Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29106 |
| ensemblid | ENSG00000104112.9 |
| hgncid | 13707 |
| symbol | SCG3 |
| name | secretogranin III |
| refseq_nuc | NM_013243.4 |
| refseq_prot | NP_037375.2 |
| ensembl_nuc | ENST00000220478.8 |
| ensembl_prot | ENSP00000220478.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 51681503 |
| end | 51721026 |
| strand | + |
| ver | v1.2 |
| region | chr15:51681503-51721026 |
| region5000 | chr15:51676503-51726026 |
| regionname0 | SCG3_chr15_51681503_51721026 |
| regionname5000 | SCG3_chr15_51676503_51726026 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 468 | 352 | 62 | 72 | 164 | 12 | 40 | 137 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| a0002 | 0/0 | 468 | 31 | 30 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| a0003 | 0/0 | 468 | 14 | 0 | 5 | 7 | 0 | 2 | 6 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| a0004 | 0/0 | 468 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| a0005 | 0/0 | 468 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| a0006 | 0/0 | 468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | MGFLG others(463): Show |
chr15 | 51676503 | 51726026 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1404 | 312 | 54 | 69 | 137 | 11 | 39 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0001c0002 | 0/0 | 1404 | 34 | 6 | 1 | 27 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0001c0005 | 0/0 | 1404 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0001c0006 | 0/0 | 1404 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0001c0010 | 0/0 | 1404 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0001c0011 | 0/0 | 1404 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0002c0003 | 0/0 | 1404 | 30 | 29 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0002c0009 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0003c0004 | 0/0 | 1404 | 14 | 0 | 5 | 7 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0004c0007 | 0/0 | 1404 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0005c0008 | 0/0 | 1404 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 | ||
| a0006c0012 | 0/0 | 1404 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ATGGG others(1399): Show |
chr15 | 51676503 | 51726026 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3160 | 111 | 19 | 29 | 45 | 7 | 10 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0002 | 1/0 | 3160 | 104 | 17 | 10 | 65 | 0 | 11 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0003 | 0/0 | 3160 | 52 | 7 | 27 | 0 | 3 | 15 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0004 | 0/0 | 3160 | 14 | 0 | 0 | 12 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0005 | 0/0 | 3160 | 13 | 2 | 0 | 9 | 1 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0006 | 0/0 | 3160 | 5 | 5 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0007 | 0/0 | 3160 | 5 | 3 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0008 | 0/0 | 3160 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0012 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0013 | 0/0 | 3160 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0014 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0001t0015 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0002t0001 | 0/0 | 3160 | 5 | 1 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0002t0002 | 0/0 | 3160 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0002t0004 | 0/0 | 3160 | 24 | 2 | 1 | 21 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0002t0009 | 0/0 | 3160 | 3 | 3 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0005t0005 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0006t0010 | 0/0 | 3160 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0010t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0001c0011t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0002c0003t0001 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0002c0003t0003 | 0/0 | 3160 | 25 | 24 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0002c0003t0005 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0002c0003t0011 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0002c0009t0003 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0003c0004t0001 | 0/0 | 3160 | 6 | 0 | 4 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0003c0004t0002 | 0/0 | 3160 | 3 | 0 | 0 | 1 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0003c0004t0003 | 0/0 | 3160 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0003c0004t0004 | 0/0 | 3160 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0004c0007t0006 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0005c0008t0001 | 0/0 | 3160 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| a0006c0012t0005 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | ACAGG others(3155): Show |
chr15 | 51676503 | 51726026 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0007g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0001t0015g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0002t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0005t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0005t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0006t0010g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0010t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0001c0011t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0003t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0002c0009t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0003c0004t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0004c0007t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0004c0007t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0005c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0005c0008t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| a0006c0012t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0259 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | FIN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0308 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0162 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01167 | hp2 | a0001 | c0006 | t0010 | g0036 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01169 | hp2 | a0001 | c0006 | t0010 | g0036 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01255 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0016 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0038 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0016 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01433 | hp2 | a0003 | c0004 | t0003 | g0227 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0068 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01517 | hp1 | a0001 | c0010 | t0001 | g0271 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01891 | hp2 | a0002 | c0003 | t0003 | g0325 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01975 | hp2 | a0003 | c0004 | t0001 | g0228 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0229 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0257 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02055 | hp1 | a0002 | c0003 | t0003 | g0083 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02055 | hp2 | a0002 | c0003 | t0003 | g0314 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02056 | hp2 | a0001 | c0002 | t0004 | g0300 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02155 | hp2 | a0003 | c0004 | t0001 | g0048 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02257 | hp1 | a0002 | c0003 | t0003 | g0002 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02280 | hp2 | a0002 | c0003 | t0003 | g0002 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02293 | hp1 | a0003 | c0004 | t0001 | g0221 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02572 | hp2 | a0002 | c0003 | t0011 | g0313 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02602 | hp2 | a0003 | c0004 | t0002 | g0231 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0296 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02622 | hp1 | a0004 | c0007 | t0006 | g0086 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0317 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02630 | hp1 | a0002 | c0003 | t0003 | g0323 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0332 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02717 | hp2 | a0004 | c0007 | t0006 | g0085 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0318 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02809 | hp2 | a0002 | c0009 | t0003 | g0320 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02818 | hp1 | a0002 | c0003 | t0003 | g0084 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02895 | hp2 | a0002 | c0003 | t0003 | g0322 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02896 | hp1 | a0002 | c0003 | t0003 | g0315 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02922 | hp1 | a0001 | c0005 | t0005 | g0109 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0316 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03098 | hp1 | a0002 | c0003 | t0003 | g0081 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03130 | hp1 | a0002 | c0003 | t0003 | g0002 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0108 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03139 | hp1 | a0002 | c0003 | t0003 | g0326 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03139 | hp2 | a0002 | c0003 | t0003 | g0282 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03195 | hp1 | a0002 | c0003 | t0003 | g0310 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0080 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0319 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03486 | hp1 | a0002 | c0003 | t0005 | g0324 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03516 | hp1 | a0001 | c0002 | t0009 | g0298 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03516 | hp2 | a0002 | c0003 | t0003 | g0312 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03540 | hp2 | a0002 | c0003 | t0003 | g0327 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03579 | hp2 | a0001 | c0005 | t0005 | g0110 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03834 | hp1 | a0001 | c0011 | t0001 | g0171 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0207 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04184 | hp1 | a0003 | c0004 | t0002 | g0232 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18906 | hp1 | a0002 | c0003 | t0003 | g0002 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0309 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0303 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18954 | hp2 | a0001 | c0002 | t0004 | g0330 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18964 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0329 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18972 | hp2 | a0001 | c0001 | t0008 | g0169 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18973 | hp2 | a0005 | c0008 | t0001 | g0224 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18978 | hp1 | a0006 | c0012 | t0005 | g0105 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0254 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18987 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18987 | hp2 | a0003 | c0004 | t0004 | g0253 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19005 | hp1 | a0001 | c0001 | t0012 | g0197 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19006 | hp2 | a0003 | c0004 | t0004 | g0242 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19009 | hp1 | a0001 | c0002 | t0004 | g0306 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19030 | hp2 | a0002 | c0003 | t0003 | g0321 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0082 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19057 | hp2 | a0003 | c0004 | t0002 | g0249 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19062 | hp2 | a0003 | c0004 | t0004 | g0246 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19072 | hp2 | a0001 | c0002 | t0004 | g0331 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19076 | hp2 | a0001 | c0002 | t0004 | g0328 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19083 | hp1 | a0005 | c0008 | t0001 | g0225 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0302 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19090 | hp2 | a0003 | c0004 | t0004 | g0240 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20129 | hp1 | a0001 | c0002 | t0009 | g0297 | AFR | ASW | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0251 | EUR | TSI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | GIH | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0096 | SAS | GIH | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02486 | hp2 | a0002 | c0003 | t0003 | g0079 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0301 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03471 | hp1 | a0002 | c0003 | t0003 | g0002 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG03471 | hp2 | a0002 | c0003 | t0011 | g0002 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0291 | REF | REF | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0070 | REF | REF | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51683411 | G | A | 1 | a0003 | 14 | HG01433.hp2 HG01975.hp2 HG01981.hp2 others(11): Show |
missense_variant | MODERATE | c.374G>A | p.Ser125Asn | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 627/3160 | 374/1407 | 125/468 | chr15 | 51683411 | |||
| chr15:51688293 | C | T | 1 | a0006 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.431C>T | p.Thr144Ile | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/12 | 684/3160 | 431/1407 | 144/468 | chr15 | 51688293 | |||
| chr15:51692165 | A | G | 1 | a0002 | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
missense_variant | MODERATE | c.697A>G | p.Met233Val | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/12 | 950/3160 | 697/1407 | 233/468 | chr15 | 51692165 | |||
| chr15:51701121 | A | G | 1 | a0005 | 2 | NA18973.hp2 NA19083.hp1 |
missense_variant | MODERATE | c.1084A>G | p.Ser362Gly | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/12 | 1337/3160 | 1084/1407 | 362/468 | chr15 | 51701121 | |||
| chr15:51719507 | G | A | 1 | a0004 | 2 | HG02622.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1388G>A | p.Arg463His | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1641/3160 | 1388/1407 | 463/468 | chr15 | 51719507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51683349 | T | C | 2 | a0001c0005 a0002c0009 |
3 | HG02809.hp2 HG02922.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.312T>C | p.Asn104Asn | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 565/3160 | 312/1407 | 104/468 | chr15 | 51683349 | |||
| chr15:51683388 | C | A | 1 | a0001c0002 | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
synonymous_variant | LOW | c.351C>A | p.Ile117Ile | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 604/3160 | 351/1407 | 117/468 | chr15 | 51683388 | |||
| chr15:51688378 | T | G | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.516T>G | p.Val172Val | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/12 | 769/3160 | 516/1407 | 172/468 | chr15 | 51688378 | |||
| chr15:51692317 | A | G | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.849A>G | p.Leu283Leu | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/12 | 1102/3160 | 849/1407 | 283/468 | chr15 | 51692317 | |||
| chr15:51695954 | T | C | 1 | a0001c0010 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.948T>C | p.Tyr316Tyr | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/12 | 1201/3160 | 948/1407 | 316/468 | chr15 | 51695954 | |||
| chr15:51719472 | C | T | 1 | a0001c0011 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1353C>T | p.Gly451Gly | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1606/3160 | 1353/1407 | 451/468 | chr15 | 51719472 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51681633 | C | A | 1 | a0001c0006t0010 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/12 | 123 | chr15 | 51681633 | ||||||
| chr15:51681688 | C | G | 1 | a0001c0001t0015 | 1 | HG03130.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/12 | chr15 | 51681688 | |||||||
| chr15:51719528 | A | G | 2 | a0001c0001t0006 a0004c0007t0006 |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 2 | chr15 | 51719528 | ||||||
| chr15:51719575 | A | G | 1 | a0001c0001t0014 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 49 | chr15 | 51719575 | ||||||
| chr15:51719610 | T | G | 2 | a0001c0001t0006 a0004c0007t0006 |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*84T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 84 | chr15 | 51719610 | ||||||
| chr15:51719779 | C | G | 1 | a0001c0001t0013 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 253 | chr15 | 51719779 | ||||||
| chr15:51719806 | T | C | 1 | a0001c0001t0007 | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*280T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 280 | chr15 | 51719806 | ||||||
| chr15:51719866 | G | A | 1 | a0001c0001t0007 | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 340 | chr15 | 51719866 | ||||||
| chr15:51720188 | G | C | 1 | a0001c0001t0013 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 662 | chr15 | 51720188 | ||||||
| chr15:51720255 | A | G | 1 | a0001c0001t0012 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*729A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 729 | chr15 | 51720255 | ||||||
| chr15:51720433 | C | G | 2 | a0001c0001t0006 a0004c0007t0006 |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*907C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 907 | chr15 | 51720433 | ||||||
| chr15:51720453 | G | A | 1 | a0001c0001t0008 | 4 | NA18972.hp2 NA18977.hp1 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*927G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 927 | chr15 | 51720453 | ||||||
