Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 342527 |
| ensemblid | ENSG00000188176.12 |
| hgncid | 24764 |
| symbol | SMTNL2 |
| name | smoothelin like 2 |
| refseq_nuc | NM_001114974.2 |
| refseq_prot | NP_001108446.1 |
| ensembl_nuc | ENST00000389313.9 |
| ensembl_prot | ENSP00000373964.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 4584529 |
| end | 4608319 |
| strand | + |
| ver | v1.2 |
| region | chr17:4584529-4608319 |
| region5000 | chr17:4579529-4613319 |
| regionname0 | SMTNL2_chr17_4584529_4608319 |
| regionname5000 | SMTNL2_chr17_4579529_4613319 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 461 | 255 | 83 | 40 | 88 | 9 | 33 | 69 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0002 | 0/0 | 461 | 167 | 7 | 41 | 102 | 7 | 10 | 74 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0003 | 0/0 | 461 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0004 | 0/0 | 461 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0005 | 0/0 | 461 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0006 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0007 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0008 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0009 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0010 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0011 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| a0012 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | MEPAP others(456): Show |
chr17 | 4579529 | 4613319 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1383 | 112 | 24 | 26 | 44 | 3 | 14 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0003 | 1/0 | 1383 | 42 | 24 | 2 | 14 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0004 | 0/0 | 1383 | 39 | 0 | 7 | 20 | 2 | 10 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0005 | 0/0 | 1383 | 17 | 11 | 1 | 5 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0006 | 0/0 | 1383 | 13 | 12 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0007 | 0/0 | 1383 | 12 | 3 | 2 | 0 | 4 | 3 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0008 | 0/0 | 1383 | 7 | 1 | 0 | 4 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0012 | 0/0 | 1383 | 4 | 1 | 0 | 0 | 0 | 3 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0013 | 0/0 | 1383 | 3 | 3 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0017 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0019 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0020 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0026 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0001c0027 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0002c0001 | 0/0 | 1383 | 154 | 3 | 39 | 98 | 4 | 10 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0002c0010 | 0/0 | 1383 | 6 | 0 | 1 | 3 | 2 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0002c0011 | 0/0 | 1383 | 5 | 4 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0002c0021 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0002c0023 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0003c0009 | 0/0 | 1383 | 7 | 6 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0003c0016 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0004c0014 | 0/0 | 1383 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0005c0015 | 0/0 | 1383 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0006c0024 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0007c0029 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0008c0018 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0009c0030 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0010c0025 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0011c0022 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 | ||
| a0012c0028 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | ATGGA others(1378): Show |
chr17 | 4579529 | 4613319 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 2295 | 75 | 20 | 17 | 25 | 3 | 9 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0002t0002 | 0/0 | 2296 | 33 | 4 | 9 | 15 | 0 | 5 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0002t0005 | 0/0 | 2298 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2293): Show |
chr17 | 4579529 | 4613319 |
| a0001c0002t0006 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0001 | 1/0 | 2295 | 18 | 13 | 0 | 3 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0002 | 0/0 | 2296 | 18 | 7 | 1 | 10 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0004 | 0/0 | 2295 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0007 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0010 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0011 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2269): Show |
chr17 | 4579529 | 4613319 |
| a0001c0003t0013 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0004t0001 | 0/0 | 2295 | 10 | 0 | 0 | 7 | 0 | 3 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0004t0002 | 0/0 | 2296 | 29 | 0 | 7 | 13 | 2 | 7 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0005t0001 | 0/0 | 2295 | 12 | 11 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0005t0002 | 0/0 | 2296 | 5 | 0 | 1 | 4 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0006t0001 | 0/0 | 2295 | 3 | 3 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0006t0003 | 0/0 | 2295 | 10 | 9 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0007t0001 | 0/0 | 2295 | 3 | 2 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0007t0002 | 0/0 | 2296 | 9 | 1 | 1 | 0 | 4 | 3 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0008t0001 | 0/0 | 2295 | 4 | 0 | 0 | 4 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0008t0002 | 0/0 | 2296 | 3 | 1 | 0 | 0 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0012t0001 | 0/0 | 2295 | 4 | 1 | 0 | 0 | 0 | 3 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0013t0001 | 0/0 | 2295 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0013t0007 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0017t0003 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0017t0009 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0019t0001 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0020t0001 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0001c0026t0002 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0001c0027t0001 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0001t0001 | 0/0 | 2295 | 126 | 1 | 30 | 85 | 1 | 9 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0001t0002 | 0/0 | 2296 | 25 | 2 | 9 | 10 | 3 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0002c0001t0006 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0001t0012 | 0/0 | 2297 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2292): Show |
