Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23295 |
| ensemblid | ENSG00000102858.13 |
| hgncid | 20254 |
| symbol | MGRN1 |
| name | mahogunin ring finger 1 |
| refseq_nuc | NM_015246.4 |
| refseq_prot | NP_056061.1 |
| ensembl_nuc | ENST00000262370.12 |
| ensembl_prot | ENSP00000262370.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 4624826 |
| end | 4690972 |
| strand | + |
| ver | v1.2 |
| region | chr16:4624826-4690972 |
| region5000 | chr16:4619826-4695972 |
| regionname0 | MGRN1_chr16_4624826_4690972 |
| regionname5000 | MGRN1_chr16_4619826_4695972 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 576 | 331 | 88 | 56 | 130 | 16 | 39 | 90 | MGRN1_chr16_4619826_4695972 | MGRN1 | MGSIL others(571): Show |
chr16 | 4619826 | 4695972 |
| a0002 | 0/0 | 576 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | MGSIL others(571): Show |
chr16 | 4619826 | 4695972 |
| a0003 | 0/0 | 168 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | MGSIL others(163): Show |
chr16 | 4619826 | 4695972 |
| a0004 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | MGSIL others(571): Show |
chr16 | 4619826 | 4695972 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1728 | 321 | 82 | 53 | 130 | 16 | 39 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0001c0002 | 0/0 | 1728 | 4 | 3 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0001c0003 | 0/0 | 1728 | 3 | 1 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0001c0004 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0001c0006 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0001c0008 | 0/1 | 1728 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0002c0007 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0003c0009 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 | ||
| a0004c0005 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | ATGGG others(1723): Show |
chr16 | 4619826 | 4695972 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3930 | 103 | 7 | 26 | 50 | 8 | 12 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0002 | 0/0 | 3930 | 77 | 9 | 14 | 38 | 2 | 14 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0003 | 1/0 | 3930 | 34 | 16 | 1 | 11 | 2 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0004 | 0/0 | 3930 | 15 | 3 | 4 | 7 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0005 | 0/0 | 3930 | 13 | 13 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0006 | 0/0 | 3930 | 11 | 1 | 3 | 7 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0007 | 0/0 | 3930 | 8 | 8 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0008 | 0/0 | 3930 | 8 | 8 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0009 | 0/0 | 3930 | 7 | 0 | 0 | 7 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0010 | 0/0 | 3930 | 4 | 0 | 1 | 0 | 0 | 3 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0011 | 0/0 | 3930 | 3 | 1 | 0 | 0 | 1 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0012 | 0/0 | 3930 | 3 | 0 | 1 | 0 | 1 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0013 | 0/0 | 3930 | 2 | 0 | 0 | 2 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0015 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0016 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0017 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0018 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0019 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0020 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0021 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0022 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0023 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0024 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0025 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0026 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0027 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0028 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0030 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0032 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0033 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0034 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0035 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0036 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0037 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0038 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0039 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0041 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0042 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0043 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0044 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0045 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0046 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0047 | 0/0 | 3930 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0048 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0049 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0001t0050 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0002t0003 | 0/0 | 3930 | 2 | 1 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0002t0004 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0002t0005 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0003t0014 | 0/0 | 3930 | 2 | 0 | 2 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0003t0031 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0004t0029 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0006t0007 | 0/0 | 3930 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0001c0008t0040 | 0/1 | 3930 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0002c0007t0001 | 0/0 | 3930 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0003c0009t0001 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| a0004c0005t0001 | 0/0 | 3930 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | GGGGG others(3925): Show |
chr16 | 4619826 | 4695972 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0010g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0012g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0013g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0021g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0022g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0023g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0024g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0025g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0026g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0027g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0028g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0030g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0032g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0033g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0035g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0036g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0037g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0038g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0039g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0041g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0042g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0043g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0044g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0045g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0046g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0047g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0048g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0049g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0001t0050g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0002t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0002t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0002t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0003t0014g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0003t0014g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0003t0031g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0004t0029g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0006t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0001c0008t0040g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0002c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0003c0009t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| a0004c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0051 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00140 | hp2 | a0001 | c0001 | t0024 | g0046 | EUR | GBR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00323 | hp2 | a0001 | c0001 | t0012 | g0164 | EUR | FIN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00423 | hp2 | a0001 | c0001 | t0013 | g0163 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0277 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0202 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00741 | hp1 | a0001 | c0001 | t0047 | g0114 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01081 | hp1 | a0001 | c0001 | t0012 | g0211 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01167 | hp1 | a0001 | c0003 | t0014 | g0136 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01169 | hp1 | a0001 | c0003 | t0014 | g0137 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0276 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0071 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0049 | EUR | IBS | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01884 | hp1 | a0001 | c0001 | t0027 | g0002 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01891 | hp1 | a0001 | c0001 | t0045 | g0329 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02055 | hp1 | a0001 | c0006 | t0007 | g0099 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02071 | hp1 | a0001 | c0001 | t0042 | g0317 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0311 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0291 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0107 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02273 | hp1 | a0001 | c0001 | t0041 | g0322 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02602 | hp2 | a0001 | c0001 | t0010 | g0177 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0011 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02630 | hp2 | a0001 | c0001 | t0034 | g0185 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02723 | hp2 | a0001 | c0001 | t0018 | g0014 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02809 | hp2 | a0001 | c0004 | t0029 | g0083 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0086 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0333 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0006 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0042 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0012 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0001 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03195 | hp2 | a0001 | c0003 | t0031 | g0017 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03225 | hp1 | a0001 | c0001 | t0033 | g0184 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0085 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0027 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03490 | hp2 | a0001 | c0001 | t0048 | g0315 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03579 | hp1 | a0001 | c0001 | t0030 | g0082 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03579 | hp2 | a0001 | c0001 | t0021 | g0032 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03654 | hp2 | a0001 | c0001 | t0050 | g0318 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03669 | hp2 | a0001 | c0001 | t0023 | g0073 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03710 | hp2 | a0001 | c0001 | t0049 | g0122 | SAS | PJL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0191 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03834 | hp1 | a0001 | c0001 | t0044 | g0116 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03927 | hp1 | a0002 | c0007 | t0001 | g0126 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0323 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0192 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | STU | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18953 | hp2 | a0001 | c0001 | t0013 | g0178 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0226 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0228 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18961 | hp2 | a0001 | c0001 | t0038 | g0254 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18964 | hp2 | a0001 | c0001 | t0039 | g0155 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0294 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18971 | hp1 | a0001 | c0001 | t0043 | g0306 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18977 | hp2 | a0003 | c0009 | t0001 | g0168 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0243 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18984 | hp1 | a0001 | c0001 | t0037 | g0171 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19002 | hp1 | a0001 | c0001 | t0035 | g0118 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19011 | hp2 | a0004 | c0005 | t0001 | g0144 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19055 | hp1 | a0001 | c0001 | t0009 | g0141 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19057 | hp1 | a0001 | c0001 | t0036 | g0198 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19063 | hp1 | a0001 | c0001 | t0009 | g0332 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19074 | hp1 | a0001 | c0001 | t0025 | g0081 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0310 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19086 | hp2 | a0001 | c0001 | t0009 | g0210 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0324 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | YRI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ASW | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20129 | hp2 | a0001 | c0001 | t0028 | g0043 | AFR | ASW | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20805 | hp1 | a0001 | c0001 | t0011 | g0056 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0174 | SAS | GIH | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0066 | SAS | GIH | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG01123 | hp2 | a0001 | c0001 | t0032 | g0124 | AMR | CLM | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0334 | AFR | MSL | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0045 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | USA | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | LWK | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| homoSapiens | chm13v2 | a0001 | c0008 | t0040 | g0182 | REF | REF | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0016 | REF | REF | MGRN1_chr16_4619826_4695972 | MGRN1 | chr16 | 4619826 | 4695972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4657307 | C | T | 1 | a0003 | 1 | NA18977.hp2 | stop_gained | HIGH | c.505C>T | p.Gln169* | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/17 | 640/3930 | 505/1731 | 169/576 | chr16 | 4657307 | |||
| chr16:4657361 | G | A | 1 | a0004 | 1 | NA19011.hp2 | missense_variant&splice_region_variant | MODERATE | c.559G>A | p.Glu187Lys | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/17 | 694/3930 | 559/1731 | 187/576 | chr16 | 4657361 | |||
| chr16:4683252 | C | T | 1 | a0002 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1511C>T | p.Ser504Leu | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/17 | 1646/3930 | 1511/1731 | 504/576 | chr16 | 4683252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4650417 | C | A | 2 | a0001c0002 a0001c0004 |
5 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.141C>A | p.Pro47Pro | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/17 | 276/3930 | 141/1731 | 47/576 | chr16 | 4650417 | |||
| chr16:4664744 | A | G | 2 | a0001c0003 a0001c0004 |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.597A>G | p.Val199Val | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/17 | 732/3930 | 597/1731 | 199/576 | chr16 | 4664744 | |||
| chr16:4688884 | C | T | 1 | a0001c0006 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1707C>T | p.Ser569Ser | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1842/3930 | 1707/1731 | 569/576 | chr16 | 4688884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4624953 | C | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(26): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/17 | 8 | chr16 | 4624953 | ||||||
| chr16:4688919 | G | A | 1 | a0001c0001t0032 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 11 | chr16 | 4688919 | ||||||
| chr16:4689176 | T | C | 5 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0017 others(2): Show |
5 | HG02622.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*268T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 268 | chr16 | 4689176 | ||||||
| chr16:4689188 | G | A | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 280 | chr16 | 4689188 | ||||||
| chr16:4689245 | A | C | 3 | a0001c0001t0049 a0001c0001t0050 a0001c0003t0014 |
4 | HG01167.hp1 HG01169.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 337 | chr16 | 4689245 | ||||||
| chr16:4689377 | C | G | 1 | a0001c0001t0010 | 4 | HG00738.hp2 HG02602.hp2 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*469C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 469 | chr16 | 4689377 | ||||||
| chr16:4689467 | C | T | 5 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 others(2): Show |
17 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*559C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 559 | chr16 | 4689467 | ||||||
| chr16:4689513 | T | C | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(30): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 605 | chr16 | 4689513 | ||||||
| chr16:4689516 | C | A | 2 | a0001c0001t0015 a0001c0001t0021 |
2 | HG02622.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*608C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 608 | chr16 | 4689516 | ||||||
| chr16:4689518 | C | G | 1 | a0001c0001t0048 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 610 | chr16 | 4689518 | ||||||
| chr16:4689638 | C | T | 1 | a0001c0001t0047 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*730C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 730 | chr16 | 4689638 | ||||||
| chr16:4689674 | A | G | 1 | a0001c0001t0030 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 766 | chr16 | 4689674 | ||||||
| chr16:4689767 | CT | C | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*874delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 874 | INFO_REALIGN_3_PRIME | chr16 | 4689767 | |||||
| chr16:4689767 | CTT | C | 4 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(1): Show |
9 | HG00323.hp2 HG01257.hp1 HG01975.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*873_*874delTT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 873 | INFO_REALIGN_3_PRIME | chr16 | 4689767 | |||||
| chr16:4689784 | A | T | 1 | a0001c0001t0046 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*876A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 876 | chr16 | 4689784 | ||||||
| chr16:4689806 | C | T | 1 | a0001c0003t0014 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*898C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 898 | chr16 | 4689806 | ||||||
| chr16:4689822 | G | A | 6 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0033 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*914G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 914 | chr16 | 4689822 | ||||||
| chr16:4689851 | C | T | 4 | a0001c0001t0007 a0001c0001t0045 a0001c0004t0029 others(1): Show |
11 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 943 | chr16 | 4689851 | ||||||
| chr16:4690054 | G | A | 1 | a0001c0001t0013 | 2 | HG00423.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1146 | chr16 | 4690054 | ||||||
| chr16:4690060 | G | A | 1 | a0001c0003t0014 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1152 | chr16 | 4690060 | ||||||
| chr16:4690096 | G | A | 2 | a0001c0001t0021 a0001c0003t0014 |
3 | HG01167.hp1 HG01169.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1188G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1188 | chr16 | 4690096 | ||||||
| chr16:4690163 | T | G | 1 | a0001c0001t0038 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1255T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1255 | chr16 | 4690163 | ||||||
| chr16:4690164 | C | T | 1 | a0001c0001t0038 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1256C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1256 | chr16 | 4690164 | ||||||
| chr16:4690170 | C | T | 1 | a0001c0001t0044 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1262 | chr16 | 4690170 | ||||||
| chr16:4690207 | T | G | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(25): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1299 | chr16 | 4690207 | ||||||
| chr16:4690285 | C | G | 1 | a0001c0001t0009 | 7 | NA18960.hp1 NA18961.hp1 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1377C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1377 | chr16 | 4690285 | ||||||
| chr16:4690307 | G | A | 1 | a0001c0003t0014 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1399G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1399 | chr16 | 4690307 | ||||||
| chr16:4690440 | G | C | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(28): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1532G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1532 | chr16 | 4690440 | ||||||
| chr16:4690443 | C | T | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(26): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1535 | chr16 | 4690443 | ||||||
| chr16:4690449 | C | T | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1541C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1541 | chr16 | 4690449 | ||||||
| chr16:4690455 | G | A | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1547 | chr16 | 4690455 | ||||||
| chr16:4690476 | T | C | 35 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(32): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1568T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1568 | chr16 | 4690476 | ||||||
| chr16:4690523 | C | T | 1 | a0001c0001t0036 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1615C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1615 | chr16 | 4690523 | ||||||
| chr16:4690540 | G | A | 1 | a0001c0001t0033 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1632 | chr16 | 4690540 | ||||||
| chr16:4690601 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1693T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1693 | chr16 | 4690601 | ||||||
| chr16:4690621 | C | G | 1 | a0001c0001t0035 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1713C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1713 | chr16 | 4690621 | ||||||
| chr16:4690640 | G | A | 1 | a0001c0001t0043 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1732G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1732 | chr16 | 4690640 | ||||||
| chr16:4690699 | G | A | 1 | a0001c0001t0041 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1791 | chr16 | 4690699 | ||||||
| chr16:4690771 | C | A | 1 | a0001c0001t0023 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1863C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1863 | chr16 | 4690771 | ||||||
| chr16:4690837 | T | G | 1 | a0001c0001t0035 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1929 | chr16 | 4690837 | ||||||
| chr16:4690863 | C | T | 1 | a0001c0001t0024 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 1955 | chr16 | 4690863 | ||||||
| chr16:4690913 | G | C | 1 | a0001c0001t0026 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 17/17 | 2005 | chr16 | 4690913 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4625104 | G | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+56G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625104 | |||||||
| chr16:4625115 | G | T | 250 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(247): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.88+67G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625115 | |||||||
| chr16:4625191 | A | G | 231 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(228): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.88+143A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625191 | |||||||
| chr16:4625202 | C | T | 1 | a0001c0001t0009g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.88+154C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625202 | |||||||
| chr16:4625212 | G | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+164G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625212 | |||||||
| chr16:4625241 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.88+193G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625241 | |||||||
| chr16:4625279 | T | C | 230 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(227): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.88+231T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625279 | |||||||
| chr16:4625291 | C | T | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+243C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625291 | |||||||
| chr16:4625295 | G | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+247G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625295 | |||||||
| chr16:4625328 | G | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+280G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625328 | |||||||
| chr16:4625371 | G | T | 1 | a0001c0001t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88+323G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625371 | |||||||
| chr16:4625410 | C | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG00408.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.88+362C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625410 | |||||||
| chr16:4625413 | A | G | 37 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+365A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625413 | |||||||
| chr16:4625565 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+517G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625565 | |||||||
| chr16:4625622 | C | T | 1 | a0001c0001t0045g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88+574C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625622 | |||||||
| chr16:4625713 | G | A | 7 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0019g0006 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+665G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625713 | |||||||
| chr16:4625721 | C | G | 251 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(248): Show |
251 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.88+673C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625721 | |||||||
| chr16:4625835 | T | C | 296 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.88+787T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625835 | |||||||
| chr16:4625875 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.88+827T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625875 | |||||||
| chr16:4625938 | C | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+890C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625938 | |||||||
| chr16:4625958 | C | T | 296 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(293): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.88+910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4625958 | |||||||
| chr16:4626008 | G | C | 1 | a0001c0001t0030g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.88+960G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626008 | |||||||
| chr16:4626233 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+1185A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626233 | |||||||
| chr16:4626292 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.88+1244A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626292 | |||||||
| chr16:4626421 | C | T | 331 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(328): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.88+1373C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626421 | |||||||
| chr16:4626458 | C | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+1410C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626458 | |||||||
| chr16:4626488 | C | T | 58 | a0001c0001t0001g0272 a0001c0001t0001g0286 a0001c0001t0001g0289 others(55): Show |
58 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.88+1440C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626488 | |||||||
| chr16:4626495 | A | G | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+1447A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626495 | |||||||
| chr16:4626525 | G | A | 23 | a0001c0001t0003g0088 a0001c0001t0003g0097 a0001c0001t0003g0098 others(20): Show |
23 | HG01175.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.88+1477G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626525 | |||||||
| chr16:4626548 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.88+1500C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626548 | |||||||
| chr16:4626555 | A | T | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+1507A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626555 | |||||||
| chr16:4626593 | C | T | 1 | a0001c0001t0002g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88+1545C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626593 | |||||||
| chr16:4626594 | A | G | 299 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(296): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.88+1546A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626594 | |||||||
| chr16:4626613 | G | T | 37 | a0001c0001t0001g0103 a0001c0001t0003g0047 a0001c0001t0003g0048 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+1565G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626613 | |||||||
| chr16:4626633 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.88+1585A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626633 | |||||||
| chr16:4626659 | G | A | 229 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(226): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.88+1611G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626659 | |||||||
| chr16:4626719 | A | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0005g0036 others(10): Show |
13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1671A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626719 | |||||||
| chr16:4626729 | C | G | 229 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(226): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.88+1681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626729 | |||||||
| chr16:4626734 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0016g0012 a0001c0001t0018g0014 |
3 | HG02723.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88+1686C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626734 | |||||||
| chr16:4626793 | A | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0005g0036 others(10): Show |
13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1745A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626793 | |||||||
| chr16:4626851 | C | A | 69 | a0001c0001t0001g0103 a0001c0001t0003g0010 a0001c0001t0003g0013 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.88+1803C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626851 | |||||||
| chr16:4626868 | G | C | 14 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0005g0036 others(11): Show |
14 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+1820G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626868 | |||||||
| chr16:4626903 | C | G | 312 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(309): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.88+1855C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626903 | |||||||
| chr16:4626971 | G | A | 66 | a0001c0001t0001g0103 a0001c0001t0003g0010 a0001c0001t0003g0013 others(63): Show |
66 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+1923G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4626971 | |||||||
| chr16:4627039 | C | T | 15 | a0001c0001t0003g0088 a0001c0001t0003g0097 a0001c0001t0003g0098 others(12): Show |
15 | HG01175.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+1991C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627039 | |||||||
| chr16:4627050 | C | T | 10 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(7): Show |
10 | HG00673.hp2 HG02074.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+2002C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627050 | |||||||
| chr16:4627080 | G | T | 2 | a0001c0001t0007g0101 a0001c0001t0008g0100 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.88+2032G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627080 | |||||||
| chr16:4627189 | C | T | 227 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(224): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.88+2141C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627189 | |||||||
| chr16:4627401 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.88+2353A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627401 | |||||||
| chr16:4627417 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+2369T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627417 | |||||||
| chr16:4627433 | G | A | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+2385G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627433 | |||||||
| chr16:4627496 | G | C | 237 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(234): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.88+2448G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627496 | |||||||
| chr16:4627510 | A | G | 4 | a0001c0001t0003g0074 a0001c0001t0004g0018 a0001c0001t0019g0006 others(1): Show |
4 | HG02809.hp1 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+2462A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627510 | |||||||
| chr16:4627514 | G | A | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+2466G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627514 | |||||||
| chr16:4627525 | C | T | 6 | a0001c0001t0001g0251 a0001c0001t0001g0270 a0001c0001t0002g0253 others(3): Show |
6 | HG00673.hp1 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+2477C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627525 | |||||||
| chr16:4627530 | A | G | 1 | a0001c0001t0041g0322 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.88+2482A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627530 | |||||||
| chr16:4627539 | TCACTTTG others(592): Show |
T | 1 | a0001c0001t0005g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.88+2506_88+3104del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4627539 | ||||||
| chr16:4627548 | G | A | 2 | a0001c0001t0002g0321 a0001c0001t0002g0326 |
2 | HG00639.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.88+2500G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627548 | |||||||
| chr16:4627558 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.88+2510C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627558 | |||||||
| chr16:4627583 | G | C | 7 | a0001c0001t0003g0010 a0001c0001t0007g0333 a0001c0001t0017g0042 others(4): Show |
7 | HG02572.hp2 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+2535G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627583 | |||||||
| chr16:4627583 | G | T | 40 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0179 others(37): Show |
40 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.88+2535G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627583 | |||||||
| chr16:4627591 | T | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0028g0043 |