| chr15:51720603 | T | C | 1 | a0001c0002t0009 | 3 | HG02615.hp2 HG03516.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1077 | chr15 | 51720603 | ||||||
| chr15:51720703 | A | C | 1 | a0002c0003t0011 | 2 | HG02572.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1177A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1177 | chr15 | 51720703 | ||||||
| chr15:51720814 | A | G | 2 | a0001c0001t0004 a0003c0004t0004 |
17 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1288A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1288 | chr15 | 51720814 | ||||||
| chr15:51720826 | T | G | 4 | a0001c0001t0005 a0001c0005t0005 a0002c0003t0005 others(1): Show |
17 | HG00140.hp1 HG02145.hp1 HG02922.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1300T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1300 | chr15 | 51720826 | ||||||
| chr15:51720904 | G | A | 5 | a0001c0001t0003 a0002c0003t0003 a0002c0003t0011 others(2): Show |
81 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1378 | chr15 | 51720904 | ||||||
| chr15:51720950 | C | T | 1 | a0001c0006t0010 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1424 | chr15 | 51720950 | ||||||
| chr15:51720951 | A | G | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(17): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1425A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1425 | chr15 | 51720951 | ||||||
| chr15:51720968 | G | A | 2 | a0001c0001t0006 a0004c0007t0006 |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1442 | chr15 | 51720968 | ||||||
| chr15:51720974 | C | T | 10 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(7): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1448C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1448 | chr15 | 51720974 | ||||||
| chr15:51721023 | T | C | 2 | a0001c0001t0006 a0004c0007t0006 |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1497T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1497 | chr15 | 51721023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:51681906 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.82+69T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681906 | |||||||
| chr15:51681916 | G | A | 8 | a0001c0002t0001g0047 a0001c0002t0002g0043 a0001c0002t0002g0044 others(5): Show |
10 | NA18939.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+79G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681916 | |||||||
| chr15:51681999 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82+162C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681999 | |||||||
| chr15:51682027 | A | G | 49 | a0001c0001t0001g0311 a0001c0002t0001g0047 a0001c0002t0001g0299 others(46): Show |
59 | HG00423.hp1 HG01255.hp1 HG01257.hp2 others(56): Show |
intron_variant | MODIFIER | c.82+190A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682027 | |||||||
| chr15:51682053 | A | G | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.82+216A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682053 | |||||||
| chr15:51682232 | G | A | 1 | a0003c0004t0001g0048 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.83-285G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682232 | |||||||
| chr15:51682236 | A | G | 299 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(296): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.83-281A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682236 | |||||||
| chr15:51682256 | A | G | 4 | a0001c0002t0004g0328 a0001c0002t0004g0329 a0001c0002t0004g0330 others(1): Show |
4 | NA18954.hp2 NA18966.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-261A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682256 | |||||||
| chr15:51682276 | G | GAA | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.83-230_83-229dupAA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 51682276 | ||||||
| chr15:51682315 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.83-202C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682315 | |||||||
| chr15:51682321 | GATAATAA others(8): Show |
G | 1 | a0001c0001t0001g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.83-192_83-178delAT others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 51682321 | ||||||
| chr15:51682442 | A | C | 25 | a0001c0002t0001g0047 a0001c0002t0001g0304 a0001c0002t0001g0305 others(22): Show |
30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.83-75A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682442 | |||||||
| chr15:51682713 | A | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0029 others(94): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.135+144A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682713 | |||||||
| chr15:51682753 | C | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.135+184C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682753 | |||||||
| chr15:51682788 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0021 others(97): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.135+219A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682788 | |||||||
| chr15:51682914 | A | T | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.136-165A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682914 | |||||||
| chr15:51683135 | A | ATCATATT others(39): Show |
1 | a0001c0001t0005g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.181+13_182-37dupCA others(44): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 51683135 | ||||||
| chr15:51683543 | G | A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.397+109G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683543 | |||||||
| chr15:51683561 | A | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+127A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683561 | |||||||
| chr15:51683714 | ATTTAT | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+285_397+289del others(5): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51683714 | ||||||
| chr15:51683770 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+336G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683770 | |||||||
| chr15:51683919 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+485G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683919 | |||||||
| chr15:51683938 | A | C | 1 | a0001c0001t0002g0112 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.397+504A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683938 | |||||||
| chr15:51683949 | T | C | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.397+515T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683949 | |||||||
| chr15:51683965 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+531C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683965 | |||||||
| chr15:51684011 | C | A | 26 | a0001c0001t0001g0311 a0002c0003t0001g0080 a0002c0003t0001g0318 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+577C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684011 | |||||||
| chr15:51684033 | G | T | 299 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(296): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.397+599G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684033 | |||||||
| chr15:51684155 | A | C | 1 | a0001c0001t0002g0194 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.397+721A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684155 | |||||||
| chr15:51684218 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397+784T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684218 | |||||||
| chr15:51684241 | G | A | 20 | a0001c0001t0001g0311 a0002c0003t0001g0318 a0002c0003t0003g0002 others(17): Show |
25 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+807G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684241 | |||||||
| chr15:51684422 | C | T | 249 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(246): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.397+988C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684422 | |||||||
| chr15:51684509 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.397+1075A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684509 | |||||||
| chr15:51684533 | C | T | 25 | a0001c0002t0001g0047 a0001c0002t0001g0304 a0001c0002t0001g0305 others(22): Show |
30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.397+1099C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684533 | |||||||
| chr15:51684555 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1121C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684555 | |||||||
| chr15:51684592 | A | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1158A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684592 | |||||||
| chr15:51684880 | A | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1446A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684880 | |||||||
| chr15:51684882 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.397+1448A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684882 | |||||||
| chr15:51684962 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1528C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684962 | |||||||
| chr15:51684974 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0111 a0001c0001t0002g0005 others(18): Show |
25 | HG01496.hp2 HG03098.hp2 HG04204.hp1 others(22): Show |
intron_variant | MODIFIER | c.397+1540G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684974 | |||||||
| chr15:51685014 | A | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1580A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685014 | |||||||
| chr15:51685115 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1681C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685115 | |||||||
| chr15:51685200 | T | A | 26 | a0001c0001t0001g0311 a0002c0003t0001g0080 a0002c0003t0001g0318 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+1766T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685200 | |||||||
| chr15:51685353 | C | G | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+1919C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685353 | |||||||
| chr15:51685396 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0003g0013 others(6): Show |
11 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+1962G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685396 | |||||||
| chr15:51685397 | A | G | 1 | a0001c0005t0005g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.397+1963A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685397 | |||||||
| chr15:51685466 | T | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+2032T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685466 | |||||||
| chr15:51685469 | A | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+2035A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685469 | |||||||
| chr15:51686104 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.398-2156T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686104 | |||||||
| chr15:51686111 | G | C | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-2149G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686111 | |||||||
| chr15:51686524 | C | A | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-1736C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686524 | |||||||
| chr15:51686565 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.398-1695G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686565 | |||||||
| chr15:51686585 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1675G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686585 | |||||||
| chr15:51686588 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.398-1672A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686588 | |||||||
| chr15:51686628 | G | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1632G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686628 | |||||||
| chr15:51686641 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.398-1619C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686641 | |||||||
| chr15:51686681 | A | ATGTT | 32 | a0001c0001t0001g0111 a0001c0001t0001g0204 a0001c0001t0002g0005 others(29): Show |
36 | HG00597.hp2 HG02145.hp1 HG02922.hp1 others(33): Show |
intron_variant | MODIFIER | c.398-1559_398-1556d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | ||||||
| chr15:51686681 | A | ATGTTTGT others(1): Show |
137 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(134): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.398-1563_398-1556d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | ||||||
| chr15:51686681 | A | ATGTTTGT others(5): Show |
91 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(88): Show |
122 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.398-1567_398-1556d others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | ||||||
| chr15:51686681 | A | ATGTTTGT others(9): Show |
5 | a0001c0001t0001g0188 a0001c0001t0002g0186 a0001c0001t0002g0187 others(2): Show |
5 | HG01261.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-1571_398-1556d others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | ||||||
| chr15:51686705 | A | T | 51 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0017 others(48): Show |
60 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(57): Show |
intron_variant | MODIFIER | c.398-1555A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686705 | |||||||
| chr15:51686709 | T | A | 4 | a0001c0002t0001g0299 a0001c0002t0009g0296 a0001c0002t0009g0297 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-1551T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686709 | |||||||
| chr15:51686713 | T | A | 25 | a0001c0002t0001g0047 a0001c0002t0001g0304 a0001c0002t0001g0305 others(22): Show |
30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.398-1547T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686713 | |||||||
| chr15:51686721 | T | TTG | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1538_398-1537i others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686721 | ||||||
| chr15:51686725 | C | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1535C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686725 | |||||||
| chr15:51686728 | A | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1532A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686728 | |||||||
| chr15:51686729 | G | GTTTCTCA others(115): Show |
6 | a0001c0002t0001g0299 a0001c0002t0004g0037 a0001c0002t0004g0300 others(3): Show |
7 | HG01891.hp1 HG02056.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1531_398-1530i others(124): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | |||||||
| chr15:51686729 | G | GTTTGTTT others(119): Show |
22 | a0001c0002t0001g0304 a0001c0002t0001g0305 a0001c0002t0001g0307 others(19): Show |
26 | HG00423.hp1 HG01257.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-1531_398-1530i others(128): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | |||||||
| chr15:51686729 | G | GTTTGTTT others(119): Show |
1 | a0001c0002t0001g0047 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.398-1531_398-1530i others(128): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | |||||||
| chr15:51686730 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1530G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686730 | |||||||
| chr15:51686731 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1529G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686731 | |||||||
| chr15:51686880 | A | G | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-1380A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686880 | |||||||
| chr15:51686950 | G | A | 3 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0012g0197 |
3 | NA18953.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.398-1310G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686950 | |||||||
| chr15:51687031 | T | C | 4 | a0001c0001t0002g0117 a0001c0001t0002g0127 a0001c0001t0002g0128 others(1): Show |
4 | HG00544.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-1229T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687031 | |||||||
| chr15:51687099 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1161G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687099 | |||||||
| chr15:51687233 | C | A | 1 | a0002c0003t0003g0310 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.398-1027C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687233 | |||||||
| chr15:51687458 | C | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(275): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.398-802C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687458 | |||||||
| chr15:51687477 | G | A | 249 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(246): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.398-783G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687477 | |||||||
| chr15:51687616 | G | A | 299 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(296): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.398-644G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687616 | |||||||
| chr15:51687621 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-639C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687621 | |||||||
| chr15:51687755 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.398-505G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687755 | |||||||
| chr15:51687791 | C | T | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-469C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687791 | |||||||
| chr15:51687797 | C | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.398-463C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687797 | |||||||
| chr15:51687912 | A | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-348A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687912 | |||||||
