Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29929 |
| ensemblid | ENSG00000088035.18 |
| hgncid | 23157 |
| symbol | ALG6 |
| name | ALG6 alpha-1,3-glucosyltransferase |
| refseq_nuc | NM_013339.4 |
| refseq_prot | NP_037471.2 |
| ensembl_nuc | ENST00000263440.6 |
| ensembl_prot | ENSP00000263440.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 63367627 |
| end | 63438553 |
| strand | + |
| ver | v1.2 |
| region | chr1:63367627-63438553 |
| region5000 | chr1:63362627-63443553 |
| regionname0 | ALG6_chr1_63367627_63438553 |
| regionname5000 | ALG6_chr1_63362627_63443553 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 507 | 307 | 75 | 44 | 145 | 7 | 36 | 113 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| a0002 | 1/1 | 507 | 74 | 9 | 16 | 37 | 3 | 7 | 33 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| a0003 | 0/0 | 507 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| a0004 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| a0005 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| a0006 | 0/0 | 507 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | MEKWY others(502): Show |
chr1 | 63362627 | 63443553 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1521 | 291 | 61 | 43 | 144 | 7 | 36 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0001c0003 | 0/0 | 1521 | 8 | 7 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0001c0004 | 0/0 | 1521 | 7 | 7 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0001c0007 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0002c0002 | 1/1 | 1521 | 74 | 9 | 16 | 37 | 3 | 7 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0003c0005 | 0/0 | 1521 | 4 | 0 | 4 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0004c0008 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0005c0009 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 | ||
| a0006c0006 | 0/0 | 1521 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | ATGGA others(1516): Show |
chr1 | 63362627 | 63443553 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3325 | 52 | 0 | 5 | 39 | 2 | 6 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0002 | 0/0 | 3325 | 119 | 17 | 23 | 58 | 4 | 17 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0003 | 0/0 | 3321 | 74 | 12 | 12 | 40 | 1 | 9 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0004 | 0/0 | 3321 | 19 | 16 | 2 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0005 | 0/0 | 3325 | 6 | 0 | 0 | 3 | 0 | 3 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0007 | 0/0 | 3321 | 6 | 5 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0008 | 0/0 | 3321 | 5 | 5 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0010 | 0/0 | 3325 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0011 | 0/0 | 3325 | 3 | 3 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0013 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0015 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0017 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0018 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0001t0019 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0003t0009 | 0/0 | 3325 | 4 | 3 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0003t0010 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0003t0012 | 0/0 | 3325 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0003t0014 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0004t0004 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0001c0004t0006 | 0/0 | 3325 | 6 | 6 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0001c0007t0001 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0002c0002t0001 | 1/1 | 3325 | 72 | 9 | 16 | 36 | 3 | 6 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0002c0002t0005 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0002c0002t0016 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| a0003c0005t0003 | 0/0 | 3321 | 4 | 0 | 4 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0004c0008t0003 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3316): Show |
chr1 | 63362627 | 63443553 |
| a0005c0009t0020 | 0/0 | 3326 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3321): Show |
chr1 | 63362627 | 63443553 |
| a0006c0006t0002 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | GCGCA others(3320): Show |
chr1 | 63362627 | 63443553 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0010g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0010g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0015g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0018g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0001t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0009g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0012g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0003t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0004t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0001c0007t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0002c0002t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0003c0005t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0003c0005t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0003c0005t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0003c0005t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0004c0008t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0005c0009t0020g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| a0006c0006t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0358 | EUR | GBR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0111 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00733 | hp1 | a0003 | c0005 | t0003 | g0142 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG00741 | hp2 | a0003 | c0005 | t0003 | g0108 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01069 | hp2 | a0003 | c0005 | t0003 | g0130 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0306 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01071 | hp1 | a0003 | c0005 | t0003 | g0001 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01192 | hp1 | a0001 | c0003 | t0009 | g0164 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0308 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0305 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01891 | hp2 | a0001 | c0004 | t0006 | g0198 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0146 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02129 | hp2 | a0002 | c0002 | t0016 | g0196 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0065 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02280 | hp2 | a0001 | c0004 | t0006 | g0317 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0327 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0229 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02615 | hp1 | a0001 | c0004 | t0006 | g0197 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0161 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02622 | hp2 | a0001 | c0003 | t0009 | g0165 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02647 | hp1 | a0001 | c0003 | t0009 | g0166 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02809 | hp2 | a0001 | c0004 | t0004 | g0199 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02818 | hp1 | a0001 | c0004 | t0006 | g0200 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0326 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0228 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0369 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02965 | hp1 | a0001 | c0004 | t0006 | g0225 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0325 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0231 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03195 | hp2 | a0001 | c0003 | t0012 | g0232 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0162 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0230 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03516 | hp1 | a0005 | c0009 | t0020 | g0315 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03579 | hp2 | a0001 | c0004 | t0006 | g0157 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0329 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0330 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03710 | hp1 | a0006 | c0006 | t0002 | g0272 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0309 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03831 | hp1 | a0002 | c0002 | t0005 | g0104 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0323 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0018 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0140 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0311 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18522 | hp2 | a0001 | c0003 | t0012 | g0233 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0226 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18956 | hp1 | a0001 | c0001 | t0018 | g0009 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18966 | hp1 | a0001 | c0007 | t0001 | g0096 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18971 | hp2 | a0001 | c0001 | t0019 | g0148 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18997 | hp1 | a0001 | c0001 | t0013 | g0156 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19011 | hp2 | a0001 | c0001 | t0017 | g0005 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | LWK | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19043 | hp2 | a0001 | c0003 | t0014 | g0234 | AFR | LWK | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | ASW | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ASW | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0121 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | GIH | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0368 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02559 | hp1 | a0004 | c0008 | t0003 | g0202 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG06807 | hp1 | a0001 | c0003 | t0010 | g0316 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| NA20300 | hp2 | a0001 | c0003 | t0009 | g0167 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0017 | REF | REF | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0173 | REF | REF | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63406361 | T | C | 1 | a0003 | 4 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
missense_variant | MODERATE | c.391T>C | p.Tyr131His | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/15 | 659/3325 | 391/1524 | 131/507 | chr1 | 63406361 | |||
| chr1:63411329 | G | T | 1 | a0005 | 1 | HG03516.hp1 | missense_variant&splice_region_variant | MODERATE | c.678G>T | p.Lys226Asn | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/15 | 946/3325 | 678/1524 | 226/507 | chr1 | 63411329 | |||
| chr1:63411996 | A | G | 1 | a0004 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.751A>G | p.Thr251Ala | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/15 | 1019/3325 | 751/1524 | 251/507 | chr1 | 63411996 | |||
| chr1:63415881 | C | T | 5 | a0001 a0003 a0004 others(2): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
missense_variant | MODERATE | c.911C>T | p.Ser304Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/15 | 1179/3325 | 911/1524 | 304/507 | chr1 | 63415881 | |||
| chr1:63419415 | G | C | 1 | a0006 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1033G>C | p.Glu345Gln | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/15 | 1301/3325 | 1033/1524 | 345/507 | chr1 | 63419415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63411971 | C | T | 1 | a0001c0004 | 7 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.726C>T | p.Phe242Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/15 | 994/3325 | 726/1524 | 242/507 | chr1 | 63411971 | |||
| chr1:63415951 | T | C | 2 | a0001c0003 a0001c0004 |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.981T>C | p.Phe327Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/15 | 1249/3325 | 981/1524 | 327/507 | chr1 | 63415951 | |||
| chr1:63436948 | C | T | 1 | a0001c0007 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1452C>T | p.Phe484Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1720/3325 | 1452/1524 | 484/507 | chr1 | 63436948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63367683 | G | C | 1 | a0001c0001t0013 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/15 | 3295 | chr1 | 63367683 | ||||||
| chr1:63367684 | C | G | 1 | a0001c0001t0013 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-211C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/15 | 3294 | chr1 | 63367684 | ||||||
| chr1:63370842 | C | G | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(8): Show |
102 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/15 | chr1 | 63370842 | |||||||
| chr1:63370857 | T | G | 2 | a0001c0003t0012 a0001c0003t0014 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-121T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/15 | 121 | chr1 | 63370857 | ||||||
| chr1:63437195 | G | T | 1 | a0001c0001t0018 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 175 | chr1 | 63437195 | ||||||
| chr1:63437207 | A | G | 1 | a0001c0001t0017 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 187 | chr1 | 63437207 | ||||||
| chr1:63437530 | T | C | 1 | a0001c0001t0015 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 510 | chr1 | 63437530 | ||||||
| chr1:63437781 | T | C | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 761 | chr1 | 63437781 | ||||||
| chr1:63437807 | CATTAT | C | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(5): Show |
111 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*795_*799delTATAT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 795 | INFO_REALIGN_3_PRIME | chr1 | 63437807 | |||||
| chr1:63437821 | T | C | 1 | a0002c0002t0016 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 801 | chr1 | 63437821 | ||||||
| chr1:63437864 | T | C | 2 | a0001c0001t0007 a0001c0001t0008 |
11 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*844T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 844 | chr1 | 63437864 | ||||||
| chr1:63437981 | C | T | 1 | a0001c0001t0011 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*961C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 961 | chr1 | 63437981 | ||||||
| chr1:63438156 | C | T | 1 | a0001c0001t0011 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1136C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1136 | chr1 | 63438156 | ||||||
| chr1:63438175 | A | AT | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(6): Show |
112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1156dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1157 | INFO_REALIGN_3_PRIME | chr1 | 63438175 | |||||
| chr1:63438342 | A | G | 3 | a0001c0003t0009 a0001c0003t0014 a0001c0004t0006 |
11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1322 | chr1 | 63438342 | ||||||
| chr1:63438435 | T | G | 3 | a0001c0001t0010 a0001c0001t0011 a0001c0003t0010 |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1415T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1415 | chr1 | 63438435 | ||||||
| chr1:63438454 | T | C | 3 | a0001c0001t0010 a0001c0001t0011 a0001c0003t0010 |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1434T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1434 | chr1 | 63438454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63367765 | C | G | 55 | a0001c0001t0001g0016 a0001c0001t0001g0328 a0001c0001t0001g0331 others(52): Show |
57 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.-208+78C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367765 | |||||||
| chr1:63367779 | G | T | 44 | a0001c0001t0001g0016 a0001c0001t0001g0328 a0001c0001t0001g0331 others(41): Show |
46 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.-208+92G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367779 | |||||||
| chr1:63367802 | C | G | 3 | a0001c0001t0004g0325 a0001c0001t0010g0326 a0001c0001t0010g0327 |
3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-208+115C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367802 | |||||||
| chr1:63367903 | G | T | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-208+216G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367903 | |||||||
| chr1:63367953 | A | C | 3 | a0001c0001t0004g0325 a0001c0001t0010g0326 a0001c0001t0010g0327 |
3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-208+266A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367953 | |||||||
| chr1:63368022 | C | T | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-208+335C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368022 | |||||||
| chr1:63368024 | C | T | 11 | a0001c0001t0001g0313 a0002c0002t0001g0003 a0002c0002t0001g0305 others(8): Show |
13 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-208+337C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368024 | |||||||
| chr1:63368409 | A | G | 71 | a0001c0001t0001g0241 a0001c0001t0001g0279 a0001c0001t0001g0280 others(68): Show |
72 | HG00408.hp2 HG00423.hp2 HG01261.hp1 others(69): Show |
intron_variant | MODIFIER | c.-208+722A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368409 | |||||||
| chr1:63368599 | C | T | 3 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-208+912C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368599 | |||||||
| chr1:63368742 | C | T | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-208+1055C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368742 | |||||||
| chr1:63368764 | G | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0019 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-208+1077G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368764 | |||||||
| chr1:63368783 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-208+1096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368783 | |||||||
| chr1:63368806 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-208+1119T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368806 | |||||||
| chr1:63368850 | G | A | 160 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(157): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-208+1163G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368850 | |||||||
| chr1:63368853 | A | G | 160 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(157): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-208+1166A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368853 | |||||||
| chr1:63368924 | G | C | 12 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(9): Show |
12 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-208+1237G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368924 | |||||||
| chr1:63369022 | C | T | 6 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(3): Show |
6 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-208+1335C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369022 | |||||||
| chr1:63369063 | C | CATATG | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-208+1382_-208+138 others(9): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369063 | ||||||
| chr1:63369143 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0084 others(23): Show |
27 | HG00408.hp1 HG00423.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-208+1456C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369143 | |||||||
| chr1:63369351 | G | A | 12 | a0001c0001t0001g0313 a0001c0001t0004g0102 a0002c0002t0001g0003 others(9): Show |
14 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-207-1420G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369351 | |||||||
| chr1:63369366 | C | T | 1 | a0001c0004t0006g0225 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-207-1405C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369366 | |||||||
| chr1:63369402 | G | T | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-1369G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369402 | |||||||
| chr1:63369438 | G | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 |
3 | NA18986.hp1 NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-207-1333G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369438 | |||||||
| chr1:63369457 | C | T | 19 | a0001c0001t0003g0002 a0001c0001t0003g0020 a0001c0001t0003g0208 others(16): Show |
21 | HG00544.hp1 HG00558.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-207-1314C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369457 | |||||||
| chr1:63369569 | C | T | 4 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 others(1): Show |
4 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207-1202C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369569 | |||||||
| chr1:63369629 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-207-1142C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369629 | |||||||
| chr1:63369639 | G | GA | 19 | a0001c0001t0001g0313 a0001c0001t0001g0331 a0001c0001t0002g0235 others(16): Show |
21 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-207-1123dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369639 | ||||||
| chr1:63369822 | A | AT | 6 | a0001c0001t0002g0014 a0001c0001t0002g0300 a0001c0001t0002g0301 others(3): Show |
7 | HG01496.hp2 HG01952.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207-940dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369822 | ||||||
| chr1:63369950 | C | T | 1 | a0001c0001t0002g0299 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-207-821C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369950 | |||||||
| chr1:63369968 | G | A | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-803G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369968 | |||||||
| chr1:63370055 | T | C | 80 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(77): Show |
85 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-207-716T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370055 | |||||||
| chr1:63370158 | C | G | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-613C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370158 | |||||||
| chr1:63370161 | T | TA | 78 | a0001c0001t0002g0238 a0001c0001t0003g0001 a0001c0001t0003g0002 others(75): Show |
83 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-207-595dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63370161 | ||||||
| chr1:63370161 | TA | T | 7 | a0001c0001t0001g0101 a0001c0001t0002g0298 a0001c0001t0003g0207 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-207-595delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63370161 | ||||||
| chr1:63370221 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-207-550C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370221 | |||||||
| chr1:63370230 | A | G | 338 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(335): Show |
353 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.-207-541A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370230 | |||||||
| chr1:63370231 | T | G | 5 | a0002c0002t0001g0333 a0002c0002t0001g0334 a0002c0002t0001g0335 others(2): Show |
5 | NA18973.hp2 NA18991.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.-207-540T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370231 | |||||||
| chr1:63370300 | A | G | 3 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-207-471A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370300 | |||||||
| chr1:63370389 | C | T | 1 | a0001c0003t0014g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-207-382C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370389 | |||||||
| chr1:63370390 | G | A | 3 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0160 |
3 | HG01167.hp1 HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-207-381G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370390 | |||||||
| chr1:63370424 | G | A | 1 | a0002c0002t0001g0321 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-207-347G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370424 | |||||||
| chr1:63370466 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-207-305A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370466 | |||||||
| chr1:63370674 | T | C | 7 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
7 | HG01192.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207-97T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370674 | |||||||
| chr1:63371079 | T | TA | 7 | a0001c0001t0001g0241 a0001c0001t0002g0021 a0001c0001t0002g0024 others(4): Show |
7 | HG01891.hp1 NA18953.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+30dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63371079 | ||||||
| chr1:63371135 | A | G | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+76A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371135 | |||||||
| chr1:63371148 | T | G | 6 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(3): Show |
6 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+89T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371148 | |||||||
| chr1:63371383 | G | A | 1 | a0002c0002t0001g0338 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.82+324G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371383 | |||||||
| chr1:63371411 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.82+352G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371411 | |||||||
| chr1:63371416 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.82+357G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371416 | |||||||
| chr1:63371532 | C | T | 1 | a0002c0002t0001g0314 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.82+473C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371532 | |||||||
| chr1:63371589 | C | T | 5 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(2): Show |
6 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+530C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371589 | |||||||
| chr1:63371625 | T | G | 1 | a0001c0001t0003g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.82+566T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371625 | |||||||
| chr1:63371627 | C | G | 1 | a0001c0001t0002g0297 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.82+568C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371627 | |||||||
| chr1:63371753 | C | T | 159 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(156): Show |
164 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.82+694C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371753 | |||||||
| chr1:63371762 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82+703G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371762 | |||||||
| chr1:63371892 | C | T | 1 | a0002c0002t0001g0368 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82+833C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371892 | |||||||
| chr1:63372025 | C | T | 7 | a0001c0004t0004g0199 a0001c0004t0006g0157 a0001c0004t0006g0197 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+966C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372025 | |||||||
| chr1:63372217 | A | G | 12 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(9): Show |
12 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+1158A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372217 | |||||||
| chr1:63372344 | A | G | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+1285A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372344 | |||||||
| chr1:63372604 | A | C | 1 | a0001c0001t0013g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.82+1545A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372604 | |||||||
| chr1:63372706 | C | T | 160 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(157): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.82+1647C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372706 | |||||||
| chr1:63372763 | T | G | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+1704T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372763 | |||||||
| chr1:63372825 | A | G | 1 | a0002c0002t0016g0196 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.82+1766A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372825 | |||||||
| chr1:63373094 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+2035G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373094 | |||||||
| chr1:63373125 | G | C | 11 | a0001c0001t0001g0313 a0002c0002t0001g0003 a0002c0002t0001g0305 others(8): Show |
13 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+2066G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373125 | |||||||
| chr1:63373136 | A | G | 1 | a0001c0001t0015g0369 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82+2077A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373136 | |||||||
| chr1:63373437 | T | C | 4 | a0002c0002t0001g0015 a0002c0002t0001g0338 a0002c0002t0001g0339 others(1): Show |
5 | NA18946.hp2 NA18962.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2378T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373437 | |||||||