3 | HG02486.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.88+2543T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627591 | |||||||
| chr16:4627598 | T | C | 72 | a0001c0001t0001g0112 a0001c0001t0001g0143 a0001c0001t0001g0153 others(69): Show |
72 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+2550T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627598 | |||||||
| chr16:4627603 | C | A | 61 | a0001c0001t0001g0143 a0001c0001t0001g0153 a0001c0001t0001g0166 others(58): Show |
61 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.88+2555C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627603 | |||||||
| chr16:4627603 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.88+2555C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627603 | |||||||
| chr16:4627606 | G | T | 82 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0001g0143 others(79): Show |
82 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.88+2558G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627606 | |||||||
| chr16:4627624 | A | G | 1 | a0001c0001t0008g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.88+2576A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627624 | |||||||
| chr16:4627658 | A | G | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+2610A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627658 | |||||||
| chr16:4627660 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88+2612G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627660 | |||||||
| chr16:4627679 | C | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+2631C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627679 | |||||||
| chr16:4627744 | T | G | 20 | a0001c0001t0002g0105 a0001c0001t0003g0007 a0001c0001t0003g0008 others(17): Show |
20 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+2696T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627744 | |||||||
| chr16:4627749 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.88+2701C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627749 | |||||||
| chr16:4627975 | G | C | 1 | a0001c0001t0002g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.88+2927G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4627975 | |||||||
| chr16:4628077 | C | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88+3029C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628077 | |||||||
| chr16:4628079 | C | CA | 11 | a0001c0001t0001g0176 a0001c0001t0001g0213 a0001c0001t0001g0217 others(8): Show |
11 | HG00280.hp2 HG01192.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+3049dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628079 | ||||||
| chr16:4628079 | CA | C | 9 | a0001c0001t0001g0207 a0001c0001t0002g0247 a0001c0001t0002g0250 others(6): Show |
9 | HG01167.hp2 HG02273.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+3049delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628079 | ||||||
| chr16:4628114 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0201 a0001c0001t0002g0113 others(4): Show |
7 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+3066C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628114 | |||||||
| chr16:4628116 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+3068G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628116 | |||||||
| chr16:4628255 | A | T | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+3207A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628255 | |||||||
| chr16:4628385 | C | CA | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+3355dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628385 | ||||||
| chr16:4628385 | CA | C | 276 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0115 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.88+3355delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4628385 | ||||||
| chr16:4628410 | G | T | 2 | a0001c0001t0004g0009 a0001c0001t0015g0011 |
2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.88+3362G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628410 | |||||||
| chr16:4628432 | A | C | 4 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0028g0043 others(1): Show |
4 | HG01167.hp2 NA18940.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+3384A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628432 | |||||||
| chr16:4628463 | G | T | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.88+3415G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628463 | |||||||
| chr16:4628475 | C | G | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+3427C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628475 | |||||||
| chr16:4628496 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.88+3448C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628496 | |||||||
| chr16:4628546 | T | G | 6 | a0001c0001t0001g0115 a0001c0001t0002g0113 a0001c0001t0002g0117 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3498T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628546 | |||||||
| chr16:4628692 | G | A | 1 | a0001c0001t0035g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.88+3644G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628692 | |||||||
| chr16:4628770 | C | G | 1 | a0001c0001t0002g0247 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.88+3722C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4628770 | |||||||
| chr16:4629029 | G | T | 1 | a0001c0002t0003g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88+3981G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629029 | |||||||
| chr16:4629147 | C | CGTGTGT | 3 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0023g0073 |
3 | HG02055.hp2 HG02258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.88+4101_88+4102ins others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629147 | ||||||
| chr16:4629148 | G | GTA | 6 | a0001c0001t0002g0105 a0001c0001t0004g0009 a0001c0001t0005g0044 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4102_88+4103dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629148 | ||||||
| chr16:4629150 | A | ATATT | 9 | a0001c0001t0003g0010 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+4103_88+4104ins others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATATTGTG others(6): Show |
1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.88+4103_88+4104ins others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATATTTGT others(3): Show |
3 | a0001c0002t0003g0003 a0001c0002t0004g0004 a0001c0002t0005g0001 |
3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+4103_88+4104ins others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATATTTGT others(5): Show |
1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+4103_88+4104ins others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATG | 58 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0145 others(55): Show |
58 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.88+4143_88+4144dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATGTG | 65 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0115 others(62): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+4141_88+4144dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATGTGTG | 48 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0201 others(45): Show |
48 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+4139_88+4144dup others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATGTGTGT others(1): Show |
16 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(13): Show |
16 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+4137_88+4144dup others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0002g0102 others(2): Show |
5 | HG02300.hp2 HG02976.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+4135_88+4144dup others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.88+4133_88+4144dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | A | G | 8 | a0001c0001t0001g0112 a0001c0001t0002g0245 a0001c0001t0002g0246 others(5): Show |
8 | HG00639.hp2 HG01167.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4102A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629150 | |||||||
| chr16:4629150 | ATG | A | 9 | a0001c0001t0001g0130 a0001c0001t0002g0131 a0001c0001t0006g0277 others(6): Show |
9 | HG00597.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+4143_88+4144del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | ATGTG | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0273 others(7): Show |
10 | HG00738.hp1 HG01081.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+4141_88+4144del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | ATGTGTG | A | 4 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0003g0078 others(1): Show |
4 | NA18975.hp1 NA18977.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+4139_88+4144del others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | ATGTGTGT others(1): Show |
A | 35 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(32): Show |
35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4137_88+4144del others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0003g0074 a0001c0001t0006g0127 a0002c0007t0001g0126 |
3 | HG02109.hp1 HG02809.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.88+4135_88+4144del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629150 | ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0002g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+4133_88+4144del others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629150 | ||||||
| chr16:4629152 | G | A | 8 | a0001c0001t0003g0013 a0001c0001t0003g0019 a0001c0001t0003g0020 others(5): Show |
8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4104G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629152 | |||||||
| chr16:4629152 | G | T | 6 | a0001c0001t0002g0105 a0001c0001t0004g0009 a0001c0001t0005g0044 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4104G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629152 | |||||||
| chr16:4629154 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4106G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629154 | |||||||
| chr16:4629154 | G | T | 8 | a0001c0001t0003g0013 a0001c0001t0003g0019 a0001c0001t0003g0020 others(5): Show |
8 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+4106G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629154 | |||||||
| chr16:4629156 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0019g0006 a0001c0001t0022g0045 others(1): Show |
4 | HG02922.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629156 | |||||||
| chr16:4629156 | G | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4108G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629156 | |||||||
| chr16:4629158 | G | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+4110G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629158 | |||||||
| chr16:4629158 | G | T | 4 | a0001c0001t0004g0018 a0001c0001t0019g0006 a0001c0001t0022g0045 others(1): Show |
4 | HG02922.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4110G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629158 | |||||||
| chr16:4629160 | G | A | 35 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(32): Show |
35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4112G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629160 | |||||||
| chr16:4629160 | G | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.88+4112G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629160 | |||||||
| chr16:4629162 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+4114G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629162 | |||||||
| chr16:4629162 | G | T | 35 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(32): Show |
35 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+4114G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629162 | |||||||
| chr16:4629164 | G | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+4116G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629164 | |||||||
| chr16:4629191 | T | A | 1 | a0001c0001t0003g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.88+4143T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629191 | |||||||
| chr16:4629236 | ATTGT | A | 7 | a0001c0001t0003g0098 a0001c0001t0008g0022 a0001c0001t0008g0023 others(4): Show |
7 | HG02559.hp2 HG02896.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+4191_88+4194del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629236 | ||||||
| chr16:4629273 | A | C | 3 | a0001c0001t0002g0105 a0001c0001t0004g0009 a0001c0001t0015g0011 |
3 | HG01243.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.88+4225A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629273 | |||||||
| chr16:4629467 | A | G | 66 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(63): Show |
66 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+4419A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629467 | |||||||
| chr16:4629511 | T | C | 12 | a0001c0001t0003g0013 a0001c0001t0004g0018 a0001c0001t0005g0044 others(9): Show |
12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+4463T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629511 | |||||||
| chr16:4629600 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+4552G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629600 | |||||||
| chr16:4629610 | A | G | 15 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+4562A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629610 | |||||||
| chr16:4629627 | T | A | 37 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(34): Show |
37 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+4579T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629627 | |||||||
| chr16:4629628 | G | A | 72 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(69): Show |
72 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.88+4580G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629628 | |||||||
| chr16:4629661 | C | A | 1 | a0001c0001t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88+4613C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629661 | |||||||
| chr16:4629693 | C | T | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+4645C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629693 | |||||||
| chr16:4629737 | C | CA | 17 | a0001c0001t0001g0108 a0001c0001t0001g0154 a0001c0001t0001g0201 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+4705dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629737 | ||||||
| chr16:4629737 | CA | C | 19 | a0001c0001t0001g0199 a0001c0001t0001g0265 a0001c0001t0002g0105 others(16): Show |
19 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+4705delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4629737 | ||||||
| chr16:4629853 | C | G | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+4805C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629853 | |||||||
| chr16:4629875 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0019g0006 a0001c0003t0031g0017 |
3 | HG02922.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+4827G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629875 | |||||||
| chr16:4629913 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88+4865G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629913 | |||||||
| chr16:4629950 | T | G | 59 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(56): Show |
59 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+4902T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4629950 | |||||||
| chr16:4630048 | C | CA | 55 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(52): Show |
55 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+5021dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | ||||||
| chr16:4630048 | C | CAA | 7 | a0001c0001t0002g0255 a0001c0001t0003g0035 a0001c0001t0004g0018 others(4): Show |
7 | HG00099.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+5020_88+5021dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | ||||||
| chr16:4630048 | CA | C | 13 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0225 others(10): Show |
13 | HG02015.hp2 HG02080.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.88+5021delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | ||||||
| chr16:4630048 | CAAA | C | 14 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(11): Show |
14 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+5019_88+5021del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630048 | ||||||
| chr16:4630072 | G | C | 65 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(62): Show |
65 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+5024G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630072 | |||||||
| chr16:4630077 | T | A | 1 | a0001c0001t0002g0309 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.88+5029T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630077 | |||||||
| chr16:4630087 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+5039C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630087 | |||||||
| chr16:4630088 | G | A | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.88+5040G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630088 | |||||||
| chr16:4630128 | G | C | 38 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(35): Show |
38 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.88+5080G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630128 | |||||||
| chr16:4630198 | A | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+5150A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630198 | |||||||
| chr16:4630252 | C | T | 9 | a0001c0001t0003g0013 a0001c0001t0005g0044 a0001c0001t0005g0084 others(6): Show |
9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+5204C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630252 | |||||||
| chr16:4630283 | C | G | 67 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(64): Show |
67 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.88+5235C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630283 | |||||||
| chr16:4630354 | C | CA | 59 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0119 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+5319dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630354 | ||||||
| chr16:4630354 | C | CAA | 10 | a0001c0001t0003g0013 a0001c0001t0003g0055 a0001c0001t0005g0044 others(7): Show |
10 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+5318_88+5319dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630354 | ||||||
| chr16:4630438 | TTTGTTG | T | 28 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0013 others(25): Show |
28 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+5406_88+5411del others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630438 | ||||||
| chr16:4630448 | T | C | 2 | a0001c0001t0002g0284 a0001c0001t0006g0285 |
2 | HG00408.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.88+5400T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630448 | |||||||
| chr16:4630493 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+5445C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630493 | |||||||
| chr16:4630531 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+5483G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630531 | |||||||
| chr16:4630570 | A | G | 5 | a0001c0001t0005g0044 a0001c0001t0005g0084 a0001c0001t0005g0085 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+5522A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630570 | |||||||
| chr16:4630604 | C | T | 5 | a0001c0001t0005g0044 a0001c0001t0005g0084 a0001c0001t0005g0085 others(2): Show |
5 | HG02280.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+5556C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630604 | |||||||
| chr16:4630638 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0233 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.88+5590G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630638 | |||||||
| chr16:4630673 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+5625C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630673 | |||||||
| chr16:4630678 | C | G | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+5630C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630678 | |||||||
| chr16:4630731 | C | T | 94 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0293 others(91): Show |
94 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.88+5683C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630731 | |||||||
| chr16:4630760 | A | G | 37 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(34): Show |
37 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.88+5712A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630760 | |||||||
| chr16:4630808 | C | CT | 10 | a0001c0001t0001g0108 a0001c0001t0001g0193 a0001c0001t0001g0203 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+5780dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | ||||||
| chr16:4630808 | CT | C | 28 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0153 others(25): Show |
28 | HG01167.hp2 HG01975.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.88+5780delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | ||||||
| chr16:4630808 | CTT | C | 10 | a0001c0001t0003g0013 a0001c0001t0005g0044 a0001c0001t0005g0084 others(7): Show |
10 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+5779_88+5780del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4630808 | ||||||
| chr16:4630875 | G | A | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+5827G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4630875 | |||||||
| chr16:4631108 | C | T | 2 | a0001c0001t0004g0018 a0001c0003t0031g0017 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+6060C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631108 | |||||||
| chr16:4631183 | G | A | 2 | a0001c0001t0004g0051 a0001c0001t0004g0052 |
2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.88+6135G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631183 | |||||||
| chr16:4631308 | A | G | 12 | a0001c0001t0003g0013 a0001c0001t0004g0018 a0001c0001t0005g0044 others(9): Show |
12 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+6260A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631308 | |||||||
| chr16:4631507 | G | A | 67 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(64): Show |
67 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.88+6459G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631507 | |||||||
| chr16:4631588 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.88+6540C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631588 | |||||||
| chr16:4631629 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0018g0014 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88+6581A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631629 | |||||||
| chr16:4631709 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.88+6661T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631709 | |||||||
| chr16:4631746 | C | G | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+6698C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631746 | |||||||
| chr16:4631796 | T | C | 1 | a0001c0001t0003g0088 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.88+6748T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631796 | |||||||
| chr16:4631845 | C | G | 11 | a0001c0001t0002g0105 a0001c0001t0004g0018 a0001c0001t0005g0036 others(8): Show |
11 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+6797C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631845 | |||||||
| chr16:4631902 | A | AGTT | 240 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(237): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.88+6858_88+6860dup others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631902 | ||||||
| chr16:4631906 | G | GTTGT | 6 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0199 others(3): Show |
6 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631906 | ||||||
| chr16:4631907 | T | TTG | 63 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(60): Show |
63 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4631907 | ||||||
| chr16:4631908 | T | TG | 9 | a0001c0001t0003g0013 a0001c0001t0005g0044 a0001c0001t0005g0084 others(6): Show |
9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6860_88+6861ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631908 | |||||||
| chr16:4631961 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+6913A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4631961 | |||||||
| chr16:4632007 | C | CT | 42 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0112 others(39): Show |
42 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+6983dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | ||||||
| chr16:4632007 | C | CTTTT | 13 | a0001c0001t0001g0221 a0001c0001t0002g0105 a0001c0001t0002g0121 others(10): Show |
13 | HG01243.hp1 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+6980_88+6983dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | ||||||
| chr16:4632007 | C | CTTTTT | 21 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0002g0157 others(18): Show |
21 | HG00544.hp1 HG00673.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.88+6979_88+6983dup others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | ||||||
| chr16:4632007 | CT | C | 36 | a0001c0001t0001g0103 a0001c0001t0001g0115 a0001c0001t0001g0119 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.88+6983delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | ||||||
| chr16:4632007 | CTTTT | C | 9 | a0001c0001t0003g0013 a0001c0001t0005g0044 a0001c0001t0005g0084 others(6): Show |
9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+6980_88+6983del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632007 | ||||||
| chr16:4632035 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.88+6987A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632035 | |||||||
| chr16:4632091 | T | G | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+7043T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632091 | |||||||
| chr16:4632106 | G | C | 74 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+7058G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632106 | |||||||
| chr16:4632127 | C | T | 1 | a0001c0001t0023g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88+7079C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632127 | |||||||
| chr16:4632143 | T | A | 73 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(70): Show |
73 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.88+7095T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632143 | |||||||
| chr16:4632205 | T | TG | 331 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(328): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.88+7160dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4632205 | ||||||
| chr16:4632215 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.88+7167C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632215 | |||||||
| chr16:4632254 | C | T | 79 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(76): Show |
79 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.88+7206C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632254 | |||||||
| chr16:4632286 | TTACAGGC | T | 36 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(33): Show |
36 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.88+7239_88+7245del others(7): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632286 | |||||||
| chr16:4632310 | G | A | 3 | a0001c0001t0003g0010 a0001c0001t0007g0333 a0001c0001t0026g0334 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+7262G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632310 | |||||||
| chr16:4632416 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.88+7368C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632416 | |||||||
| chr16:4632444 | A | T | 1 | a0001c0001t0016g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.88+7396A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632444 | |||||||
| chr16:4632455 | G | A | 2 | a0001c0002t0003g0005 a0001c0002t0004g0004 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.88+7407G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632455 | |||||||
| chr16:4632465 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.88+7417C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632465 | |||||||
| chr16:4632486 | C | T | 43 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(40): Show |
43 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.88+7438C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632486 | |||||||
| chr16:4632542 | C | T | 13 | a0001c0001t0002g0105 a0001c0001t0004g0018 a0001c0001t0005g0036 others(10): Show |
13 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+7494C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632542 | |||||||
| chr16:4632630 | T | G | 74 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+7582T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632630 | |||||||
| chr16:4632661 | G | A | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+7613G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632661 | |||||||
| chr16:4632696 | G | T | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+7648G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632696 | |||||||
| chr16:4632740 | A | C | 1 | a0001c0001t0002g0250 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.88+7692A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632740 | |||||||
| chr16:4632800 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+7752C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632800 | |||||||
| chr16:4632802 | G | A | 1 | a0001c0006t0007g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.88+7754G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4632802 | |||||||
| chr16:4633106 | G | T | 1 | a0001c0001t0002g0258 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+8058G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633106 | |||||||
| chr16:4633125 | C | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.88+8077C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633125 | |||||||
| chr16:4633126 | A | G | 74 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.88+8078A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633126 | |||||||
| chr16:4633225 | T | TA | 11 | a0001c0001t0004g0018 a0001c0001t0005g0036 a0001c0001t0005g0037 others(8): Show |
11 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+8182dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4633225 | ||||||
| chr16:4633250 | G | A | 1 | a0001c0001t0006g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.88+8202G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633250 | |||||||
| chr16:4633336 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88+8288C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633336 | |||||||
| chr16:4633463 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.88+8415G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633463 | |||||||
| chr16:4633548 | G | A | 1 | a0001c0001t0046g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.88+8500G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633548 | |||||||
| chr16:4633718 | AT | A | 13 | a0001c0001t0001g0272 a0001c0001t0002g0105 a0001c0001t0004g0018 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+8672delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4633718 | ||||||
| chr16:4633719 | T | A | 41 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(38): Show |
41 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+8671T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633719 | |||||||
| chr16:4633720 | T | A | 54 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(51): Show |
54 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.88+8672T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633720 | |||||||
| chr16:4633773 | A | C | 6 | a0001c0001t0003g0098 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+8725A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633773 | |||||||
| chr16:4633781 | T | G | 1 | a0001c0001t0049g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+8733T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633781 | |||||||
| chr16:4633784 | C | A | 1 | a0001c0001t0049g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+8736C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633784 | |||||||
| chr16:4633810 | C | T | 2 | a0001c0001t0002g0302 a0001c0001t0048g0315 |
2 | HG02735.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.88+8762C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633810 | |||||||
| chr16:4633871 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.88+8823C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633871 | |||||||
| chr16:4633879 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.88+8831G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633879 | |||||||
| chr16:4633879 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8831G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633879 | |||||||
| chr16:4633881 | C | G | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8833C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633881 | |||||||
| chr16:4633883 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+8835A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4633883 | |||||||
| chr16:4634041 | A | C | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+8993A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634041 | |||||||
| chr16:4634131 | G | A | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+9083G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634131 | |||||||
| chr16:4634247 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.88+9199A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634247 | |||||||
| chr16:4634268 | C | G | 42 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(39): Show |
42 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.88+9220C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634268 | |||||||
| chr16:4634293 | G | A | 3 | a0001c0001t0002g0279 a0001c0001t0002g0303 a0001c0001t0009g0324 |
3 | HG02027.hp1 NA19080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.88+9245G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634293 | |||||||
| chr16:4634384 | G | T | 4 | a0001c0001t0002g0105 a0001c0001t0004g0018 a0001c0001t0015g0011 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9336G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634384 | |||||||
| chr16:4634399 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+9351C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634399 | |||||||
| chr16:4634410 | T | A | 2 | a0001c0001t0002g0132 a0001c0001t0009g0141 |
2 | NA18975.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.88+9362T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634410 | |||||||
| chr16:4634447 | G | A | 70 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(67): Show |
70 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+9399G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634447 | |||||||
| chr16:4634504 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.88+9456G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634504 | |||||||
| chr16:4634575 | C | T | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+9527C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634575 | |||||||
| chr16:4634584 | GC | G | 9 | a0001c0001t0003g0013 a0001c0001t0005g0044 a0001c0001t0005g0084 others(6): Show |
9 | HG02280.hp1 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+9539delC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4634584 | ||||||
| chr16:4634596 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.88+9548G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634596 | |||||||
| chr16:4634777 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+9729C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634777 | |||||||