| chr15:51687940 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0021 others(97): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.398-320A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687940 | |||||||
| chr15:51688002 | T | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-258T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688002 | |||||||
| chr15:51688114 | G | A | 299 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(296): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.398-146G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688114 | |||||||
| chr15:51688135 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-125A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688135 | |||||||
| chr15:51688249 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.398-11G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688249 | |||||||
| chr15:51688412 | T | G | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+10T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688412 | |||||||
| chr15:51688415 | G | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+13G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688415 | |||||||
| chr15:51688416 | T | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+14T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688416 | |||||||
| chr15:51688417 | A | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+15A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688417 | |||||||
| chr15:51688503 | T | C | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.540+101T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688503 | |||||||
| chr15:51688508 | C | T | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.540+106C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688508 | |||||||
| chr15:51688522 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+120C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688522 | |||||||
| chr15:51688553 | C | G | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.540+151C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688553 | |||||||
| chr15:51688563 | TAGG | T | 93 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(90): Show |
123 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.540+164_540+166del others(3): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 51688563 | ||||||
| chr15:51688624 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(101): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.540+222C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688624 | |||||||
| chr15:51688698 | A | G | 1 | a0001c0001t0006g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+296A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688698 | |||||||
| chr15:51688737 | A | C | 1 | a0002c0003t0003g0326 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.540+335A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688737 | |||||||
| chr15:51688908 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541-311G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688908 | |||||||
| chr15:51689079 | G | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.541-140G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689079 | |||||||
| chr15:51689094 | C | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(103): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.541-125C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689094 | |||||||
| chr15:51689102 | T | C | 2 | a0001c0005t0005g0109 a0001c0005t0005g0110 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.541-117T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689102 | |||||||
| chr15:51689145 | G | A | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(2): Show |
5 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-74G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689145 | |||||||
| chr15:51689151 | T | TCCACATT others(348): Show |
1 | a0001c0001t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-54_541-53insTT others(353): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 51689151 | ||||||
| chr15:51689215 | A | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0095 others(5): Show |
12 | NA18939.hp1 NA18945.hp2 NA18947.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.541-4A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689215 | |||||||
| chr15:51689398 | G | GGT | 41 | a0001c0001t0001g0111 a0001c0001t0001g0183 a0001c0001t0001g0236 others(38): Show |
44 | HG00408.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | ||||||
| chr15:51689398 | G | GGTGT | 24 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0277 others(21): Show |
25 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | ||||||
| chr15:51689398 | G | GGTGTGT | 16 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
18 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | ||||||
| chr15:51689398 | G | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0035 |
3 | HG00140.hp2 HG03492.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.690+30G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689398 | |||||||
| chr15:51689398 | GGGGT | G | 88 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(85): Show |
116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.690+32_690+35delGG others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | ||||||
| chr15:51689398 | GGGGTGT | G | 15 | a0001c0001t0001g0150 a0001c0001t0001g0204 a0001c0001t0001g0295 others(12): Show |
15 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.690+32_690+37delGG others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | ||||||
| chr15:51689400 | G | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(192): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.690+32G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689400 | |||||||
| chr15:51689433 | A | G | 2 | a0001c0001t0005g0101 a0001c0001t0005g0102 |
2 | NA18982.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.690+65A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689433 | |||||||
| chr15:51689480 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.690+112G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689480 | |||||||
| chr15:51689602 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.690+234C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689602 | |||||||
| chr15:51689643 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0093 |
2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.690+275G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689643 | |||||||
| chr15:51689655 | G | A | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.690+287G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689655 | |||||||
| chr15:51689702 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.690+334G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689702 | |||||||
| chr15:51689790 | AAATT | A | 3 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 |
3 | HG02683.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.690+439_690+442del others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689790 | ||||||
| chr15:51689819 | T | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(102): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.690+451T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689819 | |||||||
| chr15:51689868 | T | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(91): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.690+500T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689868 | |||||||
| chr15:51689905 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.690+537T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689905 | |||||||
| chr15:51689940 | A | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.690+572A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689940 | |||||||
| chr15:51689990 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0219 a0001c0001t0001g0286 |
4 | HG02451.hp2 HG03453.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+622T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689990 | |||||||
| chr15:51690272 | G | A | 1 | a0001c0001t0004g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.690+904G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690272 | |||||||
| chr15:51690410 | C | T | 26 | a0002c0003t0001g0080 a0002c0003t0001g0318 a0002c0003t0003g0002 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.690+1042C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690410 | |||||||
| chr15:51690431 | A | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.690+1063A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690431 | |||||||
| chr15:51690652 | CA | C | 300 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(297): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.690+1295delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51690652 | ||||||
| chr15:51690663 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+1295A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690663 | |||||||
| chr15:51690765 | A | G | 4 | a0001c0001t0003g0120 a0001c0001t0003g0121 a0001c0001t0003g0122 others(1): Show |
4 | HG00738.hp1 HG01081.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1394A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690765 | |||||||
| chr15:51691401 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.691-758C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691401 | |||||||
| chr15:51691401 | C | T | 2 | a0001c0005t0005g0109 a0001c0005t0005g0110 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.691-758C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691401 | |||||||
| chr15:51691484 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0130 |
3 | NA18948.hp2 NA19001.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.691-675G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691484 | |||||||
| chr15:51691911 | CCCCTGAG others(47): Show |
C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-239_691-186del others(54): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51691911 | ||||||
| chr15:51691941 | G | T | 23 | a0001c0001t0001g0092 a0001c0001t0001g0111 a0001c0001t0002g0005 others(20): Show |
27 | HG01496.hp2 HG02145.hp1 HG03098.hp2 others(24): Show |
intron_variant | MODIFIER | c.691-218G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691941 | |||||||
| chr15:51692034 | G | C | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-125G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692034 | |||||||
| chr15:51692045 | C | T | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.691-114C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692045 | |||||||
| chr15:51692095 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-64T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692095 | |||||||
| chr15:51692096 | C | G | 5 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(2): Show |
5 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-63C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692096 | |||||||
| chr15:51692428 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.868+92A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692428 | |||||||
| chr15:51692480 | C | T | 1 | a0001c0001t0002g0028 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.868+144C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692480 | |||||||
| chr15:51692544 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.868+208T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692544 | |||||||
| chr15:51692864 | CT | C | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.868+536delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51692864 | ||||||
| chr15:51692879 | TTC | T | 13 | a0001c0001t0001g0209 a0001c0001t0001g0268 a0001c0001t0001g0272 others(10): Show |
14 | HG01074.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.868+545_868+546del others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51692879 | ||||||
| chr15:51692898 | G | A | 1 | a0001c0002t0004g0302 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.868+562G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692898 | |||||||
| chr15:51692911 | A | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.868+575A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692911 | |||||||
| chr15:51692950 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(253): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.868+614T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692950 | |||||||
| chr15:51692987 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+651A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692987 | |||||||
| chr15:51693078 | A | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(253): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.868+742A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693078 | |||||||
| chr15:51693163 | T | C | 4 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
4 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+827T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693163 | |||||||
| chr15:51693277 | A | G | 1 | a0002c0003t0003g0325 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.868+941A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693277 | |||||||
| chr15:51693367 | T | C | 249 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(246): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.868+1031T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693367 | |||||||
| chr15:51693400 | G | A | 8 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.868+1064G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693400 | |||||||
| chr15:51693403 | C | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.868+1067C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693403 | |||||||
| chr15:51693425 | ATTTGTT | A | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+1105_868+1110d others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51693425 | ||||||
| chr15:51693441 | G | T | 1 | a0001c0001t0002g0028 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.868+1105G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693441 | |||||||
| chr15:51693638 | C | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(221): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.868+1302C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693638 | |||||||
| chr15:51693693 | G | A | 4 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.868+1357G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693693 | |||||||
| chr15:51694013 | C | A | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.868+1677C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694013 | |||||||
| chr15:51694248 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | NA18945.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.869-1627A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694248 | |||||||
| chr15:51694307 | G | A | 1 | a0003c0004t0001g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.869-1568G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694307 | |||||||
| chr15:51694310 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.869-1565C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694310 | |||||||
| chr15:51694756 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.869-1119C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694756 | |||||||
| chr15:51694768 | C | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.869-1107C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694768 | |||||||
| chr15:51694800 | G | A | 1 | a0001c0001t0004g0199 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.869-1075G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694800 | |||||||
| chr15:51694811 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.869-1064G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694811 | |||||||
| chr15:51694956 | A | G | 4 | a0001c0002t0001g0299 a0001c0002t0009g0296 a0001c0002t0009g0297 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-919A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694956 | |||||||
| chr15:51695030 | C | CA | 17 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0002g0206 others(14): Show |
17 | HG00597.hp2 HG01167.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.869-830dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695030 | ||||||
| chr15:51695046 | G | A | 1 | a0001c0001t0003g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.869-829G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695046 | |||||||
| chr15:51695078 | G | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.869-797G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695078 | |||||||
| chr15:51695231 | A | G | 100 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0021 others(97): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.869-644A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695231 | |||||||
| chr15:51695254 | GTTC | G | 26 | a0002c0003t0001g0080 a0002c0003t0001g0318 a0002c0003t0003g0002 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.869-618_869-616del others(3): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695254 | ||||||
| chr15:51695475 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.869-400C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695475 | |||||||
| chr15:51695524 | A | G | 3 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0012g0197 |
3 | NA18953.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.869-351A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695524 | |||||||
| chr15:51695625 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.869-250G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695625 | |||||||
| chr15:51695710 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.869-165G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695710 | |||||||
| chr15:51695762 | G | GA | 6 | a0001c0001t0002g0133 a0001c0001t0002g0182 a0001c0001t0003g0210 others(3): Show |
