1 NA18963.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-15180G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302386 | |||||||
| chr13:31302451 | C | T | 1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065-15115C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302451 | |||||||
| chr13:31302469 | C | T | 66 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(63): Show |
67 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1065-15097C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302469 | |||||||
| chr13:31302485 | C | T | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-15081C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302485 | |||||||
| chr13:31302486 | G | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-15080G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302486 | |||||||
| chr13:31302520 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-15046G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302520 | |||||||
| chr13:31302647 | G | A | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065-14919G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302647 | |||||||
| chr13:31302692 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1065-14874G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302692 | |||||||
| chr13:31302733 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14833G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302733 | |||||||
| chr13:31302737 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(57): Show |
61 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1065-14829A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302737 | |||||||
| chr13:31302738 | C | T | 1 | a0001c0001t0006g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1065-14828C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302738 | |||||||
| chr13:31302740 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1065-14826G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302740 | |||||||
| chr13:31302762 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14804C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302762 | |||||||
| chr13:31302799 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14767G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302799 | |||||||
| chr13:31302825 | A | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14741A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302825 | |||||||
| chr13:31302881 | GACAA | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-14679_1065-14 others(10): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31302881 | ||||||
| chr13:31302966 | T | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1065-14600T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31302966 | |||||||
| chr13:31303012 | C | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-14554C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303012 | |||||||
| chr13:31303032 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-14534C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303032 | |||||||
| chr13:31303081 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(236): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1065-14485T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303081 | |||||||
| chr13:31303082 | G | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-14484G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303082 | |||||||
| chr13:31303091 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14475T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303091 | |||||||
| chr13:31303163 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-14403G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303163 | |||||||
| chr13:31303216 | A | G | 1 | a0002c0002t0003g0244 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1065-14350A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303216 | |||||||
| chr13:31303267 | T | C | 5 | a0002c0002t0003g0236 a0002c0002t0003g0243 a0002c0002t0003g0244 others(2): Show |
5 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-14299T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303267 | |||||||
| chr13:31303342 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14224G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303342 | |||||||
| chr13:31303364 | C | T | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1065-14202C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303364 | |||||||
| chr13:31303462 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-14104C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303462 | |||||||
| chr13:31303800 | A | G | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065-13766A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303800 | |||||||
| chr13:31303950 | G | GA | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-13613dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31303950 | ||||||
| chr13:31303951 | A | G | 1 | a0002c0010t0003g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1065-13615A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303951 | |||||||
| chr13:31303971 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13595C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303971 | |||||||
| chr13:31303981 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13585G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31303981 | |||||||
| chr13:31304023 | G | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-13543G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304023 | |||||||
| chr13:31304146 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-13420C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304146 | |||||||
| chr13:31304201 | C | T | 73 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(70): Show |
74 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1065-13365C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304201 | |||||||
| chr13:31304244 | C | T | 1 | a0002c0002t0003g0255 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1065-13322C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304244 | |||||||
| chr13:31304348 | T | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-13218T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304348 | |||||||
| chr13:31304416 | C | G | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1065-13150C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304416 | |||||||
| chr13:31304591 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12975C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304591 | |||||||
| chr13:31304608 | A | G | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12958A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304608 | |||||||
| chr13:31304625 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-12941T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304625 | |||||||
| chr13:31304688 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12878G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304688 | |||||||
| chr13:31304693 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12873C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31304693 | |||||||
| chr13:31305013 | G | C | 7 | a0002c0002t0001g0250 a0002c0002t0003g0096 a0002c0002t0003g0245 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-12553G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305013 | |||||||
| chr13:31305035 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-12531T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305035 | |||||||
| chr13:31305039 | C | T | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12527C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305039 | |||||||
| chr13:31305130 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0229 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-12436C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305130 | |||||||
| chr13:31305262 | A | C | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-12304A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305262 | |||||||
| chr13:31305338 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(58): Show |
62 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1065-12228T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305338 | |||||||
| chr13:31305339 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-12227G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305339 | |||||||
| chr13:31305339 | G | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0045 others(55): Show |
59 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1065-12227G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305339 | |||||||
| chr13:31305378 | A | G | 66 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(63): Show |
67 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1065-12188A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305378 | |||||||
| chr13:31305405 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-12161G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305405 | |||||||
| chr13:31305473 | A | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-12093A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305473 | |||||||
| chr13:31305488 | A | G | 74 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1065-12078A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305488 | |||||||
| chr13:31305556 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-12010T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305556 | |||||||
| chr13:31305566 | C | G | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1065-12000C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305566 | |||||||
| chr13:31305764 | G | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11802G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305764 | |||||||