chr17 | 4579529 | 4613319 |
| a0002c0001t0014 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0010t0001 | 0/0 | 2295 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0010t0002 | 0/0 | 2296 | 5 | 0 | 1 | 3 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0002c0011t0001 | 0/0 | 2295 | 4 | 4 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0011t0002 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0002c0021t0001 | 0/0 | 2295 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0002c0023t0002 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0003c0009t0001 | 0/0 | 2295 | 6 | 6 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0003c0009t0004 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0003c0016t0001 | 0/0 | 2295 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0004c0014t0001 | 0/0 | 2295 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0005c0015t0001 | 0/0 | 2295 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0006c0024t0001 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0007c0029t0002 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0008c0018t0001 | 0/0 | 2295 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0009c0030t0001 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0010c0025t0002 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| a0011c0022t0008 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2290): Show |
chr17 | 4579529 | 4613319 |
| a0012c0028t0002 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | AGTCG others(2291): Show |
chr17 | 4579529 | 4613319 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0001g0341 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0043 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0003t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0003 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0004t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0005t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0006t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0007t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0008t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0012t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0012t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0012t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0012t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0013t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0013t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0013t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0017t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0017t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0019t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0020t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0026t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0001c0027t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0001 | 0/0 | 12 | 0 | 3 | 8 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0001t0014g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0010t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0011t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0011t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0011t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0011t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0021t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0002c0023t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0009t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0016t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0003c0016t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0004c0014t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0004c0014t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0005c0015t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0005c0015t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0006c0024t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0007c0029t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0008c0018t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0009c0030t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0010c0025t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0011c0022t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| a0012c0028t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0055 | EUR | GBR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00099 | hp2 | a0001 | c0004 | t0002 | g0003 | EUR | GBR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00140 | hp1 | a0001 | c0004 | t0002 | g0117 | EUR | GBR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0073 | EUR | GBR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00280 | hp2 | a0002 | c0010 | t0001 | g0270 | EUR | FIN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00408 | hp1 | a0001 | c0008 | t0001 | g0131 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00423 | hp1 | a0002 | c0001 | t0002 | g0296 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0105 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0094 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0045 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00597 | hp1 | a0002 | c0001 | t0002 | g0205 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0115 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0098 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0072 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00673 | hp2 | a0006 | c0024 | t0001 | g0309 | EAS | CHS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0048 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00735 | hp1 | a0007 | c0029 | t0002 | g0201 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00735 | hp2 | a0002 | c0001 | t0002 | g0281 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00738 | hp1 | a0002 | c0001 | t0002 | g0276 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00738 | hp2 | a0002 | c0001 | t0002 | g0283 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0114 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0038 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01069 | hp2 | a0001 | c0004 | t0002 | g0249 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0038 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01081 | hp1 | a0002 | c0001 | t0002 | g0303 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01099 | hp1 | a0008 | c0018 | t0001 | g0118 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0116 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01109 | hp1 | a0001 | c0019 | t0001 | g0221 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0330 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01167 | hp1 | a0004 | c0014 | t0001 | g0261 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01167 | hp2 | a0001 | c0003 | t0010 | g0172 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01169 | hp2 | a0004 | c0014 | t0001 | g0018 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0253 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0322 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01243 | hp1 | a0001 | c0006 | t0003 | g0226 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01243 | hp2 | a0003 | c0009 | t0004 | g0241 | AMR | PUR | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01256 | hp2 | a0001 | c0004 | t0002 | g0119 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01261 | hp2 | a0001 | c0004 | t0002 | g0336 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0291 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01346 | hp2 | a0001 | c0005 | t0002 | g0260 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0029 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0321 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01361 | hp1 | a0002 | c0001 | t0002 | g0319 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01361 | hp2 | a0002 | c0011 | t0002 | g0277 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0324 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01433 | hp2 | a0001 | c0007 | t0002 | g0149 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01496 | hp1 | a0002 | c0001 | t0002 | g0099 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01496 | hp2 | a0002 | c0001 | t0001 | g0101 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01515 | hp1 | a0001 | c0007 | t0002 | g0150 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01515 | hp2 | a0001 | c0007 | t0002 | g0151 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0049 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01516 | hp2 | a0002 | c0021 | t0001 | g0275 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01517 | hp1 | a0001 | c0007 | t0002 | g0152 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01517 | hp2 | a0002 | c0001 | t0002 | g0049 | EUR | IBS | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0004 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01891 | hp2 | a0001 | c0006 | t0003 | g0034 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0266 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01934 | hp1 | a0002 | c0001 | t0001 | g0293 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01943 | hp2 | a0002 | c0001 | t0001 | g0314 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01952 | hp1 | a0001 | c0007 | t0001 | g0186 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0048 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0257 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0282 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01981 | hp1 | a0002 | c0010 | t0002 | g0316 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0046 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0310 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0306 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0290 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02055 | hp2 | a0001 | c0017 | t0003 | g0240 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0183 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02071 | hp1 | a0002 | c0010 | t0002 | g0286 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02071 | hp2 | a0001 | c0026 | t0002 | g0223 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02080 | hp1 | a0002 | c0001 | t0002 | g0308 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0292 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0108 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02132 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02135 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02145 | hp1 | a0001 | c0003 | t0013 | g0255 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02145 | hp2 | a0002 | c0011 | t0001 | g0230 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02148 | hp1 | a0001 | c0004 | t0002 | g0133 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | CDX | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0019 | EAS | CDX | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | CDX | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CDX | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02257 | hp2 | a0001 | c0013 | t0001 | g0132 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02258 | hp1 | a0001 | c0006 | t0003 | g0157 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02258 | hp2 | a0001 | c0003 | t0007 | g0244 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02273 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02273 | hp2 | a0002 | c0001 | t0002 | g0318 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0212 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0284 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02523 | hp2 | a0002 | c0010 | t0002 | g0272 | EAS | KHV | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02572 | hp1 | a0003 | c0009 | t0001 | g0137 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02572 | hp2 | a0001 | c0013 | t0007 | g0028 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0213 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0220 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02698 | hp1 | a0001 | c0007 | t0002 | g0025 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0088 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02717 | hp1 | a0001 | c0003 | t0004 | g0237 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02717 | hp2 | a0003 | c0009 | t0001 | g0315 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02723 | hp1 | a0003 | c0009 | t0001 | g0139 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02723 | hp2 | a0001 | c0020 | t0001 | g0165 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02735 | hp2 | a0001 | c0004 | t0002 | g0003 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0259 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02738 | hp2 | a0001 | c0007 | t0002 | g0153 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0180 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0135 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0178 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02896 | hp1 | a0001 | c0007 | t0002 | g0231 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0179 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02922 | hp1 | a0001 | c0013 | t0001 | g0028 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02970 | hp2 | a0003 | c0016 | t0001 | g0216 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02976 | hp1 | a0003 | c0009 | t0001 | g0134 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0037 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0054 