6 | HG01175.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-99dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | ||||||
| chr15:51695762 | G | GAA | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.869-100_869-99dupA others(1): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | ||||||
| chr15:51695762 | GA | G | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.869-99delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | ||||||
| chr15:51695778 | C | G | 1 | a0001c0001t0002g0180 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.869-97C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695778 | |||||||
| chr15:51696016 | T | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.985+25T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696016 | |||||||
| chr15:51696135 | A | G | 14 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(11): Show |
14 | HG00597.hp2 HG03130.hp2 HG04115.hp2 others(11): Show |
intron_variant | MODIFIER | c.985+144A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696135 | |||||||
| chr15:51696142 | T | C | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.985+151T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696142 | |||||||
| chr15:51696181 | T | C | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.985+190T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696181 | |||||||
| chr15:51696277 | C | T | 1 | a0001c0001t0006g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985+286C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696277 | |||||||
| chr15:51696543 | C | T | 19 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0017 others(16): Show |
23 | HG04204.hp1 NA18939.hp1 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.985+552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696543 | |||||||
| chr15:51696871 | A | C | 4 | a0001c0001t0001g0092 a0001c0001t0002g0093 a0001c0005t0005g0109 others(1): Show |
4 | HG01496.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.985+880A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696871 | |||||||
| chr15:51696885 | T | C | 84 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(81): Show |
95 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.985+894T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696885 | |||||||
| chr15:51696935 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.985+944G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696935 | |||||||
| chr15:51697002 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.985+1011C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697002 | |||||||
| chr15:51697132 | C | CTG | 30 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0212 others(27): Show |
33 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.985+1173_985+1174d others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTG | 28 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0003g0013 others(25): Show |
35 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.985+1171_985+1174d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTGTG | 94 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0021 others(91): Show |
122 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.985+1169_985+1174d others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTGTGT others(1): Show |
21 | a0001c0001t0001g0026 a0001c0001t0001g0172 a0001c0001t0001g0175 others(18): Show |
24 | HG00621.hp1 HG01069.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1167_985+1174d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTGTGT others(3): Show |
36 | a0001c0001t0001g0092 a0001c0001t0001g0204 a0001c0001t0002g0027 others(33): Show |
41 | HG00597.hp2 HG01496.hp2 HG02056.hp2 others(38): Show |
intron_variant | MODIFIER | c.985+1165_985+1174d others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTGTGT others(5): Show |
10 | a0001c0001t0002g0192 a0001c0001t0004g0207 a0001c0001t0005g0101 others(7): Show |
11 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.985+1163_985+1174d others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697132 | C | CTGTGTGT others(7): Show |
20 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0017 others(17): Show |
24 | HG02559.hp1 HG04204.hp1 NA18906.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1161_985+1174d others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | ||||||
| chr15:51697177 | TTCTTTCT others(106): Show |
T | 19 | a0002c0003t0001g0318 a0002c0003t0003g0002 a0002c0003t0003g0282 others(16): Show |
24 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1189_985+1301d others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697177 | ||||||
| chr15:51697283 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.985+1292C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697283 | |||||||
| chr15:51697337 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.985+1346T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697337 | |||||||
| chr15:51697440 | C | T | 1 | a0001c0011t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.985+1449C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697440 | |||||||
| chr15:51697769 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0002g0093 a0001c0005t0005g0109 others(1): Show |
4 | HG01496.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-1550A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697769 | |||||||
| chr15:51697776 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0002g0093 |
2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.986-1543C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697776 | |||||||
| chr15:51697860 | G | T | 29 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(26): Show |
33 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.986-1459G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697860 | |||||||
| chr15:51697861 | A | T | 29 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(26): Show |
33 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.986-1458A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697861 | |||||||
| chr15:51698050 | C | T | 80 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(77): Show |
90 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.986-1269C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698050 | |||||||
| chr15:51698171 | G | A | 1 | a0001c0001t0004g0200 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.986-1148G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698171 | |||||||
| chr15:51698268 | G | A | 25 | a0001c0002t0001g0047 a0001c0002t0001g0304 a0001c0002t0001g0305 others(22): Show |
30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.986-1051G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698268 | |||||||
| chr15:51698309 | A | C | 1 | a0001c0001t0004g0200 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.986-1010A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698309 | |||||||
| chr15:51698329 | G | A | 1 | a0002c0003t0003g0312 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.986-990G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698329 | |||||||
| chr15:51698366 | A | G | 21 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0017 others(18): Show |
25 | HG02145.hp1 HG03195.hp2 HG04204.hp1 others(22): Show |
intron_variant | MODIFIER | c.986-953A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698366 | |||||||
| chr15:51698452 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.986-867T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698452 | |||||||
| chr15:51698504 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.986-815C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698504 | |||||||
| chr15:51698590 | T | C | 80 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(77): Show |
90 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.986-729T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698590 | |||||||
| chr15:51698596 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.986-723G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698596 | |||||||
| chr15:51698793 | A | AAAGAGAG others(318): Show |
3 | a0001c0001t0004g0198 a0001c0001t0004g0201 a0001c0001t0004g0202 |
3 | NA18747.hp1 NA18971.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.986-510_986-509ins others(325): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | ||||||
| chr15:51698793 | A | AAAGAGAG others(319): Show |
6 | a0001c0001t0001g0204 a0001c0001t0004g0196 a0001c0001t0004g0203 others(3): Show |
6 | HG04115.hp2 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-510_986-509ins others(326): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | ||||||
| chr15:51698793 | A | AAAGAGAG others(320): Show |
4 | a0001c0001t0002g0206 a0001c0001t0004g0195 a0001c0001t0004g0199 others(1): Show |
4 | HG00597.hp2 NA18952.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-510_986-509ins others(327): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | ||||||
| chr15:51698794 | AAG | A | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-520_986-519del others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698794 | ||||||
| chr15:51699062 | T | C | 6 | a0001c0001t0001g0226 a0001c0001t0001g0266 a0001c0001t0001g0267 others(3): Show |
6 | HG02129.hp2 NA18944.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-257T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699062 | |||||||
| chr15:51699099 | T | C | 19 | a0001c0001t0001g0111 a0001c0001t0002g0005 a0001c0001t0002g0017 others(16): Show |
23 | HG04204.hp1 NA18939.hp1 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.986-220T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699099 | |||||||
| chr15:51699257 | C | T | 119 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(116): Show |
154 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.986-62C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699257 | |||||||
| chr15:51699454 | T | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+52T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699454 | |||||||
| chr15:51699551 | C | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1069+149C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699551 | |||||||
| chr15:51699687 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1069+285C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699687 | |||||||
| chr15:51699767 | A | G | 1 | a0001c0001t0007g0074 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069+365A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699767 | |||||||
| chr15:51699802 | C | T | 2 | a0001c0001t0004g0176 a0001c0001t0004g0178 |
2 | HG02165.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1069+400C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699802 | |||||||
| chr15:51699864 | C | T | 93 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(90): Show |
123 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1069+462C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699864 | |||||||
| chr15:51699903 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1069+501C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699903 | |||||||
| chr15:51700016 | T | C | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1069+614T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700016 | |||||||
| chr15:51700099 | T | C | 29 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(26): Show |
34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+697T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700099 | |||||||
| chr15:51700162 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1069+760A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700162 | |||||||
| chr15:51700229 | T | C | 105 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0058 others(102): Show |
120 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1069+827T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700229 | |||||||
| chr15:51700394 | T | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(27): Show |
37 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070-713T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700394 | |||||||
| chr15:51700555 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1070-552T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700555 | |||||||
| chr15:51700628 | T | C | 204 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0018 others(201): Show |
249 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1070-479T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700628 | |||||||
| chr15:51700807 | C | G | 3 | a0001c0002t0009g0296 a0001c0002t0009g0297 a0001c0002t0009g0298 |
3 | HG02615.hp2 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1070-300C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700807 | |||||||
| chr15:51700928 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1070-179A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700928 | |||||||
| chr15:51700962 | G | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1070-145G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700962 | |||||||
| chr15:51701331 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1207+87C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701331 | |||||||
| chr15:51701387 | A | G | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+143A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701387 | |||||||
| chr15:51701469 | G | C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+225G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701469 | |||||||
| chr15:51701521 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1207+277T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701521 | |||||||
| chr15:51701712 | C | G | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+468C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701712 | |||||||
| chr15:51701934 | G | A | 1 | a0001c0002t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207+690G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701934 | |||||||
| chr15:51701990 | G | A | 4 | a0001c0002t0001g0299 a0001c0002t0009g0296 a0001c0002t0009g0297 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+746G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701990 | |||||||
| chr15:51702046 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+802C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702046 | |||||||
| chr15:51702048 | C | A | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0281 |
3 | HG01243.hp2 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1207+804C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702048 | |||||||
| chr15:51702319 | C | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+1075C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702319 | |||||||
| chr15:51702508 | A | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0075 others(86): Show |
101 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.1207+1264A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702508 | |||||||
| chr15:51702831 | T | G | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+1587T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702831 | |||||||
| chr15:51703184 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+1940G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703184 | |||||||
| chr15:51703246 | C | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(33): Show |
43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2002C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703246 | |||||||
| chr15:51703293 | C | T | 48 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0111 others(45): Show |
51 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1207+2049C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703293 | |||||||
| chr15:51703397 | T | C | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+2153T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703397 | |||||||
| chr15:51703493 | T | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(33): Show |
43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2249T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703493 | |||||||
| chr15:51703566 | C | T | 118 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0125 others(115): Show |
155 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.1207+2322C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703566 | |||||||
| chr15:51703583 | C | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2339C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703583 | |||||||
| chr15:51703611 | T | C | 1 | a0001c0001t0004g0196 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1207+2367T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703611 | |||||||
| chr15:51703773 | A | G | 32 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(29): Show |
39 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.1207+2529A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703773 | |||||||
| chr15:51703860 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1207+2616T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703860 | |||||||
| chr15:51703953 | T | C | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+2709T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703953 | |||||||
| chr15:51703984 | C | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+2740C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703984 | |||||||
| chr15:51703987 | A | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(33): Show |
43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2743A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703987 | |||||||
| chr15:51704105 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207+2861G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704105 | |||||||
| chr15:51704118 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1207+2874C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704118 | |||||||