| chr1:63373464 | G | A | 3 | a0001c0001t0004g0325 a0001c0001t0010g0326 a0001c0001t0010g0327 |
3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+2405G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373464 | |||||||
| chr1:63373531 | G | A | 4 | a0002c0002t0001g0341 a0002c0002t0001g0342 a0002c0002t0001g0343 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2472G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373531 | |||||||
| chr1:63373594 | C | CA | 6 | a0001c0001t0002g0025 a0001c0001t0002g0169 a0001c0001t0003g0105 others(3): Show |
6 | HG01070.hp1 HG02738.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2544dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373594 | ||||||
| chr1:63373657 | C | CT | 6 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0235 others(3): Show |
6 | HG01952.hp2 HG02109.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2598_82+2599ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373657 | |||||||
| chr1:63373657 | CA | C | 5 | a0001c0001t0002g0244 a0001c0003t0012g0232 a0001c0003t0012g0233 others(2): Show |
5 | HG01070.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2599delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373657 | |||||||
| chr1:63373658 | A | AT | 8 | a0001c0001t0004g0195 a0001c0001t0008g0228 a0001c0001t0008g0229 others(5): Show |
8 | HG02145.hp2 HG02572.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2619dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | ||||||
| chr1:63373658 | A | ATT | 10 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(7): Show |
10 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2618_82+2619dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | ||||||
| chr1:63373658 | A | T | 170 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(167): Show |
177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.82+2599A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373658 | |||||||
| chr1:63373658 | AT | A | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(81): Show |
90 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.82+2619delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | ||||||
| chr1:63373658 | ATT | A | 45 | a0001c0001t0001g0016 a0001c0001t0001g0328 a0001c0001t0001g0331 others(42): Show |
47 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.82+2618_82+2619del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | ||||||
| chr1:63373714 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82+2655G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373714 | |||||||
| chr1:63373913 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82+2854C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373913 | |||||||
| chr1:63373914 | G | A | 3 | a0001c0001t0004g0325 a0001c0001t0010g0326 a0001c0001t0010g0327 |
3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+2855G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373914 | |||||||
| chr1:63373944 | A | G | 1 | a0001c0001t0005g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.82+2885A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373944 | |||||||
| chr1:63374043 | C | T | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+2984C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374043 | |||||||
| chr1:63374083 | A | T | 1 | a0001c0001t0013g0156 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.82+3024A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374083 | |||||||
| chr1:63374189 | G | A | 3 | a0001c0004t0006g0157 a0001c0004t0006g0197 a0001c0004t0006g0198 |
3 | HG01891.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+3130G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374189 | |||||||
| chr1:63374246 | A | T | 96 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(93): Show |
102 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+3187A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374246 | |||||||
| chr1:63374278 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.82+3219G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374278 | |||||||
| chr1:63374394 | G | A | 9 | a0001c0001t0002g0324 a0001c0001t0004g0318 a0001c0001t0004g0319 others(6): Show |
9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+3335G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374394 | |||||||
| chr1:63374401 | G | A | 3 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.82+3342G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374401 | |||||||
| chr1:63374456 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.82+3397C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374456 | |||||||
| chr1:63374496 | C | T | 3 | a0001c0001t0004g0325 a0001c0001t0010g0326 a0001c0001t0010g0327 |
3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+3437C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374496 | |||||||
| chr1:63374522 | G | A | 4 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+3463G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374522 | |||||||
| chr1:63374585 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82+3526G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374585 | |||||||
| chr1:63374628 | CA | C | 326 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(323): Show |
339 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.82+3581delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63374628 | ||||||
| chr1:63374734 | A | G | 3 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 |
3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.82+3675A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374734 | |||||||
| chr1:63374832 | T | C | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+3773T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374832 | |||||||
| chr1:63375026 | A | T | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82+3967A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375026 | |||||||
| chr1:63375071 | C | T | 2 | a0001c0001t0004g0318 a0001c0001t0004g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.82+4012C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375071 | |||||||
| chr1:63375093 | C | A | 5 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0011g0161 others(2): Show |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+4034C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375093 | |||||||
| chr1:63375199 | TAA | T | 132 | a0001c0001t0001g0016 a0001c0001t0001g0328 a0001c0001t0001g0331 others(129): Show |
139 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.82+4149_82+4150del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375199 | ||||||
| chr1:63375309 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82+4250A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375309 | |||||||
| chr1:63375333 | T | C | 3 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 |
3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+4274T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375333 | |||||||
| chr1:63375410 | A | AT | 79 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0097 others(76): Show |
81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.82+4378dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | ||||||
| chr1:63375410 | A | ATT | 10 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0001c0001t0002g0235 others(7): Show |
11 | HG01106.hp1 HG01175.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+4377_82+4378dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | ||||||
| chr1:63375410 | AT | A | 10 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG01358.hp1 HG01993.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+4378delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | ||||||
| chr1:63375410 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.82+4368_82+4378del others(11): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | ||||||
| chr1:63375410 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+4367_82+4378del others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | ||||||
| chr1:63375424 | TTTTTTTT others(7): Show |
T | 4 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+4366_82+4379del others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375424 | |||||||
| chr1:63375438 | C | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+4379C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375438 | |||||||
| chr1:63375740 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.82+4681A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375740 | |||||||
| chr1:63376033 | C | CAGTCATG others(282): Show |
3 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 |
3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+4985_82+4986ins others(289): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63376033 | ||||||
| chr1:63376133 | G | C | 3 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 |
3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+5074G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376133 | |||||||
| chr1:63376172 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82+5113C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376172 | |||||||
| chr1:63376339 | C | T | 1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82+5280C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376339 | |||||||
| chr1:63376581 | A | G | 1 | a0001c0001t0002g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.82+5522A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376581 | |||||||
| chr1:63376607 | A | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+5548A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376607 | |||||||
| chr1:63376745 | T | G | 1 | a0001c0001t0003g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.82+5686T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376745 | |||||||
| chr1:63376904 | T | C | 1 | a0002c0002t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5845T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376904 | |||||||
| chr1:63376905 | C | T | 1 | a0002c0002t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5846C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376905 | |||||||
| chr1:63376906 | T | C | 1 | a0002c0002t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5847T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376906 | |||||||
| chr1:63377251 | T | G | 1 | a0001c0001t0003g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.82+6192T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377251 | |||||||
| chr1:63377301 | G | A | 157 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(154): Show |
162 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.82+6242G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377301 | |||||||
| chr1:63377467 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0002g0243 |
2 | NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.82+6408A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377467 | |||||||
| chr1:63377523 | C | T | 87 | a0001c0001t0001g0313 a0001c0001t0003g0001 a0001c0001t0003g0002 others(84): Show |
92 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.82+6464C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377523 | |||||||
| chr1:63377641 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.82+6582T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377641 | |||||||
| chr1:63377764 | C | G | 1 | a0001c0001t0004g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+6705C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377764 | |||||||
| chr1:63377816 | C | G | 4 | a0001c0001t0003g0209 a0001c0001t0003g0218 a0001c0001t0003g0219 others(1): Show |
4 | HG01358.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+6757C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377816 | |||||||
| chr1:63378085 | A | G | 1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82+7026A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378085 | |||||||
| chr1:63378461 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.82+7402A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378461 | |||||||
| chr1:63378503 | T | A | 3 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0003t0010g0316 |
3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+7444T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378503 | |||||||
| chr1:63378762 | A | T | 5 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0010g0326 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+7703A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378762 | |||||||
| chr1:63378782 | C | G | 100 | a0001c0001t0001g0313 a0001c0001t0002g0186 a0001c0001t0002g0187 others(97): Show |
105 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+7723C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378782 | |||||||
| chr1:63378839 | G | C | 105 | a0001c0001t0001g0313 a0001c0001t0002g0186 a0001c0001t0002g0187 others(102): Show |
110 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+7780G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378839 | |||||||
| chr1:63378864 | G | GT | 97 | a0001c0001t0001g0313 a0001c0001t0002g0186 a0001c0001t0002g0187 others(94): Show |
102 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+7817dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63378864 | ||||||
| chr1:63378864 | G | T | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+7805G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378864 | |||||||
| chr1:63378867 | T | TG | 4 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0115 others(1): Show |
4 | NA18939.hp2 NA18957.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+7808_82+7809ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378867 | |||||||
| chr1:63378943 | C | CT | 105 | a0001c0001t0001g0313 a0001c0001t0002g0186 a0001c0001t0002g0187 others(102): Show |
110 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+7889dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63378943 | ||||||
| chr1:63379064 | G | A | 10 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(7): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+8005G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379064 | |||||||
| chr1:63379065 | T | C | 72 | a0001c0001t0001g0313 a0001c0001t0003g0001 a0001c0001t0003g0002 others(69): Show |
76 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.82+8006T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379065 | |||||||
| chr1:63379299 | C | T | 155 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(152): Show |
160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.82+8240C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379299 | |||||||
| chr1:63379370 | TAGG | T | 5 | a0001c0001t0004g0318 a0001c0001t0004g0319 a0001c0001t0010g0326 others(2): Show |
5 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+8314_82+8316del others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63379370 | ||||||
| chr1:63379396 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.82+8337G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379396 | |||||||
| chr1:63379459 | G | GAGATAGT others(6): Show |
1 | a0001c0001t0002g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+8400_82+8401ins others(13): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379459 | |||||||
| chr1:63379460 | C | A | 1 | a0001c0001t0002g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+8401C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379460 | |||||||
| chr1:63379520 | C | T | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.82+8461C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379520 | |||||||
| chr1:63379547 | C | T | 289 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(286): Show |
301 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.82+8488C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379547 | |||||||
| chr1:63379582 | G | A | 1 | a0001c0001t0001g0354 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82+8523G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379582 | |||||||
| chr1:63379659 | A | C | 1 | a0001c0001t0001g0365 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.82+8600A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379659 | |||||||
| chr1:63379721 | A | G | 4 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 others(1): Show |
4 | HG03195.hp2 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+8662A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379721 | |||||||
| chr1:63379722 | C | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+8663C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379722 | |||||||
| chr1:63380075 | G | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82+9016G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380075 | |||||||
| chr1:63380312 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.82+9253C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380312 | |||||||
| chr1:63380338 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+9279G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380338 | |||||||
| chr1:63380435 | GTAACTTA others(12): Show |
G | 6 | a0001c0004t0004g0199 a0001c0004t0006g0157 a0001c0004t0006g0197 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+9379_82+9397del others(19): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63380435 | ||||||
| chr1:63380577 | T | C | 7 | a0002c0002t0001g0201 a0002c0002t0001g0320 a0002c0002t0001g0321 others(4): Show |
7 | HG02280.hp1 HG03471.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+9518T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380577 | |||||||
| chr1:63380583 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.82+9524T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380583 | |||||||
| chr1:63380589 | G | A | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+9530G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380589 | |||||||
| chr1:63380648 | A | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+9589A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380648 | |||||||
| chr1:63380821 | A | G | 1 | a0001c0001t0002g0298 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.82+9762A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380821 | |||||||
| chr1:63381099 | T | C | 239 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(236): Show |
248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.82+10040T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381099 | |||||||
| chr1:63381122 | C | T | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+10063C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381122 | |||||||
| chr1:63381176 | C | T | 69 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(66): Show |
73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.82+10117C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381176 | |||||||
| chr1:63381181 | G | A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+10122G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381181 | |||||||
| chr1:63381182 | C | T | 1 | a0001c0004t0006g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+10123C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381182 | |||||||
| chr1:63381322 | C | T | 4 | a0002c0002t0001g0341 a0002c0002t0001g0342 a0002c0002t0001g0343 others(1): Show |
4 | NA18939.hp1 NA18953.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+10263C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381322 | |||||||
| chr1:63381326 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+10267C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381326 | |||||||
| chr1:63381334 | G | T | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+10275G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381334 | |||||||
| chr1:63381385 | C | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.82+10326C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381385 | |||||||
| chr1:63381424 | A | G | 6 | a0001c0004t0004g0199 a0001c0004t0006g0157 a0001c0004t0006g0197 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+10365A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381424 | |||||||
| chr1:63381560 | C | T | 5 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0002c0002t0001g0178 others(2): Show |
5 | NA18941.hp1 NA18950.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+10501C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381560 | |||||||
| chr1:63381643 | T | G | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.82+10584T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381643 | |||||||
| chr1:63381664 | AGGGAG | A | 141 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(138): Show |
146 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.82+10626_82+10630d others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63381664 | ||||||
| chr1:63381693 | A | G | 1 | a0002c0002t0005g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.82+10634A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381693 | |||||||
| chr1:63381747 | C | T | 23 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(20): Show |
24 | HG01167.hp2 HG02145.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.82+10688C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381747 | |||||||
| chr1:63381825 | C | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+10766C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381825 | |||||||
| chr1:63381852 | G | T | 1 | a0002c0002t0001g0175 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.82+10793G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381852 | |||||||
| chr1:63381897 | T | C | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+10838T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381897 | |||||||
| chr1:63382164 | T | A | 8 | a0001c0001t0003g0207 a0001c0001t0004g0102 a0002c0002t0001g0015 others(5): Show |
9 | HG01243.hp1 HG02559.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+11105T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382164 | |||||||
| chr1:63382165 | A | T | 4 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0004t0006g0317 others(1): Show |
4 | HG01516.hp1 HG01517.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+11106A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382165 | |||||||
| chr1:63382221 | A | G | 5 | a0001c0001t0003g0105 a0001c0001t0003g0138 a0001c0001t0003g0139 others(2): Show |
5 | HG02071.hp2 NA18964.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+11162A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382221 | |||||||
| chr1:63382286 | C | T | 1 | a0002c0002t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+11227C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382286 | |||||||
| chr1:63382505 | C | T | 17 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(14): Show |
18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+11446C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382505 | |||||||
| chr1:63382506 | G | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(2): Show |
6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+11447G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382506 | |||||||
| chr1:63382538 | G | A | 2 | a0001c0003t0012g0232 a0001c0003t0012g0233 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82+11479G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382538 | |||||||
| chr1:63382583 | C | T | 1 | a0001c0001t0001g0364 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+11524C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382583 | |||||||
| chr1:63382640 | AGTTTTTT others(17): Show |
A | 18 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(15): Show |
19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+11592_82+11615d others(26): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382640 | ||||||
| chr1:63382642 | TTTTTTTT others(6): Show |
T | 120 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(117): Show |
124 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.82+11592_82+11604d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382642 | ||||||
| chr1:63382642 | TTTTTTTT others(16): Show |
T | 1 | a0001c0001t0004g0189 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.82+11592_82+11614d others(25): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382642 | ||||||
| chr1:63382645 | TTTTTTGT others(3): Show |
T | 1 | a0001c0001t0003g0120 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.82+11592_82+11601d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382645 | ||||||
| chr1:63382650 | T | G | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+11591T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382650 | |||||||
| chr1:63382650 | TGTTTGTT others(8): Show |
T | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+11592_82+11606d others(17): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382650 | |||||||
| chr1:63382651 | G | T | 138 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(135): Show |
144 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.82+11592G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382651 | |||||||
| chr1:63382655 | G | T | 1 | a0001c0004t0004g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82+11596G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382655 | |||||||
| chr1:63382655 | GTTTTTTT others(7): Show |
G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(148): Show |
158 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.82+11620_82+11633d others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382655 | ||||||
| chr1:63382656 | TTTTTTTT others(16): Show |
T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+11606_82+11628d others(25): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382656 | ||||||
| chr1:63382659 | T | G | 3 | a0001c0001t0002g0235 a0001c0001t0002g0278 a0001c0001t0002g0290 |
3 | NA19000.hp2 NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.82+11600T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382659 | |||||||
| chr1:63382666 | TTTTTTTT others(6): Show |
T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG01168.hp2 HG01433.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+11620_82+11632d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382666 | ||||||
| chr1:63382667 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0002g0235 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.82+11620_82+11631d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382667 | ||||||
| chr1:63382669 | T | G | 128 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(125): Show |
132 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.82+11610T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382669 | |||||||
| chr1:63382673 | T | G | 125 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
129 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.82+11614T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382673 | |||||||
| chr1:63382674 | T | G | 6 | a0001c0001t0003g0119 a0001c0001t0007g0112 a0001c0001t0008g0228 others(3): Show |
6 | HG02572.hp2 HG02886.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+11615T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382674 | |||||||
| chr1:63382680 | T | G | 1 | a0001c0001t0003g0120 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.82+11621T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382680 | |||||||
| chr1:63382684 | T | G | 2 | a0001c0001t0004g0325 a0001c0001t0013g0156 |
2 | HG03098.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.82+11625T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382684 | |||||||
| chr1:63382685 | T | G | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0105 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.82+11626T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382685 | |||||||
| chr1:63382737 | G | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0328 a0001c0001t0001g0331 others(14): Show |
18 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+11678G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382737 | |||||||
| chr1:63382745 | G | A | 38 | a0001c0001t0002g0057 a0001c0001t0002g0236 a0001c0001t0002g0237 others(35): Show |
38 | HG00408.hp2 HG00423.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.82+11686G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382745 | |||||||
| chr1:63382769 | G | A | 71 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(68): Show |
75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.82+11710G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382769 | |||||||
| chr1:63382822 | C | T | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.82+11763C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382822 | |||||||
| chr1:63382833 | A | G | 25 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(22): Show |
26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.82+11774A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382833 | |||||||