| chr16:4634830 | G | A | 1 | a0004c0005t0001g0144 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.88+9782G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634830 | |||||||
| chr16:4634928 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+9880C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634928 | |||||||
| chr16:4634971 | C | A | 2 | a0001c0001t0002g0302 a0001c0001t0048g0315 |
2 | HG02735.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.88+9923C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4634971 | |||||||
| chr16:4635042 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.88+9994G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635042 | |||||||
| chr16:4635110 | A | G | 4 | a0001c0001t0004g0018 a0001c0001t0008g0026 a0001c0001t0019g0006 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10062A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635110 | |||||||
| chr16:4635325 | G | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10277G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635325 | |||||||
| chr16:4635482 | T | G | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.88+10434T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635482 | |||||||
| chr16:4635488 | G | A | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+10440G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635488 | |||||||
| chr16:4635569 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.88+10521G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635569 | |||||||
| chr16:4635617 | C | T | 63 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.88+10569C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635617 | |||||||
| chr16:4635714 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.88+10666A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635714 | |||||||
| chr16:4635746 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10698C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635746 | |||||||
| chr16:4635791 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+10743C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635791 | |||||||
| chr16:4635801 | A | AT | 69 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.88+10772dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635801 | ||||||
| chr16:4635801 | A | ATT | 24 | a0001c0001t0002g0105 a0001c0001t0002g0120 a0001c0001t0003g0019 others(21): Show |
24 | HG00544.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.88+10771_88+10772d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635801 | ||||||
| chr16:4635877 | G | C | 1 | a0001c0001t0024g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.88+10829G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635877 | |||||||
| chr16:4635937 | T | C | 7 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+10889T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4635937 | |||||||
| chr16:4635968 | G | GT | 71 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.88+10932dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635968 | ||||||
| chr16:4635968 | G | GTT | 13 | a0001c0001t0002g0105 a0001c0001t0002g0246 a0001c0001t0004g0018 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+10931_88+10932d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4635968 | ||||||
| chr16:4636084 | G | T | 7 | a0001c0001t0001g0143 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+11036G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636084 | |||||||
| chr16:4636192 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.88+11144G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636192 | |||||||
| chr16:4636215 | A | G | 14 | a0001c0001t0002g0105 a0001c0001t0004g0018 a0001c0001t0005g0036 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+11167A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636215 | |||||||
| chr16:4636267 | C | G | 1 | a0001c0001t0009g0324 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.88+11219C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636267 | |||||||
| chr16:4636275 | C | T | 6 | a0001c0001t0003g0098 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+11227C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636275 | |||||||
| chr16:4636359 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.88+11311G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636359 | |||||||
| chr16:4636410 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.88+11362G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636410 | |||||||
| chr16:4636439 | C | T | 1 | a0001c0001t0011g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88+11391C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636439 | |||||||
| chr16:4636468 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0204 |
2 | NA18967.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.88+11420A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636468 | |||||||
| chr16:4636567 | C | T | 3 | a0001c0001t0002g0161 a0001c0001t0033g0184 a0001c0001t0034g0185 |
3 | HG02630.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.88+11519C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636567 | |||||||
| chr16:4636688 | T | G | 1 | a0001c0002t0003g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.88+11640T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636688 | |||||||
| chr16:4636740 | T | C | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+11692T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636740 | |||||||
| chr16:4636806 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0233 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.88+11758G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636806 | |||||||
| chr16:4636843 | G | T | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+11795G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636843 | |||||||
| chr16:4636987 | C | T | 1 | a0001c0001t0006g0277 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.88+11939C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4636987 | |||||||
| chr16:4637049 | G | C | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+12001G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637049 | |||||||
| chr16:4637118 | C | CA | 26 | a0001c0001t0001g0108 a0001c0001t0001g0145 a0001c0001t0001g0154 others(23): Show |
26 | HG01123.hp2 HG01258.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+12093dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4637118 | ||||||
| chr16:4637118 | CA | C | 16 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0138 others(13): Show |
16 | HG00323.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+12093delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4637118 | ||||||
| chr16:4637238 | C | T | 7 | a0001c0001t0001g0183 a0001c0001t0001g0203 a0001c0001t0001g0215 others(4): Show |
7 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+12190C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637238 | |||||||
| chr16:4637306 | T | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.88+12258T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637306 | |||||||
| chr16:4637386 | C | T | 2 | a0001c0001t0007g0075 a0001c0001t0007g0076 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+12338C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637386 | |||||||
| chr16:4637485 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.88+12437C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637485 | |||||||
| chr16:4637598 | G | T | 1 | a0001c0001t0030g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.88+12550G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637598 | |||||||
| chr16:4637694 | C | T | 57 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(54): Show |
57 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.88+12646C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637694 | |||||||
| chr16:4637770 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.89-12595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637770 | |||||||
| chr16:4637956 | C | G | 6 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0002g0120 others(3): Show |
6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-12409C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4637956 | |||||||
| chr16:4638016 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0224 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.89-12349C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638016 | |||||||
| chr16:4638057 | C | A | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-12308C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638057 | |||||||
| chr16:4638067 | T | C | 17 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-12298T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638067 | |||||||
| chr16:4638113 | T | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0286 a0001c0001t0002g0200 |
3 | NA18955.hp1 NA19010.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.89-12252T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638113 | |||||||
| chr16:4638138 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-12227C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638138 | |||||||
| chr16:4638238 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0004g0080 |
2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.89-12127G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638238 | |||||||
| chr16:4638257 | G | A | 9 | a0001c0001t0002g0105 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-12108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638257 | |||||||
| chr16:4638277 | C | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0199 others(1): Show |
4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-12088C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638277 | |||||||
| chr16:4638381 | C | T | 7 | a0001c0001t0001g0143 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-11984C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638381 | |||||||
| chr16:4638464 | C | CA | 13 | a0001c0001t0001g0167 a0001c0001t0001g0234 a0001c0001t0002g0105 others(10): Show |
13 | HG00099.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-11890dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4638464 | ||||||
| chr16:4638476 | T | A | 75 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(72): Show |
75 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.89-11889T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638476 | |||||||
| chr16:4638480 | T | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-11885T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638480 | |||||||
| chr16:4638487 | C | A | 2 | a0001c0001t0003g0013 a0001c0001t0018g0014 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-11878C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638487 | |||||||
| chr16:4638491 | G | GC | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11871dupC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4638491 | ||||||
| chr16:4638492 | C | A | 48 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(45): Show |
48 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.89-11873C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638492 | |||||||
| chr16:4638550 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0002g0275 |
2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.89-11815G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638550 | |||||||
| chr16:4638674 | C | A | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11691C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638674 | |||||||
| chr16:4638760 | C | T | 1 | a0001c0001t0016g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.89-11605C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638760 | |||||||
| chr16:4638836 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.89-11529C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638836 | |||||||
| chr16:4638840 | C | T | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0003g0053 |
3 | HG01257.hp2 HG01258.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.89-11525C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638840 | |||||||
| chr16:4638841 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-11524C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638841 | |||||||
| chr16:4638847 | T | A | 1 | a0001c0001t0045g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.89-11518T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638847 | |||||||
| chr16:4638904 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-11461G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638904 | |||||||
| chr16:4638920 | A | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11445A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638920 | |||||||
| chr16:4638920 | A | G | 9 | a0001c0001t0002g0105 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-11445A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638920 | |||||||
| chr16:4638934 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-11431C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638934 | |||||||
| chr16:4638952 | A | T | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11413A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638952 | |||||||
| chr16:4638980 | T | C | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11385T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4638980 | |||||||
| chr16:4639100 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0015g0011 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-11265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639100 | |||||||
| chr16:4639139 | C | T | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11226C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639139 | |||||||
| chr16:4639191 | A | T | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11174A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639191 | |||||||
| chr16:4639317 | G | A | 16 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-11048G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639317 | |||||||
| chr16:4639318 | T | G | 93 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0123 others(90): Show |
93 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.89-11047T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639318 | |||||||
| chr16:4639342 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-11023C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639342 | |||||||
| chr16:4639470 | C | T | 6 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0002g0120 others(3): Show |
6 | HG01070.hp1 HG01123.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-10895C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639470 | |||||||
| chr16:4639568 | A | G | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.89-10797A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639568 | |||||||
| chr16:4639619 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.89-10746G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639619 | |||||||
| chr16:4639685 | C | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0234 |
2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.89-10680C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639685 | |||||||
| chr16:4639696 | T | A | 17 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-10669T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639696 | |||||||
| chr16:4639812 | T | C | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10553T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4639812 | |||||||
| chr16:4640005 | T | C | 1 | a0001c0001t0007g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.89-10360T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640005 | |||||||
| chr16:4640020 | G | A | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10345G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640020 | |||||||
| chr16:4640186 | G | T | 26 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0221 others(23): Show |
26 | HG01070.hp1 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-10179G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640186 | |||||||
| chr16:4640241 | T | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-10124T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640241 | |||||||
| chr16:4640262 | C | T | 1 | a0001c0001t0023g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.89-10103C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640262 | |||||||
| chr16:4640362 | A | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-10003A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640362 | |||||||
| chr16:4640454 | C | A | 9 | a0001c0001t0002g0105 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-9911C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640454 | |||||||
| chr16:4640455 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-9910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640455 | |||||||
| chr16:4640476 | G | C | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-9889G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640476 | |||||||
| chr16:4640599 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.89-9766C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640599 | |||||||
| chr16:4640653 | G | A | 2 | a0001c0002t0003g0005 a0001c0002t0004g0004 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-9712G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640653 | |||||||
| chr16:4640718 | A | G | 1 | a0001c0001t0005g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.89-9647A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640718 | |||||||
| chr16:4640733 | G | GT | 12 | a0001c0001t0002g0105 a0001c0001t0002g0209 a0001c0001t0002g0280 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-9626dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4640733 | ||||||
| chr16:4640764 | C | A | 3 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0034 |
3 | HG02280.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.89-9601C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640764 | |||||||
| chr16:4640766 | G | T | 3 | a0001c0001t0003g0013 a0001c0001t0016g0012 a0001c0001t0018g0014 |
3 | HG02723.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-9599G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640766 | |||||||
| chr16:4640850 | G | A | 6 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-9515G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640850 | |||||||
| chr16:4640991 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0004t0029g0083 |
3 | HG01070.hp1 HG01175.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.89-9374C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4640991 | |||||||
| chr16:4641021 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.89-9344C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641021 | |||||||
| chr16:4641052 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.89-9313A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641052 | |||||||
| chr16:4641116 | G | A | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-9249G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641116 | |||||||
| chr16:4641145 | G | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-9220G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641145 | |||||||
| chr16:4641218 | G | A | 16 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9147G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641218 | |||||||
| chr16:4641224 | G | C | 16 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9141G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641224 | |||||||
| chr16:4641252 | C | T | 9 | a0001c0001t0002g0105 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-9113C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641252 | |||||||
| chr16:4641259 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-9106C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641259 | |||||||
| chr16:4641336 | A | G | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-9029A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641336 | |||||||
| chr16:4641342 | A | AT | 16 | a0001c0001t0001g0203 a0001c0001t0002g0105 a0001c0001t0003g0019 others(13): Show |
16 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-9013dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641342 | ||||||
| chr16:4641353 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.89-9012G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641353 | |||||||
| chr16:4641402 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.89-8963C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641402 | |||||||
| chr16:4641448 | G | A | 19 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0003g0020 others(16): Show |
19 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-8917G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641448 | |||||||
| chr16:4641515 | C | CT | 7 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0002g0109 others(4): Show |
7 | HG00423.hp1 HG01952.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-8831dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | ||||||
| chr16:4641515 | CT | C | 23 | a0001c0001t0001g0156 a0001c0001t0001g0165 a0001c0001t0001g0206 others(20): Show |
23 | HG00323.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-8831delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | ||||||
| chr16:4641515 | CTT | C | 29 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0221 others(26): Show |
29 | HG01070.hp1 HG01099.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.89-8832_89-8831del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4641515 | ||||||
| chr16:4641542 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-8823C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641542 | |||||||
| chr16:4641585 | C | G | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-8780C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641585 | |||||||
| chr16:4641587 | C | T | 17 | a0001c0001t0003g0013 a0001c0001t0004g0009 a0001c0001t0005g0044 others(14): Show |
17 | HG01099.hp1 HG01243.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-8778C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641587 | |||||||
| chr16:4641621 | T | C | 24 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0019 others(21): Show |
24 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-8744T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641621 | |||||||
| chr16:4641706 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.89-8659C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641706 | |||||||
| chr16:4641809 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0199 others(1): Show |
4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8556G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641809 | |||||||
| chr16:4641879 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.89-8486C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641879 | |||||||
| chr16:4641942 | C | A | 16 | a0001c0001t0003g0010 a0001c0001t0003g0098 a0001c0001t0004g0009 others(13): Show |
16 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-8423C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4641942 | |||||||
| chr16:4642022 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89-8343A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642022 | |||||||
| chr16:4642032 | C | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.89-8333C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642032 | |||||||
| chr16:4642033 | C | G | 8 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0002g0244 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-8332C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642033 | |||||||
| chr16:4642033 | C | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-8332C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642033 | |||||||
| chr16:4642060 | G | A | 18 | a0001c0001t0003g0098 a0001c0001t0004g0018 a0001c0001t0005g0036 others(15): Show |
18 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-8305G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642060 | |||||||
| chr16:4642068 | A | G | 1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-8297A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642068 | |||||||
| chr16:4642090 | A | G | 121 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0148 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.89-8275A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642090 | |||||||
| chr16:4642112 | G | A | 43 | a0001c0001t0001g0125 a0001c0001t0001g0235 a0001c0001t0001g0259 others(40): Show |
43 | HG01070.hp1 HG01099.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-8253G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642112 | |||||||
| chr16:4642128 | C | CT | 258 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0110 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.89-8219dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642128 | ||||||
| chr16:4642128 | C | CTT | 30 | a0001c0001t0001g0108 a0001c0001t0001g0221 a0001c0001t0001g0231 others(27): Show |
30 | HG01074.hp2 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-8220_89-8219dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642128 | ||||||
| chr16:4642146 | T | TA | 7 | a0001c0001t0001g0149 a0001c0001t0001g0183 a0001c0001t0001g0215 others(4): Show |
7 | HG00738.hp2 HG01069.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-8213dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642146 | ||||||
| chr16:4642147 | A | T | 1 | a0001c0001t0036g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.89-8218A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642147 | |||||||
| chr16:4642194 | G | A | 24 | a0001c0001t0003g0013 a0001c0001t0003g0019 a0001c0001t0003g0020 others(21): Show |
24 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-8171G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642194 | |||||||
| chr16:4642258 | G | C | 3 | a0001c0001t0002g0105 a0001c0001t0004g0009 a0001c0004t0029g0083 |
3 | HG01243.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-8107G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642258 | |||||||
| chr16:4642267 | A | C | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-8098A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642267 | |||||||
| chr16:4642347 | G | C | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-8018G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642347 | |||||||
| chr16:4642374 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.89-7991G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642374 | |||||||
| chr16:4642456 | G | A | 1 | a0001c0001t0011g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89-7909G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642456 | |||||||
| chr16:4642466 | T | TTG | 30 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(27): Show |
30 | HG00140.hp1 HG00597.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-7865_89-7864dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTG | 5 | a0001c0001t0001g0251 a0001c0001t0002g0131 a0001c0001t0004g0009 others(2): Show |
5 | HG01243.hp1 HG02056.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-7867_89-7864dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTG | 11 | a0001c0001t0001g0169 a0001c0001t0004g0018 a0001c0001t0004g0089 others(8): Show |
11 | HG01891.hp2 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-7869_89-7864dup others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(1): Show |
7 | a0001c0001t0005g0033 a0001c0001t0005g0044 a0001c0001t0007g0093 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7871_89-7864dup others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(7): Show |
10 | HG02015.hp1 HG02083.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-7873_89-7864dup others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(5): Show |
6 | a0001c0001t0005g0085 a0001c0001t0016g0012 a0001c0001t0019g0006 others(3): Show |
6 | HG01099.hp1 HG02922.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7875_89-7864dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-7877_89-7864dup others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0011g0021 a0001c0002t0005g0001 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.89-7879_89-7864dup others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(11): Show |
1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7881_89-7864dup others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-7885_89-7864dup others(22): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | T | TTGTGTGT others(19): Show |
2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-7889_89-7864dup others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | TTG | T | 9 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0200 others(6): Show |
9 | HG01175.hp2 HG01361.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-7865_89-7864del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-7873_89-7864del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642466 | TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-7881_89-7864del others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642466 | ||||||
| chr16:4642526 | C | G | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7839C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642526 | |||||||
| chr16:4642556 | C | T | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7809C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642556 | |||||||
| chr16:4642571 | G | A | 1 | a0001c0001t0046g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-7794G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642571 | |||||||
| chr16:4642614 | G | A | 20 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0004g0018 others(17): Show |
20 | HG01099.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-7751G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642614 | |||||||
| chr16:4642690 | C | G | 1 | a0001c0001t0005g0094 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.89-7675C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642690 | |||||||
| chr16:4642691 | G | T | 6 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(3): Show |
6 | HG01099.hp1 HG01243.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7674G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642691 | |||||||
| chr16:4642744 | G | A | 3 | a0001c0001t0007g0333 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG02896.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-7621G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642744 | |||||||
| chr16:4642788 | A | AT | 7 | a0001c0001t0001g0110 a0001c0001t0001g0179 a0001c0001t0001g0193 others(4): Show |
7 | HG00544.hp2 HG02809.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7561dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | ||||||
| chr16:4642788 | AT | A | 14 | a0001c0001t0001g0265 a0001c0001t0002g0218 a0001c0001t0003g0098 others(11): Show |
14 | HG00673.hp1 HG01099.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-7561delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | ||||||
| chr16:4642788 | ATT | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-7562_89-7561del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642788 | ||||||
| chr16:4642934 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.89-7431G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4642934 | |||||||
| chr16:4642980 | C | CAG | 167 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0148 others(164): Show |
167 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.89-7384_89-7383dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4642980 | ||||||
| chr16:4643023 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG00673.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.89-7342T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643023 | |||||||
| chr16:4643049 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.89-7316A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643049 | |||||||
| chr16:4643168 | C | A | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7197C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643168 | |||||||
| chr16:4643190 | G | T | 27 | a0001c0001t0002g0105 a0001c0001t0003g0010 a0001c0001t0003g0013 others(24): Show |
27 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(24): Show |
intron_variant | MODIFIER | c.89-7175G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643190 | |||||||
| chr16:4643231 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-7134A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643231 | |||||||
| chr16:4643241 | C | T | 6 | a0001c0001t0027g0002 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-7124C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643241 | |||||||
| chr16:4643301 | G | A | 2 | a0001c0001t0002g0200 a0001c0001t0002g0253 |
2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.89-7064G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643301 | |||||||
| chr16:4643344 | C | G | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-7021C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643344 | |||||||
| chr16:4643391 | C | T | 2 | a0001c0001t0004g0018 a0001c0003t0031g0017 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.89-6974C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643391 | |||||||
| chr16:4643403 | A | AT | 34 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0162 others(31): Show |
34 | HG00735.hp2 HG01070.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.89-6941dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | ||||||
| chr16:4643403 | A | ATT | 6 | a0001c0001t0002g0312 a0001c0001t0004g0018 a0001c0002t0003g0003 others(3): Show |
6 | HG01099.hp1 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-6942_89-6941dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | ||||||
| chr16:4643403 | AT | A | 28 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0167 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-6941delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4643403 | ||||||
| chr16:4643456 | G | T | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6909G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643456 | |||||||
| chr16:4643594 | C | A | 310 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(307): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.89-6771C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643594 | |||||||
| chr16:4643594 | C | G | 9 | a0001c0001t0002g0105 a0001c0001t0002g0260 a0001c0001t0003g0010 others(6): Show |
9 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-6771C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643594 | |||||||
| chr16:4643595 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6770A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643595 | |||||||
| chr16:4643647 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6718C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643647 | |||||||
| chr16:4643649 | C | G | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.89-6716C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643649 | |||||||
| chr16:4643657 | T | C | 42 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(39): Show |
42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-6708T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643657 | |||||||
| chr16:4643711 | A | G | 8 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0157 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-6654A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643711 | |||||||
| chr16:4643802 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-6563A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643802 | |||||||
| chr16:4643841 | A | T | 42 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(39): Show |