| chr15:51704147 | G | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2903G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704147 | |||||||
| chr15:51704236 | C | CATATATA others(3): Show |
1 | a0001c0001t0007g0016 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1207+2995_1207+299 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | ||||||
| chr15:51704236 | CATACATA others(7): Show |
C | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2996_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | ||||||
| chr15:51704236 | CATACATA others(19): Show |
C | 3 | a0001c0001t0007g0072 a0001c0001t0007g0073 a0001c0001t0007g0074 |
3 | HG01884.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+2996_1207+302 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | ||||||
| chr15:51704240 | C | CAT | 7 | a0001c0001t0001g0058 a0001c0001t0003g0051 a0001c0001t0003g0052 others(4): Show |
7 | HG00735.hp2 HG01515.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207+2998_1207+299 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | C | CATAT | 4 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0069 others(1): Show |
4 | HG01081.hp2 HG02683.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+2999_1207+300 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | C | CATATATA others(3): Show |
4 | a0001c0001t0003g0014 a0001c0001t0003g0062 a0001c0001t0003g0067 others(1): Show |
5 | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+2999_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | C | CATATATA others(5): Show |
1 | a0001c0001t0003g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1207+2999_1207+300 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | C | T | 3 | a0001c0001t0005g0114 a0001c0001t0005g0115 a0001c0001t0007g0016 |
4 | HG01256.hp2 HG01258.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+2996C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704240 | |||||||
| chr15:51704240 | CATACAT | C | 6 | a0001c0001t0001g0075 a0001c0001t0005g0097 a0001c0001t0005g0099 others(3): Show |
6 | NA18946.hp1 NA18981.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(1): Show |
C | 10 | a0001c0001t0001g0111 a0001c0001t0004g0106 a0001c0001t0005g0094 others(7): Show |
10 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(3): Show |
C | 3 | a0001c0001t0005g0096 a0001c0001t0006g0090 a0001c0001t0006g0091 |
3 | HG02965.hp1 NA20905.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(5): Show |
C | 2 | a0001c0002t0004g0301 a0001c0002t0004g0308 |
2 | HG00423.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(9): Show |
C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(23): Show |
32 | HG01069.hp2 HG01261.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(11): Show |
C | 8 | a0001c0002t0001g0047 a0001c0002t0001g0299 a0001c0002t0001g0304 others(5): Show |
8 | HG01257.hp2 HG01891.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704240 | CATACATA others(13): Show |
C | 1 | a0001c0002t0009g0298 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207+3000_1207+301 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | ||||||
| chr15:51704242 | TAC | T | 5 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0059 others(2): Show |
5 | HG00323.hp1 HG00733.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704242 | ||||||
| chr15:51704244 | C | CAT | 27 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0211 others(24): Show |
28 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1207+3034_1207+303 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACAT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0208 others(4): Show |
10 | HG00735.hp1 HG01358.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(7): Show |
1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207+3003_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(1): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0150 others(11): Show |
18 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(3): Show |
14 | a0001c0001t0001g0011 a0001c0001t0001g0125 a0001c0001t0001g0168 others(11): Show |
14 | HG00639.hp1 HG01993.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(5): Show |
16 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0001c0001t0001g0165 others(13): Show |
19 | HG00597.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(7): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0035 others(19): Show |
24 | HG00099.hp2 HG01175.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(9): Show |
8 | a0001c0001t0001g0012 a0001c0001t0002g0017 a0001c0001t0002g0130 others(5): Show |
8 | HG01109.hp1 HG02165.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(11): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0050 others(11): Show |
16 | HG00423.hp2 HG01515.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(13): Show |
9 | a0001c0001t0001g0140 a0001c0001t0001g0167 a0001c0001t0002g0001 others(6): Show |
10 | HG01934.hp1 HG02056.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(15): Show |
4 | a0001c0001t0002g0023 a0001c0001t0002g0131 a0001c0001t0002g0173 others(1): Show |
4 | HG00621.hp1 HG03704.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(17): Show |
2 | a0001c0001t0001g0166 a0001c0001t0002g0112 |
2 | HG00544.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATACATA others(21): Show |
1 | a0001c0001t0002g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1207+3003_1207+300 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATAT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0250 a0001c0001t0001g0261 others(18): Show |
22 | HG01255.hp1 HG01517.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207+3032_1207+303 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATAT | 19 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0258 others(16): Show |
20 | HG01168.hp2 HG01256.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1207+3030_1207+303 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(1): Show |
8 | a0001c0001t0001g0144 a0001c0001t0001g0243 a0001c0001t0002g0142 others(5): Show |
9 | HG01074.hp2 HG01081.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207+3028_1207+303 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(3): Show |
8 | a0001c0001t0001g0218 a0001c0001t0001g0252 a0001c0001t0002g0104 others(5): Show |
10 | HG02027.hp1 HG02027.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3026_1207+303 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0244 a0002c0003t0003g0002 |
2 | HG03130.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1207+3024_1207+303 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(7): Show |
1 | a0002c0003t0003g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1207+3022_1207+303 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(11): Show |
1 | a0002c0003t0003g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1207+3018_1207+303 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(13): Show |
2 | a0001c0001t0001g0092 a0001c0001t0002g0156 |
2 | HG01496.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1207+3016_1207+303 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0093 a0001c0001t0003g0007 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1207+3014_1207+303 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | C | T | 25 | a0001c0001t0001g0058 a0001c0001t0003g0013 a0001c0001t0003g0014 others(22): Show |
28 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1207+3000C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704244 | |||||||
| chr15:51704244 | CAT | C | 16 | a0001c0001t0001g0029 a0001c0001t0001g0219 a0001c0001t0001g0272 others(13): Show |
16 | HG01975.hp2 HG01981.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1207+3034_1207+303 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | CATAT | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0273 a0001c0001t0001g0275 others(9): Show |
12 | HG00323.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207+3032_1207+303 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704244 | CATATATA others(1): Show |
C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0022 others(2): Show |
9 | HG00408.hp1 NA18940.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1207+3028_1207+303 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | ||||||
| chr15:51704248 | T | C | 2 | a0001c0001t0002g0010 a0001c0001t0015g0108 |
3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1207+3004T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704248 | |||||||
| chr15:51704248 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+3024_1207+302 others(46): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704248 | ||||||
| chr15:51704250 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0175 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1207+3007_1207+302 others(23): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704250 | ||||||
| chr15:51704252 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1207+3008T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704252 | |||||||
| chr15:51704254 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1207+3010T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704254 | |||||||
| chr15:51704256 | T | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0022 others(2): Show |
9 | HG00408.hp1 NA18940.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1207+3012T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704256 | |||||||
| chr15:51704278 | T | A | 9 | a0001c0001t0001g0075 a0001c0001t0004g0106 a0001c0001t0004g0201 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3034T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704278 | |||||||
| chr15:51704280 | A | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(34): Show |
44 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.1207+3036A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704280 | |||||||
| chr15:51704482 | C | T | 1 | a0001c0001t0004g0199 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1207+3238C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704482 | |||||||
| chr15:51704724 | C | T | 1 | a0002c0003t0003g0323 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+3480C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704724 | |||||||
| chr15:51704738 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1207+3494C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704738 | |||||||
| chr15:51704760 | A | AATAC | 11 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0035 others(8): Show |
18 | HG00735.hp1 HG00741.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1207+3520_1207+352 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704760 | ||||||
| chr15:51704764 | C | CAT | 32 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0118 others(29): Show |
43 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1207+3550_1207+355 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATACAT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0050 |
5 | HG00140.hp2 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+3523_1207+352 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATAT | 15 | a0001c0001t0001g0018 a0001c0001t0001g0125 a0001c0001t0001g0165 others(12): Show |
19 | HG00544.hp1 HG01070.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3548_1207+355 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATAT | 18 | a0001c0001t0001g0075 a0001c0001t0001g0175 a0001c0001t0001g0183 others(15): Show |
19 | HG01358.hp1 HG01884.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3546_1207+355 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(1): Show |
12 | a0001c0001t0001g0058 a0001c0001t0001g0223 a0001c0001t0002g0184 others(9): Show |
17 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207+3544_1207+355 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(3): Show |
8 | a0001c0001t0001g0268 a0001c0001t0001g0294 a0001c0001t0003g0060 others(5): Show |
8 | HG00642.hp2 HG01168.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+3542_1207+355 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(5): Show |
10 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
10 | HG00408.hp2 HG02109.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3540_1207+355 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(7): Show |
13 | a0001c0001t0001g0168 a0001c0001t0001g0241 a0001c0001t0003g0015 others(10): Show |
14 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1207+3538_1207+355 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(9): Show |
11 | a0001c0001t0001g0141 a0001c0001t0001g0243 a0001c0001t0001g0244 others(8): Show |
12 | HG01074.hp2 HG01361.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207+3536_1207+355 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(11): Show |
14 | a0001c0001t0001g0031 a0001c0001t0001g0247 a0001c0001t0001g0263 others(11): Show |
16 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207+3534_1207+355 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(13): Show |
8 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0002g0116 others(5): Show |
8 | HG02027.hp2 HG02486.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207+3532_1207+355 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(15): Show |
9 | a0001c0001t0001g0032 a0001c0001t0001g0218 a0001c0001t0001g0252 others(6): Show |
10 | HG02027.hp1 HG02257.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3530_1207+355 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(17): Show |
12 | a0001c0001t0001g0111 a0001c0001t0001g0256 a0001c0001t0002g0255 others(9): Show |
12 | HG00735.hp2 HG01361.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207+3528_1207+355 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(19): Show |
6 | a0001c0001t0001g0276 a0001c0001t0001g0287 a0001c0001t0003g0053 others(3): Show |
6 | HG00639.hp2 HG01081.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3526_1207+355 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(21): Show |
6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3524_1207+355 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(23): Show |
6 | a0001c0001t0001g0211 a0001c0001t0001g0273 a0001c0001t0003g0054 others(3): Show |
6 | HG00323.hp1 HG01515.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3522_1207+355 others(34): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(25): Show |
5 | a0001c0001t0001g0226 a0001c0001t0001g0279 a0001c0001t0003g0071 others(2): Show |
5 | HG01081.hp2 HG01123.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(36): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(27): Show |
3 | a0001c0001t0001g0258 a0001c0001t0005g0099 a0001c0001t0005g0100 |
3 | NA18946.hp1 NA18981.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(29): Show |
2 | a0001c0001t0001g0260 a0001c0001t0005g0259 |
2 | HG00140.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(31): Show |
1 | a0001c0001t0001g0029 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(42): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(33): Show |
1 | a0001c0001t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(44): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(35): Show |
1 | a0001c0001t0001g0280 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(46): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(39): Show |
1 | a0001c0001t0001g0215 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(50): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | C | CATATATA others(43): Show |
1 | a0001c0001t0001g0209 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(54): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | CATATAT | C | 3 | a0001c0001t0012g0197 a0001c0006t0010g0036 a0004c0007t0006g0085 |
4 | HG01167.hp2 HG01169.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+3546_1207+355 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | CATATATA others(1): Show |
C | 10 | a0001c0001t0003g0076 a0001c0001t0004g0199 a0001c0001t0015g0108 others(7): Show |
12 | HG00423.hp1 HG01243.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207+3544_1207+355 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | CATATATA others(3): Show |
C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0136 others(39): Show |
47 | HG00597.hp2 HG01069.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.1207+3542_1207+355 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704764 | CATATATA others(5): Show |
C | 19 | a0002c0003t0001g0318 a0002c0003t0003g0002 a0002c0003t0003g0282 others(16): Show |
24 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+3540_1207+355 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | ||||||
| chr15:51704779 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0261 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1207+3548_1207+354 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704779 | ||||||
| chr15:51704794 | T | C | 2 | a0001c0001t0001g0262 a0001c0002t0004g0303 |
2 | HG00735.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1207+3550T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704794 | |||||||
| chr15:51704796 | C | T | 2 | a0001c0001t0003g0033 a0001c0001t0003g0049 |
3 | HG02486.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1207+3552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704796 | |||||||
| chr15:51704806 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1207+3562T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704806 | |||||||
| chr15:51704950 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1207+3706G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704950 | |||||||
| chr15:51705444 | C | G | 2 | a0004c0007t0006g0085 a0004c0007t0006g0086 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1207+4200C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705444 | |||||||
| chr15:51705523 | T | C | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+4279T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705523 | |||||||