| chr1:63382867 | A | G | 25 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(22): Show |
26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.82+11808A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382867 | |||||||
| chr1:63382879 | T | C | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+11820T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382879 | |||||||
| chr1:63382898 | G | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.82+11839G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382898 | |||||||
| chr1:63382922 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82+11863C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382922 | |||||||
| chr1:63382927 | C | T | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+11868C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382927 | |||||||
| chr1:63382965 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82+11906C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382965 | |||||||
| chr1:63383073 | A | G | 1 | a0001c0001t0002g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82+12014A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383073 | |||||||
| chr1:63383093 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82+12034G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383093 | |||||||
| chr1:63383093 | G | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(4): Show |
9 | HG01192.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+12034G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383093 | |||||||
| chr1:63383145 | C | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+12086C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383145 | |||||||
| chr1:63383355 | C | T | 1 | a0002c0002t0001g0312 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82+12296C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383355 | |||||||
| chr1:63383357 | A | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+12298A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383357 | |||||||
| chr1:63383860 | C | T | 1 | a0002c0002t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.83-12653C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383860 | |||||||
| chr1:63383964 | C | T | 1 | a0001c0003t0012g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83-12549C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383964 | |||||||
| chr1:63384193 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-12320G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384193 | |||||||
| chr1:63384343 | A | G | 25 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(22): Show |
26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-12170A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384343 | |||||||
| chr1:63384373 | C | T | 1 | a0001c0001t0002g0293 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.83-12140C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384373 | |||||||
| chr1:63384387 | G | A | 1 | a0002c0002t0001g0347 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.83-12126G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384387 | |||||||
| chr1:63384509 | C | T | 1 | a0002c0002t0001g0336 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.83-12004C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384509 | |||||||
| chr1:63384621 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83-11892G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384621 | |||||||
| chr1:63384712 | C | T | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.83-11801C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384712 | |||||||
| chr1:63384717 | T | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-11796T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384717 | |||||||
| chr1:63385001 | A | G | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83-11512A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385001 | |||||||
| chr1:63385184 | C | CT | 13 | a0002c0002t0001g0015 a0002c0002t0001g0079 a0002c0002t0001g0080 others(10): Show |
14 | HG02280.hp1 NA18906.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.83-11296dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CT | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0090 others(35): Show |
39 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.83-11296delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTT | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.83-11297_83-11296d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTT | C | 10 | a0001c0001t0003g0170 a0001c0001t0004g0195 a0001c0001t0008g0229 others(7): Show |
10 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-11299_83-11296d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTTT | C | 47 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0013 others(44): Show |
48 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.83-11300_83-11296d others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTTTT | C | 55 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0002 others(52): Show |
57 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.83-11301_83-11296d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0286 a0006c0006t0002g0272 |
3 | HG02027.hp1 HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.83-11307_83-11296d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTTTTT others(6): Show |
C | 117 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
121 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.83-11308_83-11296d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385184 | CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0001g0356 a0001c0001t0001g0360 a0001c0001t0001g0361 others(4): Show |
7 | HG00438.hp1 HG02165.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-11309_83-11296d others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | ||||||
| chr1:63385205 | T | C | 14 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(11): Show |
16 | HG01106.hp2 HG01192.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-11308T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385205 | |||||||
| chr1:63385372 | G | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-11141G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385372 | |||||||
| chr1:63385693 | T | C | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-10820T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385693 | |||||||
| chr1:63385700 | G | C | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-10813G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385700 | |||||||
| chr1:63385749 | T | C | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-10764T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385749 | |||||||
| chr1:63385880 | A | ATTC | 302 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.83-10630_83-10628d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385880 | ||||||
| chr1:63386194 | T | C | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83-10319T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386194 | |||||||
| chr1:63386230 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.83-10283G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386230 | |||||||
| chr1:63386250 | A | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-10263A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386250 | |||||||
| chr1:63386270 | G | GT | 22 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(19): Show |
23 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.83-10234dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63386270 | ||||||
| chr1:63386562 | A | G | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-9951A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386562 | |||||||
| chr1:63386570 | G | A | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.83-9943G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386570 | |||||||
| chr1:63386574 | C | A | 1 | a0004c0008t0003g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83-9939C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386574 | |||||||
| chr1:63386710 | C | T | 2 | a0001c0001t0003g0154 a0001c0001t0013g0156 |
2 | NA18997.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.83-9803C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386710 | |||||||
| chr1:63386751 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.83-9762G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386751 | |||||||
| chr1:63386806 | C | A | 19 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(16): Show |
20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.83-9707C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386806 | |||||||
| chr1:63386888 | T | C | 6 | a0001c0001t0003g0106 a0001c0001t0003g0121 a0001c0001t0003g0122 others(3): Show |
6 | HG01884.hp1 HG02293.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-9625T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386888 | |||||||
| chr1:63386933 | C | T | 23 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0022 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.83-9580C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386933 | |||||||
| chr1:63387208 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83-9305G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387208 | |||||||
| chr1:63387532 | C | CT | 15 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0101 others(12): Show |
15 | HG00438.hp2 HG01361.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-8954dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | C | CTTT | 55 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0239 others(52): Show |
59 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.83-8956_83-8954dup others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | C | CTTTT | 32 | a0001c0001t0002g0022 a0001c0001t0002g0052 a0001c0001t0002g0053 others(29): Show |
32 | HG01168.hp2 HG01175.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.83-8957_83-8954dup others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | C | CTTTTT | 63 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(60): Show |
67 | HG00408.hp2 HG00558.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.83-8958_83-8954dup others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | C | CTTTTTT | 44 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0028 others(41): Show |
44 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.83-8959_83-8954dup others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | C | CTTTTTTT | 9 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0069 others(6): Show |
9 | HG00544.hp2 HG01358.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.83-8960_83-8954dup others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | CT | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0241 a0001c0001t0001g0279 others(5): Show |
8 | HG00738.hp2 HG01070.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-8954delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387532 | CTTTTTTT | C | 18 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(15): Show |
19 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-8960_83-8954del others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | ||||||
| chr1:63387635 | A | C | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-8878A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387635 | |||||||
| chr1:63387652 | C | T | 1 | a0001c0001t0007g0011 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.83-8861C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387652 | |||||||
| chr1:63387742 | G | C | 30 | a0002c0002t0001g0015 a0002c0002t0001g0060 a0002c0002t0001g0079 others(27): Show |
31 | HG00738.hp2 HG01517.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.83-8771G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387742 | |||||||
| chr1:63388019 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0085 a0001c0001t0001g0093 others(2): Show |
5 | NA18946.hp1 NA18956.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-8494C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388019 | |||||||
| chr1:63388076 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.83-8437C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388076 | |||||||
| chr1:63388210 | C | T | 2 | a0001c0001t0004g0318 a0001c0001t0004g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83-8303C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388210 | |||||||
| chr1:63388427 | A | G | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-8086A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388427 | |||||||
| chr1:63388493 | C | T | 2 | a0002c0002t0001g0347 a0002c0002t0001g0351 |
2 | NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.83-8020C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388493 | |||||||
| chr1:63388609 | T | G | 10 | a0002c0002t0001g0201 a0002c0002t0001g0311 a0002c0002t0001g0314 others(7): Show |
10 | HG02132.hp2 HG02280.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-7904T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388609 | |||||||
| chr1:63388651 | C | T | 1 | a0002c0002t0001g0312 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.83-7862C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388651 | |||||||
| chr1:63389075 | G | T | 3 | a0001c0001t0002g0286 a0001c0001t0002g0289 a0001c0001t0002g0297 |
3 | HG02027.hp1 NA18959.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.83-7438G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389075 | |||||||
| chr1:63389078 | C | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-7435C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389078 | |||||||
| chr1:63389165 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83-7348C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389165 | |||||||
| chr1:63389359 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83-7154C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389359 | |||||||
| chr1:63389410 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.83-7103A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389410 | |||||||
| chr1:63389746 | G | A | 1 | a0002c0002t0001g0343 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.83-6767G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389746 | |||||||
| chr1:63389830 | A | G | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-6683A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389830 | |||||||
| chr1:63389849 | G | A | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-6664G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389849 | |||||||
| chr1:63389945 | C | G | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-6568C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389945 | |||||||
| chr1:63389954 | G | C | 2 | a0001c0001t0003g0168 a0001c0001t0004g0063 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.83-6559G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389954 | |||||||
| chr1:63390029 | C | A | 2 | a0001c0001t0003g0168 a0001c0001t0004g0063 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.83-6484C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390029 | |||||||
| chr1:63390128 | G | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-6385G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390128 | |||||||
| chr1:63390154 | C | T | 2 | a0001c0001t0002g0261 a0001c0001t0002g0262 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.83-6359C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390154 | |||||||
| chr1:63390351 | G | A | 3 | a0002c0002t0001g0311 a0002c0002t0001g0314 a0002c0002t0005g0104 |
3 | HG02132.hp2 HG03831.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.83-6162G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390351 | |||||||
| chr1:63390359 | T | C | 2 | a0001c0001t0002g0005 a0001c0001t0017g0005 |
2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.83-6154T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390359 | |||||||
| chr1:63390389 | G | C | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-6124G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390389 | |||||||
| chr1:63390436 | A | G | 1 | a0002c0002t0001g0350 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.83-6077A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390436 | |||||||
| chr1:63390451 | C | G | 1 | a0001c0001t0003g0151 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.83-6062C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390451 | |||||||
| chr1:63390458 | C | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0268 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.83-6055C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390458 | |||||||
| chr1:63390609 | A | T | 1 | a0001c0001t0007g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-5904A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390609 | |||||||
| chr1:63390724 | C | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(38): Show |
42 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.83-5789C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390724 | |||||||
| chr1:63390980 | A | G | 305 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(302): Show |
317 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.83-5533A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390980 | |||||||
| chr1:63391011 | G | T | 2 | a0001c0001t0004g0318 a0001c0001t0004g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83-5502G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391011 | |||||||
| chr1:63391038 | G | A | 7 | a0001c0004t0004g0199 a0001c0004t0006g0157 a0001c0004t0006g0197 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-5475G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391038 | |||||||
| chr1:63391047 | G | T | 1 | a0001c0001t0002g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.83-5466G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391047 | |||||||
| chr1:63391184 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.83-5329C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391184 | |||||||
| chr1:63391221 | C | T | 87 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(84): Show |
92 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.83-5292C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391221 | |||||||
| chr1:63391318 | T | C | 1 | a0001c0001t0003g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.83-5195T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391318 | |||||||
| chr1:63391447 | C | T | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-5066C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391447 | |||||||
| chr1:63391483 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.83-5030C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391483 | |||||||
| chr1:63391632 | T | C | 2 | a0002c0002t0001g0188 a0002c0002t0001g0226 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83-4881T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391632 | |||||||
| chr1:63391764 | T | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-4749T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391764 | |||||||
| chr1:63391998 | A | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-4515A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391998 | |||||||
| chr1:63392172 | A | AT | 39 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0105 others(36): Show |
40 | HG01167.hp2 HG01884.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.83-4327dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63392172 | ||||||
| chr1:63392226 | A | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-4287A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392226 | |||||||
| chr1:63392239 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-4274C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392239 | |||||||
| chr1:63392451 | A | G | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.83-4062A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392451 | |||||||
| chr1:63392612 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.83-3901C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392612 | |||||||
| chr1:63392627 | T | C | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.83-3886T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392627 | |||||||
| chr1:63392631 | C | T | 1 | a0002c0002t0001g0368 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-3882C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392631 | |||||||
| chr1:63392667 | G | A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3846G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392667 | |||||||
| chr1:63393224 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-3289C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393224 | |||||||
| chr1:63393375 | C | T | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.83-3138C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393375 | |||||||
| chr1:63393469 | G | A | 2 | a0001c0001t0002g0247 a0001c0001t0002g0268 |
2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.83-3044G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393469 | |||||||
| chr1:63393500 | A | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83-3013A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393500 | |||||||
| chr1:63393817 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.83-2696G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393817 | |||||||
| chr1:63393819 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.83-2694C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393819 | |||||||
| chr1:63393927 | TAGAG | T | 5 | a0001c0001t0004g0102 a0001c0001t0008g0228 a0001c0001t0008g0229 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-2582_83-2579del others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63393927 | ||||||
| chr1:63394065 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83-2448T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394065 | |||||||
| chr1:63394187 | T | C | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2326T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394187 | |||||||
| chr1:63394246 | A | G | 1 | a0001c0001t0003g0010 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.83-2267A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394246 | |||||||
| chr1:63394376 | T | C | 1 | a0001c0001t0002g0276 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.83-2137T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394376 | |||||||
| chr1:63394440 | C | T | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2073C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394440 | |||||||
| chr1:63394652 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.83-1861G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394652 | |||||||
| chr1:63394734 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-1779A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394734 | |||||||
| chr1:63394856 | T | C | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-1657T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394856 | |||||||
| chr1:63395115 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-1398C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395115 | |||||||
| chr1:63395144 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.83-1369G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395144 | |||||||
| chr1:63395156 | G | A | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG00408.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.83-1357G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395156 | |||||||
| chr1:63395281 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83-1232G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395281 | |||||||
| chr1:63395342 | T | G | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-1171T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395342 | |||||||
| chr1:63395366 | C | T | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.83-1147C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395366 | |||||||
| chr1:63395461 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.83-1052C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395461 | |||||||
| chr1:63395540 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0056 |
2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.83-973C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395540 | |||||||
| chr1:63395550 | G | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-963G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395550 | |||||||
| chr1:63395602 | T | C | 1 | a0002c0002t0001g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.83-911T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395602 | |||||||
| chr1:63395655 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.83-858A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395655 | |||||||
| chr1:63395658 | G | T | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83-855G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395658 | |||||||
| chr1:63395790 | C | A | 23 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0022 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.83-723C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395790 | |||||||
| chr1:63396032 | A | G | 1 | a0002c0002t0001g0350 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.83-481A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396032 | |||||||
| chr1:63396096 | A | G | 1 | a0002c0002t0001g0321 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.83-417A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396096 | |||||||
| chr1:63396179 | C | T | 1 | a0001c0001t0015g0369 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.83-334C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396179 | |||||||
| chr1:63396239 | T | G | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-274T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396239 | |||||||
| chr1:63396621 | T | C | 1 | a0001c0001t0007g0146 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.167+24T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396621 | |||||||
| chr1:63396745 | T | C | 2 | a0001c0001t0004g0102 a0004c0008t0003g0202 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.167+148T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396745 | |||||||
| chr1:63396940 | G | A | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+343G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396940 | |||||||
| chr1:63397023 | G | A | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.167+426G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397023 | |||||||
| chr1:63397069 | G | A | 368 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(365): Show |
384 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(381): Show |
intron_variant | MODIFIER | c.167+472G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397069 | |||||||
| chr1:63397077 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+480G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397077 | |||||||
| chr1:63397147 | A | G | 1 | a0001c0001t0003g0020 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.167+550A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397147 | |||||||
| chr1:63397251 | T | G | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+654T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397251 | |||||||
| chr1:63397516 | A | G | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+919A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397516 | |||||||
| chr1:63397565 | T | TG | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.167+969dupG | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63397565 | ||||||
| chr1:63397592 | C | T | 1 | a0001c0001t0007g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.167+995C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397592 | |||||||
| chr1:63397593 | G | A | 1 | a0001c0003t0009g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.167+996G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397593 | |||||||
| chr1:63397847 | T | C | 1 | a0001c0001t0001g0362 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.167+1250T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397847 | |||||||
| chr1:63397850 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.167+1253A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397850 | |||||||
| chr1:63397897 | T | C | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.167+1300T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397897 | |||||||
| chr1:63397911 | C | T | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+1314C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397911 | |||||||
| chr1:63397928 | C | T | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.167+1331C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397928 | |||||||