42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-6524A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643841 | |||||||
| chr16:4643868 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.89-6497T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643868 | |||||||
| chr16:4643973 | TG | T | 41 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(38): Show |
41 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-6391delG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643973 | |||||||
| chr16:4643974 | G | T | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-6391G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643974 | |||||||
| chr16:4643986 | T | G | 7 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(4): Show |
7 | HG00597.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-6379T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4643986 | |||||||
| chr16:4644004 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.89-6361G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644004 | |||||||
| chr16:4644124 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.89-6241T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644124 | |||||||
| chr16:4644154 | G | T | 23 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(20): Show |
23 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-6211G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644154 | |||||||
| chr16:4644227 | A | C | 1 | a0001c0002t0003g0003 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-6138A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644227 | |||||||
| chr16:4644276 | G | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0327 a0001c0001t0002g0195 others(7): Show |
10 | HG00597.hp1 HG02027.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-6089G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644276 | |||||||
| chr16:4644277 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-6088C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644277 | |||||||
| chr16:4644305 | G | GT | 33 | a0001c0001t0001g0133 a0001c0001t0001g0197 a0001c0001t0001g0203 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.89-6039dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4644305 | ||||||
| chr16:4644305 | GT | G | 16 | a0001c0001t0001g0238 a0001c0001t0002g0102 a0001c0001t0002g0309 others(13): Show |
16 | HG01884.hp1 HG02056.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-6039delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4644305 | ||||||
| chr16:4644310 | T | G | 1 | a0001c0001t0010g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.89-6055T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644310 | |||||||
| chr16:4644312 | T | G | 1 | a0001c0001t0047g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.89-6053T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644312 | |||||||
| chr16:4644341 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02723.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.89-6024C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644341 | |||||||
| chr16:4644373 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-5992C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644373 | |||||||
| chr16:4644386 | C | T | 1 | a0001c0001t0006g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.89-5979C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644386 | |||||||
| chr16:4644387 | G | C | 42 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(39): Show |
42 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.89-5978G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644387 | |||||||
| chr16:4644413 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.89-5952C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644413 | |||||||
| chr16:4644508 | C | G | 4 | a0001c0001t0004g0089 a0001c0001t0005g0033 a0001c0001t0005g0091 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-5857C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644508 | |||||||
| chr16:4644611 | C | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-5754C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644611 | |||||||
| chr16:4644703 | C | G | 30 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(27): Show |
30 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-5662C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644703 | |||||||
| chr16:4644827 | A | G | 2 | a0001c0001t0002g0121 a0001c0001t0049g0122 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.89-5538A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644827 | |||||||
| chr16:4644875 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.89-5490T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644875 | |||||||
| chr16:4644915 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-5450C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644915 | |||||||
| chr16:4644932 | A | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.89-5433A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644932 | |||||||
| chr16:4644990 | T | C | 44 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(41): Show |
44 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.89-5375T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4644990 | |||||||
| chr16:4645019 | A | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-5346A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645019 | |||||||
| chr16:4645030 | A | T | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-5335A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645030 | |||||||
| chr16:4645088 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0050g0318 |
2 | HG02056.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.89-5277T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645088 | |||||||
| chr16:4645104 | T | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-5261T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645104 | |||||||
| chr16:4645115 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.89-5250G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645115 | |||||||
| chr16:4645168 | G | T | 1 | a0001c0001t0009g0228 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.89-5197G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645168 | |||||||
| chr16:4645183 | CAG | C | 19 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(16): Show |
19 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-5181_89-5180del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645183 | |||||||
| chr16:4645222 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-5143G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645222 | |||||||
| chr16:4645238 | C | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-5127C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645238 | |||||||
| chr16:4645407 | G | A | 12 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(9): Show |
12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-4958G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645407 | |||||||
| chr16:4645519 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.89-4846C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645519 | |||||||
| chr16:4645534 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.89-4831C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645534 | |||||||
| chr16:4645589 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.89-4776T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645589 | |||||||
| chr16:4645652 | G | A | 1 | a0001c0001t0011g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89-4713G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645652 | |||||||
| chr16:4645678 | T | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-4687T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645678 | |||||||
| chr16:4645690 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-4675G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645690 | |||||||
| chr16:4645699 | G | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-4666G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645699 | |||||||
| chr16:4645705 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.89-4660C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645705 | |||||||
| chr16:4645829 | G | T | 8 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0157 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-4536G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645829 | |||||||
| chr16:4645831 | G | A | 3 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0246 |
3 | HG02055.hp2 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.89-4534G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645831 | |||||||
| chr16:4645889 | A | G | 1 | a0001c0001t0024g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.89-4476A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645889 | |||||||
| chr16:4645925 | A | G | 2 | a0001c0001t0002g0260 a0001c0001t0003g0098 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-4440A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645925 | |||||||
| chr16:4645948 | A | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-4417A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645948 | |||||||
| chr16:4645961 | T | C | 38 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(35): Show |
38 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.89-4404T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4645961 | |||||||
| chr16:4646009 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.89-4356C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646009 | |||||||
| chr16:4646076 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.89-4289C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646076 | |||||||
| chr16:4646107 | C | CG | 16 | a0001c0001t0002g0200 a0001c0001t0003g0013 a0001c0001t0005g0036 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-4252dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646107 | ||||||
| chr16:4646198 | A | G | 1 | a0003c0009t0001g0168 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.89-4167A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646198 | |||||||
| chr16:4646209 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0259 |
2 | HG01192.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.89-4156T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646209 | |||||||
| chr16:4646223 | C | A | 43 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(40): Show |
43 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-4142C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646223 | |||||||
| chr16:4646422 | C | CA | 20 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(17): Show |
20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-3930dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646422 | ||||||
| chr16:4646422 | C | CAAA | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3932_89-3930dup others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4646422 | ||||||
| chr16:4646476 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3889A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646476 | |||||||
| chr16:4646566 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.89-3799T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646566 | |||||||
| chr16:4646653 | T | C | 41 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(38): Show |
41 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-3712T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646653 | |||||||
| chr16:4646658 | A | G | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-3707A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646658 | |||||||
| chr16:4646771 | C | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3594C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646771 | |||||||
| chr16:4646803 | G | A | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3562G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646803 | |||||||
| chr16:4646973 | C | T | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-3392C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4646973 | |||||||
| chr16:4647004 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-3361C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647004 | |||||||
| chr16:4647050 | G | A | 1 | a0001c0001t0006g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-3315G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647050 | |||||||
| chr16:4647087 | A | C | 1 | a0001c0001t0004g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-3278A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647087 | |||||||
| chr16:4647100 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-3265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647100 | |||||||
| chr16:4647188 | A | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.89-3177A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647188 | |||||||
| chr16:4647212 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.89-3153C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647212 | |||||||
| chr16:4647255 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-3110A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647255 | |||||||
| chr16:4647258 | A | T | 6 | a0001c0001t0027g0002 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3107A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647258 | |||||||
| chr16:4647370 | T | C | 11 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0002g0260 others(8): Show |
11 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-2995T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647370 | |||||||
| chr16:4647377 | CTT | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-2986_89-2985del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4647377 | ||||||
| chr16:4647511 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0018g0014 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.89-2854C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647511 | |||||||
| chr16:4647516 | G | T | 1 | a0001c0001t0001g0264 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.89-2849G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647516 | |||||||
| chr16:4647672 | C | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-2693C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647672 | |||||||
| chr16:4647675 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0003g0047 a0001c0001t0003g0048 |
3 | NA18978.hp1 NA18978.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.89-2690T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647675 | |||||||
| chr16:4647793 | G | A | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-2572G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647793 | |||||||
| chr16:4647829 | C | A | 2 | a0001c0002t0003g0005 a0001c0002t0004g0004 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-2536C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4647829 | |||||||
| chr16:4648174 | A | G | 6 | a0001c0001t0027g0002 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2191A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648174 | |||||||
| chr16:4648191 | T | C | 14 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(11): Show |
14 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-2174T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648191 | |||||||
| chr16:4648258 | C | G | 9 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2107C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648258 | |||||||
| chr16:4648273 | A | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2092A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648273 | |||||||
| chr16:4648276 | C | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-2089C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648276 | |||||||
| chr16:4648294 | C | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2071C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648294 | |||||||
| chr16:4648296 | C | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-2069C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648296 | |||||||
| chr16:4648304 | CGCGGGCT others(423): Show |
C | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-2059_89-1630del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648304 | ||||||
| chr16:4648305 | GCGGGCTC others(208): Show |
G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2059_89-1845del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648305 | |||||||
| chr16:4648306 | C | G | 19 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0002g0260 others(16): Show |
19 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.89-2059C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648306 | |||||||
| chr16:4648339 | T | C | 17 | a0001c0001t0001g0115 a0001c0001t0001g0201 a0001c0001t0002g0113 others(14): Show |
17 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-2026T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648339 | |||||||
| chr16:4648345 | A | G | 4 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(1): Show |
4 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2020A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648345 | |||||||
| chr16:4648381 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1984A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648381 | |||||||
| chr16:4648402 | G | GTCCTCCT others(29): Show |
1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1953_89-1952ins others(36): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648402 | ||||||
| chr16:4648413 | G | C | 1 | a0001c0001t0004g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1952G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648413 | |||||||
| chr16:4648447 | T | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1918T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648447 | |||||||
| chr16:4648449 | G | C | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1916G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648449 | |||||||
| chr16:4648453 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1912A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648453 | |||||||
| chr16:4648454 | C | G | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-1911C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648454 | |||||||
| chr16:4648471 | T | C | 24 | a0001c0001t0001g0133 a0001c0001t0001g0159 a0001c0001t0001g0201 others(21): Show |
24 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-1894T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648471 | |||||||
| chr16:4648474 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0027g0002 |
2 | HG01884.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.89-1891C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648474 | |||||||
| chr16:4648475 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.89-1890T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648475 | |||||||
| chr16:4648476 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.89-1889C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648476 | |||||||
| chr16:4648485 | G | C | 1 | a0001c0001t0004g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1880G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648485 | |||||||
| chr16:4648509 | G | GCTCCTCC others(493): Show |
1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(500): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | |||||||
| chr16:4648509 | G | GCTCCTCC others(387): Show |
1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(394): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | |||||||
| chr16:4648509 | G | GCTCCTCC others(315): Show |
1 | a0001c0001t0004g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1856_89-1855ins others(322): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648509 | |||||||
| chr16:4648510 | G | C | 6 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(3): Show |
6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1855G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648510 | |||||||
| chr16:4648511 | G | T | 5 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(2): Show |
5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1854G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648511 | |||||||
| chr16:4648512 | G | C | 5 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(2): Show |
5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1853G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648512 | |||||||
| chr16:4648512 | GCTCCTCC others(64): Show |
G | 2 | a0001c0001t0002g0284 a0001c0001t0006g0285 |
2 | HG00408.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.89-1806_89-1736del others(71): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648512 | ||||||
| chr16:4648520 | C | CG | 5 | a0001c0001t0027g0002 a0001c0002t0003g0003 a0001c0002t0004g0004 others(2): Show |
5 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1841dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648520 | ||||||
| chr16:4648524 | G | GGCTCTTC others(30): Show |
1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1841_89-1840ins others(37): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648524 | |||||||
| chr16:4648533 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1832G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648533 | |||||||
| chr16:4648533 | G | T | 2 | a0001c0001t0002g0260 a0001c0001t0003g0098 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1832G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648533 | |||||||
| chr16:4648545 | G | C | 5 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(2): Show |
5 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1820G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648545 | |||||||
| chr16:4648549 | T | A | 11 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0002g0260 others(8): Show |
11 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-1816T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648549 | |||||||
| chr16:4648556 | G | GGGGGCTC others(135): Show |
2 | a0001c0001t0002g0260 a0001c0001t0003g0098 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1740_89-1739ins others(142): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648556 | ||||||
| chr16:4648560 | G | A | 3 | a0001c0002t0003g0003 a0001c0002t0004g0004 a0001c0002t0005g0001 |
3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1805G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648560 | |||||||
| chr16:4648581 | G | C | 6 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1784G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648581 | |||||||
| chr16:4648591 | C | CG | 6 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(3): Show |
6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1770dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648591 | ||||||
| chr16:4648595 | G | GA | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1770_89-1769ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648595 | |||||||
| chr16:4648616 | G | C | 10 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-1749G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648616 | |||||||
| chr16:4648623 | T | TCTCCGGG others(30): Show |
1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1741_89-1740ins others(37): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648623 | ||||||
| chr16:4648624 | C | CT | 7 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1741_89-1740ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648624 | |||||||
| chr16:4648626 | C | CG | 6 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(3): Show |
6 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1736dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648626 | ||||||
| chr16:4648626 | C | G | 7 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-1739C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648626 | |||||||
| chr16:4648626 | C | T | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-1739C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648626 | |||||||
| chr16:4648630 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1735A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648630 | |||||||
| chr16:4648651 | C | G | 1 | a0001c0001t0007g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-1714C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648651 | |||||||
| chr16:4648660 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1705C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648660 | |||||||
| chr16:4648666 | A | G | 14 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0109 others(11): Show |
14 | HG00280.hp2 HG01099.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-1699A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648666 | |||||||
| chr16:4648666 | ACTCTTCC others(170): Show |
A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1678_89-1502del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648666 | ||||||
| chr16:4648687 | G | C | 5 | a0001c0001t0004g0018 a0001c0002t0003g0003 a0001c0002t0004g0004 others(2): Show |
5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1678G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648687 | |||||||
| chr16:4648696 | C | T | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1669C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648696 | |||||||
| chr16:4648698 | G | C | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1667G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648698 | |||||||
| chr16:4648701 | G | T | 1 | a0001c0001t0002g0288 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.89-1664G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648701 | |||||||
| chr16:4648723 | C | G | 3 | a0001c0002t0003g0003 a0001c0002t0004g0004 a0001c0002t0005g0001 |
3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1642C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648723 | |||||||
| chr16:4648728 | C | T | 1 | a0001c0001t0012g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-1637C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648728 | |||||||
| chr16:4648732 | T | C | 5 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0005 others(2): Show |
5 | HG01884.hp1 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-1633T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648732 | |||||||
| chr16:4648734 | G | C | 3 | a0001c0002t0003g0003 a0001c0002t0004g0004 a0001c0002t0005g0001 |
3 | HG01099.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1631G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648734 | |||||||
| chr16:4648738 | A | G | 24 | a0001c0001t0001g0286 a0001c0001t0003g0013 a0001c0001t0004g0018 others(21): Show |
24 | HG01099.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-1627A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648738 | |||||||
| chr16:4648738 | ACTCTTCC others(28): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.89-1606_89-1572del others(35): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648738 | ||||||
| chr16:4648738 | ACTCTTCC others(98): Show |
A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-1597_89-1493del | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648738 | ||||||
| chr16:4648741 | C | G | 1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1624C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648741 | |||||||
| chr16:4648756 | C | CGGCTCCT others(1035): Show |
1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(1042): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648756 | ||||||
| chr16:4648759 | C | G | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-1606C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648759 | |||||||
| chr16:4648769 | C | CGGGGGCT others(916): Show |
1 | a0001c0002t0003g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(923): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | ||||||
| chr16:4648769 | C | CGGGGGCT others(485): Show |
1 | a0001c0001t0004g0018 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(492): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | ||||||
| chr16:4648769 | C | CGGGGGCT others(952): Show |
2 | a0001c0002t0003g0003 a0001c0002t0004g0004 |
2 | HG01099.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.89-1592_89-1591ins others(959): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | ||||||
| chr16:4648769 | C | CGGGGGCT others(952): Show |
1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.89-1592_89-1591ins others(959): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648769 | ||||||
| chr16:4648781 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.89-1584C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648781 | |||||||
| chr16:4648794 | G | C | 9 | a0001c0001t0002g0260 a0001c0001t0003g0098 a0001c0001t0004g0018 others(6): Show |
9 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-1571G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648794 | |||||||
| chr16:4648804 | C | CG | 5 | a0001c0001t0004g0018 a0001c0002t0003g0003 a0001c0002t0003g0005 others(2): Show |
5 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1557dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648804 | ||||||
| chr16:4648804 | C | CGGGGGCT others(881): Show |
1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-1557_89-1556ins others(888): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648804 | ||||||
| chr16:4648808 | G | GA | 3 | a0001c0001t0002g0260 a0001c0001t0003g0098 a0001c0004t0029g0083 |
3 | HG02809.hp2 NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1557_89-1556ins others(1): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648808 | |||||||
| chr16:4648829 | G | C | 6 | a0001c0001t0004g0018 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1536G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648829 | |||||||
| chr16:4648838 | C | T | 2 | a0001c0001t0002g0260 a0001c0001t0003g0098 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1527C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648838 | |||||||
| chr16:4648839 | C | CG | 6 | a0001c0001t0004g0018 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-1522dupG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(529): Show |
1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(529): Show |
2 | a0001c0001t0002g0105 a0001c0001t0015g0011 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(529): Show |
1 | a0001c0001t0008g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(423): Show |
1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(430): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(529): Show |
1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGACTC others(529): Show |
3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-1523_89-1522ins others(536): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGGACT others(341): Show |
1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-1522_89-1521ins others(348): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648839 | C | CGGGGGCT others(521): Show |
1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-1522_89-1521ins others(528): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648839 | ||||||
| chr16:4648843 | G | A | 9 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0003g0010 others(6): Show |
9 | HG01243.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-1522G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648843 | |||||||
| chr16:4648843 | G | GACTCTTC others(351): Show |
2 | a0001c0001t0002g0260 a0001c0001t0003g0098 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.89-1522_89-1521ins others(358): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648843 | |||||||
| chr16:4648843 | G | GCTCTTCC others(29): Show |
3 | a0001c0001t0007g0333 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG02896.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-1465_89-1430dup others(36): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4648843 | ||||||
| chr16:4648864 | C | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1501C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648864 | |||||||
| chr16:4648873 | T | C | 25 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0233 others(22): Show |
25 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.89-1492T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648873 | |||||||
| chr16:4648879 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1486A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648879 | |||||||
| chr16:4648900 | C | G | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0002g0109 others(3): Show |
6 | HG00280.hp2 HG02602.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1465C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648900 | |||||||
| chr16:4648909 | T | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1456T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648909 | |||||||
| chr16:4648915 | A | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-1450A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4648915 | |||||||
| chr16:4649149 | T | G | 2 | a0001c0001t0001g0223 a0001c0001t0030g0082 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89-1216T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649149 | |||||||
| chr16:4649152 | C | T | 2 | a0001c0001t0004g0018 a0001c0003t0031g0017 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.89-1213C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649152 | |||||||
| chr16:4649153 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.89-1212G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649153 | |||||||
| chr16:4649163 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89-1202G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649163 | |||||||
| chr16:4649167 | G | T | 1 | a0001c0001t0003g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89-1198G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649167 | |||||||
| chr16:4649291 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.89-1074A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649291 | |||||||
| chr16:4649318 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.89-1047A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649318 | |||||||
| chr16:4649378 | A | C | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-987A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649378 | |||||||
| chr16:4649389 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-976C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649389 | |||||||
| chr16:4649412 | C | T | 4 | a0001c0002t0003g0003 a0001c0002t0003g0005 a0001c0002t0004g0004 others(1): Show |
4 | HG01099.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-953C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649412 | |||||||
| chr16:4649421 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-944C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649421 | |||||||
| chr16:4649507 | G | C | 48 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(45): Show |
48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.89-858G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649507 | |||||||
| chr16:4649554 | C | T | 1 | a0002c0007t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.89-811C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649554 | |||||||
| chr16:4649593 | T | A | 15 | a0001c0001t0003g0013 a0001c0001t0005g0036 a0001c0001t0005g0037 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-772T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649593 | |||||||
| chr16:4649657 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.89-708C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649657 | |||||||
| chr16:4649761 | T | C | 2 | a0001c0001t0002g0249 a0001c0001t0006g0291 |
2 | HG02165.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.89-604T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649761 | |||||||
| chr16:4649770 | G | T | 2 | a0001c0001t0002g0309 a0001c0001t0042g0317 |