| chr13:31305782 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-11784C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305782 | |||||||
| chr13:31305783 | T | G | 74 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1065-11783T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305783 | |||||||
| chr13:31305824 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1065-11742T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305824 | |||||||
| chr13:31305859 | G | A | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-11707G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305859 | |||||||
| chr13:31305916 | T | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-11650T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305916 | |||||||
| chr13:31305955 | G | A | 1 | a0002c0002t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1065-11611G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305955 | |||||||
| chr13:31305980 | C | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11586C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31305980 | |||||||
| chr13:31306100 | G | T | 1 | a0001c0001t0005g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1065-11466G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306100 | |||||||
| chr13:31306127 | C | G | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1065-11439C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306127 | |||||||
| chr13:31306131 | C | G | 74 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1065-11435C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306131 | |||||||
| chr13:31306282 | C | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-11284C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306282 | |||||||
| chr13:31306293 | C | T | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1065-11273C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306293 | |||||||
| chr13:31306300 | A | C | 7 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(4): Show |
7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-11266A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306300 | |||||||
| chr13:31306310 | C | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-11256C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306310 | |||||||
| chr13:31306366 | A | G | 1 | a0002c0003t0002g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1065-11200A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306366 | |||||||
| chr13:31306430 | C | T | 1 | a0001c0001t0005g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1065-11136C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306430 | |||||||
| chr13:31306436 | G | A | 1 | a0001c0001t0004g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1065-11130G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306436 | |||||||
| chr13:31306478 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-11088G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306478 | |||||||
| chr13:31306544 | A | AATCAT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11022_1065-11 others(11): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306544 | |||||||
| chr13:31306545 | C | G | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11021C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306545 | |||||||
| chr13:31306551 | G | A | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-11015G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306551 | |||||||
| chr13:31306570 | C | G | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-10996C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306570 | |||||||
| chr13:31306583 | A | G | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-10983A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306583 | |||||||
| chr13:31306612 | C | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-10954C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306612 | |||||||
| chr13:31306673 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10893A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306673 | |||||||
| chr13:31306686 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-10880T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306686 | |||||||
| chr13:31306735 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10831C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306735 | |||||||
| chr13:31306768 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1065-10798C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306768 | |||||||
| chr13:31306858 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10708G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306858 | |||||||
| chr13:31306868 | G | A | 1 | a0002c0002t0002g0231 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1065-10698G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306868 | |||||||
| chr13:31306879 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10687C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306879 | |||||||
| chr13:31306999 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-10567C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31306999 | |||||||
| chr13:31307098 | C | T | 5 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0002t0002g0177 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-10468C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307098 | |||||||
| chr13:31307158 | T | C | 3 | a0002c0003t0003g0028 a0005c0006t0003g0224 a0005c0006t0003g0225 |
3 | HG01256.hp2 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1065-10408T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307158 | |||||||
| chr13:31307167 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1065-10399T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307167 | |||||||
| chr13:31307208 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-10358G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307208 | |||||||
| chr13:31307315 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-10251G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307315 | |||||||
| chr13:31307319 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-10247A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307319 | |||||||
| chr13:31307338 | A | C | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-10228A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307338 | |||||||
| chr13:31307343 | A | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0229 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-10223A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307343 | |||||||
| chr13:31307347 | C | A | 3 | a0001c0001t0001g0182 a0002c0002t0003g0238 a0002c0002t0018g0251 |
3 | HG01496.hp2 HG03130.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1065-10219C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307347 | |||||||
| chr13:31307411 | A | G | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-10155A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307411 | |||||||
| chr13:31307420 | G | A | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1065-10146G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307420 | |||||||
| chr13:31307433 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1065-10133C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307433 | |||||||
| chr13:31307498 | A | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1065-10068A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307498 | |||||||
| chr13:31307509 | A | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-10057A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307509 | |||||||
| chr13:31307614 | A | T | 5 | a0002c0002t0002g0066 a0002c0002t0002g0067 a0002c0002t0002g0177 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-9952A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307614 | |||||||
| chr13:31307712 | G | A | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9854G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307712 | |||||||
| chr13:31307727 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-9839G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307727 | |||||||
| chr13:31307757 | T | G | 1 | a0002c0002t0002g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1065-9809T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307757 | |||||||
| chr13:31307765 | T | A | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9801T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307765 | |||||||
| chr13:31307767 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.1065-9799A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307767 | |||||||
| chr13:31307779 | C | A | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9787C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307779 | |||||||
| chr13:31307779 | C | T | 1 | a0002c0002t0003g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1065-9787C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307779 | |||||||
| chr13:31307788 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-9778T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307788 | |||||||
| chr13:31307867 | G | A | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-9699G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307867 | |||||||
| chr13:31307874 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1065-9692C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307874 | |||||||
| chr13:31307883 | G | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-9683G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307883 | |||||||
| chr13:31307883 | G | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9683G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307883 | |||||||