| chr1:63398253 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+1656G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398253 | |||||||
| chr1:63398262 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+1665T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398262 | |||||||
| chr1:63398507 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.167+1910C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398507 | |||||||
| chr1:63398589 | T | C | 1 | a0001c0001t0003g0124 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.167+1992T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398589 | |||||||
| chr1:63398597 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.167+2000C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398597 | |||||||
| chr1:63398666 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+2069A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398666 | |||||||
| chr1:63398715 | T | G | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.167+2118T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398715 | |||||||
| chr1:63398717 | C | T | 68 | a0001c0001t0002g0025 a0001c0001t0002g0035 a0001c0001t0002g0036 others(65): Show |
69 | HG00408.hp2 HG00423.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.167+2120C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398717 | |||||||
| chr1:63398770 | T | C | 1 | a0002c0002t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.167+2173T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398770 | |||||||
| chr1:63398871 | A | C | 10 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(7): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.167+2274A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398871 | |||||||
| chr1:63398888 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167+2291A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398888 | |||||||
| chr1:63399055 | A | G | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.167+2458A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399055 | |||||||
| chr1:63399332 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | NA18986.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.167+2735A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399332 | |||||||
| chr1:63399384 | G | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.167+2787G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399384 | |||||||
| chr1:63399650 | G | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.168-2604G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399650 | |||||||
| chr1:63399689 | TA | T | 19 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(16): Show |
20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.168-2562delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63399689 | ||||||
| chr1:63399694 | A | C | 19 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(16): Show |
20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.168-2560A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399694 | |||||||
| chr1:63399714 | T | A | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2540T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399714 | |||||||
| chr1:63399786 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-2468G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399786 | |||||||
| chr1:63399834 | A | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-2420A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399834 | |||||||
| chr1:63399911 | G | A | 7 | a0001c0001t0002g0035 a0001c0001t0004g0004 a0001c0001t0004g0034 others(4): Show |
8 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.168-2343G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399911 | |||||||
| chr1:63399923 | G | A | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2331G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399923 | |||||||
| chr1:63399934 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.168-2320C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399934 | |||||||
| chr1:63399939 | G | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.168-2315G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399939 | |||||||
| chr1:63400086 | C | T | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-2168C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400086 | |||||||
| chr1:63400092 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.168-2162G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400092 | |||||||
| chr1:63400194 | C | CA | 28 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0059 others(25): Show |
29 | HG00140.hp1 HG01192.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-2047dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400194 | ||||||
| chr1:63400205 | A | T | 1 | a0002c0002t0005g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.168-2049A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400205 | |||||||
| chr1:63400206 | A | AT | 6 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0099 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2048_168-2047i others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400206 | |||||||
| chr1:63400206 | A | T | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0002c0002t0001g0180 others(1): Show |
4 | HG03209.hp1 HG03453.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-2048A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400206 | |||||||
| chr1:63400207 | AT | A | 113 | a0001c0001t0001g0356 a0001c0001t0002g0005 a0001c0001t0002g0006 others(110): Show |
116 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.168-2046delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | |||||||
| chr1:63400207 | ATAT | A | 5 | a0001c0001t0002g0353 a0001c0001t0003g0103 a0001c0001t0003g0138 others(2): Show |
5 | HG01934.hp2 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2046_168-2044d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | |||||||
| chr1:63400207 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0357 |
2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.168-2046_168-2028d others(21): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | |||||||
| chr1:63400207 | ATATATAT others(106): Show |
A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0070 others(13): Show |
17 | HG00423.hp1 HG02027.hp2 HG04184.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-2046_168-1934d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | |||||||
| chr1:63400208 | T | A | 125 | a0001c0001t0001g0016 a0001c0001t0001g0291 a0001c0001t0001g0328 others(122): Show |
132 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.168-2046T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400208 | |||||||
| chr1:63400209 | ATATATAT others(105): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.168-2032_168-1921d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400209 | ||||||
| chr1:63400210 | T | A | 197 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0014 others(194): Show |
204 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.168-2044T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400210 | |||||||
| chr1:63400212 | T | A | 120 | a0001c0001t0002g0014 a0001c0001t0002g0021 a0001c0001t0002g0037 others(117): Show |
126 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.168-2042T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400212 | |||||||
| chr1:63400213 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0004g0319 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.168-2032_168-2001d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400213 | ||||||
| chr1:63400214 | T | A | 95 | a0001c0001t0002g0057 a0001c0001t0002g0186 a0001c0001t0002g0187 others(92): Show |
100 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.168-2040T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400214 | |||||||
| chr1:63400215 | ATATATAC others(23): Show |
A | 5 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(2): Show |
6 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2032_168-2003d others(32): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400215 | ||||||
| chr1:63400215 | ATATATAC others(61): Show |
A | 2 | a0001c0001t0001g0313 a0001c0001t0005g0140 |
2 | HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.168-2032_168-1965d others(70): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400215 | ||||||
| chr1:63400216 | T | A | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.168-2038T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400216 | |||||||
| chr1:63400218 | T | A | 84 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.168-2036T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400218 | |||||||
| chr1:63400219 | ATACG | A | 6 | a0001c0001t0001g0328 a0001c0001t0001g0362 a0001c0001t0001g0367 others(3): Show |
7 | HG01106.hp1 HG01952.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2032_168-2029d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400219 | ||||||
| chr1:63400220 | T | A | 84 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.168-2034T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400220 | |||||||
| chr1:63400221 | ACG | A | 94 | a0001c0001t0001g0016 a0001c0001t0001g0291 a0001c0001t0001g0331 others(91): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.168-2032_168-2031d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | |||||||
| chr1:63400221 | ACGT | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(42): Show |
46 | HG00544.hp1 HG00733.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.168-2032_168-2030d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | |||||||
| chr1:63400221 | ACGTATAT others(27): Show |
A | 1 | a0001c0001t0004g0318 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.168-2032_168-1999d others(36): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | |||||||
| chr1:63400221 | ACGTATAT others(55): Show |
A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-2032_168-1971d others(64): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | |||||||
| chr1:63400221 | ACGTATAT others(79): Show |
A | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-2032_168-1947d others(88): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | |||||||
| chr1:63400222 | C | A | 39 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(36): Show |
40 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.168-2032C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | |||||||
| chr1:63400222 | C | T | 58 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0025 others(55): Show |
60 | HG00408.hp2 HG01070.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-2032C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | |||||||
| chr1:63400222 | CGTATATA others(109): Show |
C | 2 | a0001c0001t0001g0092 a0001c0007t0001g0096 |
2 | HG00408.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.168-2031_168-1916d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | |||||||
| chr1:63400222 | CGTATATA others(133): Show |
C | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.168-2031_168-1892d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | |||||||
| chr1:63400223 | G | A | 121 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0059 others(118): Show |
124 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.168-2031G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400223 | |||||||
| chr1:63400223 | G | GTA | 6 | a0002c0002t0001g0012 a0002c0002t0001g0079 a0002c0002t0001g0178 others(3): Show |
6 | HG01243.hp2 HG02132.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2012_168-2011d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400223 | ||||||
| chr1:63400224 | T | A | 15 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(12): Show |
15 | HG00738.hp1 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-2030T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400224 | |||||||
| chr1:63400226 | T | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(42): Show |
46 | HG00544.hp1 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.168-2028T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400226 | |||||||
| chr1:63400226 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0291 a0001c0001t0001g0331 others(8): Show |
12 | HG00140.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-2028T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400226 | |||||||
| chr1:63400228 | T | A | 8 | a0001c0001t0003g0116 a0001c0001t0003g0133 a0001c0001t0003g0207 others(5): Show |
8 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2026T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400228 | |||||||
| chr1:63400228 | T | C | 7 | a0001c0001t0001g0328 a0001c0001t0001g0356 a0001c0001t0001g0362 others(4): Show |
8 | HG00438.hp1 HG01106.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2026T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400228 | |||||||
| chr1:63400230 | T | A | 3 | a0001c0001t0003g0207 a0001c0003t0009g0164 a0001c0003t0009g0167 |
3 | HG01192.hp1 HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168-2024T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400230 | |||||||
| chr1:63400230 | T | C | 5 | a0001c0001t0007g0146 a0001c0001t0007g0147 a0001c0001t0011g0161 others(2): Show |
5 | HG01934.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-2024T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400230 | |||||||
| chr1:63400231 | ATATATAT others(45): Show |
A | 1 | a0002c0002t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.168-1972_168-1921d others(54): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400231 | ||||||
| chr1:63400232 | T | A | 2 | a0001c0003t0009g0164 a0001c0003t0009g0167 |
2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168-2022T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400232 | |||||||
| chr1:63400233 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0361 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.168-2010_168-1975d others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400233 | ||||||
| chr1:63400233 | ATATATAT others(43): Show |
A | 1 | a0002c0002t0001g0311 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.168-2010_168-1961d others(52): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400233 | ||||||
| chr1:63400234 | T | C | 2 | a0001c0001t0004g0102 a0004c0008t0003g0202 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-2020T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400234 | |||||||
| chr1:63400235 | ATATATAT others(41): Show |
A | 1 | a0002c0002t0005g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.168-2010_168-1963d others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400235 | ||||||
| chr1:63400235 | ATATATAT others(107): Show |
A | 1 | a0001c0001t0001g0099 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.168-2010_168-1897d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400235 | ||||||
| chr1:63400236 | T | C | 2 | a0001c0001t0004g0102 a0004c0008t0003g0202 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-2018T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400236 | |||||||
| chr1:63400237 | ATATATAC others(25): Show |
A | 1 | a0001c0001t0001g0360 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.168-2010_168-1979d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400237 | ||||||
| chr1:63400237 | ATATATAC others(105): Show |
A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0094 a0001c0001t0001g0101 |
3 | NA18957.hp1 NA18978.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.168-2010_168-1899d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400237 | ||||||
| chr1:63400238 | T | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0353 a0001c0001t0004g0102 others(1): Show |
5 | HG01192.hp2 HG02559.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2016T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400238 | |||||||
| chr1:63400239 | ATATACGT others(23): Show |
A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-2010_168-1981d others(32): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400239 | ||||||
| chr1:63400239 | ATATACGT others(37): Show |
A | 27 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0241 others(24): Show |
27 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.168-2010_168-1967d others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400239 | ||||||
| chr1:63400240 | T | C | 12 | a0001c0001t0002g0007 a0001c0001t0002g0353 a0001c0001t0003g0168 others(9): Show |
13 | HG01167.hp2 HG01192.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.168-2014T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400240 | |||||||
| chr1:63400241 | A | G | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-2013A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400241 | |||||||
| chr1:63400241 | ATACGTAT others(21): Show |
A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0331 |
2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.168-2010_168-1983d others(30): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | ||||||
| chr1:63400241 | ATACGTAT others(35): Show |
A | 42 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(39): Show |
42 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.168-2010_168-1969d others(44): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | ||||||
| chr1:63400241 | ATACGTAT others(49): Show |
A | 5 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0002g0302 others(2): Show |
5 | HG01496.hp2 HG01952.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2010_168-1955d others(58): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | ||||||
| chr1:63400242 | T | C | 10 | a0001c0001t0002g0007 a0001c0001t0002g0353 a0001c0001t0003g0168 others(7): Show |
11 | HG01167.hp2 HG01192.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-2012T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400242 | |||||||
| chr1:63400243 | ACG | A | 27 | a0001c0001t0001g0328 a0001c0001t0001g0355 a0001c0001t0001g0356 others(24): Show |
28 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.168-2010_168-2009d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | |||||||
| chr1:63400243 | ACGTATAT others(5): Show |
A | 1 | a0001c0003t0009g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168-2010_168-1999d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | |||||||
| chr1:63400243 | ACGTATAT others(19): Show |
A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0364 |
2 | HG02165.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.168-2010_168-1985d others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | |||||||
| chr1:63400243 | ACGTATAT others(33): Show |
A | 82 | a0001c0001t0001g0059 a0001c0001t0001g0291 a0001c0001t0002g0005 others(79): Show |
83 | HG00544.hp1 HG00558.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.168-2010_168-1971d others(42): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | |||||||
| chr1:63400243 | ACGTATAT others(47): Show |
A | 5 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(2): Show |
6 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2010_168-1957d others(56): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | |||||||
| chr1:63400244 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0011g0161 a0001c0001t0011g0162 others(2): Show |
5 | HG00639.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-2010C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | |||||||
| chr1:63400244 | CGTATATA others(15): Show |
C | 2 | a0001c0001t0002g0324 a0001c0001t0004g0325 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.168-2009_168-1988d others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | |||||||
| chr1:63400244 | CGTATATA others(19): Show |
C | 7 | a0001c0001t0003g0168 a0001c0001t0004g0189 a0001c0001t0004g0190 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-2009_168-1984d others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | |||||||
| chr1:63400244 | CGTATATA others(39): Show |
C | 50 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0031 others(47): Show |
51 | HG00408.hp2 HG01070.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.168-2009_168-1964d others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | |||||||
| chr1:63400245 | G | A | 14 | a0001c0001t0001g0354 a0001c0001t0001g0357 a0001c0001t0002g0007 others(11): Show |
15 | HG00639.hp2 HG00738.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-2009G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400245 | |||||||
| chr1:63400246 | T | C | 5 | a0001c0001t0002g0035 a0001c0001t0002g0048 a0001c0001t0002g0186 others(2): Show |
5 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2008T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400246 | |||||||
| chr1:63400247 | A | ATATATAC others(1): Show |
3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-2001_168-2000i others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400247 | ||||||
| chr1:63400248 | T | C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0048 a0001c0001t0002g0186 others(3): Show |
6 | HG00738.hp1 HG02155.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2006T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400248 | |||||||
| chr1:63400250 | T | C | 7 | a0001c0001t0002g0035 a0001c0001t0002g0039 a0001c0001t0002g0048 others(4): Show |
7 | HG00639.hp2 HG00738.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2004T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400250 | |||||||
| chr1:63400252 | T | C | 8 | a0001c0001t0002g0035 a0001c0001t0002g0039 a0001c0001t0002g0048 others(5): Show |
8 | HG00639.hp2 HG00738.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2002T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400252 | |||||||
| chr1:63400254 | T | C | 7 | a0001c0001t0002g0039 a0001c0001t0003g0153 a0001c0001t0004g0102 others(4): Show |
7 | HG00639.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2000T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400254 | |||||||
| chr1:63400255 | G | A | 36 | a0001c0001t0001g0328 a0001c0001t0001g0354 a0001c0001t0001g0355 others(33): Show |
37 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.168-1999G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400255 | |||||||
| chr1:63400255 | G | GTA | 2 | a0001c0001t0002g0007 a0001c0001t0002g0353 |
3 | HG01192.hp2 HG02683.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.168-1988_168-1987d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400255 | ||||||
| chr1:63400256 | T | C | 3 | a0001c0001t0002g0039 a0001c0001t0003g0153 a0001c0004t0006g0317 |
3 | HG00639.hp2 HG02280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.168-1998T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400256 | |||||||
| chr1:63400258 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168-1996T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400258 | |||||||
| chr1:63400262 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1992T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400262 | |||||||
| chr1:63400263 | A | G | 5 | a0001c0001t0002g0035 a0001c0001t0002g0048 a0001c0001t0002g0186 others(2): Show |
5 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-1991A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400263 | |||||||
| chr1:63400264 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1990T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400264 | |||||||
| chr1:63400265 | ATACG | A | 7 | a0001c0001t0001g0354 a0001c0001t0001g0357 a0001c0001t0002g0035 others(4): Show |
7 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1986_168-1983d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400265 | ||||||
| chr1:63400266 | T | C | 9 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(6): Show |
10 | HG01243.hp1 HG02647.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1988T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400266 | |||||||
| chr1:63400267 | A | G | 2 | a0001c0001t0002g0039 a0001c0004t0006g0317 |
2 | HG00639.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.168-1987A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400267 | |||||||
| chr1:63400267 | ACG | A | 4 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0167 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1986_168-1985d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400267 | |||||||
| chr1:63400268 | C | T | 3 | a0001c0001t0002g0039 a0001c0001t0003g0153 a0001c0004t0006g0317 |
3 | HG00639.hp2 HG02280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.168-1986C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | |||||||
| chr1:63400268 | CGTATATA others(15): Show |
C | 2 | a0001c0003t0012g0233 a0001c0003t0014g0234 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.168-1985_168-1964d others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | |||||||
| chr1:63400268 | CGTATATA others(17): Show |
C | 1 | a0001c0003t0009g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.168-1985_168-1962d others(26): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | |||||||
| chr1:63400269 | G | A | 11 | a0001c0001t0002g0039 a0001c0001t0002g0324 a0001c0001t0003g0013 others(8): Show |
12 | HG00639.hp2 HG01243.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-1985G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400269 | |||||||
| chr1:63400269 | G | GTA | 7 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0160 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1974_168-1973d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400269 | ||||||
| chr1:63400269 | G | GTATA | 40 | a0002c0002t0001g0003 a0002c0002t0001g0012 a0002c0002t0001g0015 others(37): Show |
44 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.168-1976_168-1973d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400269 | ||||||
| chr1:63400270 | T | C | 8 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(5): Show |
9 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1984T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400270 | |||||||
| chr1:63400271 | ATATATAT others(43): Show |
A | 7 | a0002c0002t0001g0188 a0002c0002t0001g0226 a0002c0002t0001g0227 others(4): Show |
7 | HG02280.hp1 HG03516.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1972_168-1923d others(52): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400271 | ||||||
| chr1:63400273 | A | ATATATAT others(21): Show |
3 | a0002c0002t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0081 |
3 | NA18944.hp1 NA18945.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.168-1973_168-1972i others(30): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | ||||||
| chr1:63400273 | ATATATAT others(41): Show |
A | 2 | a0002c0002t0001g0314 a0002c0002t0001g0323 |
2 | HG02132.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.168-1972_168-1925d others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | ||||||
| chr1:63400273 | ATATATAT others(57): Show |
A | 3 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 |
4 | HG02559.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1972_168-1909d others(66): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | ||||||
| chr1:63400278 | TATAC | T | 13 | a0001c0001t0001g0328 a0001c0001t0001g0355 a0001c0001t0001g0356 others(10): Show |
13 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-1975_168-1972d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400278 | |||||||
| chr1:63400279 | A | G | 3 | a0001c0001t0003g0207 a0001c0001t0004g0102 a0004c0008t0003g0202 |
3 | HG01243.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-1975A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400279 | |||||||
| chr1:63400280 | T | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0353 a0001c0001t0011g0161 others(5): Show |
9 | HG01192.hp1 HG01192.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1974T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400280 | |||||||
| chr1:63400281 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1973A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | |||||||
| chr1:63400281 | ACG | A | 7 | a0001c0001t0001g0354 a0001c0001t0001g0357 a0001c0001t0001g0360 others(4): Show |
7 | HG01243.hp1 HG02165.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1972_168-1971d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | |||||||
| chr1:63400281 | ACGTATAT others(83): Show |
A | 2 | a0001c0001t0004g0102 a0004c0008t0003g0202 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-1972_168-1883d others(92): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | |||||||
| chr1:63400282 | C | T | 9 | a0001c0001t0002g0324 a0001c0001t0004g0325 a0001c0001t0011g0161 others(6): Show |
9 | HG02622.hp1 HG02976.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1972C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | |||||||
| chr1:63400282 | CGTAT | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0331 |