2 | HG02071.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.89-595G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649770 | |||||||
| chr16:4649902 | A | G | 51 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(48): Show |
51 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(48): Show |
intron_variant | MODIFIER | c.89-463A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649902 | |||||||
| chr16:4649905 | C | T | 1 | a0001c0001t0009g0228 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.89-460C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649905 | |||||||
| chr16:4649918 | G | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-447G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649918 | |||||||
| chr16:4649955 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.89-410G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649955 | |||||||
| chr16:4649967 | C | T | 1 | a0001c0001t0006g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.89-398C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4649967 | |||||||
| chr16:4650006 | C | G | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-359C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650006 | |||||||
| chr16:4650008 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.89-357A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650008 | |||||||
| chr16:4650031 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.89-334C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650031 | |||||||
| chr16:4650055 | A | C | 30 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(27): Show |
30 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-310A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650055 | |||||||
| chr16:4650065 | GGCTGAGG others(11): Show |
G | 4 | a0001c0001t0002g0161 a0001c0001t0005g0094 a0001c0001t0033g0184 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-299_89-282delGC others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650065 | |||||||
| chr16:4650092 | C | T | 11 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0004g0018 others(8): Show |
11 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-273C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650092 | |||||||
| chr16:4650131 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-234C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650131 | |||||||
| chr16:4650179 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.89-186G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650179 | |||||||
| chr16:4650195 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.89-170C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | chr16 | 4650195 | |||||||
| chr16:4650317 | C | CA | 16 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0134 others(13): Show |
16 | HG00558.hp2 HG01109.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-30dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4650317 | ||||||
| chr16:4650317 | CAAA | C | 7 | a0001c0001t0004g0018 a0001c0002t0003g0003 a0001c0002t0003g0005 others(4): Show |
7 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-32_89-30delAAA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 4650317 | ||||||
| chr16:4650524 | G | A | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+41G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650524 | |||||||
| chr16:4650540 | A | C | 2 | a0001c0001t0002g0121 a0001c0001t0049g0122 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.207+57A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650540 | |||||||
| chr16:4650609 | C | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+126C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650609 | |||||||
| chr16:4650624 | G | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.207+141G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650624 | |||||||
| chr16:4650660 | T | C | 5 | a0001c0001t0001g0223 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+177T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650660 | |||||||
| chr16:4650674 | C | G | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.207+191C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650674 | |||||||
| chr16:4650878 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.207+395G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650878 | |||||||
| chr16:4650904 | T | G | 8 | a0001c0001t0001g0251 a0001c0001t0001g0330 a0001c0001t0001g0331 others(5): Show |
8 | HG00408.hp2 HG00621.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+421T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4650904 | |||||||
| chr16:4651057 | C | T | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.207+574C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651057 | |||||||
| chr16:4651072 | A | G | 48 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(45): Show |
48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.207+589A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651072 | |||||||
| chr16:4651110 | G | GA | 21 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(18): Show |
21 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.207+641dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651110 | ||||||
| chr16:4651110 | GA | G | 12 | a0001c0001t0001g0115 a0001c0001t0001g0138 a0001c0001t0002g0280 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+641delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651110 | ||||||
| chr16:4651127 | A | T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.207+644A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651127 | |||||||
| chr16:4651147 | A | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+664A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651147 | |||||||
| chr16:4651247 | C | T | 14 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0225 others(11): Show |
14 | HG00621.hp2 HG02015.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.208-716C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651247 | |||||||
| chr16:4651248 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.208-715G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651248 | |||||||
| chr16:4651264 | C | CTGTT | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-698_208-695dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 4651264 | ||||||
| chr16:4651284 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0008g0025 |
3 | HG02965.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.208-679A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651284 | |||||||
| chr16:4651346 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-617C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651346 | |||||||
| chr16:4651348 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.208-615G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651348 | |||||||
| chr16:4651349 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.208-614G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651349 | |||||||
| chr16:4651361 | A | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0217 |
3 | HG00280.hp1 HG00323.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.208-602A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651361 | |||||||
| chr16:4651408 | G | A | 6 | a0001c0001t0027g0002 a0001c0002t0003g0003 a0001c0002t0003g0005 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-555G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651408 | |||||||
| chr16:4651479 | T | A | 48 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(45): Show |
48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.208-484T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651479 | |||||||
| chr16:4651565 | G | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-398G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651565 | |||||||
| chr16:4651574 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.208-389G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651574 | |||||||
| chr16:4651578 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.208-385C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651578 | |||||||
| chr16:4651584 | G | T | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.208-379G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651584 | |||||||
| chr16:4651743 | T | C | 48 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(45): Show |
48 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.208-220T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651743 | |||||||
| chr16:4651773 | C | T | 12 | a0001c0001t0001g0307 a0001c0001t0002g0132 a0001c0001t0002g0227 others(9): Show |
12 | HG02071.hp1 HG02129.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.208-190C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651773 | |||||||
| chr16:4651826 | T | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-137T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651826 | |||||||
| chr16:4651849 | T | C | 14 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0001g0256 others(11): Show |
14 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-114T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651849 | |||||||
| chr16:4651855 | T | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-108T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651855 | |||||||
| chr16:4651858 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0008g0025 others(1): Show |
4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208-105A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651858 | |||||||
| chr16:4651859 | T | G | 14 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(11): Show |
14 | HG01099.hp1 HG01175.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-104T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651859 | |||||||
| chr16:4651928 | G | C | 1 | a0001c0001t0011g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.208-35G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651928 | |||||||
| chr16:4651930 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.208-33G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 2/16 | chr16 | 4651930 | |||||||
| chr16:4652066 | C | A | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.296+15C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652066 | |||||||
| chr16:4652095 | G | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.296+44G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652095 | |||||||
| chr16:4652101 | T | A | 1 | a0001c0001t0005g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.296+50T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652101 | |||||||
| chr16:4652172 | C | T | 2 | a0001c0001t0004g0018 a0001c0003t0031g0017 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.296+121C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652172 | |||||||
| chr16:4652214 | G | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.296+163G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652214 | |||||||
| chr16:4652474 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297-204G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652474 | |||||||
| chr16:4652544 | G | C | 1 | a0001c0001t0005g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.297-134G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652544 | |||||||
| chr16:4652546 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.297-132C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 3/16 | chr16 | 4652546 | |||||||
| chr16:4652836 | G | A | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.443+12G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652836 | |||||||
| chr16:4652933 | G | C | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+109G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652933 | |||||||
| chr16:4652942 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0003t0014g0136 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+118C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4652942 | |||||||
| chr16:4653012 | C | CT | 4 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0003t0014g0136 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+189dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4653012 | ||||||
| chr16:4653081 | C | A | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+257C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653081 | |||||||
| chr16:4653152 | C | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.443+328C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653152 | |||||||
| chr16:4653172 | C | G | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+348C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653172 | |||||||
| chr16:4653177 | T | C | 12 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0004g0018 others(9): Show |
12 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+353T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653177 | |||||||
| chr16:4653491 | TGTTTTGT others(4): Show |
T | 2 | a0001c0001t0007g0333 a0001c0001t0026g0334 |
2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.443+668_443+678del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653491 | |||||||
| chr16:4653539 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0007g0075 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+715C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653539 | |||||||
| chr16:4653596 | C | CT | 4 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0008g0025 others(1): Show |
4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+773dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4653596 | ||||||
| chr16:4653636 | G | A | 8 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.443+812G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653636 | |||||||
| chr16:4653715 | C | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.443+891C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653715 | |||||||
| chr16:4653832 | A | C | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443+1008A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653832 | |||||||
| chr16:4653848 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443+1024G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653848 | |||||||
| chr16:4653878 | G | A | 2 | a0001c0001t0001g0179 a0003c0009t0001g0168 |
2 | NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.443+1054G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653878 | |||||||
| chr16:4653942 | G | A | 14 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.443+1118G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653942 | |||||||
| chr16:4653957 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.443+1133G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653957 | |||||||
| chr16:4653969 | C | G | 2 | a0001c0001t0027g0002 a0001c0004t0029g0083 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.443+1145C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653969 | |||||||
| chr16:4653976 | G | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0035 |
3 | HG02647.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.443+1152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4653976 | |||||||
| chr16:4654083 | C | T | 1 | a0001c0001t0006g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.443+1259C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654083 | |||||||
| chr16:4654085 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.443+1261G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654085 | |||||||
| chr16:4654129 | C | G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+1305C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654129 | |||||||
| chr16:4654172 | C | T | 7 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+1348C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654172 | |||||||
| chr16:4654192 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.443+1368A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654192 | |||||||
| chr16:4654223 | C | G | 7 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.443+1399C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654223 | |||||||
| chr16:4654432 | T | G | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+1608T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654432 | |||||||
| chr16:4654466 | T | C | 36 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0186 others(33): Show |
36 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.443+1642T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654466 | |||||||
| chr16:4654666 | C | T | 2 | a0001c0001t0004g0018 a0001c0003t0031g0017 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.443+1842C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654666 | |||||||
| chr16:4654729 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0002g0105 a0001c0001t0008g0025 others(1): Show |
4 | HG02965.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+1905G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654729 | |||||||
| chr16:4654744 | T | A | 43 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(40): Show |
43 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.443+1920T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654744 | |||||||
| chr16:4654768 | T | C | 27 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0143 others(24): Show |
27 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+1944T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654768 | |||||||
| chr16:4654782 | G | T | 9 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(6): Show |
9 | HG01099.hp1 HG01175.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.443+1958G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654782 | |||||||
| chr16:4654800 | A | G | 1 | a0002c0007t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.443+1976A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654800 | |||||||
| chr16:4654908 | T | C | 17 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0186 others(14): Show |
17 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.443+2084T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654908 | |||||||
| chr16:4654925 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443+2101G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4654925 | |||||||
| chr16:4655015 | A | T | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0004g0009 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.443+2191A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655015 | |||||||
| chr16:4655022 | G | C | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.443+2198G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655022 | |||||||
| chr16:4655028 | G | A | 1 | a0002c0007t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.443+2204G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655028 | |||||||
| chr16:4655099 | T | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0003t0014g0136 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-2147T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655099 | |||||||
| chr16:4655138 | G | A | 1 | a0001c0002t0005g0001 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.444-2108G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655138 | |||||||
| chr16:4655183 | C | A | 4 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0026 others(1): Show |
4 | HG02559.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-2063C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655183 | |||||||
| chr16:4655236 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.444-2010G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655236 | |||||||
| chr16:4655279 | A | G | 7 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-1967A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655279 | |||||||
| chr16:4655297 | G | A | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1949G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655297 | |||||||
| chr16:4655381 | C | G | 7 | a0001c0001t0004g0018 a0001c0001t0027g0002 a0001c0002t0003g0003 others(4): Show |
7 | HG01099.hp1 HG01884.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.444-1865C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655381 | |||||||
| chr16:4655381 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.444-1865C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655381 | |||||||
| chr16:4655408 | G | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0003t0014g0136 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-1838G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655408 | |||||||
| chr16:4655416 | C | A | 1 | a0001c0001t0002g0260 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.444-1830C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655416 | |||||||
| chr16:4655447 | CT | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0233 a0001c0001t0015g0011 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-1798delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655447 | |||||||
| chr16:4655458 | AATCACAG others(75): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.444-1746_444-1665d others(84): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4655458 | ||||||
| chr16:4655574 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.444-1672C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655574 | |||||||
| chr16:4655597 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.444-1649G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655597 | |||||||
| chr16:4655622 | C | T | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1624C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655622 | |||||||
| chr16:4655702 | G | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.444-1544G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655702 | |||||||
| chr16:4655945 | G | A | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-1301G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655945 | |||||||
| chr16:4655946 | G | T | 1 | a0001c0006t0007g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444-1300G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655946 | |||||||
| chr16:4655986 | G | A | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0275 |
3 | HG01975.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.444-1260G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4655986 | |||||||
| chr16:4656097 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.444-1149C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656097 | |||||||
| chr16:4656179 | A | C | 5 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0199 others(2): Show |
5 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-1067A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656179 | |||||||
| chr16:4656302 | A | G | 198 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(195): Show |
198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.444-944A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656302 | |||||||
| chr16:4656316 | A | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0193 a0001c0001t0011g0066 others(1): Show |
4 | HG01175.hp1 HG02622.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-930A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656316 | |||||||
| chr16:4656330 | A | C | 37 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(34): Show |
37 | HG01099.hp1 HG01175.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.444-916A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656330 | |||||||
| chr16:4656356 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0199 others(1): Show |
4 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.444-890G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656356 | |||||||
| chr16:4656565 | C | G | 2 | a0001c0001t0003g0010 a0001c0001t0021g0032 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.444-681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656565 | |||||||
| chr16:4656710 | A | G | 11 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(8): Show |
11 | HG01175.hp1 HG01243.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-536A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656710 | |||||||
| chr16:4656787 | G | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.444-459G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656787 | |||||||
| chr16:4656882 | A | AAAAT | 4 | a0001c0001t0002g0132 a0001c0001t0002g0227 a0001c0001t0002g0244 others(1): Show |
4 | HG01175.hp2 HG02976.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.444-320_444-317dup others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656882 | AAAAT | A | 53 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0138 others(50): Show |
53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.444-320_444-317del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656882 | AAAATAAA others(1): Show |
A | 131 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0110 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.444-324_444-317del others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656882 | AAAATAAA others(5): Show |
A | 93 | a0001c0001t0001g0106 a0001c0001t0001g0133 a0001c0001t0001g0206 others(90): Show |
93 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.444-328_444-317del others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656882 | AAAATAAA others(9): Show |
A | 25 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(22): Show |
25 | HG00558.hp1 HG01099.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.444-332_444-317del others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656882 | AAAATAAA others(13): Show |
A | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.444-336_444-317del others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 4656882 | ||||||
| chr16:4656910 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.444-336T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656910 | |||||||
| chr16:4656926 | T | C | 3 | a0001c0001t0003g0058 a0001c0001t0008g0022 a0001c0001t0027g0002 |
3 | HG01884.hp1 HG02896.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.444-320T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656926 | |||||||
| chr16:4656938 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.444-308C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656938 | |||||||
| chr16:4656945 | C | T | 1 | a0001c0001t0046g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.444-301C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4656945 | |||||||
| chr16:4657019 | T | C | 29 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(26): Show |
29 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.444-227T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657019 | |||||||
| chr16:4657083 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.444-163G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657083 | |||||||
| chr16:4657186 | A | C | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(6): Show |
9 | HG01099.hp1 HG01884.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.444-60A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657186 | |||||||
| chr16:4657225 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.444-21C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 4/16 | chr16 | 4657225 | |||||||
| chr16:4657379 | C | T | 4 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0008g0024 others(1): Show |
4 | HG00408.hp2 HG00621.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+16C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657379 | |||||||
| chr16:4657431 | A | G | 109 | a0001c0001t0001g0153 a0001c0001t0001g0176 a0001c0001t0001g0197 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.561+68A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657431 | |||||||
| chr16:4657516 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.561+153G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657516 | |||||||
| chr16:4657593 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0170 |
2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.561+230G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657593 | |||||||
| chr16:4657738 | C | CT | 101 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(98): Show |
101 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.561+402dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | C | CTT | 26 | a0001c0001t0001g0142 a0001c0001t0001g0170 a0001c0001t0001g0213 others(23): Show |
26 | HG00544.hp2 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.561+401_561+402dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | C | CTTTTTTT others(8): Show |
1 | a0001c0003t0014g0137 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.561+388_561+402dup others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | C | CTTTTTTT others(9): Show |
1 | a0001c0003t0014g0136 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.561+387_561+402dup others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | CT | C | 37 | a0001c0001t0001g0183 a0001c0001t0001g0190 a0001c0001t0001g0201 others(34): Show |
37 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.561+402delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | CTT | C | 7 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0004g0009 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+401_561+402del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657738 | CTTT | C | 10 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(7): Show |
10 | HG01175.hp1 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+400_561+402del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4657738 | ||||||
| chr16:4657763 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.561+400T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657763 | |||||||
| chr16:4657784 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+421C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657784 | |||||||
| chr16:4657784 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.561+421C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657784 | |||||||
| chr16:4657807 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+444G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657807 | |||||||
| chr16:4657808 | C | T | 3 | a0001c0001t0003g0010 a0001c0001t0021g0032 a0001c0001t0027g0002 |
3 | HG01884.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.561+445C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657808 | |||||||
| chr16:4657814 | C | T | 1 | a0001c0001t0006g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.561+451C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657814 | |||||||
| chr16:4657848 | G | C | 40 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(37): Show |
40 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.561+485G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657848 | |||||||
| chr16:4657932 | C | T | 25 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(22): Show |
25 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.561+569C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657932 | |||||||
| chr16:4657943 | C | T | 2 | a0001c0001t0006g0127 a0001c0001t0006g0152 |
2 | HG01074.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.561+580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657943 | |||||||
| chr16:4657979 | T | A | 26 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(23): Show |
26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+616T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657979 | |||||||
| chr16:4657985 | G | A | 26 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(23): Show |
26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+622G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4657985 | |||||||
| chr16:4658033 | T | C | 7 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+670T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658033 | |||||||
| chr16:4658110 | T | C | 26 | a0001c0001t0001g0123 a0001c0001t0001g0133 a0001c0001t0001g0186 others(23): Show |
26 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.561+747T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658110 | |||||||
| chr16:4658179 | C | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG01175.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+816C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658179 | |||||||
| chr16:4658241 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.561+878A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658241 | |||||||
| chr16:4658263 | C | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.561+900C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658263 | |||||||
| chr16:4658273 | T | C | 1 | a0001c0001t0012g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.561+910T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658273 | |||||||
| chr16:4658278 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.561+915G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658278 | |||||||
| chr16:4658376 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.561+1013A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658376 | |||||||
| chr16:4658404 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.561+1041C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658404 | |||||||
| chr16:4658428 | G | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+1065G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658428 | |||||||
| chr16:4658484 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.561+1121C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658484 | |||||||
| chr16:4658487 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.561+1124G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658487 | |||||||
| chr16:4658493 | G | A | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.561+1130G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658493 | |||||||
| chr16:4658522 | T | C | 141 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.561+1159T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658522 | |||||||
| chr16:4658537 | G | GA | 29 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(26): Show |
29 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+1186dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4658537 | ||||||
| chr16:4658538 | A | G | 1 | a0001c0001t0002g0325 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.561+1175A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658538 | |||||||
| chr16:4658541 | A | AG | 129 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.561+1178_561+1179i others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658541 | |||||||
| chr16:4658736 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.561+1373G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658736 | |||||||
| chr16:4658958 | G | C | 156 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.561+1595G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658958 | |||||||
| chr16:4658969 | C | T | 1 | a0001c0001t0035g0118 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.561+1606C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4658969 | |||||||
| chr16:4659093 | T | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+1730T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659093 | |||||||
| chr16:4659130 | C | A | 145 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.561+1767C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659130 | |||||||
| chr16:4659160 | TA | T | 157 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.561+1807delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4659160 | ||||||
| chr16:4659249 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0328 |
2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.561+1886G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659249 | |||||||
| chr16:4659284 | C | A | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+1921C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659284 | |||||||