| chr13:31307895 | C | T | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1065-9671C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307895 | |||||||
| chr13:31307902 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9664A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307902 | |||||||
| chr13:31307926 | C | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-9640C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31307926 | |||||||
| chr13:31308015 | A | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9551A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308015 | |||||||
| chr13:31308098 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9468C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308098 | |||||||
| chr13:31308131 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(157): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1065-9435A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308131 | |||||||
| chr13:31308173 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9393T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308173 | |||||||
| chr13:31308176 | C | A | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1065-9390C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308176 | |||||||
| chr13:31308176 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9390C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308176 | |||||||
| chr13:31308179 | T | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9387T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308179 | |||||||
| chr13:31308188 | C | G | 5 | a0001c0001t0005g0198 a0001c0001t0005g0200 a0001c0001t0005g0204 others(2): Show |
5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9378C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308188 | |||||||
| chr13:31308195 | G | C | 5 | a0001c0001t0005g0198 a0001c0001t0005g0200 a0001c0001t0005g0204 others(2): Show |
5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9371G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308195 | |||||||
| chr13:31308245 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9321G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308245 | |||||||
| chr13:31308313 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-9253C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308313 | |||||||
| chr13:31308331 | A | ATAAAAAA others(7): Show |
1 | a0001c0001t0001g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1065-9223_1065-922 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308331 | ||||||
| chr13:31308332 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0015g0247 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1065-9223_1065-922 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308332 | ||||||
| chr13:31308332 | TA | T | 18 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(15): Show |
18 | HG00639.hp1 HG02015.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1065-9221delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308332 | ||||||
| chr13:31308333 | A | AAAAAAAA others(6): Show |
6 | a0001c0001t0001g0088 a0001c0001t0001g0172 a0001c0001t0001g0176 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308333 | ||||||
| chr13:31308334 | A | AAAAAAAA others(5): Show |
26 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0214 others(23): Show |
26 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308334 | ||||||
| chr13:31308335 | A | AAAAAAAA others(4): Show |
6 | a0001c0001t0001g0110 a0001c0001t0004g0001 a0001c0001t0004g0040 others(3): Show |
7 | HG01943.hp1 HG02129.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1065-9223_1065-922 others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308335 | ||||||
| chr13:31308345 | A | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1065-9221A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308345 | |||||||
| chr13:31308346 | T | A | 48 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0122 others(45): Show |
49 | HG00558.hp1 HG00558.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1065-9220T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308346 | |||||||
| chr13:31308347 | T | A | 120 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0110 others(117): Show |
122 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1065-9219T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308347 | |||||||
| chr13:31308347 | T | TA | 6 | a0002c0002t0004g0170 a0002c0002t0004g0181 a0002c0002t0012g0173 others(3): Show |
6 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-9206dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | ||||||
| chr13:31308347 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0230 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1065-9209_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | ||||||
| chr13:31308347 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1065-9210_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | ||||||
| chr13:31308347 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1065-9211_1065-921 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308347 | ||||||
| chr13:31308355 | A | C | 1 | a0002c0002t0008g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1065-9211A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308355 | |||||||
| chr13:31308356 | A | AACAAAAA others(1): Show |
65 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(62): Show |
66 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1065-9209_1065-920 others(12): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308356 | ||||||
| chr13:31308356 | A | AACAAAAA others(7): Show |
4 | a0002c0003t0002g0160 a0002c0003t0002g0169 a0002c0007t0023g0006 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065-9209_1065-920 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308356 | ||||||
| chr13:31308358 | A | C | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9208A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308358 | |||||||
| chr13:31308361 | C | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(142): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1065-9205C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308361 | |||||||
| chr13:31308361 | CA | C | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-9195delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308361 | ||||||
| chr13:31308362 | A | AAAAAAAA others(6): Show |
80 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.1065-9195_1065-919 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAAAAAAA others(5): Show |
12 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0123 others(9): Show |
12 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065-9195_1065-919 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0071 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1065-9195_1065-919 others(15): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAAAAAAC others(6): Show |
1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1065-9198_1065-919 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAAAC | 69 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(66): Show |
70 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1065-9201_1065-920 others(8): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAACAAAA others(7): Show |
1 | a0001c0001t0010g0116 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAACAAAA others(6): Show |
1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(17): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | AAACAAAA others(5): Show |
1 | a0002c0002t0002g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1065-9202_1065-920 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31308362 | ||||||
| chr13:31308362 | A | ACAAAAAC others(16): Show |
4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-9204_1065-920 others(27): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308362 | |||||||
| chr13:31308362 | A | C | 34 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0182 others(31): Show |
34 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1065-9204A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308362 | |||||||
| chr13:31308414 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01074.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1065-9152A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308414 | |||||||
| chr13:31308441 | T | C | 5 | a0001c0001t0005g0198 a0001c0001t0005g0200 a0001c0001t0005g0204 others(2): Show |
5 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-9125T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308441 | |||||||
| chr13:31308647 | A | G | 2 | a0002c0002t0012g0173 a0002c0002t0012g0174 |
2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1065-8919A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308647 | |||||||
| chr13:31308862 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-8704C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308862 | |||||||
| chr13:31308875 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG00099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1065-8691C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308875 | |||||||
| chr13:31308907 | G | T | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-8659G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308907 | |||||||
| chr13:31308933 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8633T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308933 | |||||||
| chr13:31308956 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8610G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31308956 | |||||||
| chr13:31309028 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0229 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1065-8538G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309028 | |||||||