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03098 | hp2 | a0003 | c0009 | t0001 | g0138 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0219 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03139 | hp1 | a0001 | c0006 | t0003 | g0158 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03139 | hp2 | a0001 | c0017 | t0009 | g0166 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0140 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03195 | hp2 | a0001 | c0006 | t0003 | g0224 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03209 | hp1 | a0001 | c0005 | t0001 | g0206 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03225 | hp1 | a0001 | c0006 | t0003 | g0156 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0195 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0029 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0222 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03453 | hp2 | a0002 | c0011 | t0001 | g0233 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03486 | hp1 | a0001 | c0006 | t0003 | g0225 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0342 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03491 | hp2 | a0001 | c0008 | t0002 | g0031 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03492 | hp1 | a0001 | c0008 | t0002 | g0031 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0298 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03516 | hp1 | a0009 | c0030 | t0001 | g0218 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0032 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0120 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0129 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03704 | hp2 | a0001 | c0007 | t0002 | g0025 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0297 | SAS | PJL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03834 | hp2 | a0001 | c0012 | t0001 | g0065 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0125 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03942 | hp2 | a0001 | c0004 | t0002 | g0122 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0030 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04115 | hp2 | a0001 | c0012 | t0001 | g0064 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04199 | hp1 | a0001 | c0012 | t0001 | g0063 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0030 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0251 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG04228 | hp2 | a0002 | c0001 | t0002 | g0307 | SAS | STU | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0033 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18522 | hp2 | a0001 | c0027 | t0001 | g0009 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | CHB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0170 | EAS | CHB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0295 | EAS | CHB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0287 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18939 | hp1 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0328 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18941 | hp1 | a0001 | c0003 | t0011 | g0171 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18945 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18946 | hp1 | a0001 | c0005 | t0002 | g0110 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0036 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18948 | hp1 | a0001 | c0005 | t0002 | g0016 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18949 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18949 | hp2 | a0002 | c0001 | t0002 | g0265 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0335 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0274 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18956 | hp1 | a0005 | c0015 | t0001 | g0279 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18956 | hp2 | a0001 | c0002 | t0005 | g0188 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18957 | hp1 | a0002 | c0001 | t0002 | g0299 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0111 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18959 | hp1 | a0002 | c0001 | t0002 | g0339 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18960 | hp2 | a0002 | c0001 | t0002 | g0050 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0109 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0327 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18968 | hp1 | a0001 | c0008 | t0001 | g0127 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0267 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18970 | hp2 | a0002 | c0001 | t0002 | g0340 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18971 | hp1 | a0001 | c0002 | t0006 | g0173 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18973 | hp2 | a0002 | c0001 | t0001 | g0035 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18974 | hp2 | a0001 | c0005 | t0001 | g0126 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0045 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0313 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0325 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0269 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18984 | hp1 | a0002 | c0001 | t0014 | g0288 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18987 | hp2 | a0002 | c0001 | t0001 | g0300 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0337 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0334 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18997 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18998 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18999 | hp1 | a0002 | c0010 | t0002 | g0285 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0278 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0035 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0164 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19003 | hp2 | a0001 | c0004 | t0002 | g0121 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19004 | hp1 | a0001 | c0008 | t0001 | g0123 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0333 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0332 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19011 | hp1 | a0002 | c0001 | t0002 | g0050 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0311 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19012 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19030 | hp1 | a0003 | c0009 | t0001 | g0235 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19030 | hp2 | a0001 | c0006 | t0003 | g0160 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19043 | hp1 | a0002 | c0011 | t0001 | g0229 