| chr15:51705536 | T | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(33): Show |
43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+4292T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705536 | |||||||
| chr15:51705540 | G | A | 46 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0111 others(43): Show |
49 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1207+4296G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705540 | |||||||
| chr15:51705749 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1207+4505C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705749 | |||||||
| chr15:51705938 | C | T | 2 | a0001c0001t0003g0015 a0001c0001t0003g0059 |
3 | HG00733.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1207+4694C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705938 | |||||||
| chr15:51706219 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1207+4975C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706219 | |||||||
| chr15:51706320 | G | C | 1 | a0002c0003t0003g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1207+5076G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706320 | |||||||
| chr15:51706380 | C | T | 3 | a0001c0002t0001g0304 a0001c0002t0001g0305 a0001c0002t0001g0307 |
3 | HG02074.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1207+5136C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706380 | |||||||
| chr15:51706444 | G | C | 1 | a0001c0001t0006g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1207+5200G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706444 | |||||||
| chr15:51706592 | C | T | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+5348C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706592 | |||||||
| chr15:51706593 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
24 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1207+5349G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706593 | |||||||
| chr15:51707060 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1207+5816G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707060 | |||||||
| chr15:51707112 | T | G | 5 | a0002c0003t0001g0080 a0002c0003t0003g0079 a0002c0003t0003g0081 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+5868T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707112 | |||||||
| chr15:51707296 | A | T | 4 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-6037A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707296 | |||||||
| chr15:51707330 | C | A | 1 | a0003c0004t0003g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-6003C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707330 | |||||||
| chr15:51707471 | G | A | 26 | a0002c0003t0001g0080 a0002c0003t0001g0318 a0002c0003t0003g0002 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1208-5862G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707471 | |||||||
| chr15:51707542 | T | A | 1 | a0003c0004t0003g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-5791T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707542 | |||||||
| chr15:51707682 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-5651C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707682 | |||||||
| chr15:51707773 | C | T | 222 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(219): Show |
271 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1208-5560C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707773 | |||||||
| chr15:51707950 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-5383T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707950 | |||||||
| chr15:51707991 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1208-5342C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707991 | |||||||
| chr15:51708026 | G | A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-5307G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708026 | |||||||
| chr15:51708257 | A | G | 1 | a0002c0003t0003g0322 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1208-5076A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708257 | |||||||
| chr15:51708415 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1208-4918G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708415 | |||||||
| chr15:51708537 | G | T | 4 | a0002c0003t0003g0319 a0002c0003t0003g0321 a0002c0003t0003g0325 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-4796G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708537 | |||||||
| chr15:51708594 | G | A | 1 | a0001c0001t0002g0010 | 3 | HG01109.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1208-4739G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708594 | |||||||
| chr15:51708623 | A | T | 1 | a0001c0001t0002g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1208-4710A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708623 | |||||||
| chr15:51708851 | T | TC | 26 | a0002c0003t0001g0080 a0002c0003t0001g0318 a0002c0003t0003g0002 others(23): Show |
31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1208-4480dupC | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51708851 | ||||||
| chr15:51708857 | T | TA | 45 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0003g0007 others(42): Show |
51 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1208-4465dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51708857 | ||||||
| chr15:51708919 | T | A | 62 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0151 others(59): Show |
85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1208-4414T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708919 | |||||||
| chr15:51708936 | T | C | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1208-4397T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708936 | |||||||
| chr15:51709210 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0219 a0001c0001t0001g0286 |
4 | HG02451.hp2 HG03453.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-4123C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709210 | |||||||
| chr15:51709314 | A | G | 1 | a0001c0002t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1208-4019A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709314 | |||||||
| chr15:51709401 | C | G | 121 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0125 others(118): Show |
158 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1208-3932C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709401 | |||||||
| chr15:51709516 | ATATC | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(37): Show |
48 | HG00423.hp1 HG01069.hp2 HG01256.hp2 others(45): Show |
intron_variant | MODIFIER | c.1208-3812_1208-380 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709516 | ||||||
| chr15:51709633 | TA | T | 225 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(222): Show |
277 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1208-3691delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709633 | ||||||
| chr15:51709662 | C | CAT | 4 | a0001c0001t0001g0268 a0001c0001t0002g0216 a0001c0002t0001g0305 others(1): Show |
4 | HG01433.hp1 HG01884.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-363 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709662 | C | CATAT | 4 | a0001c0001t0001g0035 a0001c0001t0007g0016 a0003c0004t0002g0232 others(1): Show |
6 | HG01256.hp2 HG01258.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3634_1208-363 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709662 | CAT | C | 3 | a0001c0001t0006g0087 a0001c0002t0004g0045 a0001c0002t0004g0046 |
3 | NA18964.hp1 NA19012.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1208-3632_1208-363 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709662 | CATATATA others(1): Show |
C | 9 | a0001c0001t0001g0058 a0001c0001t0003g0065 a0001c0001t0003g0067 others(6): Show |
9 | HG00639.hp2 HG01081.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1208-3638_1208-363 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709662 | CATATATA others(3): Show |
C | 8 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0052 others(5): Show |
10 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1208-3640_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709662 | CATATATA others(5): Show |
C | 3 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0113 |
3 | NA18981.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1208-3642_1208-363 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | ||||||
| chr15:51709675 | ATATATAT others(21): Show |
A | 2 | a0002c0003t0003g0079 a0002c0003t0003g0083 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1208-3656_1208-362 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | ||||||
| chr15:51709675 | ATATATAT others(22): Show |
A | 3 | a0002c0003t0001g0080 a0002c0003t0003g0081 a0002c0003t0003g0082 |
3 | HG03098.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1208-3656_1208-362 others(33): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | ||||||
| chr15:51709675 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0214 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1208-3656_1208-362 others(35): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | ||||||
| chr15:51709675 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1208-3656_1208-362 others(36): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | ||||||
| chr15:51709677 | ATATATAT others(20): Show |
A | 1 | a0003c0004t0001g0229 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1208-3654_1208-362 others(31): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709677 | ||||||
| chr15:51709679 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0003g0154 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1208-3652_1208-362 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709679 | ||||||
| chr15:51709681 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1208-3650_1208-362 others(27): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709681 | ||||||
| chr15:51709681 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0004g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1208-3650_1208-362 others(29): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709681 | ||||||
| chr15:51709683 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0124 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1208-3648_1208-362 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709683 | ||||||
| chr15:51709683 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0005g0096 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1208-3648_1208-362 others(31): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709683 | ||||||
| chr15:51709684 | TATATATA others(4): Show |
T | 1 | a0001c0001t0003g0077 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1208-3648_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709684 | |||||||
| chr15:51709685 | ATATATAT others(15): Show |
A | 1 | a0003c0004t0003g0227 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-3646_1208-362 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709685 | ||||||
| chr15:51709685 | ATATATAT others(29): Show |
A | 4 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0199 others(1): Show |
4 | NA18952.hp2 NA18953.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3646_1208-361 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709685 | ||||||
| chr15:51709686 | TATATATA others(2): Show |
T | 6 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(3): Show |
6 | HG00733.hp2 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3646_1208-363 others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709686 | |||||||
| chr15:51709686 | TATATATA others(4): Show |
T | 4 | a0001c0001t0001g0111 a0001c0001t0005g0100 a0001c0001t0005g0101 others(1): Show |
4 | NA18946.hp1 NA18982.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3646_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709686 | |||||||
| chr15:51709687 | ATATATAT others(8): Show |
A | 1 | a0003c0004t0002g0249 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | ||||||
| chr15:51709687 | ATATATAT others(27): Show |
A | 6 | a0001c0001t0004g0198 a0001c0001t0004g0201 a0001c0001t0004g0202 others(3): Show |
6 | HG04115.hp2 NA18747.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3644_1208-361 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | ||||||
| chr15:51709687 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0004g0200 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1208-3644_1208-360 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | ||||||
| chr15:51709688 | TATATATA others(2): Show |
T | 7 | a0001c0001t0003g0013 a0001c0001t0003g0049 a0001c0001t0003g0051 others(4): Show |
8 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3644_1208-363 others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | |||||||
| chr15:51709688 | TATATATA others(4): Show |
T | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | |||||||
| chr15:51709688 | TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | |||||||
| chr15:51709689 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0027 |
3 | HG01109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1208-3642_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | ||||||
| chr15:51709689 | ATATATAT others(9): Show |
A | 1 | a0001c0011t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1208-3642_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | ||||||
| chr15:51709689 | ATATATAT others(27): Show |
A | 2 | a0001c0001t0001g0204 a0001c0001t0002g0206 |
2 | HG00597.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1208-3642_1208-360 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | ||||||
| chr15:51709690 | TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0247 a0004c0007t0006g0085 |
2 | HG02717.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1208-3642_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709690 | |||||||
| chr15:51709691 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0183 a0002c0003t0003g0316 |
2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | ||||||
| chr15:51709691 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1208-3640_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | ||||||
| chr15:51709691 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0166 a0001c0001t0002g0010 |
2 | HG00544.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | ||||||
| chr15:51709691 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0179 a0001c0001t0002g0010 others(1): Show |
4 | HG02074.hp2 HG02895.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | ||||||
| chr15:51709693 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0261 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1208-3639_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0245 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1208-3639_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0003g0057 a0001c0001t0003g0062 |
3 | HG03688.hp2 HG04115.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1208-3640A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709693 | |||||||
| chr15:51709693 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0181 a0001c0001t0008g0170 |
3 | HG03490.hp1 NA19062.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0104 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1208-3638_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0185 a0002c0003t0003g0282 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0182 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1208-3638_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | ATATATAT others(8): Show |
A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709693 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0013g0162 a0002c0003t0011g0313 |
2 | HG00741.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | ||||||
| chr15:51709695 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0288 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1208-3637_1208-363 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | A | T | 14 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0243 others(11): Show |
15 | HG00639.hp2 HG01515.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208-3638A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709695 | |||||||
| chr15:51709695 | ATATATAT others(3): Show |
A | 7 | a0001c0001t0001g0018 a0001c0001t0002g0006 a0001c0001t0002g0152 others(4): Show |
7 | HG00423.hp2 HG01099.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0001 a0002c0003t0003g0002 |
2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(5): Show |
A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0208 a0001c0001t0002g0001 others(2): Show |
5 | HG01978.hp2 HG03130.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0165 a0003c0004t0001g0048 |
2 | HG02155.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1208-3636_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1208-3636_1208-361 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709695 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0021 a0001c0001t0002g0024 |
3 | HG01192.hp2 HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1208-3636_1208-361 others(25): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | ||||||
| chr15:51709697 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0238 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1208-3635_1208-363 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0239 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1208-3635_1208-363 others(21): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | A | T | 33 | a0001c0001t0001g0032 a0001c0001t0001g0058 a0001c0001t0001g0075 others(30): Show |
37 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1208-3636A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709697 | |||||||
| chr15:51709697 | ATATATT | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0294 a0001c0001t0002g0022 others(3): Show |