| chr13:31309037 | A | T | 3 | a0001c0001t0004g0183 a0001c0001t0004g0212 a0001c0001t0004g0215 |
3 | HG02280.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1065-8529A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309037 | |||||||
| chr13:31309358 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-8208C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309358 | |||||||
| chr13:31309396 | C | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-8170C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309396 | |||||||
| chr13:31309466 | C | T | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1065-8100C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309466 | |||||||
| chr13:31309488 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1065-8078G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309488 | |||||||
| chr13:31309560 | C | T | 2 | a0002c0002t0003g0027 a0002c0002t0017g0021 |
2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1065-8006C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309560 | |||||||
| chr13:31309603 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7963T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309603 | |||||||
| chr13:31309654 | T | C | 1 | a0002c0002t0003g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1065-7912T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309654 | |||||||
| chr13:31309678 | T | A | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-7888T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309678 | |||||||
| chr13:31309694 | C | T | 1 | a0002c0002t0002g0231 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1065-7872C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309694 | |||||||
| chr13:31309726 | A | G | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-7840A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309726 | |||||||
| chr13:31309960 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0235 |
2 | HG03927.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1065-7606C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31309960 | |||||||
| chr13:31310087 | C | T | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-7479C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310087 | |||||||
| chr13:31310175 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1065-7391C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310175 | |||||||
| chr13:31310182 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1065-7384G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310182 | |||||||
| chr13:31310270 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7296G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310270 | |||||||
| chr13:31310525 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-7041G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310525 | |||||||
| chr13:31310574 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6992C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310574 | |||||||
| chr13:31310685 | A | T | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1065-6881A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310685 | |||||||
| chr13:31310780 | G | A | 1 | a0001c0001t0005g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1065-6786G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310780 | |||||||
| chr13:31310944 | G | A | 1 | a0001c0001t0015g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1065-6622G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31310944 | |||||||
| chr13:31311016 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6550C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311016 | |||||||
| chr13:31311017 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(161): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1065-6549G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311017 | |||||||
| chr13:31311029 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6537A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311029 | |||||||
| chr13:31311055 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6511C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311055 | |||||||
| chr13:31311078 | T | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-6488T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311078 | |||||||
| chr13:31311112 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-6454T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311112 | |||||||
| chr13:31311381 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1065-6185G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311381 | |||||||
| chr13:31311467 | T | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-6099T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311467 | |||||||
| chr13:31311687 | C | T | 2 | a0002c0002t0003g0238 a0002c0003t0003g0186 |
2 | HG01496.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1065-5879C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311687 | |||||||
| chr13:31311746 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5820A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311746 | |||||||
| chr13:31311770 | A | G | 69 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(66): Show |
70 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1065-5796A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31311770 | |||||||
| chr13:31312040 | A | G | 4 | a0002c0002t0003g0236 a0002c0002t0003g0243 a0002c0002t0003g0244 others(1): Show |
4 | HG01516.hp1 HG01943.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-5526A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312040 | |||||||
| chr13:31312092 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5474G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312092 | |||||||
| chr13:31312107 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1065-5459G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312107 | |||||||
| chr13:31312166 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1065-5400A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312166 | |||||||
| chr13:31312222 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5344C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312222 | |||||||
| chr13:31312365 | A | T | 8 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0172 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-5201A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312365 | |||||||
| chr13:31312469 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-5097T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312469 | |||||||
| chr13:31312677 | G | A | 1 | a0001c0001t0005g0196 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1065-4889G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312677 | |||||||
| chr13:31312713 | A | G | 71 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(68): Show |
72 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1065-4853A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312713 | |||||||
| chr13:31312772 | A | G | 1 | a0002c0003t0002g0169 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1065-4794A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312772 | |||||||
| chr13:31312901 | C | T | 1 | a0002c0002t0004g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1065-4665C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312901 | |||||||
| chr13:31312930 | C | T | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1065-4636C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31312930 | |||||||
| chr13:31313084 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-4482T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313084 | |||||||
| chr13:31313096 | G | A | 1 | a0002c0002t0003g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1065-4470G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313096 | |||||||
| chr13:31313225 | G | C | 1 | a0002c0002t0003g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1065-4341G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313225 | |||||||
| chr13:31313450 | G | C | 1 | a0002c0002t0008g0098 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1065-4116G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313450 | |||||||
| chr13:31313537 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-4029A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313537 | |||||||
| chr13:31313704 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-3862G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313704 | |||||||
| chr13:31313771 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1065-3795A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313771 | |||||||
| chr13:31313889 | G | A | 1 | a0002c0002t0002g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1065-3677G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313889 | |||||||
| chr13:31313997 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-3569G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31313997 | |||||||
| chr13:31314022 | C | T | 1 | a0002c0002t0003g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1065-3544C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314022 | |||||||
| chr13:31314190 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1065-3376A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314190 | |||||||
| chr13:31314359 | G | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1065-3207G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314359 | |||||||
| chr13:31314465 | G | A | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-3101G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314465 | |||||||
| chr13:31314630 | G | A | 68 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(65): Show |