3 | HG03490.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.168-1971_168-1968d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | |||||||
| chr1:63400282 | CGTATATA others(51): Show |
C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0353 |
3 | HG01192.hp2 HG02683.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.168-1971_168-1914d others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | |||||||
| chr1:63400283 | G | A | 10 | a0001c0001t0002g0324 a0001c0001t0011g0161 a0001c0001t0011g0162 others(7): Show |
10 | HG01192.hp1 HG02622.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-1971G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400283 | |||||||
| chr1:63400284 | T | C | 3 | a0001c0003t0009g0164 a0001c0003t0009g0167 a0001c0003t0012g0232 |
3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1970T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400284 | |||||||
| chr1:63400285 | A | ACG | 3 | a0002c0002t0001g0345 a0002c0002t0001g0347 a0002c0002t0001g0351 |
3 | NA18985.hp2 NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.168-1969_168-1968i others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400285 | |||||||
| chr1:63400286 | T | C | 3 | a0001c0003t0009g0164 a0001c0003t0009g0167 a0001c0003t0012g0232 |
3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1968T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400286 | |||||||
| chr1:63400288 | T | C | 7 | a0001c0001t0003g0143 a0001c0004t0004g0199 a0001c0004t0006g0157 others(4): Show |
7 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1966T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400288 | |||||||
| chr1:63400289 | A | G | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1965A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400289 | |||||||
| chr1:63400290 | T | C | 130 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0021 others(127): Show |
135 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.168-1964T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400290 | |||||||
| chr1:63400292 | T | C | 186 | a0001c0001t0001g0056 a0001c0001t0002g0005 a0001c0001t0002g0006 others(183): Show |
192 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.168-1962T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400292 | |||||||
| chr1:63400294 | T | C | 212 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0059 others(209): Show |
218 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.168-1960T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400294 | |||||||
| chr1:63400296 | C | T | 6 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 others(3): Show |
6 | HG01192.hp1 HG02622.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1958C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400296 | |||||||
| chr1:63400296 | CGTATATA others(37): Show |
C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0048 a0001c0001t0002g0186 others(3): Show |
6 | HG00738.hp1 HG02155.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1957_168-1914d others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400296 | |||||||
| chr1:63400297 | G | A | 190 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0021 others(187): Show |
196 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.168-1957G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400297 | |||||||
| chr1:63400298 | T | C | 2 | a0001c0001t0003g0123 a0001c0003t0010g0316 |
2 | HG03834.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1956T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400298 | |||||||
| chr1:63400299 | ATATATAT others(1): Show |
A | 3 | a0001c0003t0009g0164 a0001c0003t0009g0167 a0001c0003t0012g0232 |
3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1947_168-1940d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400299 | ||||||
| chr1:63400301 | ATATATGT others(29): Show |
A | 13 | a0001c0001t0001g0328 a0001c0001t0001g0355 a0001c0001t0001g0356 others(10): Show |
13 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-1947_168-1912d others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400301 | ||||||
| chr1:63400304 | T | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(7): Show |
11 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-1950T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400304 | |||||||
| chr1:63400305 | ATGTATAT others(25): Show |
A | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1947_168-1916d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400305 | ||||||
| chr1:63400306 | T | C | 29 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(26): Show |
31 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.168-1948T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400306 | |||||||
| chr1:63400306 | T | TATAC | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1948_168-1947i others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400306 | |||||||
| chr1:63400307 | G | A | 14 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(11): Show |
15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1947G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400307 | |||||||
| chr1:63400308 | T | C | 14 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(11): Show |
15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1946T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400308 | |||||||
| chr1:63400310 | T | C | 14 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(11): Show |
15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1944T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400310 | |||||||
| chr1:63400316 | T | C | 1 | a0002c0002t0001g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.168-1938T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400316 | |||||||
| chr1:63400317 | A | G | 4 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 others(1): Show |
4 | HG01261.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1937A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400317 | |||||||
| chr1:63400319 | ACG | A | 117 | a0001c0001t0002g0006 a0001c0001t0002g0021 a0001c0001t0002g0022 others(114): Show |
119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.168-1934_168-1933d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400319 | |||||||
| chr1:63400320 | C | T | 17 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0044 others(14): Show |
18 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.168-1934C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400320 | |||||||
| chr1:63400321 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0070 others(20): Show |
24 | HG00423.hp1 HG02027.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.168-1933G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400321 | |||||||
| chr1:63400321 | G | GTA | 40 | a0002c0002t0001g0012 a0002c0002t0001g0015 a0002c0002t0001g0060 others(37): Show |
40 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.168-1920_168-1919d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400321 | ||||||
| chr1:63400322 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1932T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400322 | |||||||
| chr1:63400324 | T | C | 120 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0021 others(117): Show |
122 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-1930T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400324 | |||||||
| chr1:63400325 | A | G | 119 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0021 others(116): Show |
121 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.168-1929A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400325 | |||||||
| chr1:63400325 | ATATATAT others(5): Show |
A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0331 a0001c0001t0001g0354 others(4): Show |
8 | HG03490.hp2 HG03491.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-1918_168-1907d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400325 | ||||||
| chr1:63400327 | ATATATAT others(3): Show |
A | 10 | a0001c0001t0001g0241 a0001c0001t0001g0279 a0001c0001t0001g0280 others(7): Show |
10 | HG02083.hp1 HG02129.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1918_168-1909d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400327 | ||||||
| chr1:63400329 | ATATATAC others(1): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0059 others(1): Show |
4 | HG00140.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1918_168-1911d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400329 | ||||||
| chr1:63400330 | T | C | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1924T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400330 | |||||||
| chr1:63400331 | A | G | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1923A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400331 | |||||||
| chr1:63400331 | ATATACG | A | 91 | a0001c0001t0001g0364 a0001c0001t0002g0039 a0001c0001t0002g0324 others(88): Show |
96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.168-1918_168-1913d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400331 | ||||||
| chr1:63400336 | C | T | 4 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1918C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400336 | |||||||
| chr1:63400336 | CGT | C | 120 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0006 others(117): Show |
122 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-1917_168-1916d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400336 | |||||||
| chr1:63400337 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0070 others(18): Show |
22 | HG00423.hp1 HG02027.hp2 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1917G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400337 | |||||||
| chr1:63400338 | T | C | 71 | a0001c0001t0002g0039 a0001c0001t0003g0001 a0001c0001t0003g0002 others(68): Show |
75 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.168-1916T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400338 | |||||||
| chr1:63400339 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1915A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400339 | |||||||
| chr1:63400340 | T | C | 205 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0021 others(202): Show |
212 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.168-1914T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400340 | |||||||
| chr1:63400342 | T | C | 4 | a0001c0001t0003g0207 a0001c0001t0011g0161 a0001c0001t0011g0162 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1912T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400342 | |||||||
| chr1:63400347 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1907A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400347 | |||||||
| chr1:63400348 | T | C | 15 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(12): Show |
16 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-1906T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400348 | |||||||
| chr1:63400349 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0070 others(36): Show |
41 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.168-1905G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400349 | |||||||
| chr1:63400350 | T | C | 17 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(14): Show |
18 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.168-1904T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400350 | |||||||
| chr1:63400351 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1903A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400351 | |||||||
| chr1:63400359 | A | G | 13 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(10): Show |
14 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-1895A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400359 | |||||||
| chr1:63400361 | G | A | 11 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(8): Show |
12 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-1893G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400361 | |||||||
| chr1:63400361 | G | GTA | 21 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(18): Show |
22 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1885_168-1884d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400361 | ||||||
| chr1:63400370 | T | C | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.168-1884T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400370 | |||||||
| chr1:63400370 | T | TAC | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1884_168-1883i others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400370 | |||||||
| chr1:63400427 | A | C | 1 | a0002c0002t0001g0308 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.168-1827A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400427 | |||||||
| chr1:63400587 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1667G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400587 | |||||||
| chr1:63400788 | T | C | 2 | a0001c0001t0003g0121 a0001c0001t0003g0149 |
2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.168-1466T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400788 | |||||||
| chr1:63400930 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1324G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400930 | |||||||
| chr1:63400931 | C | G | 1 | a0001c0001t0002g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168-1323C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400931 | |||||||
| chr1:63400994 | G | A | 1 | a0001c0001t0001g0360 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.168-1260G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400994 | |||||||
| chr1:63401015 | CA | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.168-1235delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63401015 | ||||||
| chr1:63401020 | G | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1234G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401020 | |||||||
| chr1:63401041 | A | T | 1 | a0001c0001t0003g0154 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.168-1213A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401041 | |||||||
| chr1:63401157 | T | A | 1 | a0001c0001t0002g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168-1097T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401157 | |||||||
| chr1:63401179 | G | C | 1 | a0001c0001t0002g0353 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-1075G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401179 | |||||||
| chr1:63401264 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168-990G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401264 | |||||||
| chr1:63401414 | G | A | 1 | a0002c0002t0001g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168-840G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401414 | |||||||
| chr1:63401503 | T | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-751T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401503 | |||||||
| chr1:63401580 | C | T | 2 | a0001c0001t0007g0146 a0001c0001t0007g0147 |
2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.168-674C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401580 | |||||||
| chr1:63401584 | T | TA | 17 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(14): Show |
18 | HG00544.hp1 HG01074.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.168-656dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63401584 | ||||||
| chr1:63401599 | C | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-655C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401599 | |||||||
| chr1:63401610 | G | A | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.168-644G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401610 | |||||||
| chr1:63401614 | T | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.168-640T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401614 | |||||||
| chr1:63401642 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(2): Show |
6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-612A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401642 | |||||||
| chr1:63401671 | C | T | 2 | a0001c0001t0003g0121 a0001c0001t0003g0149 |
2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.168-583C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401671 | |||||||
| chr1:63401740 | T | C | 1 | a0001c0001t0002g0285 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.168-514T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401740 | |||||||
| chr1:63401822 | T | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-432T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401822 | |||||||
| chr1:63401946 | A | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.168-308A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401946 | |||||||
| chr1:63401947 | C | T | 238 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(235): Show |
247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.168-307C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401947 | |||||||
| chr1:63402385 | C | T | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.257+42C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402385 | |||||||
| chr1:63402460 | A | AT | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(143): Show |
154 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.257+141dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | ||||||
| chr1:63402460 | A | ATT | 13 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0346 others(10): Show |
13 | HG01168.hp2 HG01169.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+140_257+141dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | ||||||
| chr1:63402460 | AT | A | 30 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0071 others(27): Show |
31 | HG01069.hp1 HG01070.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.257+141delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | ||||||
| chr1:63402515 | G | GGA | 4 | a0001c0001t0003g0103 a0001c0001t0003g0120 a0001c0001t0003g0124 others(1): Show |
4 | NA18947.hp1 NA18981.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+174_257+175dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402515 | ||||||
| chr1:63402518 | G | A | 1 | a0001c0001t0008g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.257+175G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402518 | |||||||
| chr1:63402586 | C | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.257+243C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402586 | |||||||
| chr1:63402655 | C | T | 1 | a0001c0001t0003g0020 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.257+312C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402655 | |||||||
| chr1:63402677 | A | G | 302 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.257+334A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402677 | |||||||
| chr1:63402849 | C | G | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.257+506C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402849 | |||||||
| chr1:63402924 | A | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+581A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402924 | |||||||
| chr1:63402938 | T | C | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.257+595T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402938 | |||||||
| chr1:63403027 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0024 others(4): Show |
9 | HG01192.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+684G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403027 | |||||||
| chr1:63403052 | G | A | 1 | a0001c0001t0003g0220 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.257+709G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403052 | |||||||
| chr1:63403087 | T | G | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.257+744T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403087 | |||||||
| chr1:63403094 | C | CA | 15 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0291 others(12): Show |
15 | HG00438.hp1 HG00741.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+777dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | ||||||
| chr1:63403094 | CA | C | 102 | a0001c0001t0001g0360 a0001c0001t0002g0032 a0001c0001t0002g0040 others(99): Show |
107 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.257+777delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | ||||||
| chr1:63403094 | CAA | C | 119 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(116): Show |
123 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.257+776_257+777del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | ||||||
| chr1:63403179 | T | C | 239 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(236): Show |
248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.257+836T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403179 | |||||||
| chr1:63403315 | G | A | 25 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(22): Show |
26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.257+972G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403315 | |||||||
| chr1:63403502 | A | G | 239 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(236): Show |
248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.258-951A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403502 | |||||||
| chr1:63403534 | A | G | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-919A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403534 | |||||||
| chr1:63403674 | G | C | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.258-779G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403674 | |||||||
| chr1:63403695 | C | CT | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.258-758_258-757ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403695 | |||||||
| chr1:63403751 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258-702T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403751 | |||||||
| chr1:63403767 | T | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0296 |
3 | HG02683.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.258-686T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403767 | |||||||
| chr1:63403816 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258-637C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403816 | |||||||
| chr1:63403817 | G | A | 86 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.258-636G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403817 | |||||||
| chr1:63403893 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.258-560G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403893 | |||||||
| chr1:63404168 | A | G | 7 | a0001c0001t0002g0274 a0001c0001t0002g0276 a0001c0001t0002g0286 others(4): Show |
7 | HG02027.hp1 HG02056.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-285A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404168 | |||||||
| chr1:63404428 | T | C | 6 | a0002c0002t0001g0060 a0002c0002t0001g0333 a0002c0002t0001g0334 others(3): Show |
6 | NA18973.hp2 NA18991.hp2 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-25T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404428 | |||||||
| chr1:63404431 | G | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.258-22G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404431 | |||||||
| chr1:63404624 | TACTG | T | 20 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(17): Show |
21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+87_346+90delGA others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr1 | 63404624 | ||||||
| chr1:63404780 | C | G | 1 | a0001c0001t0002g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.346+239C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63404780 | |||||||
| chr1:63404893 | G | A | 1 | a0001c0004t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.346+352G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63404893 | |||||||
| chr1:63405086 | A | T | 1 | a0001c0001t0002g0286 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346+545A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405086 | |||||||
| chr1:63405223 | C | T | 1 | a0004c0008t0003g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.346+682C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405223 | |||||||
| chr1:63405242 | C | T | 113 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(110): Show |
118 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.346+701C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405242 | |||||||
| chr1:63405285 | C | G | 1 | a0001c0001t0005g0110 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.346+744C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405285 | |||||||
| chr1:63405459 | T | A | 1 | a0001c0001t0002g0243 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.347-858T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405459 | |||||||
| chr1:63405478 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.347-839C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405478 | |||||||
| chr1:63405794 | A | G | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-523A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405794 | |||||||
| chr1:63405879 | T | A | 1 | a0001c0001t0001g0364 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.347-438T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405879 | |||||||
| chr1:63405948 | T | C | 1 | a0001c0001t0003g0213 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.347-369T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405948 | |||||||
| chr1:63405951 | C | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347-366C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405951 | |||||||
| chr1:63405969 | T | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-348T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405969 | |||||||
| chr1:63406087 | T | C | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.347-230T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406087 | |||||||
| chr1:63406109 | G | A | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-208G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406109 | |||||||
| chr1:63406153 | A | G | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.347-164A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406153 | |||||||
| chr1:63406210 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-107A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406210 | |||||||
| chr1:63406427 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.429+28G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406427 | |||||||
| chr1:63406445 | T | C | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.429+46T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406445 | |||||||
| chr1:63406617 | C | A | 3 | a0001c0001t0001g0356 a0001c0001t0001g0361 a0001c0001t0001g0364 |
3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.429+218C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406617 | |||||||
| chr1:63406655 | T | C | 3 | a0001c0001t0003g0106 a0001c0001t0003g0123 a0001c0001t0003g0153 |
3 | HG02738.hp2 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.429+256T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406655 | |||||||
| chr1:63406688 | T | C | 17 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(14): Show |
18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.429+289T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406688 | |||||||
| chr1:63406929 | T | C | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.430-133T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406929 | |||||||
| chr1:63406944 | G | T | 1 | a0001c0001t0002g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.430-118G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406944 | |||||||
| chr1:63407059 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG02698.hp2 | splice_region_variant&intron_variant | LOW | c.430-3C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63407059 | |||||||
| chr1:63407194 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.494+68G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407194 | |||||||
| chr1:63407195 | C | T | 1 | a0002c0002t0001g0347 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.494+69C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407195 | |||||||
| chr1:63407200 | A | G | 239 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(236): Show |
248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.494+74A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407200 | |||||||
| chr1:63407343 | T | C | 1 | a0003c0005t0003g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.494+217T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407343 | |||||||
| chr1:63407779 | T | C | 147 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(144): Show |
152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.494+653T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407779 | |||||||