6 | HG01517.hp1 HG02109.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0280 a0001c0001t0002g0005 others(4): Show |
7 | HG00642.hp2 HG01496.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(3): Show |
A | 11 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0190 others(8): Show |
12 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(4): Show |
A | 2 | a0001c0001t0001g0092 a0001c0001t0002g0001 |
2 | HG00639.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0002g0001 a0002c0003t0011g0002 |
2 | HG03471.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(6): Show |
A | 3 | a0002c0003t0001g0318 a0002c0003t0003g0322 a0002c0003t0003g0323 |
3 | HG02630.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(7): Show |
A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0161 |
2 | HG04199.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(8): Show |
A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0175 a0001c0001t0002g0163 |
3 | HG01934.hp2 HG02056.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(9): Show |
A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0004g0178 |
3 | HG01952.hp2 HG02165.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-361 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709697 | ATATATTT others(12): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1208-3634_1208-361 others(23): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | ||||||
| chr15:51709699 | A | AT | 3 | a0001c0001t0001g0260 a0001c0002t0002g0044 a0001c0002t0004g0042 |
3 | HG02135.hp2 NA18974.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1208-3633dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0258 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-3633_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0250 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1208-3633_1208-363 others(21): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | A | T | 62 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0058 others(59): Show |
69 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1208-3634A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709699 | |||||||
| chr15:51709699 | ATATTTT | A | 6 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0022 others(3): Show |
9 | HG01175.hp1 NA18941.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | ATATTTTT | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0295 a0001c0001t0002g0001 others(3): Show |
6 | HG03098.hp2 NA18747.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | ATATTTTT others(3): Show |
A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0167 a0001c0001t0002g0001 others(4): Show |
7 | HG00099.hp1 HG02809.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | ATATTTTT others(4): Show |
A | 2 | a0001c0001t0004g0056 a0002c0003t0003g0002 |
4 | HG02257.hp1 HG02280.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | ATATTTTT others(7): Show |
A | 3 | a0001c0001t0002g0023 a0001c0001t0002g0040 a0001c0001t0002g0174 |
4 | HG00642.hp1 HG03704.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-361 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709699 | ATATTTTT others(9): Show |
A | 1 | a0001c0001t0004g0176 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1208-3632_1208-361 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | ||||||
| chr15:51709701 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0011 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATATTT others(3): Show |
1 | a0001c0001t0001g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0290 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATATTT others(13): Show |
1 | a0001c0001t0001g0241 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0215 a0001c0001t0001g0292 |
2 | HG01261.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | A | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0029 others(74): Show |
84 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1208-3632A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709701 | |||||||
| chr15:51709701 | AT | A | 7 | a0001c0001t0001g0275 a0001c0001t0002g0116 a0001c0001t0002g0157 others(4): Show |
7 | HG02027.hp2 HG02056.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3595delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATT | A | 9 | a0001c0001t0001g0188 a0001c0001t0002g0117 a0001c0001t0002g0128 others(6): Show |
9 | HG01261.hp1 HG01934.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-3596_1208-359 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTT | A | 6 | a0001c0001t0001g0136 a0001c0001t0001g0236 a0001c0001t0002g0145 others(3): Show |
6 | HG00408.hp2 NA18941.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3597_1208-359 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTT | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0209 a0001c0001t0001g0211 others(5): Show |
8 | HG01123.hp2 HG01192.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-3599_1208-359 others(9): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTTTT | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0172 a0001c0001t0002g0001 others(5): Show |
8 | HG00621.hp2 HG01069.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3601_1208-359 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0148 others(3): Show |
7 | HG02735.hp1 HG02922.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3602_1208-359 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0311 a0001c0001t0002g0028 a0001c0001t0002g0191 others(2): Show |
5 | HG02258.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-3604_1208-359 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1208-3605_1208-359 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709701 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0020 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1208-3606_1208-359 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | ||||||
| chr15:51709702 | T | TA | 5 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0219 others(2): Show |
5 | HG00099.hp2 HG02451.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(5): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709702 | |||||||
| chr15:51709702 | T | TATA | 8 | a0001c0001t0001g0277 a0001c0001t0001g0279 a0001c0001t0001g0281 others(5): Show |
8 | HG02074.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709702 | |||||||
| chr15:51709703 | T | A | 14 | a0001c0001t0001g0144 a0001c0001t0001g0268 a0001c0001t0001g0276 others(11): Show |
15 | HG00544.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208-3630T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709703 | |||||||
| chr15:51709704 | T | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0275 a0001c0001t0001g0281 others(10): Show |
13 | HG00099.hp2 HG02027.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1208-3629T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709704 | |||||||
| chr15:51709705 | T | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0268 a0001c0001t0001g0276 others(12): Show |
15 | HG00544.hp2 HG01243.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1208-3628T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709705 | |||||||
| chr15:51709706 | T | A | 10 | a0001c0001t0001g0136 a0001c0001t0001g0236 a0001c0001t0001g0275 others(7): Show |
10 | HG00408.hp2 HG02273.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-3627T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709706 | |||||||
| chr15:51709707 | T | A | 8 | a0001c0001t0001g0137 a0001c0001t0002g0127 a0001c0001t0002g0142 others(5): Show |
8 | HG00544.hp2 HG02004.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3626T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709707 | |||||||
| chr15:51709708 | T | A | 7 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0156 others(4): Show |
7 | HG01192.hp1 HG03195.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3625T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709708 | |||||||
| chr15:51709709 | T | A | 3 | a0001c0001t0001g0137 a0001c0001t0002g0146 a0002c0003t0003g0319 |
3 | HG00597.hp1 HG02004.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1208-3624T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709709 | |||||||
| chr15:51709710 | T | A | 3 | a0001c0001t0002g0145 a0001c0001t0002g0147 a0001c0001t0002g0158 |
3 | NA18951.hp2 NA19077.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1208-3623T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709710 | |||||||
| chr15:51709711 | T | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0148 |
2 | HG00597.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1208-3622T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709711 | |||||||
| chr15:51709712 | T | A | 33 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0002g0158 others(30): Show |
36 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208-3621T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709712 | |||||||
| chr15:51709713 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1208-3620T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709713 | |||||||
| chr15:51709715 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1208-3618T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709715 | |||||||
| chr15:51709718 | T | A | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3615T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709718 | |||||||
| chr15:51709725 | T | A | 46 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0111 others(43): Show |
52 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1208-3608T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709725 | |||||||
| chr15:51709781 | C | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(26): Show |
36 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208-3552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709781 | |||||||
| chr15:51709806 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1208-3527C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709806 | |||||||
| chr15:51709845 | C | T | 1 | a0001c0001t0006g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1208-3488C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709845 | |||||||
| chr15:51709878 | G | A | 1 | a0003c0004t0001g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1208-3455G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709878 | |||||||
| chr15:51709887 | A | AT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0058 others(40): Show |
52 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1208-3424dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | ||||||
| chr15:51709887 | A | ATT | 18 | a0001c0001t0001g0208 a0001c0001t0003g0007 a0001c0001t0003g0049 others(15): Show |
21 | HG01123.hp1 HG01243.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1208-3425_1208-342 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | ||||||
| chr15:51709887 | A | ATTT | 8 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(5): Show |
8 | HG00597.hp2 HG02145.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3426_1208-342 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | ||||||
| chr15:51709887 | AT | A | 107 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0125 others(104): Show |
144 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1208-3424delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | ||||||
| chr15:51709926 | C | T | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3407C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709926 | |||||||
| chr15:51710035 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1208-3298C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710035 | |||||||
| chr15:51710038 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0191 a0001c0001t0002g0192 |
3 | HG03704.hp1 HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1208-3295C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710038 | |||||||
| chr15:51710073 | G | A | 7 | a0001c0001t0003g0013 a0001c0001t0003g0049 a0001c0001t0003g0051 others(4): Show |
8 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3260G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710073 | |||||||
| chr15:51710341 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1208-2992T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710341 | |||||||
| chr15:51710355 | G | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1208-2978G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710355 | |||||||
| chr15:51710593 | T | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(29): Show |
39 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.1208-2740T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710593 | |||||||
| chr15:51710655 | T | C | 48 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0111 others(45): Show |
54 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1208-2678T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710655 | |||||||
| chr15:51710752 | A | AT | 90 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0136 others(87): Show |
103 | HG00423.hp1 HG01069.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.1208-2558dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | ||||||
| chr15:51710752 | A | ATT | 118 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1208-2559_1208-255 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | ||||||
| chr15:51710752 | A | ATTT | 12 | a0001c0001t0001g0111 a0001c0001t0001g0239 a0001c0001t0001g0247 others(9): Show |
12 | HG00639.hp2 HG01358.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208-2560_1208-255 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | ||||||
| chr15:51710752 | ATTTTTT | A | 90 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0125 others(87): Show |
122 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1208-2563_1208-255 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | ||||||
| chr15:51711042 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1208-2291A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711042 | |||||||
| chr15:51711079 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1208-2254C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711079 | |||||||
| chr15:51711353 | A | G | 1 | a0002c0003t0003g0314 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1208-1980A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711353 | |||||||
| chr15:51711568 | A | T | 3 | a0001c0001t0003g0251 a0001c0001t0003g0269 a0001c0001t0003g0270 |
3 | HG01074.hp2 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1208-1765A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711568 | |||||||
| chr15:51711650 | A | G | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1208-1683A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711650 | |||||||
| chr15:51711726 | C | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG02135.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1208-1607C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711726 | |||||||
| chr15:51711814 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1208-1519C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711814 | |||||||
| chr15:51711846 | T | C | 1 | a0001c0001t0013g0162 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1208-1487T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711846 | |||||||
| chr15:51712053 | G | A | 222 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(219): Show |
274 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1208-1280G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712053 | |||||||
| chr15:51712209 | C | A | 1 | a0001c0001t0002g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1208-1124C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712209 | |||||||
| chr15:51712363 | G | T | 37 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0003g0007 others(34): Show |
43 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1208-970G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712363 | |||||||
| chr15:51712420 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0177 |
3 | HG02970.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1208-913C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712420 | |||||||
| chr15:51712452 | T | C | 1 | a0001c0001t0005g0094 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-881T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712452 | |||||||
| chr15:51712587 | G | A | 4 | a0003c0004t0004g0240 a0003c0004t0004g0242 a0003c0004t0004g0246 others(1): Show |
4 | NA18987.hp2 NA19006.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-746G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712587 | |||||||
| chr15:51712700 | T | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0243 a0001c0001t0001g0248 others(4): Show |
8 | HG02135.hp2 NA18956.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-633T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712700 | |||||||
| chr15:51712709 | A | T | 1 | a0001c0002t0004g0042 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1208-624A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712709 | |||||||
| chr15:51712953 | T | C | 1 | a0002c0003t0003g0084 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1208-380T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712953 | |||||||
| chr15:51713085 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
24 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1208-248C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713085 | |||||||
| chr15:51713089 | T | A | 1 | a0002c0003t0003g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1208-244T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713089 | |||||||
| chr15:51713130 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1208-203C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713130 | |||||||
| chr15:51713511 | C | T | 4 | a0001c0002t0001g0299 a0001c0002t0009g0296 a0001c0002t0009g0297 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+98C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713511 | |||||||