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19054 | hp1 | a0001 | c0008 | t0001 | g0130 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19054 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19055 | hp1 | a0001 | c0005 | t0002 | g0113 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19055 | hp2 | a0002 | c0001 | t0001 | g0294 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19057 | hp1 | a0002 | c0001 | t0012 | g0044 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19057 | hp2 | a0001 | c0005 | t0002 | g0016 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19063 | hp1 | a0002 | c0001 | t0006 | g0102 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0326 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0037 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0163 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0305 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0329 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19079 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0268 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19082 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19082 | hp2 | a0001 | c0002 | t0005 | g0040 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0046 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19085 | hp2 | a0001 | c0004 | t0002 | g0128 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0312 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19086 | hp2 | a0005 | c0015 | t0001 | g0023 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19087 | hp1 | a0002 | c0023 | t0002 | g0289 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19088 | hp1 | a0001 | c0002 | t0005 | g0040 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19091 | hp2 | a0001 | c0004 | t0002 | g0112 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19240 | hp1 | a0002 | c0011 | t0001 | g0234 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA19240 | hp2 | a0011 | c0022 | t0008 | g0236 | AFR | YRI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | ASW | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20129 | hp2 | a0002 | c0001 | t0002 | g0051 | AFR | ASW | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20752 | hp1 | a0002 | c0010 | t0002 | g0271 | EUR | TSI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20752 | hp2 | a0002 | c0001 | t0002 | g0304 | EUR | TSI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20805 | hp1 | a0001 | c0007 | t0002 | g0106 | EUR | TSI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0302 | EUR | TSI | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20905 | hp1 | a0012 | c0028 | t0002 | g0238 | SAS | GIH | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0323 | SAS | GIH | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG01123 | hp2 | a0002 | c0001 | t0002 | g0051 | AMR | CLM | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02109 | hp1 | a0001 | c0012 | t0001 | g0059 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0004 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG02559 | hp2 | a0001 | c0006 | t0003 | g0159 | AFR | ACB | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03471 | hp1 | a0001 | c0006 | t0003 | g0033 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0242 | AFR | MSL | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | USA | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| HG06807 | hp2 | a0001 | c0008 | t0002 | g0217 | AFR | USA | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA18955 | hp2 | a0010 | c0025 | t0002 | g0273 | EAS | JPT | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20300 | hp1 | a0003 | c0016 | t0001 | g0147 | AFR | USA | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA20300 | hp2 | a0002 | c0001 | t0002 | g0320 | AFR | USA | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA21309 | hp1 | a0001 | c0007 | t0001 | g0243 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | LWK | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0341 | REF | REF | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0043 | REF | REF | SMTNL2_chr17_4579529_4613319 | SMTNL2 | chr17 | 4579529 | 4613319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4584710 | G | C | 1 | a0004 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.105G>C | p.Met35Ile | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 182/2295 | 105/1386 | 35/461 | chr17 | 4584710 | |||
| chr17:4584832 | G | A | 1 | a0005 | 2 | NA18956.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.227G>A | p.Arg76His | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 304/2295 | 227/1386 | 76/461 | chr17 | 4584832 | |||
| chr17:4584912 | C | G | 1 | a0009 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.307C>G | p.Pro103Ala | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 384/2295 | 307/1386 | 103/461 | chr17 | 4584912 | |||
| chr17:4592368 | A | G | 1 | a0007 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.407A>G | p.Asp136Gly | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/8 | 484/2295 | 407/1386 | 136/461 | chr17 | 4592368 | |||
| chr17:4592445 | G | A | 5 | a0002 a0005 a0006 others(2): Show |
172 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(169): Show |
missense_variant | MODERATE | c.484G>A | p.Ala162Thr | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/8 | 561/2295 | 484/1386 | 162/461 | chr17 | 4592445 | |||
| chr17:4592944 | C | G | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.503C>G | p.Pro168Arg | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/8 | 580/2295 | 503/1386 | 168/461 | chr17 | 4592944 | |||
| chr17:4592966 | C | A | 1 | a0008 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.525C>A | p.Phe175Leu | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/8 | 602/2295 | 525/1386 | 175/461 | chr17 | 4592966 | |||
| chr17:4593109 | C | T | 1 | a0012 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.668C>T | p.Thr223Ile | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/8 | 745/2295 | 668/1386 | 223/461 | chr17 | 4593109 | |||
| chr17:4593842 | T | C | 2 | a0003 a0011 |
10 | HG01243.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
missense_variant | MODERATE | c.751T>C | p.Trp251Arg | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/8 | 828/2295 | 751/1386 | 251/461 | chr17 | 4593842 | |||
| chr17:4597322 | G | A | 1 | a0006 | 1 | HG00673.hp2 | missense_variant&splice_region_variant | MODERATE | c.1258G>A | p.Glu420Lys | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/8 | 1335/2295 | 1258/1386 | 420/461 | chr17 | 4597322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4584711 | C | A | 1 | a0001c0012 | 4 | HG02109.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