69 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1065-2936G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314630 | |||||||
| chr13:31314803 | C | T | 1 | a0006c0009t0002g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1065-2763C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314803 | |||||||
| chr13:31314903 | G | A | 66 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(63): Show |
67 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1065-2663G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314903 | |||||||
| chr13:31314963 | C | T | 1 | a0002c0002t0003g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-2603C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31314963 | |||||||
| chr13:31315082 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1065-2484C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315082 | |||||||
| chr13:31315197 | A | C | 1 | a0002c0002t0002g0168 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1065-2369A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315197 | |||||||
| chr13:31315211 | T | G | 1 | a0001c0001t0004g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-2355T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315211 | |||||||
| chr13:31315295 | A | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1065-2271A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315295 | |||||||
| chr13:31315368 | G | A | 15 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(12): Show |
15 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1065-2198G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315368 | |||||||
| chr13:31315389 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-2177T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315389 | |||||||
| chr13:31315626 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-1940T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315626 | |||||||
| chr13:31315688 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-1878T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315688 | |||||||
| chr13:31315806 | G | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1065-1760G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315806 | |||||||
| chr13:31315939 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1065-1627A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31315939 | |||||||
| chr13:31316259 | C | T | 1 | a0002c0003t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1065-1307C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316259 | |||||||
| chr13:31316405 | T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0060 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1065-1160_1065-115 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316405 | ||||||
| chr13:31316407 | T | A | 1 | a0001c0001t0004g0060 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1065-1159T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | |||||||
| chr13:31316407 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0240 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | |||||||
| chr13:31316407 | T | TATATATA others(10): Show |
2 | a0001c0001t0001g0122 a0001c0001t0007g0149 |
2 | HG01192.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1065-1159_1065-115 others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | |||||||
| chr13:31316407 | T | TATATATA others(18): Show |
1 | a0004c0004t0004g0207 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(29): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | |||||||
| chr13:31316407 | T | TATATATA others(28): Show |
1 | a0001c0001t0001g0094 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1065-1159_1065-115 others(39): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316407 | |||||||
| chr13:31316407 | T | TTA | 6 | a0001c0001t0005g0100 a0002c0002t0004g0025 a0002c0002t0004g0170 others(3): Show |
6 | HG01106.hp2 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-1136_1065-113 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(3): Show |
1 | a0002c0003t0003g0186 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1065-1144_1065-113 others(14): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(5): Show |
1 | a0002c0003t0021g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1065-1146_1065-113 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0150 a0001c0001t0001g0176 a0002c0002t0011g0008 |
3 | HG02280.hp1 NA18990.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1065-1148_1065-113 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(9): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0082 others(17): Show |
21 | HG00558.hp2 HG00673.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1065-1150_1065-113 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(11): Show |
10 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0045 others(7): Show |
10 | HG01123.hp2 HG02015.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1065-1152_1065-113 others(22): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(13): Show |
9 | a0001c0001t0001g0051 a0001c0001t0001g0086 a0001c0001t0001g0090 others(6): Show |
9 | HG00735.hp1 HG01167.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065-1154_1065-113 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(15): Show |
9 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0115 others(6): Show |
9 | HG00741.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1065-1156_1065-113 others(26): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(17): Show |
12 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0110 others(9): Show |
12 | HG00621.hp2 HG01074.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1065-1158_1065-113 others(28): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(19): Show |
8 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0087 others(5): Show |
8 | HG00099.hp2 HG01071.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(30): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(21): Show |
8 | a0001c0001t0001g0048 a0001c0001t0001g0088 a0001c0001t0001g0102 others(5): Show |
8 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(32): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(23): Show |
8 | a0001c0001t0001g0077 a0001c0001t0001g0191 a0001c0001t0004g0043 others(5): Show |
8 | HG00639.hp2 HG02145.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(34): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(25): Show |
5 | a0001c0001t0005g0200 a0001c0001t0007g0017 a0001c0001t0007g0029 others(2): Show |
5 | HG01361.hp1 HG02818.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(36): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(27): Show |
10 | a0001c0001t0001g0229 a0001c0001t0005g0252 a0001c0001t0007g0019 others(7): Show |
10 | HG00738.hp1 HG01175.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(38): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(29): Show |
8 | a0001c0001t0001g0254 a0001c0001t0005g0198 a0001c0001t0007g0020 others(5): Show |
8 | HG00140.hp2 HG00639.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(40): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(31): Show |
3 | a0001c0001t0004g0041 a0001c0001t0005g0101 a0001c0001t0005g0196 |
3 | HG02027.hp1 NA18612.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(42): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(33): Show |
1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(44): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(35): Show |
2 | a0001c0001t0001g0071 a0001c0001t0001g0117 |
2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(46): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(37): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0014g0184 |
3 | HG00140.hp1 HG01255.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(48): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(39): Show |
1 | a0002c0002t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(50): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTATATAT others(43): Show |
1 | a0001c0001t0001g0104 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(54): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(3): Show |
9 | a0002c0002t0003g0004 a0002c0002t0003g0092 a0002c0002t0003g0236 others(6): Show |
10 | HG00738.hp2 HG01123.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(14): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(5): Show |
15 | a0002c0002t0002g0018 a0002c0002t0002g0118 a0002c0002t0002g0136 others(12): Show |
15 | HG00621.hp1 HG01516.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(16): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(7): Show |
24 | a0002c0002t0002g0126 a0002c0002t0002g0127 a0002c0002t0002g0128 others(21): Show |
24 | HG00099.hp1 HG00609.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(18): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(9): Show |
5 | a0002c0002t0002g0066 a0002c0002t0002g0135 a0002c0002t0002g0139 others(2): Show |
5 | HG02698.hp2 HG02886.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(11): Show |
6 | a0002c0002t0002g0067 a0002c0002t0002g0131 a0002c0002t0003g0242 others(3): Show |
6 | HG01358.hp2 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(22): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(13): Show |
3 | a0002c0002t0003g0241 a0002c0002t0003g0245 a0002c0002t0003g0253 |
3 | HG01255.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1065-1158_1065-115 others(24): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | T | TTTTATAT others(15): Show |
1 | a0002c0002t0001g0250 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1065-1158_1065-115 others(26): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316407 | TTA | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-1136_1065-113 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr13 | 31316407 | ||||||