| chr1:63407795 | GT | G | 69 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(66): Show |
73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.494+673delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 63407795 | ||||||
| chr1:63407835 | G | A | 4 | a0001c0001t0001g0313 a0001c0001t0005g0018 a0001c0001t0005g0019 others(1): Show |
4 | HG03491.hp2 HG04115.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+709G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407835 | |||||||
| chr1:63408040 | G | A | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.494+914G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408040 | |||||||
| chr1:63408405 | A | T | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.494+1279A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408405 | |||||||
| chr1:63408511 | A | G | 147 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(144): Show |
152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.494+1385A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408511 | |||||||
| chr1:63408530 | A | G | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.494+1404A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408530 | |||||||
| chr1:63409071 | T | C | 92 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(89): Show |
96 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.494+1945T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409071 | |||||||
| chr1:63409245 | T | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.495-1901T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409245 | |||||||
| chr1:63409352 | G | A | 2 | a0002c0002t0001g0348 a0002c0002t0001g0352 |
2 | NA18961.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.495-1794G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409352 | |||||||
| chr1:63409357 | A | G | 2 | a0002c0002t0001g0172 a0002c0002t0001g0183 |
2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.495-1789A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409357 | |||||||
| chr1:63409403 | T | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495-1743T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409403 | |||||||
| chr1:63409565 | A | C | 1 | a0002c0002t0001g0350 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.495-1581A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409565 | |||||||
| chr1:63409604 | A | G | 1 | a0001c0004t0004g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495-1542A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409604 | |||||||
| chr1:63409643 | A | T | 1 | a0001c0001t0002g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.495-1503A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409643 | |||||||
| chr1:63409669 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495-1477C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409669 | |||||||
| chr1:63409695 | T | C | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-1451T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409695 | |||||||
| chr1:63409746 | A | G | 1 | a0001c0001t0001g0283 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.495-1400A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409746 | |||||||
| chr1:63409880 | C | A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1266C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409880 | |||||||
| chr1:63409965 | A | G | 3 | a0002c0002t0001g0334 a0002c0002t0001g0335 a0002c0002t0001g0337 |
3 | NA18973.hp2 NA19054.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.495-1181A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409965 | |||||||
| chr1:63410031 | C | T | 4 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0160 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1115C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410031 | |||||||
| chr1:63410050 | G | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.495-1096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410050 | |||||||
| chr1:63410164 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0022 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.495-982T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410164 | |||||||
| chr1:63410312 | T | A | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.495-834T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410312 | |||||||
| chr1:63410394 | C | G | 1 | a0001c0001t0002g0285 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495-752C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410394 | |||||||
| chr1:63410444 | T | C | 83 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(80): Show |
87 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.495-702T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410444 | |||||||
| chr1:63410500 | C | T | 4 | a0001c0001t0002g0240 a0001c0001t0002g0244 a0001c0001t0002g0250 others(1): Show |
4 | HG02071.hp1 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-646C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410500 | |||||||
| chr1:63410617 | G | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.495-529G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410617 | |||||||
| chr1:63410678 | T | C | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.495-468T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410678 | |||||||
| chr1:63410696 | T | G | 303 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.495-450T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410696 | |||||||
| chr1:63410729 | A | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495-417A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410729 | |||||||
| chr1:63410753 | G | T | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-393G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410753 | |||||||
| chr1:63410803 | C | T | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.495-343C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410803 | |||||||
| chr1:63410823 | T | C | 1 | a0001c0001t0001g0363 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.495-323T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410823 | |||||||
| chr1:63410913 | G | A | 1 | a0002c0002t0016g0196 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.495-233G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410913 | |||||||
| chr1:63411008 | G | A | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.495-138G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63411008 | |||||||
| chr1:63411015 | T | C | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495-131T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63411015 | |||||||
| chr1:63411400 | A | C | 1 | a0001c0001t0002g0007 | 2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.680+69A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411400 | |||||||
| chr1:63411459 | G | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.680+128G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411459 | |||||||
| chr1:63411483 | T | G | 1 | a0001c0001t0001g0358 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.680+152T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411483 | |||||||
| chr1:63411716 | T | A | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.681-210T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411716 | |||||||
| chr1:63411718 | A | G | 1 | a0002c0002t0001g0340 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.681-208A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411718 | |||||||
| chr1:63411743 | C | T | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.681-183C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411743 | |||||||
| chr1:63411829 | A | G | 1 | a0001c0001t0003g0105 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.681-97A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411829 | |||||||
| chr1:63412128 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.816+67G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412128 | |||||||
| chr1:63412262 | C | T | 18 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(15): Show |
19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+201C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412262 | |||||||
| chr1:63412360 | A | C | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816+299A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412360 | |||||||
| chr1:63412380 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.816+319C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412380 | |||||||
| chr1:63412431 | G | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.816+370G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412431 | |||||||
| chr1:63412896 | A | G | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.816+835A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412896 | |||||||
| chr1:63412960 | C | T | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.816+899C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412960 | |||||||
| chr1:63413056 | T | A | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.816+995T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413056 | |||||||
| chr1:63413096 | T | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.817-965T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413096 | |||||||
| chr1:63413106 | T | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.817-955T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413106 | |||||||
| chr1:63413194 | A | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.817-867A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413194 | |||||||
| chr1:63413393 | T | G | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-668T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413393 | |||||||
| chr1:63413435 | C | T | 84 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(81): Show |
88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.817-626C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413435 | |||||||
| chr1:63413436 | A | G | 1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.817-625A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413436 | |||||||
| chr1:63413451 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.817-610G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413451 | |||||||
| chr1:63413562 | A | G | 1 | a0001c0001t0008g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-499A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413562 | |||||||
| chr1:63413732 | A | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.817-329A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413732 | |||||||
| chr1:63413769 | A | G | 147 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(144): Show |
152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.817-292A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413769 | |||||||
| chr1:63413783 | G | T | 1 | a0001c0001t0003g0118 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.817-278G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413783 | |||||||
| chr1:63413788 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0039 others(2): Show |
5 | HG00639.hp2 HG01255.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-273G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413788 | |||||||
| chr1:63413795 | G | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-266G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413795 | |||||||
| chr1:63413902 | G | A | 1 | a0001c0001t0015g0369 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817-159G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413902 | |||||||
| chr1:63414021 | C | T | 1 | a0001c0001t0007g0146 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.817-40C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63414021 | |||||||
| chr1:63414213 | T | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.902+67T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414213 | |||||||
| chr1:63414331 | A | G | 6 | a0001c0001t0002g0324 a0001c0001t0010g0326 a0001c0001t0010g0327 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.902+185A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414331 | |||||||
| chr1:63414400 | C | T | 2 | a0001c0001t0002g0274 a0001c0001t0002g0288 |
2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.902+254C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414400 | |||||||
| chr1:63414485 | G | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.902+339G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414485 | |||||||
| chr1:63414739 | A | G | 1 | a0001c0001t0003g0131 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.902+593A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414739 | |||||||
| chr1:63414754 | A | C | 216 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(213): Show |
225 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.902+608A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414754 | |||||||
| chr1:63414851 | A | G | 5 | a0001c0001t0002g0240 a0001c0001t0002g0244 a0001c0001t0002g0250 others(2): Show |
5 | HG02071.hp1 NA18948.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.902+705A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414851 | |||||||
| chr1:63414881 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0056 |
2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.902+735G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414881 | |||||||
| chr1:63414932 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0278 |
2 | NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.902+786G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414932 | |||||||
| chr1:63414977 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.902+831A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414977 | |||||||
| chr1:63415027 | G | A | 68 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(65): Show |
72 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.903-846G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415027 | |||||||
| chr1:63415100 | A | G | 1 | a0001c0001t0003g0010 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.903-773A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415100 | |||||||
| chr1:63415145 | C | A | 13 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(10): Show |
13 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903-728C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415145 | |||||||
| chr1:63415224 | T | C | 22 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(19): Show |
22 | HG00738.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.903-649T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415224 | |||||||
| chr1:63415226 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0039 others(2): Show |
5 | HG00639.hp2 HG01255.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.903-647G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415226 | |||||||
| chr1:63415662 | G | A | 1 | a0002c0002t0001g0323 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.903-211G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415662 | |||||||
| chr1:63415678 | G | C | 1 | a0002c0002t0001g0175 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.903-195G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415678 | |||||||
| chr1:63415678 | GTA | G | 121 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(118): Show |
125 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.903-183_903-182del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 63415678 | ||||||
| chr1:63415837 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.903-36A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415837 | |||||||
| chr1:63415843 | A | T | 13 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(10): Show |
13 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903-30A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415843 | |||||||
| chr1:63415850 | T | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.903-23T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415850 | |||||||
| chr1:63415993 | C | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.987+36C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63415993 | |||||||
| chr1:63416193 | A | G | 2 | a0001c0001t0003g0137 a0001c0001t0004g0062 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.987+236A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416193 | |||||||
| chr1:63416244 | A | G | 3 | a0001c0001t0002g0027 a0001c0001t0002g0029 a0001c0001t0002g0296 |
3 | HG02683.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.987+287A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416244 | |||||||
| chr1:63416263 | G | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(38): Show |
42 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.987+306G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416263 | |||||||
| chr1:63416313 | T | G | 1 | a0002c0002t0001g0336 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.987+356T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416313 | |||||||
| chr1:63416319 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0002g0040 |
2 | HG01884.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.987+362C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416319 | |||||||
| chr1:63416332 | T | C | 5 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(2): Show |
6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+375T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416332 | |||||||
| chr1:63416559 | G | A | 1 | a0002c0002t0001g0305 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.987+602G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416559 | |||||||
| chr1:63416614 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.987+657G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416614 | |||||||
| chr1:63416665 | G | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(2): Show |
6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+708G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416665 | |||||||
| chr1:63416841 | TA | T | 115 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(112): Show |
120 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.987+886delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 63416841 | ||||||
| chr1:63416984 | A | G | 1 | a0001c0001t0004g0042 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.987+1027A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416984 | |||||||
| chr1:63417007 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.987+1050T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417007 | |||||||
| chr1:63417085 | G | A | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1128G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417085 | |||||||
| chr1:63417201 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.987+1244T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417201 | |||||||
| chr1:63417402 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.987+1445G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417402 | |||||||
| chr1:63417459 | T | C | 10 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(7): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+1502T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417459 | |||||||
| chr1:63417651 | A | G | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+1694A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417651 | |||||||
| chr1:63417744 | C | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.988-1626C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417744 | |||||||
| chr1:63418048 | C | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.988-1322C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418048 | |||||||
| chr1:63418048 | C | T | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-1322C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418048 | |||||||
| chr1:63418091 | G | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.988-1279G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418091 | |||||||
| chr1:63418099 | A | G | 1 | a0001c0001t0002g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.988-1271A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418099 | |||||||
| chr1:63418244 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.988-1126G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418244 | |||||||
| chr1:63418255 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.988-1115G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418255 | |||||||
| chr1:63418267 | T | C | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-1103T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418267 | |||||||
| chr1:63418341 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.988-1029A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418341 | |||||||
| chr1:63418393 | A | G | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.988-977A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418393 | |||||||
| chr1:63418422 | T | C | 10 | a0002c0002t0001g0201 a0002c0002t0001g0311 a0002c0002t0001g0314 others(7): Show |
10 | HG02132.hp2 HG02280.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-948T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418422 | |||||||
| chr1:63418614 | A | G | 2 | a0002c0002t0001g0226 a0002c0002t0001g0227 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.988-756A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418614 | |||||||
| chr1:63418616 | G | T | 1 | a0001c0001t0002g0046 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.988-754G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418616 | |||||||
| chr1:63418750 | G | T | 11 | a0001c0001t0002g0014 a0001c0001t0002g0075 a0001c0001t0002g0076 others(8): Show |
12 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-620G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418750 | |||||||
| chr1:63418785 | T | C | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-585T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418785 | |||||||
| chr1:63418914 | T | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-456T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418914 | |||||||
| chr1:63418988 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.988-382A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418988 | |||||||
| chr1:63419038 | G | T | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-332G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419038 | |||||||
| chr1:63419097 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.988-273G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419097 | |||||||
| chr1:63419129 | G | A | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-241G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419129 | |||||||
| chr1:63419205 | T | C | 2 | a0001c0003t0010g0316 a0001c0004t0006g0317 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.988-165T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419205 | |||||||
| chr1:63419228 | G | A | 1 | a0002c0002t0001g0322 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.988-142G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419228 | |||||||
| chr1:63419551 | T | G | 77 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(74): Show |
81 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1058+111T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419551 | |||||||
| chr1:63419594 | G | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+154G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419594 | |||||||
| chr1:63419828 | T | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+388T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419828 | |||||||
| chr1:63419841 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+401C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419841 | |||||||
| chr1:63419847 | CT | C | 115 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(112): Show |
120 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1058+414delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63419847 | ||||||
| chr1:63419920 | A | C | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+480A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419920 | |||||||
| chr1:63420132 | T | A | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+692T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420132 | |||||||
| chr1:63420200 | G | C | 92 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(89): Show |
97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1058+760G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420200 | |||||||
| chr1:63420363 | G | A | 1 | a0001c0004t0004g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1058+923G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420363 | |||||||
| chr1:63420418 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+978G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420418 | |||||||
| chr1:63420444 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+1004G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420444 | |||||||
| chr1:63420536 | T | C | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+1096T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420536 | |||||||
| chr1:63420545 | A | G | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+1105A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420545 | |||||||
| chr1:63420625 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1058+1185C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420625 | |||||||
| chr1:63420662 | C | T | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+1222C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420662 | |||||||
| chr1:63420775 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1335T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420775 | |||||||
| chr1:63420778 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1338T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420778 | |||||||
| chr1:63420779 | T | C | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1339T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420779 | |||||||
| chr1:63420786 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1346A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420786 | |||||||
| chr1:63420840 | G | A | 1 | a0002c0002t0001g0339 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1058+1400G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420840 | |||||||
| chr1:63420860 | C | CA | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1058+1436dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | ||||||
| chr1:63420860 | CA | C | 86 | a0001c0001t0002g0187 a0001c0001t0002g0324 a0001c0001t0003g0001 others(83): Show |
90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1058+1436delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | ||||||
| chr1:63420860 | CAA | C | 28 | a0001c0001t0002g0186 a0001c0001t0003g0013 a0001c0001t0003g0116 others(25): Show |
29 | HG01069.hp2 HG01167.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1058+1435_1058+143 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | ||||||
| chr1:63420892 | T | A | 3 | a0001c0001t0001g0356 a0001c0001t0001g0361 a0001c0001t0001g0364 |
3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1058+1452T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420892 | |||||||
| chr1:63420896 | G | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+1456G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420896 | |||||||
| chr1:63420975 | C | T | 4 | a0001c0001t0002g0235 a0001c0001t0002g0277 a0001c0001t0002g0287 others(1): Show |
4 | NA18942.hp1 NA18990.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+1535C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420975 | |||||||
| chr1:63421029 | T | C | 2 | a0002c0002t0001g0158 a0002c0002t0001g0160 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1058+1589T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421029 | |||||||
| chr1:63421161 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0313 a0001c0001t0005g0018 others(2): Show |
5 | HG01433.hp2 HG03491.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1721C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421161 | |||||||
| chr1:63421330 | T | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+1890T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421330 | |||||||
| chr1:63421396 | T | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1058+1956T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421396 | |||||||
| chr1:63421584 | T | A | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+2144T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421584 | |||||||
| chr1:63421728 | A | G | 1 | a0001c0001t0002g0256 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1058+2288A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421728 | |||||||
| chr1:63421843 | A | G | 345 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(342): Show |