synonymous_variant | LOW | c.106C>A | p.Arg36Arg | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 183/2295 | 106/1386 | 36/461 | chr17 | 4584711 | |||
| chr17:4592387 | G | A | 8 | a0001c0004 a0001c0005 a0001c0008 others(5): Show |
71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
synonymous_variant | LOW | c.426G>A | p.Glu142Glu | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/8 | 503/2295 | 426/1386 | 142/461 | chr17 | 4592387 | |||
| chr17:4592390 | G | A | 1 | a0001c0020 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.429G>A | p.Ser143Ser | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/8 | 506/2295 | 429/1386 | 143/461 | chr17 | 4592390 | |||
| chr17:4593012 | C | A | 1 | a0002c0021 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.571C>A | p.Arg191Arg | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/8 | 648/2295 | 571/1386 | 191/461 | chr17 | 4593012 | |||
| chr17:4593865 | T | C | 18 | a0001c0002 a0001c0006 a0001c0008 others(15): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
synonymous_variant | LOW | c.774T>C | p.Tyr258Tyr | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/8 | 851/2295 | 774/1386 | 258/461 | chr17 | 4593865 | |||
| chr17:4595316 | G | A | 8 | a0001c0004 a0001c0007 a0001c0013 others(5): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
synonymous_variant | LOW | c.978G>A | p.Thr326Thr | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/8 | 1055/2295 | 978/1386 | 326/461 | chr17 | 4595316 | |||
| chr17:4597174 | C | T | 1 | a0001c0027 | 1 | NA18522.hp2 | splice_region_variant&synonymous_variant | LOW | c.1110C>T | p.His370His | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/8 | 1187/2295 | 1110/1386 | 370/461 | chr17 | 4597174 | |||
| chr17:4597210 | C | T | 1 | a0001c0019 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1146C>T | p.Asp382Asp | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/8 | 1223/2295 | 1146/1386 | 382/461 | chr17 | 4597210 | |||
| chr17:4597264 | C | T | 5 | a0001c0006 a0001c0013 a0001c0017 others(2): Show |
20 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
synonymous_variant | LOW | c.1200C>T | p.Tyr400Tyr | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/8 | 1277/2295 | 1200/1386 | 400/461 | chr17 | 4597264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4584560 | T | C | 2 | a0001c0003t0004 a0003c0009t0004 |
3 | HG01243.hp2 HG02717.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-46T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 46 | chr17 | 4584560 | ||||||
| chr17:4584566 | C | A | 3 | a0001c0003t0004 a0003c0009t0004 a0011c0022t0008 |
4 | HG01243.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 40 | chr17 | 4584566 | ||||||
| chr17:4584588 | C | A | 2 | a0001c0006t0003 a0001c0017t0003 |
11 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-18C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | 18 | chr17 | 4584588 | ||||||
| chr17:4584599 | C | T | 1 | a0002c0001t0014 | 1 | NA18984.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/8 | chr17 | 4584599 | |||||||
| chr17:4607581 | C | T | 1 | a0001c0003t0013 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 94 | chr17 | 4607581 | ||||||
| chr17:4607596 | C | T | 2 | a0001c0003t0007 a0001c0013t0007 |
2 | HG02258.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*109C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 109 | chr17 | 4607596 | ||||||
| chr17:4607726 | T | TGA | 2 | a0001c0002t0005 a0002c0001t0012 |
4 | NA18956.hp2 NA19057.hp1 NA19082.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*252_*253dupGA | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 254 | INFO_REALIGN_3_PRIME | chr17 | 4607726 | |||||
| chr17:4607733 | G | C | 1 | a0001c0017t0009 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 246 | chr17 | 4607733 | ||||||
| chr17:4607855 | G | A | 1 | a0001c0003t0010 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 368 | chr17 | 4607855 | ||||||
| chr17:4607868 | G | GT | 15 | a0001c0002t0002 a0001c0002t0005 a0001c0003t0002 others(12): Show |
136 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*390dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 391 | INFO_REALIGN_3_PRIME | chr17 | 4607868 | |||||
| chr17:4607930 | T | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*443T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 443 | chr17 | 4607930 | ||||||
| chr17:4607931 | C | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 444 | chr17 | 4607931 | ||||||
| chr17:4607935 | C | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 448 | chr17 | 4607935 | ||||||
| chr17:4607938 | T | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 451 | chr17 | 4607938 | ||||||
| chr17:4607939 | C | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 452 | chr17 | 4607939 | ||||||
| chr17:4607940 | T | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 453 | chr17 | 4607940 | ||||||
| chr17:4607942 | G | GAACCGCT others(4): Show |
1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455_*456insAACCGC others(5): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 456 | chr17 | 4607942 | ||||||
| chr17:4607946 | A | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 459 | chr17 | 4607946 | ||||||
| chr17:4607948 | T | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*461T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 461 | chr17 | 4607948 | ||||||
| chr17:4607957 | A | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 470 | chr17 | 4607957 | ||||||
| chr17:4607958 | C | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*471C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 471 | chr17 | 4607958 | ||||||
| chr17:4607974 | T | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*487T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 487 | chr17 | 4607974 | ||||||
| chr17:4607975 | C | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*488C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 488 | chr17 | 4607975 | ||||||
| chr17:4607976 | A | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*489A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 489 | chr17 | 4607976 | ||||||
| chr17:4607977 | G | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 490 | chr17 | 4607977 | ||||||
| chr17:4607987 | A | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 500 | chr17 | 4607987 | ||||||
| chr17:4607997 | T | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*510T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 510 | chr17 | 4607997 | ||||||
| chr17:4608008 | G | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 521 | chr17 | 4608008 | ||||||
| chr17:4608010 | A | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*523A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 523 | chr17 | 4608010 | ||||||