| chr15:51713516 | C | T | 46 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0111 others(43): Show |
52 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1288+103C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713516 | |||||||
| chr15:51713517 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1288+104G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713517 | |||||||
| chr15:51713639 | G | T | 39 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0137 others(36): Show |
47 | HG00423.hp1 HG01069.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1288+226G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713639 | |||||||
| chr15:51713701 | T | A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1288+288T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713701 | |||||||
| chr15:51713762 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0001g0264 |
4 | NA18612.hp2 NA18972.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+349T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713762 | |||||||
| chr15:51713872 | G | T | 13 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0195 others(10): Show |
13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1288+459G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713872 | |||||||
| chr15:51714150 | C | T | 37 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0003g0007 others(34): Show |
43 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1288+737C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714150 | |||||||
| chr15:51714419 | G | A | 1 | a0002c0003t0011g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1288+1006G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714419 | |||||||
| chr15:51714467 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1288+1054G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714467 | |||||||
| chr15:51714472 | AG | A | 17 | a0001c0001t0001g0183 a0001c0005t0005g0109 a0002c0003t0003g0002 others(14): Show |
22 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1288+1061delG | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51714472 | ||||||
| chr15:51714554 | C | T | 4 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+1141C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714554 | |||||||
| chr15:51714581 | T | C | 2 | a0001c0005t0005g0109 a0001c0005t0005g0110 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1288+1168T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714581 | |||||||
| chr15:51714613 | C | T | 222 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0026 others(219): Show |
274 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1288+1200C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714613 | |||||||
| chr15:51715020 | G | A | 180 | a0001c0001t0001g0026 a0001c0001t0001g0075 a0001c0001t0001g0111 others(177): Show |
223 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1288+1607G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715020 | |||||||
| chr15:51715325 | G | A | 159 | a0001c0001t0001g0026 a0001c0001t0001g0125 a0001c0001t0001g0132 others(156): Show |
201 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1288+1912G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715325 | |||||||
| chr15:51715381 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0003g0062 a0001c0001t0003g0063 others(15): Show |
19 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1288+1968T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715381 | |||||||
| chr15:51715426 | T | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(209): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1288+2013T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715426 | |||||||
| chr15:51715498 | C | T | 13 | a0001c0001t0004g0176 a0001c0001t0004g0178 a0001c0001t0004g0195 others(10): Show |
13 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1288+2085C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715498 | |||||||
| chr15:51715529 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1288+2116T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715529 | |||||||
| chr15:51715609 | C | G | 20 | a0001c0001t0001g0111 a0001c0001t0005g0094 a0001c0001t0005g0096 others(17): Show |
21 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1288+2196C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715609 | |||||||
| chr15:51715671 | C | G | 14 | a0001c0001t0001g0111 a0001c0001t0005g0094 a0001c0001t0005g0096 others(11): Show |
15 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+2258C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715671 | |||||||
| chr15:51715861 | C | CT | 8 | a0001c0001t0007g0016 a0001c0001t0007g0072 a0001c0001t0007g0073 others(5): Show |
9 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288+2462dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51715861 | ||||||
| chr15:51715861 | CT | C | 15 | a0001c0001t0001g0111 a0001c0001t0005g0094 a0001c0001t0005g0096 others(12): Show |
16 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1288+2462delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51715861 | ||||||
| chr15:51715889 | G | A | 14 | a0001c0001t0001g0111 a0001c0001t0005g0094 a0001c0001t0005g0096 others(11): Show |
15 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+2476G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715889 | |||||||
| chr15:51715911 | G | A | 1 | a0001c0002t0002g0043 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1288+2498G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715911 | |||||||
| chr15:51716014 | T | A | 1 | a0001c0001t0013g0162 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1288+2601T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716014 | |||||||
| chr15:51716065 | G | T | 14 | a0001c0001t0001g0204 a0001c0001t0004g0176 a0001c0001t0004g0178 others(11): Show |
14 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1288+2652G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716065 | |||||||
| chr15:51716147 | G | A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1288+2734G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716147 | |||||||
| chr15:51716176 | T | C | 4 | a0001c0001t0001g0141 a0001c0001t0001g0268 a0001c0001t0001g0273 others(1): Show |
4 | HG01433.hp1 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+2763T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716176 | |||||||
| chr15:51716270 | A | G | 2 | a0002c0003t0003g0084 a0002c0003t0003g0327 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1288+2857A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716270 | |||||||
| chr15:51716363 | G | A | 1 | a0001c0001t0015g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1288+2950G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716363 | |||||||
| chr15:51716368 | G | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(33): Show |
42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1288+2955G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716368 | |||||||
| chr15:51716544 | A | G | 37 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(34): Show |
43 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1289-2864A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716544 | |||||||
| chr15:51716745 | T | G | 36 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(33): Show |
42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2663T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716745 | |||||||
| chr15:51716838 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1289-2570T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716838 | |||||||
| chr15:51716955 | G | A | 36 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(33): Show |
42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2453G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716955 | |||||||
| chr15:51716959 | C | CTCACACC others(281): Show |
1 | a0001c0001t0002g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1289-2273_1289-227 others(292): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51716959 | ||||||
| chr15:51717046 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1289-2362C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717046 | |||||||
| chr15:51717050 | A | AC | 14 | a0001c0001t0001g0204 a0001c0001t0004g0176 a0001c0001t0004g0178 others(11): Show |
14 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1289-2354dupC | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717050 | ||||||
| chr15:51717165 | C | T | 36 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(33): Show |
42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2243C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717165 | |||||||
| chr15:51717281 | T | C | 37 | a0001c0001t0003g0007 a0001c0001t0003g0013 a0001c0001t0003g0014 others(34): Show |
43 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1289-2127T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717281 | |||||||
| chr15:51717367 | C | CA | 22 | a0001c0001t0001g0263 a0001c0001t0002g0191 a0001c0001t0005g0094 others(19): Show |
23 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1289-2025dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717367 | ||||||
| chr15:51717384 | T | A | 1 | a0001c0001t0006g0091 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1289-2024T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717384 | |||||||
| chr15:51717388 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1289-2020C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717388 | |||||||
| chr15:51717441 | G | A | 12 | a0001c0001t0005g0094 a0001c0001t0005g0096 a0001c0001t0005g0097 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-1967G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717441 | |||||||
| chr15:51717548 | G | GA | 315 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(312): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1289-1851dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717548 | ||||||
| chr15:51717570 | T | TTCAGAGA others(6): Show |
1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-1836_1289-182 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717570 | ||||||
| chr15:51717689 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1289-1719C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717689 | |||||||
| chr15:51717761 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1289-1647C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717761 | |||||||
| chr15:51717762 | G | A | 1 | a0001c0001t0003g0033 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1289-1646G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717762 | |||||||
| chr15:51717859 | T | C | 1 | a0003c0004t0002g0249 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1289-1549T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717859 | |||||||
| chr15:51718183 | T | A | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1225T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718183 | |||||||
| chr15:51718184 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-1224G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718184 | |||||||
| chr15:51718187 | T | C | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-1221T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718187 | |||||||
| chr15:51718195 | T | C | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1213T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718195 | |||||||
| chr15:51718195 | TAGATAGA others(9): Show |
T | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-1209_1289-119 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718195 | ||||||
| chr15:51718199 | T | C | 2 | a0001c0001t0002g0159 a0001c0001t0004g0202 |
2 | NA18747.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1289-1209T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718199 | |||||||
| chr15:51718199 | T | TAGAC | 45 | a0001c0001t0002g0025 a0001c0001t0002g0206 a0001c0001t0002g0217 others(42): Show |
51 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1289-1173_1289-117 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718199 | T | TAGACAGA others(1): Show |
16 | a0001c0001t0003g0069 a0001c0001t0003g0285 a0002c0003t0003g0002 others(13): Show |
19 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1289-1177_1289-117 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718199 | T | TAGACAGA others(5): Show |
2 | a0002c0003t0003g0002 a0002c0003t0003g0322 |
3 | HG02280.hp2 HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1289-1181_1289-117 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718199 | TAGAC | T | 54 | a0001c0001t0001g0031 a0001c0001t0001g0111 a0001c0001t0001g0237 others(51): Show |
61 | HG00140.hp1 HG00423.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.1289-1173_1289-117 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718199 | TAGACAGA others(1): Show |
T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(100): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1289-1177_1289-117 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718199 | TAGACAGA others(5): Show |
T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0179 |
2 | HG02074.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1289-1181_1289-117 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | ||||||
| chr15:51718203 | C | T | 1 | a0001c0006t0010g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1205C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718203 | |||||||
| chr15:51718207 | C | T | 5 | a0001c0001t0005g0114 a0001c0001t0005g0115 a0001c0005t0005g0109 others(2): Show |
5 | HG02145.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-1201C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718207 | |||||||
| chr15:51718239 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-1169T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718239 | |||||||
| chr15:51718296 | A | G | 2 | a0001c0002t0004g0301 a0001c0002t0004g0309 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1289-1112A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718296 | |||||||
| chr15:51718443 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-965T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718443 | |||||||
| chr15:51718561 | CAACT | C | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-843_1289-840d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718561 | ||||||
| chr15:51718602 | G | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(57): Show |
84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1289-806G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718602 | |||||||
| chr15:51718610 | C | T | 185 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(182): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1289-798C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718610 | |||||||
| chr15:51718641 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-767G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718641 | |||||||
| chr15:51718646 | TA | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(164): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1289-758delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718646 | ||||||
| chr15:51718730 | T | TTTTG | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-662_1289-659d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718730 | ||||||
| chr15:51718753 | G | T | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-655G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718753 | |||||||
| chr15:51718802 | C | A | 1 | a0001c0001t0002g0159 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1289-606C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718802 | |||||||
| chr15:51718807 | A | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(112): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1289-601A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718807 | |||||||
| chr15:51718835 | CTT | C | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-572_1289-571d others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718835 | |||||||
| chr15:51718890 | TAAGTCAG others(1): Show |
T | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-502_1289-495d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718890 | ||||||
| chr15:51719011 | C | T | 17 | a0001c0001t0004g0056 a0001c0001t0004g0176 a0001c0001t0004g0178 others(14): Show |
17 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-397C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719011 | |||||||
| chr15:51719021 | G | A | 1 | a0001c0002t0002g0043 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1289-387G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719021 | |||||||
| chr15:51719158 | A | C | 143 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(140): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1289-250A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719158 | |||||||
| chr15:51719215 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1289-193G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719215 | |||||||
| chr15:51719229 | A | T | 7 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-179A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719229 | |||||||
| chr15:51719293 | G | A | 17 | a0001c0001t0005g0094 a0001c0001t0005g0096 a0001c0001t0005g0097 others(14): Show |
17 | HG00140.hp1 HG02145.hp1 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-115G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719293 | |||||||
| chr15:51719321 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0279 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1289-87T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719321 | |||||||
| chr15:51719397 | A | T | 1 | a0002c0003t0003g0316 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1289-11A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719397 |