358 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(355): Show |
intron_variant | MODIFIER | c.1058+2403A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421843 | |||||||
| chr1:63421911 | G | A | 1 | a0002c0002t0001g0350 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1058+2471G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421911 | |||||||
| chr1:63422082 | AATAAATA others(1): Show |
A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+2660_1058+266 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422082 | ||||||
| chr1:63422088 | TATATAAA others(7): Show |
T | 7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2662_1058+267 others(18): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422088 | ||||||
| chr1:63422098 | TATAAATA others(3): Show |
T | 1 | a0001c0001t0001g0086 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1058+2662_1058+267 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422098 | ||||||
| chr1:63422108 | AAT | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(60): Show |
66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1058+2676_1058+267 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422108 | ||||||
| chr1:63422110 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1058+2670T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422110 | |||||||
| chr1:63422114 | TATAAATA others(5): Show |
T | 70 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(67): Show |
74 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1058+2690_1058+270 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422114 | ||||||
| chr1:63422120 | T | TATATATA others(55): Show |
1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2685_1058+268 others(66): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422120 | ||||||
| chr1:63422124 | T | TATAA | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2685_1058+268 others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422124 | ||||||
| chr1:63422126 | A | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2686A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422126 | |||||||
| chr1:63422130 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2690A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422130 | |||||||
| chr1:63422135 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2695A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422135 | |||||||
| chr1:63422137 | A | ATAACTAT others(1): Show |
6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2697_1058+269 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422137 | |||||||
| chr1:63422138 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2698A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422138 | |||||||
| chr1:63422141 | A | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2701A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422141 | |||||||
| chr1:63422142 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2702T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422142 | |||||||
| chr1:63422147 | A | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2707A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422147 | |||||||
| chr1:63422148 | A | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2708A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422148 | |||||||
| chr1:63422154 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2714A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422154 | |||||||
| chr1:63422154 | AAT | A | 273 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(270): Show |
285 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1058+2724_1058+272 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422154 | ||||||
| chr1:63422154 | AATATAT | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+2720_1058+272 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422154 | ||||||
| chr1:63422157 | A | C | 1 | a0001c0001t0002g0057 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2717A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422157 | |||||||
| chr1:63422160 | T | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+2720T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422160 | |||||||
| chr1:63422160 | T | TATCTATA others(3): Show |
6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(3): Show |
6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2722_1058+272 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422160 | ||||||
| chr1:63422167 | C | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2727C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422167 | |||||||
| chr1:63422167 | CTA | C | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+2729_1058+273 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422167 | ||||||
| chr1:63422168 | T | G | 1 | a0001c0001t0002g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1058+2728T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422168 | |||||||
| chr1:63422171 | G | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2731G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422171 | |||||||
| chr1:63422172 | A | T | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2732A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422172 | |||||||
| chr1:63422181 | T | A | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2741T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422181 | |||||||
| chr1:63422182 | T | G | 7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2742T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422182 | |||||||
| chr1:63422197 | CTA | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0331 |
3 | HG03490.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1058+2761_1058+276 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422197 | ||||||
| chr1:63422202 | T | G | 2 | a0001c0001t0004g0318 a0001c0001t0004g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1058+2762T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422202 | |||||||
| chr1:63422204 | AATATAAA others(103): Show |
A | 2 | a0001c0001t0004g0318 a0001c0001t0004g0319 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1058+2770_1058+287 others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422204 | ||||||
| chr1:63422210 | A | AATATATA others(61): Show |
1 | a0006c0006t0002g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1058+2785_1058+278 others(72): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422210 | ||||||
| chr1:63422210 | A | G | 1 | a0001c0001t0004g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1058+2770A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422210 | |||||||
| chr1:63422210 | AATATATA others(39): Show |
A | 1 | a0002c0002t0005g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1058+2776_1058+282 others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422210 | ||||||
| chr1:63422219 | T | C | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2779T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422219 | |||||||
| chr1:63422220 | TATATAAA others(5): Show |
T | 90 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(87): Show |
95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2786_1058+279 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422220 | ||||||
| chr1:63422226 | A | AATATAAA others(29): Show |
1 | a0002c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1058+2837_1058+287 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422226 | ||||||
| chr1:63422226 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(121): Show |
128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1058+2786A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422226 | |||||||
| chr1:63422232 | A | AATATATA others(57): Show |
1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(68): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422232 | ||||||
| chr1:63422237 | A | C | 90 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(87): Show |
95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2797A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422237 | |||||||
| chr1:63422238 | T | G | 75 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(72): Show |
79 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.1058+2798T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422238 | |||||||
| chr1:63422238 | T | TATATTTA others(5): Show |
7 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2802_1058+280 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(3): Show |
14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(49): Show |
1 | a0001c0001t0002g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(49): Show |
104 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0014 others(101): Show |
108 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(73): Show |
3 | a0001c0001t0002g0029 a0001c0001t0002g0261 a0001c0001t0002g0298 |
3 | HG03704.hp1 NA18964.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(84): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(93): Show |
2 | a0001c0001t0002g0028 a0001c0001t0002g0072 |
2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(104): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422238 | T | TATCTATA others(71): Show |
1 | a0001c0001t0002g0242 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(82): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | ||||||
| chr1:63422240 | T | TCTATATG others(1): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0044 a0001c0001t0002g0276 others(2): Show |
5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422240 | |||||||
| chr1:63422244 | A | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0044 a0001c0001t0002g0276 others(2): Show |
5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2804A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422244 | |||||||
| chr1:63422246 | T | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0044 a0001c0001t0002g0276 others(2): Show |
5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2806T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422246 | |||||||
| chr1:63422261 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0100 |
2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1058+2821A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422261 | |||||||
| chr1:63422262 | G | A | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2822G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422262 | |||||||
| chr1:63422262 | G | T | 1 | a0001c0001t0001g0361 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1058+2822G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422262 | |||||||
| chr1:63422270 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+2830T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422270 | |||||||
| chr1:63422273 | A | C | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1058+2833A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422273 | |||||||
| chr1:63422274 | T | G | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2834T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422274 | |||||||
| chr1:63422274 | T | TATATAAA others(17): Show |
1 | a0001c0001t0001g0281 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1058+2849_1058+287 others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | ||||||
| chr1:63422274 | T | TATATTTA others(5): Show |
1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2838_1058+283 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | ||||||
| chr1:63422274 | T | TATATTTA others(65): Show |
5 | a0001c0001t0002g0005 a0001c0001t0002g0044 a0001c0001t0002g0276 others(2): Show |
5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2838_1058+283 others(76): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | ||||||
| chr1:63422277 | A | C | 96 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(93): Show |
101 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.1058+2837A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422277 | |||||||
| chr1:63422283 | ATATATAT others(23): Show |
A | 96 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(93): Show |
101 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.1058+2851_1058+288 others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422283 | ||||||
| chr1:63422297 | A | C | 1 | a0001c0001t0002g0287 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1058+2857A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422297 | |||||||
| chr1:63422313 | C | A | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2873C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422313 | |||||||
| chr1:63422315 | A | T | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2875A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422315 | |||||||
| chr1:63422320 | T | TA | 11 | a0001c0003t0010g0316 a0001c0003t0012g0232 a0001c0003t0012g0233 others(8): Show |
11 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1058+2880_1058+288 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422320 | |||||||
| chr1:63422320 | T | TC | 4 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2880_1058+288 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422320 | |||||||
| chr1:63422322 | A | ATATAAAT | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2882_1058+288 others(11): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422322 | |||||||
| chr1:63422331 | C | T | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2891C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422331 | |||||||
| chr1:63422336 | G | T | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2896G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422336 | |||||||
| chr1:63422337 | G | A | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0167 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2897G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422337 | |||||||
| chr1:63422337 | G | C | 1 | a0001c0003t0009g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1058+2897G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422337 | |||||||
| chr1:63422338 | A | G | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2898A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422338 | |||||||
| chr1:63422344 | A | AAT | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2911_1058+291 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422344 | ||||||
| chr1:63422353 | C | T | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2913C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422353 | |||||||
| chr1:63422354 | TATATAA | T | 90 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(87): Show |
95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2926_1058+293 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422354 | ||||||
| chr1:63422360 | A | G | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2920A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422360 | |||||||
| chr1:63422360 | A | T | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2920A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422360 | |||||||
| chr1:63422364 | TAAATATA others(37): Show |
T | 2 | a0001c0001t0003g0212 a0001c0001t0003g0214 |
2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2926_1058+296 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422364 | ||||||
| chr1:63422365 | A | G | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2925A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422365 | |||||||
| chr1:63422375 | A | ATTTATAT others(12): Show |
4 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2935_1058+293 others(23): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422375 | |||||||
| chr1:63422375 | A | G | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2935A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422375 | |||||||
| chr1:63422376 | A | T | 10 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+2936A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422376 | |||||||
| chr1:63422377 | G | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2937G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | |||||||
| chr1:63422377 | G | GA | 4 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2937_1058+293 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | |||||||
| chr1:63422377 | G | T | 10 | a0001c0003t0012g0232 a0001c0003t0012g0233 a0001c0003t0014g0234 others(7): Show |
10 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+2937G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | |||||||
| chr1:63422379 | A | ATATAGAT others(61): Show |
2 | a0001c0003t0012g0232 a0001c0004t0006g0225 |
2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(72): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | ||||||
| chr1:63422379 | A | ATATAGAT others(37): Show |
6 | a0001c0003t0012g0233 a0001c0004t0004g0199 a0001c0004t0006g0157 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | ||||||
| chr1:63422379 | A | ATATAGAT others(13): Show |
2 | a0001c0003t0014g0234 a0001c0004t0006g0317 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | ||||||
| chr1:63422388 | TATAAATA others(37): Show |
T | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+2952_1058+299 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422388 | ||||||
| chr1:63422391 | A | ATG | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2951_1058+295 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422391 | |||||||
| chr1:63422396 | TATATCTA others(29): Show |
T | 10 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0204 others(7): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1058+2961_1058+299 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422396 | ||||||
| chr1:63422397 | A | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+2957A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422397 | |||||||
| chr1:63422398 | T | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2958T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422398 | |||||||
| chr1:63422398 | TATCTATA others(27): Show |
T | 76 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(73): Show |
80 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1058+2961_1058+299 others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422398 | ||||||
| chr1:63422398 | TATCTATA others(39): Show |
T | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+2961_1058+300 others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422398 | ||||||
| chr1:63422401 | C | A | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2961C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422401 | |||||||
| chr1:63422402 | TATATAA | T | 62 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(59): Show |
65 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1058+2974_1058+297 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422402 | ||||||
| chr1:63422406 | T | G | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2966T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422406 | |||||||
| chr1:63422407 | A | G | 14 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(11): Show |
14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2967A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422407 | |||||||
| chr1:63422408 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0313 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1058+2973_1058+297 others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | ||||||
| chr1:63422408 | AATATAAA others(23): Show |
A | 129 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(126): Show |
133 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1058+3016_1058+304 others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | ||||||
| chr1:63422408 | AATATAAA others(35): Show |
A | 1 | a0001c0001t0010g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1058+2980_1058+302 others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | ||||||
| chr1:63422409 | A | G | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2969A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422409 | |||||||
| chr1:63422414 | AATATATA others(29): Show |
A | 1 | a0001c0001t0010g0327 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1058+2980_1058+301 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422414 | ||||||
| chr1:63422415 | A | G | 2 | a0001c0001t0003g0212 a0001c0001t0003g0214 |
2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2975A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422415 | |||||||
| chr1:63422420 | T | A | 2 | a0001c0001t0003g0212 a0001c0001t0003g0214 |
2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2980T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422420 | |||||||
| chr1:63422426 | A | T | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2986A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422426 | |||||||
| chr1:63422426 | AATATAAA others(5): Show |
A | 2 | a0002c0002t0001g0181 a0002c0002t0001g0185 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1058+3010_1058+302 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422426 | ||||||
| chr1:63422431 | A | C | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2991A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422431 | |||||||
| chr1:63422432 | A | T | 3 | a0001c0001t0003g0212 a0001c0001t0003g0214 a0001c0003t0010g0316 |
3 | HG06807.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2992A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422432 | |||||||
| chr1:63422434 | T | TATATATA others(7): Show |
1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3001_1058+300 others(18): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422434 | ||||||
| chr1:63422438 | T | A | 93 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(90): Show |
98 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.1058+2998T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422438 | |||||||
| chr1:63422438 | T | TATAAGTA others(29): Show |
6 | a0001c0004t0004g0199 a0001c0004t0006g0157 a0001c0004t0006g0197 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+3001_1058+300 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422438 | ||||||
| chr1:63422438 | T | TATAAGTA others(29): Show |
7 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+3001_1058+300 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422438 | ||||||
| chr1:63422450 | T | A | 4 | a0001c0001t0003g0170 a0001c0001t0011g0161 a0001c0001t0011g0162 others(1): Show |
4 | HG02622.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+3010T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422450 | |||||||
| chr1:63422450 | T | TATCTATA others(3): Show |
1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3012_1058+301 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422450 | ||||||
| chr1:63422462 | A | T | 1 | a0001c0004t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3022A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422462 | |||||||
| chr1:63422493 | A | G | 1 | a0004c0008t0003g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1058+3053A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422493 | |||||||
| chr1:63422638 | C | T | 1 | a0001c0003t0009g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1058+3198C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422638 | |||||||
| chr1:63422895 | C | T | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+3455C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422895 | |||||||
| chr1:63422936 | C | T | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3496C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422936 | |||||||
| chr1:63422937 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+3497G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422937 | |||||||
| chr1:63423020 | T | C | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3580T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423020 | |||||||
| chr1:63423024 | A | AT | 173 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(170): Show |
181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1058+3601dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | ||||||
| chr1:63423024 | A | ATT | 9 | a0001c0001t0001g0070 a0001c0001t0001g0291 a0001c0001t0002g0186 others(6): Show |
9 | HG00738.hp1 HG01243.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1058+3600_1058+360 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | ||||||
| chr1:63423024 | AT | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+3601delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | ||||||
| chr1:63423169 | G | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0036 a0001c0001t0002g0040 |
3 | HG01070.hp1 HG01884.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1058+3729G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423169 | |||||||
| chr1:63423181 | G | A | 1 | a0001c0001t0002g0014 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1058+3741G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423181 | |||||||
| chr1:63423346 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0070 others(20): Show |
24 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1058+3906A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423346 | |||||||
| chr1:63423473 | G | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(120): Show |
127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+4033G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423473 | |||||||
| chr1:63423808 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1058+4368C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423808 | |||||||
| chr1:63423963 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1058+4523C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423963 | |||||||
| chr1:63423989 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+4549C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423989 | |||||||
| chr1:63424265 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1059-4468C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424265 | |||||||
| chr1:63424274 | G | A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-4459G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424274 | |||||||
| chr1:63424286 | G | A | 15 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(12): Show |
15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059-4447G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424286 | |||||||
| chr1:63424375 | G | A | 68 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(65): Show |
72 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059-4358G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424375 | |||||||
| chr1:63424419 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-4314G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424419 | |||||||
| chr1:63424439 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1059-4294G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424439 | |||||||
| chr1:63424496 | A | C | 1 | a0001c0003t0014g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059-4237A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424496 | |||||||
| chr1:63424704 | C | T | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1059-4029C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424704 | |||||||
| chr1:63424774 | A | AT | 28 | a0001c0001t0002g0187 a0001c0001t0002g0324 a0001c0001t0003g0106 others(25): Show |
28 | HG00738.hp1 HG01192.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059-3937dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424774 | A | ATT | 7 | a0001c0001t0003g0119 a0001c0001t0008g0228 a0001c0001t0008g0229 others(4): Show |
7 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3938_1059-393 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424774 | A | ATTT | 7 | a0001c0003t0010g0316 a0001c0004t0004g0199 a0001c0004t0006g0157 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3939_1059-393 others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424774 | AT | A | 16 | a0001c0001t0001g0346 a0001c0001t0002g0058 a0001c0001t0002g0304 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1059-3937delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424774 | ATT | A | 128 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(125): Show |
133 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1059-3938_1059-393 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424774 | ATTT | A | 9 | a0001c0001t0002g0046 a0001c0001t0002g0053 a0001c0001t0002g0082 others(6): Show |
9 | HG01167.hp2 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-3939_1059-393 others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | ||||||
| chr1:63424820 | C | T | 1 | a0006c0006t0002g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1059-3913C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424820 | |||||||