| chr16:4659417 | G | A | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+2054G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659417 | |||||||
| chr16:4659458 | T | G | 191 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(188): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.561+2095T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659458 | |||||||
| chr16:4659503 | T | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2140T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659503 | |||||||
| chr16:4659578 | C | A | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.561+2215C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659578 | |||||||
| chr16:4659625 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG00673.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.561+2262C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659625 | |||||||
| chr16:4659635 | A | G | 166 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.561+2272A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659635 | |||||||
| chr16:4659675 | G | A | 1 | a0001c0001t0002g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.561+2312G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659675 | |||||||
| chr16:4659963 | T | C | 31 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(28): Show |
31 | HG01099.hp1 HG01175.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.561+2600T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659963 | |||||||
| chr16:4659992 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2629C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4659992 | |||||||
| chr16:4660008 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+2645C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660008 | |||||||
| chr16:4660097 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.561+2734C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660097 | |||||||
| chr16:4660192 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.561+2829C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660192 | |||||||
| chr16:4660218 | A | G | 1 | a0001c0001t0011g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.561+2855A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660218 | |||||||
| chr16:4660240 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.561+2877G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660240 | |||||||
| chr16:4660276 | G | A | 2 | a0001c0001t0007g0075 a0001c0001t0007g0076 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.561+2913G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660276 | |||||||
| chr16:4660294 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.561+2931G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660294 | |||||||
| chr16:4660338 | T | A | 16 | a0001c0001t0003g0013 a0001c0001t0004g0009 a0001c0001t0005g0036 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.561+2975T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660338 | |||||||
| chr16:4660348 | C | T | 1 | a0001c0001t0011g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.561+2985C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660348 | |||||||
| chr16:4660349 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.561+2986G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660349 | |||||||
| chr16:4660364 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.561+3001G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660364 | |||||||
| chr16:4660376 | G | C | 2 | a0001c0001t0002g0121 a0001c0001t0049g0122 |
2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.561+3013G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660376 | |||||||
| chr16:4660381 | T | A | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.561+3018T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660381 | |||||||
| chr16:4660403 | C | T | 1 | a0001c0001t0024g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.561+3040C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660403 | |||||||
| chr16:4660492 | A | G | 7 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+3129A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660492 | |||||||
| chr16:4660589 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.561+3226C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660589 | |||||||
| chr16:4660607 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0008g0025 a0001c0001t0022g0045 |
3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.561+3244C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660607 | |||||||
| chr16:4660609 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.561+3246C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660609 | |||||||
| chr16:4660621 | C | T | 1 | a0001c0001t0017g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.561+3258C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660621 | |||||||
| chr16:4660622 | G | T | 1 | a0001c0001t0010g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.561+3259G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660622 | |||||||
| chr16:4660636 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.561+3273T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660636 | |||||||
| chr16:4660646 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.561+3283G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660646 | |||||||
| chr16:4660772 | T | C | 13 | a0001c0001t0004g0009 a0001c0001t0005g0036 a0001c0001t0005g0037 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+3409T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660772 | |||||||
| chr16:4660778 | CAG | C | 133 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.561+3416_561+3417d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660778 | |||||||
| chr16:4660897 | T | G | 233 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.561+3534T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660897 | |||||||
| chr16:4660982 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.561+3619A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4660982 | |||||||
| chr16:4661024 | C | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.561+3661C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661024 | |||||||
| chr16:4661034 | T | C | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.561+3671T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661034 | |||||||
| chr16:4661143 | AT | A | 142 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.562-3551delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4661143 | ||||||
| chr16:4661249 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0008g0025 a0001c0001t0022g0045 |
3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3460G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661249 | |||||||
| chr16:4661270 | C | T | 3 | a0001c0001t0001g0264 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG02922.hp1 HG03471.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.562-3439C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661270 | |||||||
| chr16:4661325 | G | C | 174 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.562-3384G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661325 | |||||||
| chr16:4661344 | C | T | 2 | a0001c0001t0008g0025 a0001c0001t0022g0045 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3365C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661344 | |||||||
| chr16:4661357 | C | CGCACCCT others(8): Show |
1 | a0001c0001t0002g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.562-3344_562-3330d others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4661357 | ||||||
| chr16:4661392 | C | T | 115 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.562-3317C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661392 | |||||||
| chr16:4661405 | G | T | 2 | a0001c0001t0002g0189 a0001c0001t0011g0056 |
2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.562-3304G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661405 | |||||||
| chr16:4661407 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0008g0025 a0001c0001t0022g0045 |
3 | HG03139.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-3302C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661407 | |||||||
| chr16:4661511 | C | T | 11 | a0001c0001t0004g0009 a0001c0001t0005g0036 a0001c0001t0005g0037 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-3198C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661511 | |||||||
| chr16:4661630 | C | T | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.562-3079C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661630 | |||||||
| chr16:4661642 | C | G | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.562-3067C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661642 | |||||||
| chr16:4661736 | T | G | 157 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.562-2973T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661736 | |||||||
| chr16:4661790 | C | T | 140 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.562-2919C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661790 | |||||||
| chr16:4661814 | G | A | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-2895G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661814 | |||||||
| chr16:4661863 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-2846T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661863 | |||||||
| chr16:4661902 | T | A | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-2807T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4661902 | |||||||
| chr16:4662055 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-2654G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662055 | |||||||
| chr16:4662147 | G | A | 140 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(137): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.562-2562G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662147 | |||||||
| chr16:4662177 | T | G | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.562-2532T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662177 | |||||||
| chr16:4662306 | G | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.562-2403G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662306 | |||||||
| chr16:4662311 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.562-2398T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662311 | |||||||
| chr16:4662400 | C | T | 126 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.562-2309C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662400 | |||||||
| chr16:4662459 | C | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.562-2250C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662459 | |||||||
| chr16:4662515 | CA | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0233 a0001c0001t0003g0007 others(5): Show |
8 | HG02155.hp1 HG02486.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2179delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4662515 | ||||||
| chr16:4662543 | TACTC | T | 3 | a0001c0001t0003g0057 a0001c0001t0004g0063 a0001c0001t0004g0070 |
3 | NA18967.hp1 NA18971.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.562-2163_562-2160d others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4662543 | ||||||
| chr16:4662549 | C | A | 1 | a0001c0001t0025g0081 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.562-2160C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662549 | |||||||
| chr16:4662790 | G | C | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.562-1919G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662790 | |||||||
| chr16:4662845 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.562-1864G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662845 | |||||||
| chr16:4662939 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1770C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662939 | |||||||
| chr16:4662950 | G | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.562-1759G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4662950 | |||||||
| chr16:4663086 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-1623C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663086 | |||||||
| chr16:4663114 | A | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1595A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663114 | |||||||
| chr16:4663123 | G | C | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-1586G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663123 | |||||||
| chr16:4663132 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.562-1577C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663132 | |||||||
| chr16:4663225 | G | C | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.562-1484G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663225 | |||||||
| chr16:4663295 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-1414C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663295 | |||||||
| chr16:4663300 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-1409G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663300 | |||||||
| chr16:4663358 | T | C | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-1351T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663358 | |||||||
| chr16:4663365 | G | GT | 106 | a0001c0001t0001g0125 a0001c0001t0001g0183 a0001c0001t0001g0203 others(103): Show |
106 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.562-1318dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | ||||||
| chr16:4663365 | G | GTT | 46 | a0001c0001t0001g0216 a0001c0001t0001g0221 a0001c0001t0001g0223 others(43): Show |
46 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.562-1319_562-1318d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | ||||||
| chr16:4663365 | G | GTTT | 22 | a0001c0001t0001g0224 a0001c0001t0002g0104 a0001c0001t0002g0113 others(19): Show |
22 | HG00558.hp1 HG01123.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.562-1320_562-1318d others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | ||||||
| chr16:4663365 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0123 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.562-1327_562-1318d others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 4663365 | ||||||
| chr16:4663391 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.562-1318T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | |||||||
| chr16:4663391 | T | TTTTA | 92 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.562-1318_562-1317i others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | |||||||
| chr16:4663391 | T | TTTTTA | 20 | a0001c0001t0001g0108 a0001c0001t0001g0159 a0001c0001t0001g0160 others(17): Show |
20 | HG00408.hp2 HG00423.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.562-1318_562-1317i others(7): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663391 | |||||||
| chr16:4663435 | G | A | 1 | a0001c0001t0043g0306 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.562-1274G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663435 | |||||||
| chr16:4663527 | A | G | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-1182A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663527 | |||||||
| chr16:4663607 | G | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.562-1102G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663607 | |||||||
| chr16:4663634 | A | T | 2 | a0001c0001t0003g0013 a0001c0001t0018g0014 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.562-1075A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663634 | |||||||
| chr16:4663757 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.562-952C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663757 | |||||||
| chr16:4663915 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0234 |
2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.562-794C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663915 | |||||||
| chr16:4663923 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-786C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663923 | |||||||
| chr16:4663929 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-780G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663929 | |||||||
| chr16:4663934 | C | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.562-775C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4663934 | |||||||
| chr16:4664105 | G | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.562-604G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664105 | |||||||
| chr16:4664138 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.562-571C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664138 | |||||||
| chr16:4664138 | C | T | 12 | a0001c0001t0002g0151 a0001c0001t0005g0036 a0001c0001t0005g0037 others(9): Show |
12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.562-571C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664138 | |||||||
| chr16:4664183 | G | A | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.562-526G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664183 | |||||||
| chr16:4664346 | G | T | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.562-363G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664346 | |||||||
| chr16:4664364 | T | C | 162 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.562-345T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664364 | |||||||
| chr16:4664391 | C | T | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.562-318C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664391 | |||||||
| chr16:4664552 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.562-157C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664552 | |||||||
| chr16:4664577 | C | T | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-132C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664577 | |||||||
| chr16:4664638 | T | C | 162 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.562-71T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 5/16 | chr16 | 4664638 | |||||||
| chr16:4664835 | T | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+60T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664835 | |||||||
| chr16:4664864 | A | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+89A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664864 | |||||||
| chr16:4664997 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.629-105G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4664997 | |||||||
| chr16:4665009 | C | T | 1 | a0001c0006t0007g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.629-93C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665009 | |||||||
| chr16:4665011 | C | T | 139 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.629-91C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665011 | |||||||
| chr16:4665013 | G | C | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.629-89G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 6/16 | chr16 | 4665013 | |||||||
| chr16:4665218 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.678+67C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665218 | |||||||
| chr16:4665318 | C | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.678+167C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665318 | |||||||
| chr16:4665339 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0032g0124 |
2 | HG01123.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.678+188G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665339 | |||||||
| chr16:4665362 | CT | C | 16 | a0001c0001t0002g0121 a0001c0001t0005g0036 a0001c0001t0005g0037 others(13): Show |
16 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.678+226delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665362 | ||||||
| chr16:4665418 | T | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+267T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665418 | |||||||
| chr16:4665426 | G | A | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.678+275G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665426 | |||||||
| chr16:4665509 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.678+358C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665509 | |||||||
| chr16:4665667 | C | CT | 47 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0159 others(44): Show |
47 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.678+536dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665667 | ||||||
| chr16:4665667 | CT | C | 6 | a0001c0001t0001g0183 a0001c0001t0002g0128 a0001c0001t0004g0009 others(3): Show |
6 | HG01069.hp1 HG01243.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+536delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4665667 | ||||||
| chr16:4665668 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.678+517T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665668 | |||||||
| chr16:4665669 | T | C | 1 | a0001c0001t0002g0308 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.678+518T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665669 | |||||||
| chr16:4665704 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.678+553C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665704 | |||||||
| chr16:4665833 | C | G | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.678+682C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665833 | |||||||
| chr16:4665912 | C | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.678+761C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665912 | |||||||
| chr16:4665969 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.678+818A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665969 | |||||||
| chr16:4665976 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.678+825C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4665976 | |||||||
| chr16:4666061 | C | T | 131 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.678+910C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666061 | |||||||
| chr16:4666075 | T | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+924T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666075 | |||||||
| chr16:4666102 | T | C | 146 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.678+951T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666102 | |||||||
| chr16:4666123 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.678+972C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666123 | |||||||
| chr16:4666202 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.678+1051G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666202 | |||||||
| chr16:4666209 | C | A | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.678+1058C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666209 | |||||||
| chr16:4666225 | T | C | 2 | a0001c0001t0003g0088 a0001c0001t0045g0329 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.678+1074T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666225 | |||||||
| chr16:4666253 | C | T | 131 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.678+1102C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666253 | |||||||
| chr16:4666291 | T | G | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1140T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666291 | |||||||
| chr16:4666316 | G | C | 1 | a0001c0001t0002g0323 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.678+1165G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666316 | |||||||
| chr16:4666328 | C | T | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.678+1177C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666328 | |||||||
| chr16:4666361 | G | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.678+1210G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666361 | |||||||
| chr16:4666516 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0154 |
2 | NA18978.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.678+1365G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666516 | |||||||
| chr16:4666543 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.678+1392A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666543 | |||||||
| chr16:4666616 | G | A | 1 | a0001c0001t0008g0022 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.678+1465G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666616 | |||||||
| chr16:4666633 | T | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+1482T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666633 | |||||||
| chr16:4666754 | CA | C | 5 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0220 others(2): Show |
5 | NA18942.hp2 NA18995.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-1510delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666754 | |||||||
| chr16:4666760 | C | G | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-1505C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666760 | |||||||
| chr16:4666889 | A | G | 238 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.679-1376A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666889 | |||||||
| chr16:4666926 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679-1339C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666926 | |||||||
| chr16:4666968 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.679-1297C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666968 | |||||||
| chr16:4666973 | G | C | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1292G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666973 | |||||||
| chr16:4666991 | T | C | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1274T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4666991 | |||||||
| chr16:4667028 | G | A | 1 | a0001c0001t0046g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.679-1237G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667028 | |||||||
| chr16:4667059 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.679-1206G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667059 | |||||||
| chr16:4667074 | T | G | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-1191T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667074 | |||||||
| chr16:4667085 | C | T | 2 | a0001c0003t0031g0017 a0001c0004t0029g0083 |
2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.679-1180C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667085 | |||||||
| chr16:4667140 | C | T | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-1125C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667140 | |||||||
| chr16:4667144 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.679-1121G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667144 | |||||||
| chr16:4667339 | G | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.679-926G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667339 | |||||||
| chr16:4667396 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.679-869G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667396 | |||||||
| chr16:4667446 | C | T | 2 | a0001c0001t0002g0325 a0001c0001t0003g0053 |
2 | HG00597.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.679-819C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667446 | |||||||
| chr16:4667452 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.679-813C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667452 | |||||||
| chr16:4667467 | T | C | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-798T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667467 | |||||||
| chr16:4667550 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.679-715A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667550 | |||||||
| chr16:4667616 | G | C | 1 | a0001c0001t0002g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-649G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667616 | |||||||
| chr16:4667685 | C | T | 1 | a0002c0007t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.679-580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667685 | |||||||
| chr16:4667686 | T | A | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.679-579T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667686 | |||||||
| chr16:4667710 | T | C | 7 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.679-555T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667710 | |||||||
| chr16:4667895 | G | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.679-370G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667895 | |||||||
| chr16:4667964 | C | T | 1 | a0001c0001t0004g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.679-301C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4667964 | |||||||
| chr16:4668096 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.679-169G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4668096 | |||||||
| chr16:4668124 | C | CT | 8 | a0001c0001t0001g0154 a0001c0001t0001g0267 a0001c0001t0002g0209 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.679-127dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4668124 | ||||||
| chr16:4668124 | CTT | C | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.679-128_679-127del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 4668124 | ||||||
| chr16:4668194 | A | T | 2 | a0001c0003t0031g0017 a0001c0004t0029g0083 |
2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.679-71A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 7/16 | chr16 | 4668194 | |||||||
| chr16:4668387 | A | G | 136 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.726+75A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668387 | |||||||
| chr16:4668428 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.726+116C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668428 | |||||||
| chr16:4668429 | GCTCATAC others(3): Show |
G | 1 | a0001c0001t0036g0198 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.726+128_726+137del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668429 | ||||||
| chr16:4668436 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+124C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668436 | |||||||
| chr16:4668442 | C | G | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.726+130C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668442 | |||||||
| chr16:4668470 | GAC | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+164_726+165del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668470 | ||||||
| chr16:4668484 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+172C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668484 | |||||||
| chr16:4668491 | ACACT | A | 18 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0225 others(15): Show |
18 | HG00621.hp2 HG02027.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.726+183_726+186del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668491 | ||||||
| chr16:4668508 | T | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+196T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668508 | |||||||
| chr16:4668540 | T | C | 1 | a0001c0001t0011g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.726+228T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668540 | |||||||
| chr16:4668558 | CCTA | C | 5 | a0001c0001t0001g0138 a0001c0001t0012g0164 a0001c0001t0012g0191 others(2): Show |
5 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+249_726+251del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668558 | ||||||
| chr16:4668578 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0216 |
2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.726+266C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668578 | |||||||
| chr16:4668610 | ACT | A | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+300_726+301del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668610 | ||||||
| chr16:4668655 | T | C | 158 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.726+343T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668655 | |||||||
| chr16:4668669 | CAT | C | 5 | a0001c0001t0001g0166 a0001c0003t0014g0136 a0001c0003t0014g0137 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+361_726+362del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668669 | ||||||
| chr16:4668677 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.726+365T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668677 | |||||||
| chr16:4668702 | A | G | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.726+390A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668702 | |||||||
| chr16:4668710 | ACACT | A | 10 | a0001c0001t0001g0248 a0001c0001t0002g0147 a0001c0001t0003g0019 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.726+406_726+409del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668710 | ||||||
| chr16:4668727 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0002g0189 |
3 | HG01257.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.726+415C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668727 | |||||||
| chr16:4668727 | CAT | C | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+417_726+418del others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668727 | ||||||
| chr16:4668741 | G | C | 5 | a0001c0001t0022g0045 a0001c0003t0014g0136 a0001c0003t0014g0137 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+429G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668741 | |||||||
| chr16:4668762 | T | TCA | 153 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.726+459_726+460dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668762 | ||||||
| chr16:4668769 | C | CACACAG | 4 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+460_726+461ins others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4668769 | ||||||
| chr16:4668796 | A | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00558.hp2 HG02155.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+484A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668796 | |||||||
| chr16:4668904 | G | A | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.726+592G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668904 | |||||||
| chr16:4668935 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.726+623C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4668935 | |||||||
| chr16:4669009 | GACAC | G | 134 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.726+705_726+708del others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669009 | ||||||
| chr16:4669024 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.726+712A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669024 | |||||||
| chr16:4669036 | A | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0156 a0001c0001t0001g0159 others(1): Show |
4 | NA18939.hp2 NA18949.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+724A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669036 | |||||||
| chr16:4669200 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.726+888G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669200 | |||||||
| chr16:4669348 | G | C | 154 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.726+1036G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669348 | |||||||
| chr16:4669370 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.726+1058G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669370 | |||||||
| chr16:4669383 | G | A | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1071G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669383 | |||||||
| chr16:4669431 | C | CA | 7 | a0001c0001t0002g0113 a0001c0001t0002g0131 a0001c0001t0002g0260 others(4): Show |
7 | HG01123.hp1 HG02622.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+1136dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669431 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0005g0036 a0001c0001t0005g0038 a0001c0001t0005g0039 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.726+1126_726+1136d others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669431 | C | CAAAAAAA others(5): Show |