| chr13:31316409 | A | T | 1 | a0002c0002t0003g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-1157A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316409 | |||||||
| chr13:31316431 | A | ATATATAT others(8): Show |
2 | a0001c0001t0004g0183 a0001c0001t0004g0215 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(19): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(10): Show |
2 | a0001c0001t0006g0059 a0001c0001t0022g0056 |
2 | NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(21): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(12): Show |
1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(23): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(14): Show |
1 | a0001c0001t0004g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(25): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(16): Show |
1 | a0004c0004t0004g0206 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(27): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(22): Show |
8 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0049 others(5): Show |
8 | HG01071.hp2 HG02056.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(33): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(24): Show |
5 | a0001c0001t0004g0159 a0001c0001t0006g0044 a0001c0001t0006g0147 others(2): Show |
5 | HG01361.hp2 HG01943.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(35): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(26): Show |
3 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0162 |
3 | HG03209.hp1 NA18522.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(37): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(28): Show |
1 | a0001c0001t0006g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(39): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(30): Show |
4 | a0001c0001t0004g0001 a0001c0001t0006g0055 a0001c0001t0006g0167 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(41): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(32): Show |
3 | a0001c0001t0004g0161 a0001c0001t0006g0050 a0001c0001t0006g0058 |
3 | HG00558.hp1 HG03130.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1065-1135_1065-113 others(43): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(34): Show |
1 | a0001c0001t0006g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(45): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316431 | A | ATATATAT others(38): Show |
1 | a0001c0001t0004g0063 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1065-1135_1065-113 others(49): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316431 | |||||||
| chr13:31316432 | A | T | 6 | a0001c0001t0001g0166 a0001c0001t0004g0041 a0001c0001t0004g0042 others(3): Show |
6 | HG00673.hp1 HG01169.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-1134A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316432 | |||||||
| chr13:31316434 | T | A | 34 | a0001c0001t0004g0001 a0001c0001t0004g0033 a0001c0001t0004g0039 others(31): Show |
35 | HG00558.hp1 HG01071.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.1065-1132T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | |||||||
| chr13:31316434 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1065-1132_1065-113 others(29): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | |||||||
| chr13:31316434 | T | TATATATA others(45): Show |
1 | a0001c0001t0004g0042 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1065-1132_1065-113 others(56): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316434 | |||||||
| chr13:31316435 | T | A | 2 | a0001c0001t0004g0041 a0001c0001t0004g0043 |
2 | HG02602.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1065-1131T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316435 | |||||||
| chr13:31316439 | T | C | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1065-1127T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316439 | |||||||
| chr13:31316680 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-886T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316680 | |||||||
| chr13:31316718 | A | T | 2 | a0002c0002t0003g0227 a0002c0002t0003g0263 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1065-848A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316718 | |||||||
| chr13:31316777 | C | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1065-789C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31316777 | |||||||
| chr13:31317062 | G | T | 1 | a0002c0002t0003g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1065-504G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317062 | |||||||
| chr13:31317118 | G | A | 1 | a0002c0003t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1065-448G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317118 | |||||||
| chr13:31317424 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(258): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1065-142T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 12/14 | chr13 | 31317424 | |||||||
| chr13:31317892 | T | TAAAAAAA others(138): Show |
1 | a0002c0002t0008g0085 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1184+213_1184+214i others(147): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | ||||||
| chr13:31317892 | T | TAAAAAAG others(136): Show |
54 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(51): Show |
54 | HG00099.hp1 HG00609.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1184+223_1184+224i others(145): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | ||||||
| chr13:31317892 | T | TAAAAAAG others(137): Show |
10 | a0002c0002t0002g0067 a0002c0002t0002g0118 a0002c0002t0002g0141 others(7): Show |
11 | HG00621.hp1 HG01123.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184+223_1184+224i others(146): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | ||||||
| chr13:31317892 | T | TAAAAAAG others(138): Show |
1 | a0002c0002t0003g0246 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1184+223_1184+224i others(147): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317892 | ||||||
| chr13:31317933 | G | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+248G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31317933 | |||||||
| chr13:31317977 | G | GA | 79 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(76): Show |
80 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1184+302dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31317977 | ||||||
| chr13:31318030 | T | C | 1 | a0001c0001t0004g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1184+345T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318030 | |||||||
| chr13:31318264 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1184+579G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318264 | |||||||
| chr13:31318271 | CA | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+590delA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31318271 | ||||||
| chr13:31318311 | G | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+626G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318311 | |||||||
| chr13:31318581 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+896C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318581 | |||||||
| chr13:31318719 | A | AT | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1184+1035dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31318719 | ||||||
| chr13:31318893 | T | C | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1184+1208T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318893 | |||||||
| chr13:31318933 | A | G | 3 | a0001c0001t0005g0198 a0001c0001t0005g0200 a0002c0002t0018g0251 |
3 | HG00140.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1184+1248A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31318933 | |||||||
| chr13:31319046 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1184+1361A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319046 | |||||||
| chr13:31319070 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1385A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319070 | |||||||
| chr13:31319109 | C | T | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1184+1424C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319109 | |||||||
| chr13:31319187 | G | C | 18 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0005g0003 others(15): Show |
19 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+1502G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319187 | |||||||
| chr13:31319245 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1560C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319245 | |||||||
| chr13:31319252 | T | C | 13 | a0001c0001t0006g0044 a0001c0001t0006g0050 a0001c0001t0006g0053 others(10): Show |
13 | HG00558.hp1 HG01943.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+1567T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319252 | |||||||
| chr13:31319364 | G | C | 70 | a0002c0002t0001g0250 a0002c0002t0002g0018 a0002c0002t0002g0066 others(67): Show |
71 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1184+1679G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319364 | |||||||
| chr13:31319390 | A | ATAAACTA others(9): Show |
144 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1184+1711_1184+171 others(20): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31319390 | ||||||
| chr13:31319444 | C | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+1759C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319444 | |||||||
| chr13:31319628 | A | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(2): Show |
5 | NA18950.hp2 NA18952.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184+1943A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319628 | |||||||