| chr1:63424821 | G | A | 92 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(89): Show |
97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1059-3912G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424821 | |||||||
| chr1:63425092 | A | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-3641A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425092 | |||||||
| chr1:63425164 | C | T | 22 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(19): Show |
22 | HG00738.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-3569C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425164 | |||||||
| chr1:63425409 | A | G | 92 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(89): Show |
97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1059-3324A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425409 | |||||||
| chr1:63425491 | G | A | 2 | a0001c0001t0004g0102 a0004c0008t0003g0202 |
2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1059-3242G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425491 | |||||||
| chr1:63425524 | G | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-3209G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425524 | |||||||
| chr1:63425706 | A | G | 238 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(235): Show |
247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.1059-3027A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425706 | |||||||
| chr1:63425721 | A | G | 111 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(108): Show |
116 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.1059-3012A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425721 | |||||||
| chr1:63425813 | C | A | 67 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(64): Show |
71 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.1059-2920C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425813 | |||||||
| chr1:63425827 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1059-2906G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425827 | |||||||
| chr1:63425838 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1059-2895G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425838 | |||||||
| chr1:63425876 | G | A | 18 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(15): Show |
19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1059-2857G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425876 | |||||||
| chr1:63425903 | C | T | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-2830C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425903 | |||||||
| chr1:63425923 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-2810C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425923 | |||||||
| chr1:63425963 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1059-2770G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425963 | |||||||
| chr1:63426129 | A | G | 1 | a0001c0001t0003g0151 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1059-2604A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426129 | |||||||
| chr1:63426151 | G | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-2582G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426151 | |||||||
| chr1:63426184 | G | T | 70 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(67): Show |
74 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1059-2549G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426184 | |||||||
| chr1:63426301 | T | C | 238 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(235): Show |
247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.1059-2432T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426301 | |||||||
| chr1:63426498 | G | A | 4 | a0001c0001t0003g0117 a0001c0001t0003g0119 a0001c0001t0003g0126 others(1): Show |
4 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-2235G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426498 | |||||||
| chr1:63426569 | G | A | 3 | a0001c0001t0001g0356 a0001c0001t0001g0361 a0001c0001t0001g0364 |
3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1059-2164G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426569 | |||||||
| chr1:63426643 | A | C | 1 | a0001c0003t0010g0316 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1059-2090A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426643 | |||||||
| chr1:63426681 | C | A | 64 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-2052C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426681 | |||||||
| chr1:63427040 | C | T | 17 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(14): Show |
18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059-1693C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427040 | |||||||
| chr1:63427069 | C | T | 1 | a0001c0007t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1059-1664C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427069 | |||||||
| chr1:63427086 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-1647C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427086 | |||||||
| chr1:63427167 | A | AT | 36 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0070 others(33): Show |
39 | HG00438.hp1 HG00738.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-1547dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | ||||||
| chr1:63427167 | AT | A | 22 | a0001c0001t0001g0241 a0001c0001t0003g0122 a0001c0001t0003g0131 others(19): Show |
22 | HG01069.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-1547delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | ||||||
| chr1:63427167 | ATT | A | 69 | a0001c0001t0002g0324 a0001c0001t0003g0001 a0001c0001t0003g0002 others(66): Show |
73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059-1548_1059-154 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | ||||||
| chr1:63427204 | G | A | 7 | a0001c0001t0002g0324 a0001c0004t0004g0199 a0001c0004t0006g0157 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-1529G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427204 | |||||||
| chr1:63427282 | C | A | 1 | a0002c0002t0001g0368 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1059-1451C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427282 | |||||||
| chr1:63427329 | T | C | 117 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
120 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059-1404T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427329 | |||||||
| chr1:63427537 | C | A | 1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059-1196C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427537 | |||||||
| chr1:63427647 | G | A | 1 | a0001c0001t0007g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1059-1086G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427647 | |||||||
| chr1:63427649 | C | A | 4 | a0001c0001t0008g0228 a0001c0001t0008g0229 a0001c0001t0008g0230 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-1084C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427649 | |||||||
| chr1:63427723 | A | G | 297 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(294): Show |
309 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1059-1010A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427723 | |||||||
| chr1:63427757 | T | C | 243 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0006 others(240): Show |
253 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(250): Show |
intron_variant | MODIFIER | c.1059-976T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427757 | |||||||
| chr1:63427787 | C | CT | 39 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0001g0291 others(36): Show |
39 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1059-923dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | ||||||
| chr1:63427787 | C | CTT | 7 | a0001c0001t0002g0235 a0001c0004t0004g0199 a0001c0004t0006g0157 others(4): Show |
7 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-924_1059-923d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | ||||||
| chr1:63427787 | CT | C | 30 | a0001c0001t0002g0022 a0001c0001t0002g0037 a0001c0001t0002g0186 others(27): Show |
31 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059-923delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | ||||||
| chr1:63427944 | T | G | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-789T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427944 | |||||||
| chr1:63428016 | G | A | 1 | a0002c0002t0001g0310 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1059-717G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428016 | |||||||
| chr1:63428253 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-480T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428253 | |||||||
| chr1:63428488 | T | G | 117 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(114): Show |
120 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059-245T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428488 | |||||||
| chr1:63428502 | G | T | 1 | a0001c0001t0002g0290 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1059-231G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428502 | |||||||
| chr1:63428822 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1127+21T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 13/14 | chr1 | 63428822 | |||||||
| chr1:63428887 | T | C | 13 | a0001c0001t0002g0324 a0001c0003t0009g0164 a0001c0003t0009g0165 others(10): Show |
13 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1128-41T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 13/14 | chr1 | 63428887 | |||||||
| chr1:63429334 | A | G | 1 | a0001c0001t0007g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1326+208A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429334 | |||||||
| chr1:63429534 | C | G | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326+408C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429534 | |||||||
| chr1:63429550 | G | T | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1326+424G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429550 | |||||||
| chr1:63429800 | A | G | 105 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(102): Show |
112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1326+674A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429800 | |||||||
| chr1:63429850 | A | AGT | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(77): Show |
84 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1326+757_1326+758d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | A | AGTGT | 128 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0328 others(125): Show |
133 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.1326+755_1326+758d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | A | AGTGTGT | 21 | a0001c0001t0002g0028 a0001c0001t0002g0041 a0001c0001t0002g0045 others(18): Show |
21 | HG00558.hp2 HG00738.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1326+753_1326+758d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | A | AGTGTGTG others(1): Show |
38 | a0001c0001t0001g0358 a0001c0001t0002g0027 a0001c0001t0002g0030 others(35): Show |
40 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1326+751_1326+758d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | A | AGTGTGTG others(3): Show |
5 | a0001c0001t0002g0069 a0001c0001t0002g0186 a0001c0001t0003g0129 others(2): Show |
5 | HG00544.hp2 HG00558.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+749_1326+758d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0004g0325 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1326+747_1326+758d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | AGTGT | A | 7 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(4): Show |
8 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326+755_1326+758d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0085 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1326+749_1326+758d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429850 | AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0002g0292 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1326+741_1326+758d others(20): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | ||||||
| chr1:63429975 | T | C | 1 | a0001c0001t0003g0010 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1326+849T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429975 | |||||||
| chr1:63430031 | C | T | 2 | a0001c0001t0003g0168 a0001c0001t0004g0063 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1326+905C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430031 | |||||||
| chr1:63430037 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1326+911C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430037 | |||||||
| chr1:63430171 | G | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(68): Show |
75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1326+1045G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430171 | |||||||
| chr1:63430179 | T | C | 241 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(238): Show |
251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1326+1053T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430179 | |||||||
| chr1:63430235 | T | C | 13 | a0001c0001t0002g0324 a0001c0003t0009g0164 a0001c0003t0009g0165 others(10): Show |
13 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1326+1109T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430235 | |||||||
| chr1:63430258 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1326+1132A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430258 | |||||||
| chr1:63430530 | G | T | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1326+1404G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430530 | |||||||
| chr1:63430735 | T | C | 1 | a0005c0009t0020g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326+1609T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430735 | |||||||
| chr1:63430772 | T | C | 1 | a0001c0001t0002g0251 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1326+1646T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430772 | |||||||
| chr1:63430830 | CTG | C | 5 | a0001c0004t0006g0157 a0001c0004t0006g0197 a0001c0004t0006g0198 others(2): Show |
5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326+1710_1326+171 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63430830 | ||||||
| chr1:63430903 | A | G | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1326+1777A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430903 | |||||||
| chr1:63431452 | T | C | 6 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(3): Show |
7 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326+2326T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431452 | |||||||
| chr1:63431458 | C | T | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326+2332C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431458 | |||||||
| chr1:63431620 | G | A | 1 | a0002c0002t0001g0350 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1326+2494G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431620 | |||||||
| chr1:63431654 | G | T | 1 | a0001c0001t0001g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2528G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431654 | |||||||
| chr1:63431655 | G | A | 1 | a0001c0001t0001g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2529G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431655 | |||||||
| chr1:63431656 | A | G | 1 | a0001c0001t0001g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2530A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431656 | |||||||
| chr1:63431761 | G | A | 105 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(102): Show |
112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1326+2635G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431761 | |||||||
| chr1:63431848 | A | T | 1 | a0002c0002t0001g0345 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1326+2722A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431848 | |||||||
| chr1:63431885 | C | T | 7 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0010g0326 others(4): Show |
7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1326+2759C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431885 | |||||||
| chr1:63431938 | A | T | 17 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(14): Show |
18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1326+2812A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431938 | |||||||
| chr1:63432245 | T | A | 2 | a0001c0003t0010g0316 a0001c0004t0006g0317 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1326+3119T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432245 | |||||||
| chr1:63432258 | G | GT | 214 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(211): Show |
223 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.1326+3133dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | ||||||
| chr1:63432258 | G | GTT | 6 | a0001c0001t0002g0240 a0001c0001t0003g0121 a0001c0001t0003g0135 others(3): Show |
6 | HG01884.hp1 HG02015.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326+3133_1326+313 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | ||||||
| chr1:63432258 | G | GTTTTTT | 6 | a0001c0001t0004g0004 a0001c0001t0004g0034 a0001c0001t0004g0042 others(3): Show |
7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326+3133_1326+313 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | ||||||
| chr1:63432260 | G | T | 343 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(340): Show |
356 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(353): Show |
intron_variant | MODIFIER | c.1326+3134G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432260 | |||||||
| chr1:63432283 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1326+3157T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432283 | |||||||
| chr1:63432739 | C | T | 125 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(122): Show |
132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1326+3613C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432739 | |||||||
| chr1:63432920 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1326+3794T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432920 | |||||||
| chr1:63433053 | C | G | 2 | a0002c0002t0001g0181 a0002c0002t0001g0185 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1327-3770C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433053 | |||||||
| chr1:63433158 | G | A | 2 | a0001c0001t0010g0326 a0001c0001t0010g0327 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1327-3665G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433158 | |||||||
| chr1:63433221 | G | A | 125 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(122): Show |
132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1327-3602G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433221 | |||||||
| chr1:63433230 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1327-3593C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433230 | |||||||
| chr1:63433238 | G | T | 105 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(102): Show |
112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1327-3585G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433238 | |||||||
| chr1:63433260 | A | G | 17 | a0001c0001t0003g0013 a0001c0001t0003g0168 a0001c0001t0003g0170 others(14): Show |
18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1327-3563A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433260 | |||||||
| chr1:63433270 | G | A | 6 | a0001c0001t0007g0011 a0001c0001t0007g0107 a0001c0001t0007g0112 others(3): Show |
7 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-3553G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433270 | |||||||
| chr1:63433475 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1327-3348G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433475 | |||||||
| chr1:63433663 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1327-3160C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433663 | |||||||
| chr1:63433714 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1327-3109T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433714 | |||||||
| chr1:63433752 | G | A | 6 | a0001c0001t0004g0004 a0001c0001t0004g0034 a0001c0001t0004g0042 others(3): Show |
7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-3071G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433752 | |||||||
| chr1:63433973 | T | C | 10 | a0001c0001t0002g0023 a0001c0001t0002g0239 a0001c0001t0002g0246 others(7): Show |
10 | HG00423.hp2 NA18963.hp1 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1327-2850T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433973 | |||||||
| chr1:63433981 | G | C | 1 | a0002c0002t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1327-2842G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433981 | |||||||
| chr1:63434111 | T | A | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-2712T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434111 | |||||||
| chr1:63434149 | A | G | 2 | a0001c0003t0010g0316 a0001c0004t0006g0317 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1327-2674A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434149 | |||||||
| chr1:63434337 | A | G | 2 | a0001c0001t0003g0118 a0001c0001t0003g0127 |
2 | HG01256.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1327-2486A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434337 | |||||||
| chr1:63434399 | G | A | 88 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(85): Show |
94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-2424G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434399 | |||||||
| chr1:63434462 | A | G | 241 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(238): Show |
251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1327-2361A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434462 | |||||||
| chr1:63434479 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1327-2344G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434479 | |||||||
| chr1:63434588 | T | C | 5 | a0001c0001t0010g0326 a0001c0001t0010g0327 a0001c0001t0011g0161 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-2235T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434588 | |||||||
| chr1:63434603 | G | GT | 116 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1327-2213dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63434603 | ||||||
| chr1:63434639 | C | T | 3 | a0001c0001t0011g0161 a0001c0001t0011g0162 a0001c0001t0011g0163 |
3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1327-2184C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434639 | |||||||
| chr1:63434640 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1327-2183G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434640 | |||||||
| chr1:63434666 | G | A | 1 | a0002c0002t0001g0311 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1327-2157G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434666 | |||||||
| chr1:63434727 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1327-2096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434727 | |||||||
| chr1:63434823 | G | T | 29 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(26): Show |
30 | HG01167.hp2 HG01192.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-2000G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434823 | |||||||
| chr1:63434824 | T | C | 29 | a0001c0001t0002g0324 a0001c0001t0003g0013 a0001c0001t0003g0168 others(26): Show |
30 | HG01167.hp2 HG01192.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-1999T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434824 | |||||||
| chr1:63434850 | G | A | 5 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0357 others(2): Show |
5 | NA18940.hp2 NA18944.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1973G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434850 | |||||||
| chr1:63434875 | G | T | 1 | a0001c0001t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1327-1948G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434875 | |||||||
| chr1:63434963 | G | T | 1 | a0001c0001t0010g0327 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1327-1860G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434963 | |||||||
| chr1:63434973 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1327-1850A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434973 | |||||||
| chr1:63435060 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(58): Show |
63 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1327-1763T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435060 | |||||||
| chr1:63435068 | G | A | 241 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(238): Show |
251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1327-1755G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435068 | |||||||
| chr1:63435087 | A | T | 1 | a0002c0002t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1327-1736A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435087 | |||||||
| chr1:63435111 | T | C | 1 | a0001c0001t0002g0353 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1327-1712T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435111 | |||||||
| chr1:63435116 | A | T | 88 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(85): Show |
94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-1707A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435116 | |||||||
| chr1:63435164 | G | A | 82 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(79): Show |
87 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1327-1659G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435164 | |||||||
| chr1:63435230 | G | A | 88 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(85): Show |
94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-1593G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435230 | |||||||
| chr1:63435680 | A | G | 1 | a0001c0001t0004g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1327-1143A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435680 | |||||||
| chr1:63435723 | T | A | 116 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(113): Show |
119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1327-1100T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435723 | |||||||
| chr1:63435757 | T | A | 302 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.1327-1066T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435757 | |||||||
| chr1:63435762 | C | CTCAG | 5 | a0001c0003t0009g0164 a0001c0003t0009g0165 a0001c0003t0009g0166 others(2): Show |
5 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1057_1327-105 others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63435762 | ||||||
| chr1:63435820 | A | C | 1 | a0001c0001t0002g0048 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1327-1003A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435820 | |||||||
| chr1:63435951 | G | C | 125 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0324 others(122): Show |
132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1327-872G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435951 | |||||||
| chr1:63436085 | C | T | 2 | a0001c0003t0012g0232 a0001c0003t0012g0233 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1327-738C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436085 | |||||||
| chr1:63436086 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0255 |
2 | NA18945.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1327-737G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436086 | |||||||
| chr1:63436250 | A | T | 6 | a0001c0001t0004g0004 a0001c0001t0004g0034 a0001c0001t0004g0042 others(3): Show |
7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-573A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436250 | |||||||
| chr1:63436274 | T | C | 3 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0111 |
3 | HG00438.hp2 NA18747.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1327-549T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436274 | |||||||
| chr1:63436382 | C | G | 1 | a0001c0003t0009g0166 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327-441C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436382 | |||||||
| chr1:63436526 | G | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0010 others(68): Show |
75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1327-297G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436526 | |||||||
| chr1:63436596 | A | G | 2 | a0002c0002t0001g0329 a0002c0002t0001g0330 |
2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1327-227A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436596 | |||||||
| chr1:63436760 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(33): Show |
37 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.1327-63A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436760 |