96 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0115 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.726+1125_726+1136d others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669431 | C | CAAAAAAA others(6): Show |
37 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0123 others(34): Show |
37 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.726+1124_726+1136d others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669431 | C | CAAAAAAA others(7): Show |
10 | a0001c0001t0001g0108 a0001c0001t0001g0146 a0001c0001t0001g0154 others(7): Show |
10 | HG00280.hp1 HG03688.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+1123_726+1136d others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669431 | C | CAAAAAAA others(12): Show |
2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.726+1136_726+1137i others(21): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669431 | ||||||
| chr16:4669458 | C | G | 159 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.726+1146C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669458 | |||||||
| chr16:4669521 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1209C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669521 | |||||||
| chr16:4669526 | A | G | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.726+1214A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669526 | |||||||
| chr16:4669674 | C | T | 1 | a0001c0001t0003g0008 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.726+1362C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669674 | |||||||
| chr16:4669682 | T | C | 2 | a0001c0001t0001g0179 a0003c0009t0001g0168 |
2 | NA18977.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.726+1370T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669682 | |||||||
| chr16:4669697 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.726+1385A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669697 | |||||||
| chr16:4669748 | T | C | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.726+1436T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669748 | |||||||
| chr16:4669804 | C | G | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.726+1492C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669804 | |||||||
| chr16:4669947 | A | G | 4 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0022g0045 others(1): Show |
4 | HG01243.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1444A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669947 | |||||||
| chr16:4669972 | G | GT | 111 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.727-1417dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4669972 | ||||||
| chr16:4669980 | G | A | 124 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.727-1411G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4669980 | |||||||
| chr16:4670093 | C | T | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.727-1298C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670093 | |||||||
| chr16:4670127 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-1264C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670127 | |||||||
| chr16:4670177 | T | TGCC | 20 | a0001c0001t0003g0013 a0001c0001t0004g0009 a0001c0001t0005g0036 others(17): Show |
20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.727-1214_727-1213i others(5): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670177 | |||||||
| chr16:4670373 | G | C | 3 | a0001c0001t0004g0009 a0001c0001t0022g0045 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.727-1018G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670373 | |||||||
| chr16:4670389 | C | T | 127 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.727-1002C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670389 | |||||||
| chr16:4670432 | G | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-959G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670432 | |||||||
| chr16:4670546 | A | G | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.727-845A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670546 | |||||||
| chr16:4670673 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.727-718A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670673 | |||||||
| chr16:4670675 | C | G | 1 | a0001c0001t0002g0309 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.727-716C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670675 | |||||||
| chr16:4670743 | CCAGGTCC others(3): Show |
C | 3 | a0001c0003t0014g0136 a0001c0003t0014g0137 a0001c0003t0031g0017 |
3 | HG01167.hp1 HG01169.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.727-642_727-633del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4670743 | ||||||
| chr16:4670789 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.727-602C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670789 | |||||||
| chr16:4670795 | C | T | 2 | a0001c0001t0002g0250 a0001c0001t0003g0097 |
2 | HG01167.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.727-596C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670795 | |||||||
| chr16:4670801 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-590T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670801 | |||||||
| chr16:4670818 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-573C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670818 | |||||||
| chr16:4670921 | C | T | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.727-470C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670921 | |||||||
| chr16:4670982 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.727-409A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670982 | |||||||
| chr16:4670992 | C | T | 159 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(156): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.727-399C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4670992 | |||||||
| chr16:4671024 | A | C | 162 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.727-367A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671024 | |||||||
| chr16:4671119 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.727-272C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671119 | |||||||
| chr16:4671126 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.727-265G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671126 | |||||||
| chr16:4671173 | G | A | 2 | a0001c0001t0010g0174 a0001c0001t0010g0192 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.727-218G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671173 | |||||||
| chr16:4671218 | TG | T | 4 | a0001c0001t0001g0138 a0001c0001t0012g0164 a0001c0001t0012g0191 others(1): Show |
4 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-168delG | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 4671218 | ||||||
| chr16:4671258 | C | T | 8 | a0001c0001t0001g0153 a0001c0001t0001g0225 a0001c0001t0003g0057 others(5): Show |
8 | HG00621.hp2 HG02027.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-133C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671258 | |||||||
| chr16:4671276 | C | G | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-115C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671276 | |||||||
| chr16:4671287 | T | G | 7 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0022g0045 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.727-104T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671287 | |||||||
| chr16:4671352 | A | G | 3 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0026g0334 |
3 | HG01243.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.727-39A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 8/16 | chr16 | 4671352 | |||||||
| chr16:4671467 | T | C | 169 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
splice_region_variant&intron_variant | LOW | c.795+8T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671467 | |||||||
| chr16:4671537 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0219 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.795+78G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671537 | |||||||
| chr16:4671582 | ACAT | A | 68 | a0001c0001t0001g0304 a0001c0001t0001g0307 a0001c0001t0001g0314 others(65): Show |
68 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.795+127_795+129del others(3): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 4671582 | ||||||
| chr16:4671589 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.795+130T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671589 | |||||||
| chr16:4671654 | C | G | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.795+195C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671654 | |||||||
| chr16:4671692 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.795+233G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671692 | |||||||
| chr16:4671739 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.795+280G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671739 | |||||||
| chr16:4671755 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0006g0252 |
2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.795+296C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671755 | |||||||
| chr16:4671757 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0046g0107 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.795+298G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671757 | |||||||
| chr16:4671764 | C | G | 1 | a0001c0001t0002g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.795+305C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671764 | |||||||
| chr16:4671770 | TC | T | 4 | a0001c0001t0005g0036 a0001c0001t0005g0038 a0001c0001t0005g0039 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+315delC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 4671770 | ||||||
| chr16:4671779 | A | G | 1 | a0001c0001t0003g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.795+320A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671779 | |||||||
| chr16:4671839 | T | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795+380T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671839 | |||||||
| chr16:4671884 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0328 a0001c0001t0009g0332 |
3 | HG02165.hp2 NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.795+425T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671884 | |||||||
| chr16:4671932 | G | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.795+473G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4671932 | |||||||
| chr16:4672054 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.795+595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672054 | |||||||
| chr16:4672067 | G | A | 1 | a0001c0001t0004g0070 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.795+608G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672067 | |||||||
| chr16:4672106 | A | G | 1 | a0001c0001t0033g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795+647A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672106 | |||||||
| chr16:4672156 | G | A | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.795+697G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672156 | |||||||
| chr16:4672166 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.795+707A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672166 | |||||||
| chr16:4672184 | G | T | 3 | a0001c0001t0002g0279 a0001c0001t0002g0303 a0001c0001t0006g0277 |
3 | HG00597.hp1 HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.795+725G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672184 | |||||||
| chr16:4672196 | G | A | 1 | a0001c0001t0002g0308 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.795+737G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672196 | |||||||
| chr16:4672200 | A | G | 162 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.795+741A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672200 | |||||||
| chr16:4672203 | C | A | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.795+744C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672203 | |||||||
| chr16:4672381 | G | A | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.795+922G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672381 | |||||||
| chr16:4672405 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0035 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.795+946T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672405 | |||||||
| chr16:4672491 | G | C | 11 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(8): Show |
11 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-1007G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672491 | |||||||
| chr16:4672591 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.796-907G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4672591 | |||||||
| chr16:4673016 | T | G | 1 | a0001c0001t0019g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.796-482T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673016 | |||||||
| chr16:4673096 | C | T | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.796-402C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673096 | |||||||
| chr16:4673180 | A | C | 1 | a0001c0001t0041g0322 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.796-318A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673180 | |||||||
| chr16:4673450 | A | G | 159 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.796-48A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 9/16 | chr16 | 4673450 | |||||||
| chr16:4673748 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.955+91C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673748 | |||||||
| chr16:4673758 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.955+101T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673758 | |||||||
| chr16:4673775 | C | G | 1 | a0001c0001t0045g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.955+118C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673775 | |||||||
| chr16:4673816 | G | A | 3 | a0001c0001t0002g0194 a0001c0001t0002g0218 a0001c0001t0002g0219 |
3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955+159G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673816 | |||||||
| chr16:4673816 | G | C | 1 | a0001c0001t0002g0309 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.955+159G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673816 | |||||||
| chr16:4673823 | G | C | 2 | a0001c0003t0031g0017 a0001c0004t0029g0083 |
2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.955+166G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673823 | |||||||
| chr16:4673834 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.955+177A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673834 | |||||||
| chr16:4673869 | T | A | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0242 |
3 | NA18942.hp2 NA18995.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.955+212T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673869 | |||||||
| chr16:4673902 | C | T | 3 | a0001c0001t0002g0194 a0001c0001t0002g0218 a0001c0001t0002g0219 |
3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.955+245C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673902 | |||||||
| chr16:4673910 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.955+253A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4673910 | |||||||
| chr16:4673977 | CTTATTTT others(4): Show |
C | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+326_955+336del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4673977 | ||||||
| chr16:4674001 | G | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+344G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674001 | |||||||
| chr16:4674076 | C | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.955+419C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674076 | |||||||
| chr16:4674165 | T | G | 157 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.955+508T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674165 | |||||||
| chr16:4674199 | G | A | 1 | a0001c0001t0007g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.955+542G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674199 | |||||||
| chr16:4674216 | T | TCAAGTAA others(5): Show |
1 | a0001c0001t0002g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.955+561_955+572dup others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674216 | ||||||
| chr16:4674276 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955+619G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674276 | |||||||
| chr16:4674320 | G | A | 1 | a0001c0001t0037g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.955+663G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674320 | |||||||
| chr16:4674337 | G | A | 3 | a0001c0001t0021g0032 a0001c0003t0031g0017 a0001c0004t0029g0083 |
3 | HG02809.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955+680G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674337 | |||||||
| chr16:4674353 | G | A | 152 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(149): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.955+696G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674353 | |||||||
| chr16:4674370 | A | C | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+713A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674370 | |||||||
| chr16:4674370 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+713A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674370 | |||||||
| chr16:4674522 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0154 a0001c0001t0035g0118 |
3 | NA18978.hp2 NA18999.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.955+865C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674522 | |||||||
| chr16:4674567 | G | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG01175.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+910G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674567 | |||||||
| chr16:4674578 | C | CT | 7 | a0001c0001t0001g0231 a0001c0001t0002g0301 a0001c0001t0019g0006 others(4): Show |
7 | HG02809.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+933dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674578 | ||||||
| chr16:4674581 | TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0003g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.955+949_955+968del others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674581 | ||||||
| chr16:4674586 | T | TTTTTTTC others(5): Show |
1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955+933_955+934ins others(12): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674586 | ||||||
| chr16:4674587 | TTTTCTTT others(7): Show |
T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.955+934_955+947del others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674587 | ||||||
| chr16:4674596 | CTTTTCTT others(3): Show |
C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0299 |
2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.955+949_955+958del others(10): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674596 | ||||||
| chr16:4674601 | C | CT | 30 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0115 others(27): Show |
30 | HG00140.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.955+953dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674601 | ||||||
| chr16:4674601 | CTTTTTTT others(21): Show |
C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+954_955+981del others(28): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674601 | ||||||
| chr16:4674602 | T | TTTTTTTT others(17): Show |
1 | a0001c0001t0001g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.955+958_955+959ins others(24): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674602 | ||||||
| chr16:4674606 | T | C | 2 | a0001c0001t0004g0009 a0001c0001t0027g0002 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.955+949T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674606 | |||||||
| chr16:4674611 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.955+954C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674611 | |||||||
| chr16:4674616 | C | A | 5 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0330 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+959C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674616 | |||||||
| chr16:4674616 | CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0002g0253 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.955+964_955+974del others(11): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674616 | ||||||
| chr16:4674626 | C | CT | 125 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0110 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.955+994dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | ||||||
| chr16:4674626 | C | CTT | 35 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0138 others(32): Show |
35 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.955+993_955+994dup others(2): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | ||||||
| chr16:4674626 | C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0169 others(1): Show |
4 | HG00408.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+978_955+979ins others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | ||||||
| chr16:4674626 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0331 a0004c0005t0001g0144 |
2 | HG00621.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.955+978_955+979ins others(27): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4674626 | ||||||
| chr16:4674626 | C | T | 2 | a0001c0001t0004g0009 a0001c0001t0019g0006 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.955+969C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674626 | |||||||
| chr16:4674631 | T | C | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(6): Show |
9 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+974T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674631 | |||||||
| chr16:4674634 | T | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.955+977T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674634 | |||||||
| chr16:4674636 | T | C | 1 | a0001c0001t0016g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.955+979T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674636 | |||||||
| chr16:4674664 | C | T | 112 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.955+1007C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674664 | |||||||
| chr16:4674786 | G | A | 18 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0225 others(15): Show |
18 | HG00621.hp2 HG02027.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.955+1129G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674786 | |||||||
| chr16:4674790 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.955+1133G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674790 | |||||||
| chr16:4674796 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0004g0080 a0001c0001t0018g0014 |
3 | HG02723.hp2 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.955+1139G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674796 | |||||||
| chr16:4674825 | A | G | 4 | a0001c0001t0004g0009 a0001c0001t0019g0006 a0001c0001t0022g0045 others(1): Show |
4 | HG01243.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+1168A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674825 | |||||||
| chr16:4674831 | G | A | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.955+1174G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674831 | |||||||
| chr16:4674947 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.955+1290C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4674947 | |||||||
| chr16:4675393 | C | T | 13 | a0001c0001t0005g0036 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
13 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.955+1736C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675393 | |||||||
| chr16:4675449 | T | C | 154 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.955+1792T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675449 | |||||||
| chr16:4675610 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1853A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675610 | |||||||
| chr16:4675650 | G | C | 2 | a0001c0001t0019g0006 a0001c0001t0026g0334 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1813G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675650 | |||||||
| chr16:4675653 | C | G | 2 | a0001c0001t0006g0127 a0001c0001t0006g0152 |
2 | HG01074.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.956-1810C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675653 | |||||||
| chr16:4675698 | C | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1765C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675698 | |||||||
| chr16:4675733 | C | CA | 7 | a0001c0001t0001g0110 a0001c0001t0001g0203 a0001c0001t0001g0215 others(4): Show |
7 | HG00735.hp2 HG02074.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.956-1713dupA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 4675733 | ||||||
| chr16:4675735 | A | G | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-1728A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675735 | |||||||
| chr16:4675817 | A | G | 4 | a0001c0001t0003g0057 a0001c0001t0004g0063 a0001c0001t0004g0069 others(1): Show |
4 | HG02027.hp2 NA18967.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-1646A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675817 | |||||||
| chr16:4675843 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1620A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675843 | |||||||
| chr16:4675857 | G | T | 2 | a0001c0001t0002g0113 a0001c0001t0047g0114 |
2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.956-1606G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675857 | |||||||
| chr16:4675862 | C | T | 129 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.956-1601C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675862 | |||||||
| chr16:4675900 | T | C | 1 | a0001c0001t0007g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.956-1563T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675900 | |||||||
| chr16:4675910 | G | A | 2 | a0001c0001t0019g0006 a0001c0001t0026g0334 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1553G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675910 | |||||||
| chr16:4675919 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1544C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4675919 | |||||||
| chr16:4676001 | C | T | 2 | a0001c0001t0019g0006 a0001c0001t0026g0334 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.956-1462C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676001 | |||||||
| chr16:4676007 | A | G | 166 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.956-1456A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676007 | |||||||
| chr16:4676045 | C | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0008g0022 |
3 | HG02486.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.956-1418C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676045 | |||||||
| chr16:4676102 | C | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-1361C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676102 | |||||||
| chr16:4676227 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.956-1236G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676227 | |||||||
| chr16:4676374 | T | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-1089T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676374 | |||||||
| chr16:4676450 | C | G | 150 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.956-1013C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676450 | |||||||
| chr16:4676466 | G | T | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.956-997G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676466 | |||||||
| chr16:4676470 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.956-993G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676470 | |||||||
| chr16:4676477 | C | T | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-986C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676477 | |||||||
| chr16:4676556 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-907C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676556 | |||||||
| chr16:4676578 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.956-885C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676578 | |||||||
| chr16:4676611 | C | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.956-852C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676611 | |||||||
| chr16:4676612 | T | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-851T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676612 | |||||||
| chr16:4676626 | C | G | 2 | a0001c0001t0004g0009 a0001c0001t0027g0002 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.956-837C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676626 | |||||||
| chr16:4676635 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.956-828C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676635 | |||||||
| chr16:4676636 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-827A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676636 | |||||||
| chr16:4676703 | A | C | 1 | a0001c0001t0003g0067 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.956-760A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676703 | |||||||
| chr16:4676805 | C | G | 1 | a0001c0001t0003g0031 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.956-658C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676805 | |||||||
| chr16:4676837 | G | A | 2 | a0001c0001t0021g0032 a0001c0004t0029g0083 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.956-626G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676837 | |||||||
| chr16:4676848 | G | A | 1 | a0001c0001t0008g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.956-615G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676848 | |||||||
| chr16:4676875 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.956-588C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676875 | |||||||
| chr16:4676876 | G | A | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.956-587G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676876 | |||||||
| chr16:4676970 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0002g0121 |
2 | HG01952.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.956-493G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676970 | |||||||
| chr16:4676975 | C | T | 14 | a0001c0001t0003g0088 a0001c0001t0005g0033 a0001c0001t0005g0091 others(11): Show |
14 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.956-488C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4676975 | |||||||
| chr16:4677037 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.956-426G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677037 | |||||||
| chr16:4677047 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.956-416G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677047 | |||||||
| chr16:4677075 | A | T | 1 | a0001c0001t0004g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.956-388A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677075 | |||||||
| chr16:4677101 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-362C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677101 | |||||||
| chr16:4677127 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.956-336G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677127 | |||||||
| chr16:4677179 | A | G | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.956-284A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677179 | |||||||
| chr16:4677331 | G | A | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.956-132G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677331 | |||||||
| chr16:4677359 | G | A | 1 | a0001c0001t0013g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.956-104G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677359 | |||||||
| chr16:4677399 | G | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.956-64G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677399 | |||||||
| chr16:4677460 | C | T | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.956-3C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 10/16 | chr16 | 4677460 | |||||||
| chr16:4677677 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1065+105G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677677 | |||||||
| chr16:4677799 | A | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1065+227A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677799 | |||||||
| chr16:4677836 | C | CT | 29 | a0001c0001t0002g0113 a0001c0001t0002g0151 a0001c0001t0002g0242 others(26): Show |
29 | HG00408.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1065+282dupT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4677836 | ||||||
| chr16:4677836 | CT | C | 147 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1065+282delT | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4677836 | ||||||
| chr16:4677856 | T | C | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+284T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677856 | |||||||
| chr16:4677884 | C | T | 2 | a0001c0001t0021g0032 a0001c0004t0029g0083 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1065+312C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677884 | |||||||
| chr16:4677885 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1065+313G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677885 | |||||||
| chr16:4677912 | A | T | 1 | a0001c0001t0002g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1065+340A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677912 | |||||||
| chr16:4677948 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1065+376A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677948 | |||||||
| chr16:4677952 | A | G | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1065+380A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677952 | |||||||
| chr16:4677986 | C | A | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1065+414C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677986 | |||||||
| chr16:4677988 | C | T | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1065+416C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677988 | |||||||
| chr16:4677989 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1065+417G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4677989 | |||||||
| chr16:4678165 | A | G | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+593A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678165 | |||||||
| chr16:4678166 | G | T | 2 | a0001c0001t0016g0012 a0001c0001t0017g0042 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1065+594G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678166 | |||||||
| chr16:4678223 | C | T | 1 | a0001c0001t0003g0058 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1065+651C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678223 | |||||||
| chr16:4678224 | G | A | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1065+652G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678224 | |||||||
| chr16:4678287 | A | AGG | 125 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.1065+717_1065+718d others(4): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4678287 | ||||||
| chr16:4678318 | AAGAC | A | 3 | a0001c0001t0005g0094 a0001c0001t0016g0012 a0001c0001t0017g0042 |
3 | HG03098.hp1 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1065+754_1065+757d others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4678318 | ||||||
| chr16:4678357 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1065+785A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678357 | |||||||
| chr16:4678526 | T | C | 151 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1065+954T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678526 | |||||||