| chr13:31319644 | T | C | 1 | a0002c0002t0002g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1184+1959T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319644 | |||||||
| chr13:31319821 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2136C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319821 | |||||||
| chr13:31319917 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2232C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319917 | |||||||
| chr13:31319918 | T | C | 7 | a0002c0002t0004g0170 a0002c0002t0004g0175 a0002c0002t0004g0180 others(4): Show |
7 | HG01106.hp2 HG01243.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+2233T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31319918 | |||||||
| chr13:31320165 | G | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2480G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320165 | |||||||
| chr13:31320378 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(160): Show |
166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1184+2693C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320378 | |||||||
| chr13:31320382 | A | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2697A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320382 | |||||||
| chr13:31320439 | C | T | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1184+2754C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320439 | |||||||
| chr13:31320577 | G | A | 1 | a0001c0001t0007g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1184+2892G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320577 | |||||||
| chr13:31320608 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1184+2923T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320608 | |||||||
| chr13:31320814 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1185-2937C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320814 | |||||||
| chr13:31320997 | A | G | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1185-2754A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31320997 | |||||||
| chr13:31321325 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-2426C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321325 | |||||||
| chr13:31321330 | T | C | 1 | a0002c0010t0003g0012 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1185-2421T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321330 | |||||||
| chr13:31321490 | T | C | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1185-2261T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321490 | |||||||
| chr13:31321682 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1185-2069C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321682 | |||||||
| chr13:31321693 | T | C | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG00639.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1185-2058T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321693 | |||||||
| chr13:31321838 | AT | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(235): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1185-1903delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr13 | 31321838 | ||||||
| chr13:31321947 | T | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(2): Show |
5 | NA18950.hp2 NA18952.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-1804T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321947 | |||||||
| chr13:31321954 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-1797C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321954 | |||||||
| chr13:31321990 | C | A | 1 | a0001c0001t0007g0022 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1185-1761C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31321990 | |||||||
| chr13:31322058 | T | C | 1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1185-1693T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322058 | |||||||
| chr13:31322084 | T | C | 1 | a0002c0002t0003g0243 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1185-1667T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322084 | |||||||
| chr13:31322644 | A | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-1107A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322644 | |||||||
| chr13:31322680 | A | G | 1 | a0002c0002t0004g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1185-1071A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322680 | |||||||
| chr13:31322685 | C | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1185-1066C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322685 | |||||||
| chr13:31322841 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-910G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322841 | |||||||
| chr13:31322962 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1185-789G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31322962 | |||||||
| chr13:31323177 | A | G | 3 | a0001c0001t0004g0183 a0001c0001t0004g0212 a0001c0001t0004g0215 |
3 | HG02280.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1185-574A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323177 | |||||||
| chr13:31323245 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1185-506T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323245 | |||||||
| chr13:31323257 | A | G | 4 | a0002c0002t0004g0175 a0002c0002t0004g0181 a0002c0002t0012g0173 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-494A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323257 | |||||||
| chr13:31323356 | T | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1185-395T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323356 | |||||||
| chr13:31323479 | C | G | 1 | a0001c0001t0007g0017 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1185-272C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 13/14 | chr13 | 31323479 | |||||||
| chr13:31324108 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1329+213G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324108 | |||||||
| chr13:31324230 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+335A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324230 | |||||||
| chr13:31324231 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(74): Show |
78 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1329+336A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324231 | |||||||
| chr13:31324232 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+337T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324232 | |||||||
| chr13:31324234 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+339T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324234 | |||||||
| chr13:31324235 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+340A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324235 | |||||||
| chr13:31324236 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+341T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324236 | |||||||
| chr13:31324237 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+342A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324237 | |||||||
| chr13:31324238 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+343G>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324238 | |||||||
| chr13:31324240 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+345A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324240 | |||||||
| chr13:31324241 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+346C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324241 | |||||||
| chr13:31324242 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+347T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324242 | |||||||
| chr13:31324243 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+348G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324243 | |||||||
| chr13:31324244 | A | G | 67 | a0002c0002t0002g0018 a0002c0002t0002g0066 a0002c0002t0002g0067 others(64): Show |
68 | HG00099.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1329+349A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324244 | |||||||
| chr13:31324245 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+350C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324245 | |||||||
| chr13:31324246 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+351C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324246 | |||||||
| chr13:31324273 | C | G | 3 | a0002c0002t0003g0034 a0002c0002t0003g0035 a0002c0002t0003g0255 |
3 | HG02717.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1329+378C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324273 | |||||||
| chr13:31324344 | C | T | 1 | a0002c0002t0002g0127 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1329+449C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324344 | |||||||
| chr13:31324374 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+479G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324374 | |||||||
| chr13:31324444 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(226): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1329+549C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324444 | |||||||
| chr13:31324451 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+556C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324451 | |||||||
| chr13:31324543 | C | T | 1 | a0002c0002t0002g0128 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1329+648C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324543 | |||||||
| chr13:31324568 | A | G | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1329+673A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324568 | |||||||
| chr13:31324701 | CT | C | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+813delT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31324701 | ||||||