| chr16:4678536 | C | T | 3 | a0001c0001t0002g0131 a0001c0001t0006g0127 a0001c0001t0006g0152 |
3 | HG01074.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1065+964C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678536 | |||||||
| chr16:4678704 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1065+1132G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678704 | |||||||
| chr16:4678705 | C | T | 1 | a0001c0001t0028g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1065+1133C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678705 | |||||||
| chr16:4678836 | C | G | 1 | a0001c0001t0004g0052 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1066-1196C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678836 | |||||||
| chr16:4678857 | C | T | 3 | a0001c0001t0027g0002 a0001c0003t0014g0136 a0001c0003t0014g0137 |
3 | HG01167.hp1 HG01169.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1066-1175C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678857 | |||||||
| chr16:4678861 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-1171C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678861 | |||||||
| chr16:4678931 | A | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1066-1101A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678931 | |||||||
| chr16:4678945 | T | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-1087T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678945 | |||||||
| chr16:4678976 | A | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-1056A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4678976 | |||||||
| chr16:4679129 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1066-903G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679129 | |||||||
| chr16:4679142 | G | A | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1066-890G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679142 | |||||||
| chr16:4679319 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0234 |
2 | HG00099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1066-713C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679319 | |||||||
| chr16:4679453 | C | T | 1 | a0001c0001t0002g0305 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1066-579C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679453 | |||||||
| chr16:4679480 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-552C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679480 | |||||||
| chr16:4679508 | C | T | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-524C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679508 | |||||||
| chr16:4679627 | C | T | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-405C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679627 | |||||||
| chr16:4679669 | C | A | 1 | a0001c0001t0023g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1066-363C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679669 | |||||||
| chr16:4679680 | C | T | 1 | a0001c0001t0023g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1066-352C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679680 | |||||||
| chr16:4679680 | CCCTGCAC others(4): Show |
C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-345_1066-335d others(13): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr16 | 4679680 | ||||||
| chr16:4679769 | G | A | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-263G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679769 | |||||||
| chr16:4679779 | A | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1066-253A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679779 | |||||||
| chr16:4679780 | T | A | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-252T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679780 | |||||||
| chr16:4679781 | G | T | 1 | a0001c0001t0002g0301 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1066-251G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679781 | |||||||
| chr16:4679828 | C | G | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-204C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679828 | |||||||
| chr16:4679905 | G | A | 1 | a0001c0001t0047g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1066-127G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679905 | |||||||
| chr16:4679910 | C | T | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1066-122C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679910 | |||||||
| chr16:4679991 | G | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1066-41G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 11/16 | chr16 | 4679991 | |||||||
| chr16:4680134 | C | G | 1 | a0001c0001t0045g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1131+37C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680134 | |||||||
| chr16:4680135 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1131+38C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680135 | |||||||
| chr16:4680172 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1131+75C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680172 | |||||||
| chr16:4680201 | A | C | 4 | a0001c0001t0002g0161 a0001c0001t0002g0298 a0001c0001t0002g0300 others(1): Show |
4 | HG02647.hp1 HG03195.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131+104A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680201 | |||||||
| chr16:4680233 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1131+136G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680233 | |||||||
| chr16:4680263 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1131+166G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680263 | |||||||
| chr16:4680269 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1131+172G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680269 | |||||||
| chr16:4680325 | C | G | 2 | a0001c0001t0002g0189 a0001c0001t0011g0056 |
2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1131+228C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680325 | |||||||
| chr16:4680397 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1131+300A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680397 | |||||||
| chr16:4680419 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1131+322G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680419 | |||||||
| chr16:4680464 | C | T | 2 | a0001c0001t0002g0247 a0001c0001t0003g0068 |
2 | HG02083.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1131+367C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680464 | |||||||
| chr16:4680576 | C | T | 1 | a0001c0006t0007g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+479C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680576 | |||||||
| chr16:4680578 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1131+481C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680578 | |||||||
| chr16:4680579 | C | T | 3 | a0001c0001t0004g0051 a0001c0001t0004g0060 a0001c0001t0004g0061 |
3 | HG00099.hp2 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1131+482C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680579 | |||||||
| chr16:4680685 | A | T | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1131+588A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680685 | |||||||
| chr16:4680790 | C | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1131+693C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680790 | |||||||
| chr16:4680791 | G | A | 1 | a0001c0001t0045g0329 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1131+694G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680791 | |||||||
| chr16:4680869 | C | G | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1132-681C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680869 | |||||||
| chr16:4680979 | C | T | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1132-571C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4680979 | |||||||
| chr16:4681128 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1132-422C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681128 | |||||||
| chr16:4681154 | G | A | 150 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(147): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1132-396G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681154 | |||||||
| chr16:4681181 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1132-369C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681181 | |||||||
| chr16:4681253 | G | A | 1 | a0002c0007t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1132-297G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681253 | |||||||
| chr16:4681296 | G | T | 1 | a0001c0001t0002g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1132-254G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681296 | |||||||
| chr16:4681335 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1132-215C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681335 | |||||||
| chr16:4681375 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1132-175C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681375 | |||||||
| chr16:4681400 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1132-150C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681400 | |||||||
| chr16:4681493 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-57G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681493 | |||||||
| chr16:4681532 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-18C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 12/16 | chr16 | 4681532 | |||||||
| chr16:4681907 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1358+131C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681907 | |||||||
| chr16:4681928 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1358+152G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681928 | |||||||
| chr16:4681975 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+199G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681975 | |||||||
| chr16:4681978 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1358+202C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4681978 | |||||||
| chr16:4682009 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1358+233G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682009 | |||||||
| chr16:4682121 | T | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+345T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682121 | |||||||
| chr16:4682156 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1358+380G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682156 | |||||||
| chr16:4682180 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1358+404A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682180 | |||||||
| chr16:4682223 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1358+447C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682223 | |||||||
| chr16:4682244 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0011g0021 |
3 | HG02615.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1358+468C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682244 | |||||||
| chr16:4682326 | C | T | 2 | a0001c0001t0033g0184 a0001c0001t0034g0185 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1359-497C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682326 | |||||||
| chr16:4682356 | C | T | 6 | a0001c0001t0001g0108 a0001c0001t0001g0154 a0001c0001t0001g0179 others(3): Show |
6 | NA18977.hp2 NA18978.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.1359-467C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682356 | |||||||
| chr16:4682507 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1359-316G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682507 | |||||||
| chr16:4682598 | G | C | 3 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0034 |
3 | HG02280.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1359-225G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | chr16 | 4682598 | |||||||
| chr16:4682600 | G | GTGTCGGG others(8): Show |
1 | a0001c0001t0011g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1359-215_1359-201d others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 4682600 | ||||||
| chr16:4682957 | C | G | 2 | a0001c0001t0006g0310 a0001c0001t0006g0311 |
2 | HG02155.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1482+11C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682957 | |||||||
| chr16:4682978 | C | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1482+32C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682978 | |||||||
| chr16:4682989 | G | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1482+43G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4682989 | |||||||
| chr16:4683055 | T | C | 1 | a0001c0001t0002g0298 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1482+109T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683055 | |||||||
| chr16:4683068 | C | G | 1 | a0001c0006t0007g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1482+122C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683068 | |||||||
| chr16:4683076 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1482+130C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 14/16 | chr16 | 4683076 | |||||||
| chr16:4683281 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528+12C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683281 | |||||||
| chr16:4683310 | C | T | 3 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0326 |
3 | HG01074.hp2 HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1528+41C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683310 | |||||||
| chr16:4683326 | T | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0289 |
2 | NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1528+57T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683326 | |||||||
| chr16:4683344 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | HG00735.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1528+75C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683344 | |||||||
| chr16:4683375 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1528+106C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683375 | |||||||
| chr16:4683422 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1528+153C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683422 | |||||||
| chr16:4683537 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528+268C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683537 | |||||||
| chr16:4683541 | T | G | 155 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1528+272T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683541 | |||||||
| chr16:4683551 | A | T | 3 | a0001c0001t0019g0006 a0001c0001t0026g0334 a0001c0001t0027g0002 |
3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1528+282A>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683551 | |||||||
| chr16:4683556 | CA | C | 158 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(155): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1529-275delA | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr16 | 4683556 | ||||||
| chr16:4683700 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1529-143G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 15/16 | chr16 | 4683700 | |||||||
| chr16:4683946 | G | A | 1 | a0001c0003t0031g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1618+14G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4683946 | |||||||
| chr16:4684184 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1618+252G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684184 | |||||||
| chr16:4684270 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0193 |
3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1618+338C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684270 | |||||||
| chr16:4684271 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+339G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684271 | |||||||
| chr16:4684310 | G | C | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+378G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684310 | |||||||
| chr16:4684332 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0003g0035 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1618+400C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684332 | |||||||
| chr16:4684391 | G | A | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+459G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684391 | |||||||
| chr16:4684414 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+482C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684414 | |||||||
| chr16:4684419 | G | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+487G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684419 | |||||||
| chr16:4684428 | G | C | 3 | a0001c0001t0007g0075 a0001c0001t0007g0076 a0001c0001t0021g0032 |
3 | HG03209.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1618+496G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684428 | |||||||
| chr16:4684464 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+532G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684464 | |||||||
| chr16:4684512 | C | T | 147 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(144): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1618+580C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684512 | |||||||
| chr16:4684546 | C | T | 3 | a0001c0001t0019g0006 a0001c0001t0026g0334 a0001c0001t0027g0002 |
3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1618+614C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684546 | |||||||
| chr16:4684552 | C | T | 5 | a0001c0001t0008g0023 a0001c0001t0008g0024 a0001c0001t0008g0026 others(2): Show |
5 | HG02559.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1618+620C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684552 | |||||||
| chr16:4684578 | G | A | 1 | a0001c0001t0009g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1618+646G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684578 | |||||||
| chr16:4684589 | T | C | 300 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(297): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1618+657T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684589 | |||||||
| chr16:4684631 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1618+699G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684631 | |||||||
| chr16:4684694 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1618+762C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684694 | |||||||
| chr16:4684705 | C | T | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1618+773C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684705 | |||||||
| chr16:4684726 | G | C | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1618+794G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684726 | |||||||
| chr16:4684743 | T | C | 1 | a0001c0001t0003g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1618+811T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684743 | |||||||
| chr16:4684786 | C | G | 3 | a0001c0001t0019g0006 a0001c0001t0026g0334 a0001c0001t0027g0002 |
3 | HG01884.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1618+854C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684786 | |||||||
| chr16:4684944 | G | T | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1618+1012G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4684944 | |||||||
| chr16:4685004 | AGTGGCCT others(6): Show |
A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA19064.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1618+1073_1618+108 others(17): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685004 | |||||||
| chr16:4685186 | T | G | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1618+1254T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685186 | |||||||
| chr16:4685264 | T | C | 4 | a0001c0001t0019g0006 a0001c0001t0021g0032 a0001c0001t0026g0334 others(1): Show |
4 | HG01884.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1618+1332T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685264 | |||||||
| chr16:4685299 | TCTCAGAG others(12): Show |
T | 1 | a0001c0001t0002g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1618+1371_1618+138 others(23): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4685299 | ||||||
| chr16:4685385 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1618+1453C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685385 | |||||||
| chr16:4685499 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1618+1567C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685499 | |||||||
| chr16:4685527 | C | T | 154 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1618+1595C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685527 | |||||||
| chr16:4685552 | T | C | 1 | a0001c0001t0001g0328 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1618+1620T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685552 | |||||||
| chr16:4685630 | T | C | 1 | a0001c0004t0029g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1618+1698T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685630 | |||||||
| chr16:4685630 | T | G | 156 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1618+1698T>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685630 | |||||||
| chr16:4685633 | G | A | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1618+1701G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685633 | |||||||
| chr16:4685643 | C | T | 10 | a0001c0001t0001g0145 a0001c0001t0001g0169 a0001c0001t0001g0172 others(7): Show |
10 | HG01070.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1618+1711C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685643 | |||||||
| chr16:4685702 | C | G | 1 | a0001c0001t0006g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1618+1770C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685702 | |||||||
| chr16:4685904 | C | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0227 a0001c0001t0039g0155 |
3 | NA18964.hp2 NA18975.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1618+1972C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685904 | |||||||
| chr16:4685948 | C | G | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1618+2016C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4685948 | |||||||
| chr16:4686018 | G | T | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1618+2086G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686018 | |||||||
| chr16:4686063 | G | A | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1618+2131G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686063 | |||||||
| chr16:4686079 | TTCTGGCT others(4): Show |
T | 132 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1618+2152_1618+216 others(15): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4686079 | ||||||
| chr16:4686096 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1618+2164C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686096 | |||||||
| chr16:4686114 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+2182C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686114 | |||||||
| chr16:4686214 | G | C | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1618+2282G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686214 | |||||||
| chr16:4686224 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1618+2292C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686224 | |||||||
| chr16:4686250 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1618+2318T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686250 | |||||||
| chr16:4686315 | C | T | 162 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1618+2383C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686315 | |||||||
| chr16:4686365 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1619-2431T>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686365 | |||||||
| chr16:4686419 | G | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1619-2377G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686419 | |||||||
| chr16:4686531 | C | T | 1 | a0001c0001t0020g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1619-2265C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686531 | |||||||
| chr16:4686694 | C | A | 1 | a0001c0001t0003g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1619-2102C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686694 | |||||||
| chr16:4686716 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0002g0132 a0001c0001t0002g0227 others(1): Show |
4 | HG02683.hp1 NA18964.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1619-2080G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686716 | |||||||
| chr16:4686822 | G | A | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1619-1974G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686822 | |||||||
| chr16:4686833 | G | A | 157 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1619-1963G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4686833 | |||||||
| chr16:4687016 | C | T | 1 | a0001c0001t0021g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1619-1780C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687016 | |||||||
| chr16:4687134 | C | T | 3 | a0001c0001t0016g0012 a0001c0001t0017g0042 a0001c0003t0031g0017 |
3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-1662C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687134 | |||||||
| chr16:4687207 | T | TC | 153 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1619-1582dupC | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687207 | ||||||
| chr16:4687221 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0213 others(3): Show |
6 | HG00280.hp1 HG00323.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-1575C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687221 | |||||||
| chr16:4687299 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1619-1497C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687299 | |||||||
| chr16:4687312 | G | A | 3 | a0001c0001t0016g0012 a0001c0001t0017g0042 a0001c0003t0031g0017 |
3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-1484G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687312 | |||||||
| chr16:4687364 | C | G | 2 | a0001c0001t0003g0013 a0001c0001t0018g0014 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1619-1432C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687364 | |||||||
| chr16:4687382 | G | A | 154 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1619-1414G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687382 | |||||||
| chr16:4687405 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1619-1391C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687405 | |||||||
| chr16:4687463 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1619-1333C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687463 | |||||||
| chr16:4687528 | A | C | 16 | a0001c0001t0003g0088 a0001c0001t0004g0089 a0001c0001t0005g0033 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1619-1268A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687528 | |||||||
| chr16:4687534 | A | C | 1 | a0001c0001t0038g0254 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-1262A>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687534 | |||||||
| chr16:4687578 | T | TAC | 26 | a0001c0001t0001g0203 a0001c0001t0001g0215 a0001c0001t0001g0269 others(23): Show |
26 | HG00544.hp1 HG00673.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1619-1189_1619-118 others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACAC | 6 | a0001c0001t0002g0173 a0001c0001t0002g0273 a0001c0001t0002g0274 others(3): Show |
6 | HG00738.hp1 HG01081.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1619-1191_1619-118 others(8): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(3): Show |
10 | a0001c0001t0001g0233 a0001c0001t0001g0293 a0001c0001t0005g0036 others(7): Show |
10 | HG01943.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1619-1197_1619-118 others(14): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(5): Show |
11 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0251 others(8): Show |
11 | HG01891.hp2 HG02056.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1619-1199_1619-118 others(16): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(7): Show |
88 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1619-1201_1619-118 others(18): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(9): Show |
19 | a0001c0001t0001g0133 a0001c0001t0001g0149 a0001c0001t0001g0159 others(16): Show |
19 | HG00099.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1619-1203_1619-118 others(20): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(11): Show |
8 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0125 others(5): Show |
8 | HG00280.hp2 HG00621.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1619-1205_1619-118 others(22): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(13): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0217 others(2): Show |
5 | HG00280.hp1 HG00323.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-1207_1619-118 others(24): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0270 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1619-1209_1619-118 others(26): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | T | TACACACA others(21): Show |
2 | a0001c0001t0001g0213 a0001c0001t0001g0259 |
2 | HG01192.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1619-1215_1619-118 others(32): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687578 | TAC | T | 5 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0034 others(2): Show |
5 | HG00544.hp2 HG02083.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-1189_1619-118 others(6): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 4687578 | ||||||
| chr16:4687580 | C | T | 1 | a0001c0001t0038g0254 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-1216C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687580 | |||||||
| chr16:4687608 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0110 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1619-1188_1619-118 others(19): Show |
MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687608 | |||||||
| chr16:4687678 | C | G | 1 | a0001c0001t0002g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1619-1118C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687678 | |||||||
| chr16:4687721 | C | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1619-1075C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687721 | |||||||
| chr16:4687736 | C | T | 9 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0157 others(6): Show |
9 | HG00544.hp1 HG00673.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1619-1060C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687736 | |||||||
| chr16:4687759 | C | T | 1 | a0001c0001t0003g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1619-1037C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687759 | |||||||
| chr16:4687949 | G | A | 2 | a0001c0003t0014g0136 a0001c0003t0014g0137 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1619-847G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687949 | |||||||
| chr16:4687954 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1619-842C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687954 | |||||||
| chr16:4687975 | G | T | 1 | a0001c0001t0002g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1619-821G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687975 | |||||||
| chr16:4687980 | G | A | 116 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0001g0115 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1619-816G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687980 | |||||||
| chr16:4687983 | C | T | 1 | a0001c0001t0004g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1619-813C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4687983 | |||||||
| chr16:4688010 | C | T | 1 | a0001c0001t0007g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1619-786C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688010 | |||||||
| chr16:4688053 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1619-743C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688053 | |||||||
| chr16:4688105 | C | T | 1 | a0001c0001t0027g0002 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1619-691C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688105 | |||||||
| chr16:4688123 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1619-673C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688123 | |||||||
| chr16:4688194 | C | T | 3 | a0001c0001t0002g0194 a0001c0001t0002g0218 a0001c0001t0002g0219 |
3 | HG01106.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1619-602C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688194 | |||||||
| chr16:4688195 | G | A | 1 | a0001c0001t0026g0334 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1619-601G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688195 | |||||||
| chr16:4688250 | T | C | 207 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(204): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1619-546T>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688250 | |||||||
| chr16:4688251 | G | C | 1 | a0001c0001t0038g0254 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1619-545G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688251 | |||||||
| chr16:4688324 | C | T | 1 | a0001c0001t0034g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1619-472C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688324 | |||||||
| chr16:4688330 | A | G | 1 | a0001c0001t0022g0045 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1619-466A>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688330 | |||||||
| chr16:4688386 | C | T | 5 | a0001c0001t0001g0235 a0001c0001t0004g0052 a0001c0001t0012g0164 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1619-410C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688386 | |||||||
| chr16:4688387 | C | A | 3 | a0001c0001t0002g0109 a0001c0001t0002g0180 a0001c0001t0002g0181 |
3 | HG04184.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1619-409C>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688387 | |||||||
| chr16:4688387 | C | G | 328 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0108 others(325): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1619-409C>G | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688387 | |||||||
| chr16:4688485 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0224 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1619-311G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688485 | |||||||
| chr16:4688517 | C | T | 1 | a0001c0001t0024g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1619-279C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688517 | |||||||
| chr16:4688528 | C | T | 3 | a0001c0001t0016g0012 a0001c0001t0017g0042 a0001c0003t0031g0017 |
3 | HG03098.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1619-268C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688528 | |||||||
| chr16:4688593 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1619-203G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688593 | |||||||
| chr16:4688689 | G | C | 1 | a0001c0001t0003g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1619-107G>C | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688689 | |||||||
| chr16:4688755 | G | T | 1 | a0001c0001t0002g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1619-41G>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688755 | |||||||
| chr16:4688785 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1619-11C>T | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688785 | |||||||
| chr16:4688792 | G | A | 1 | a0001c0001t0011g0066 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.1619-4G>A | MGRN1 | ENSG00000102858.13 | transcript | ENST00000262370.12 | protein_coding | 16/16 | chr16 | 4688792 |