| chr13:31324850 | G | A | 14 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0002c0002t0002g0084 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1329+955G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324850 | |||||||
| chr13:31324861 | T | C | 2 | a0002c0002t0012g0173 a0002c0002t0012g0174 |
2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1329+966T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324861 | |||||||
| chr13:31324886 | T | G | 1 | a0002c0002t0002g0232 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1329+991T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324886 | |||||||
| chr13:31324895 | G | A | 2 | a0002c0002t0002g0066 a0002c0002t0002g0067 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1329+1000G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324895 | |||||||
| chr13:31324897 | G | A | 4 | a0002c0003t0003g0028 a0002c0003t0003g0226 a0005c0006t0003g0224 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1002G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324897 | |||||||
| chr13:31324922 | G | T | 4 | a0002c0002t0009g0016 a0002c0002t0009g0208 a0002c0002t0009g0209 others(1): Show |
4 | HG02015.hp1 NA18963.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1027G>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324922 | |||||||
| chr13:31324958 | C | T | 2 | a0001c0001t0005g0201 a0001c0001t0005g0202 |
2 | NA18979.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1329+1063C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31324958 | |||||||
| chr13:31325088 | T | C | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0228 |
3 | HG00639.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1329+1193T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325088 | |||||||
| chr13:31325196 | A | G | 1 | a0002c0002t0006g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1329+1301A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325196 | |||||||
| chr13:31325227 | G | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0150 a0001c0001t0001g0152 others(1): Show |
4 | NA18983.hp1 NA18990.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+1332G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325227 | |||||||
| chr13:31325333 | C | G | 1 | a0002c0002t0003g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1329+1438C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325333 | |||||||
| chr13:31325465 | C | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(146): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1329+1570C>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31325465 | |||||||
| chr13:31326090 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+2195G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326090 | |||||||
| chr13:31326108 | G | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(208): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1329+2213G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326108 | |||||||
| chr13:31326156 | T | A | 1 | a0002c0002t0003g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1329+2261T>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326156 | |||||||
| chr13:31326275 | C | CT | 170 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(167): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1329+2406dupT | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31326275 | ||||||
| chr13:31326275 | C | CTT | 33 | a0001c0001t0001g0048 a0001c0001t0001g0071 a0001c0001t0001g0093 others(30): Show |
33 | HG00558.hp2 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1329+2405_1329+240 others(6): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31326275 | ||||||
| chr13:31326483 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1329+2588G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326483 | |||||||
| chr13:31326498 | G | A | 1 | a0002c0002t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1329+2603G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326498 | |||||||
| chr13:31326532 | C | T | 2 | a0002c0002t0003g0027 a0002c0002t0017g0021 |
2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1329+2637C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326532 | |||||||
| chr13:31326900 | C | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2601C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326900 | |||||||
| chr13:31326931 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2570T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31326931 | |||||||
| chr13:31327068 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1330-2433T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327068 | |||||||
| chr13:31327073 | C | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(218): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1330-2428C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327073 | |||||||
| chr13:31327104 | C | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(208): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1330-2397C>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327104 | |||||||
| chr13:31327365 | T | G | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-2136T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327365 | |||||||
| chr13:31327625 | G | A | 3 | a0002c0002t0011g0007 a0002c0002t0011g0008 a0002c0002t0011g0009 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1330-1876G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327625 | |||||||
| chr13:31327631 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1330-1870G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327631 | |||||||
| chr13:31327696 | G | A | 2 | a0002c0002t0002g0233 a0002c0002t0002g0264 |
2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1330-1805G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327696 | |||||||
| chr13:31327721 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(204): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1330-1780A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327721 | |||||||
| chr13:31327899 | C | T | 2 | a0002c0003t0002g0160 a0002c0003t0002g0169 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1330-1602C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327899 | |||||||
| chr13:31327905 | T | C | 15 | a0001c0001t0005g0003 a0001c0001t0005g0047 a0001c0001t0005g0068 others(12): Show |
16 | HG00140.hp2 HG00609.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1330-1596T>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327905 | |||||||
| chr13:31327992 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-1509G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31327992 | |||||||
| chr13:31328286 | A | T | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-1215A>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328286 | |||||||
| chr13:31328398 | T | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(204): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1330-1103T>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328398 | |||||||
| chr13:31328524 | G | A | 3 | a0004c0004t0004g0203 a0004c0004t0004g0206 a0004c0004t0004g0207 |
3 | HG01071.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1330-977G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328524 | |||||||
| chr13:31328690 | C | T | 1 | a0002c0002t0003g0257 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1330-811C>T | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328690 | |||||||
| chr13:31328692 | C | CA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0024 others(166): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1330-784dupA | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | ||||||
| chr13:31328692 | C | CAA | 32 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0107 others(29): Show |
33 | HG00558.hp1 HG00673.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1330-785_1330-784d others(4): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | ||||||
| chr13:31328692 | C | CAAA | 8 | a0001c0001t0001g0108 a0001c0001t0005g0101 a0002c0002t0003g0263 others(5): Show |
8 | HG02074.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1330-786_1330-784d others(5): Show |
B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr13 | 31328692 | ||||||
| chr13:31328717 | A | C | 2 | a0002c0002t0009g0208 a0002c0002t0009g0209 |
2 | HG02015.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1330-784A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328717 | |||||||
| chr13:31328760 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1330-741A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328760 | |||||||
| chr13:31328764 | G | A | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-737G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328764 | |||||||
| chr13:31328847 | A | G | 3 | a0002c0002t0004g0170 a0002c0002t0004g0180 a0002c0011t0004g0179 |
3 | HG01106.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1330-654A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328847 | |||||||
| chr13:31328885 | A | G | 3 | a0002c0002t0003g0034 a0002c0002t0003g0035 a0002c0002t0003g0255 |
3 | HG02717.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1330-616A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31328885 | |||||||
| chr13:31329075 | A | G | 1 | a0002c0002t0004g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1330-426A>G | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329075 | |||||||
| chr13:31329116 | A | C | 1 | a0002c0002t0018g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1330-385A>C | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329116 | |||||||
| chr13:31329286 | G | A | 1 | a0002c0007t0023g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1330-215G>A | B3GLCT | ENSG00000187676.8 | transcript | ENST00000343307.5 | protein_coding | 14/14 | chr13 | 31329286 |