| chr17:4608011 | G | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 524 | chr17 | 4608011 | ||||||
| chr17:4608014 | A | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 527 | chr17 | 4608014 | ||||||
| chr17:4608016 | A | G | 2 | a0001c0002t0006 a0002c0001t0006 |
2 | NA18971.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*529A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 529 | chr17 | 4608016 | ||||||
| chr17:4608018 | T | A | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 531 | chr17 | 4608018 | ||||||
| chr17:4608023 | T | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 536 | chr17 | 4608023 | ||||||
| chr17:4608038 | G | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 551 | chr17 | 4608038 | ||||||
| chr17:4608042 | A | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 555 | chr17 | 4608042 | ||||||
| chr17:4608044 | CAGATGAC others(25): Show |
C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558_*589delAGATGA others(26): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 558 | chr17 | 4608044 | ||||||
| chr17:4608074 | G | A | 3 | a0001c0017t0003 a0001c0017t0009 a0001c0020t0001 |
3 | HG02055.hp2 HG02723.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 587 | chr17 | 4608074 | ||||||
| chr17:4608098 | C | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 611 | chr17 | 4608098 | ||||||
| chr17:4608099 | G | T | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 612 | chr17 | 4608099 | ||||||
| chr17:4608100 | G | C | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 613 | chr17 | 4608100 | ||||||
| chr17:4608104 | C | G | 1 | a0001c0003t0011 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 8/8 | 617 | chr17 | 4608104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4585033 | G | C | 1 | a0002c0001t0001g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.399+29G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585033 | |||||||
| chr17:4585034 | C | G | 1 | a0002c0001t0001g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.399+30C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585034 | |||||||
| chr17:4585090 | G | A | 1 | a0001c0007t0001g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.399+86G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585090 | |||||||
| chr17:4585119 | C | G | 110 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0256 others(107): Show |
152 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.399+115C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585119 | |||||||
| chr17:4585221 | C | T | 1 | a0001c0003t0013g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+217C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585221 | |||||||
| chr17:4585548 | T | C | 334 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(331): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.399+544T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585548 | |||||||
| chr17:4585589 | T | C | 61 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(58): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.399+585T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585589 | |||||||
| chr17:4585621 | T | C | 47 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(44): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.399+617T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585621 | |||||||
| chr17:4585733 | G | A | 1 | a0001c0004t0002g0105 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.399+729G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585733 | |||||||
| chr17:4585756 | C | G | 1 | a0001c0002t0002g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.399+752C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585756 | |||||||
| chr17:4585878 | C | T | 336 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(333): Show |
424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.399+874C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585878 | |||||||
| chr17:4585879 | T | C | 336 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(333): Show |
424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.399+875T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4585879 | |||||||
| chr17:4586000 | G | A | 45 | a0001c0002t0001g0107 a0001c0003t0001g0136 a0001c0003t0002g0135 others(42): Show |
59 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.399+996G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586000 | |||||||
| chr17:4586023 | G | C | 1 | a0001c0003t0013g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.399+1019G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586023 | |||||||
| chr17:4586064 | T | C | 1 | a0001c0003t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.399+1060T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586064 | |||||||
| chr17:4586097 | A | G | 7 | a0001c0002t0001g0239 a0001c0003t0004g0237 a0001c0003t0004g0242 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+1093A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586097 | |||||||
| chr17:4586140 | G | A | 1 | a0002c0001t0001g0027 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.399+1136G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586140 | |||||||
| chr17:4586179 | G | T | 3 | a0002c0011t0001g0233 a0002c0011t0001g0234 a0003c0009t0001g0235 |
3 | HG03453.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.399+1175G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586179 | |||||||
| chr17:4586331 | G | A | 5 | a0001c0002t0001g0239 a0001c0003t0004g0237 a0001c0017t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+1327G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586331 | |||||||
| chr17:4586364 | A | C | 2 | a0001c0002t0001g0042 a0001c0002t0001g0232 |
3 | HG01099.hp2 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.399+1360A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586364 | |||||||
| chr17:4586459 | TA | T | 20 | a0001c0002t0001g0042 a0001c0002t0001g0228 a0001c0002t0001g0232 others(17): Show |
21 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.399+1466delA | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586459 | ||||||
| chr17:4586510 | CAAAGAGA others(3): Show |
C | 3 | a0001c0006t0003g0224 a0001c0006t0003g0225 a0001c0006t0003g0226 |
3 | HG01243.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.399+1508_399+1517d others(12): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586510 | ||||||
| chr17:4586512 | A | AAG | 7 | a0001c0002t0002g0252 a0001c0003t0001g0250 a0001c0003t0001g0251 others(4): Show |
9 | HG01069.hp2 HG01175.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+1535_399+1536d others(4): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586512 | ||||||
| chr17:4586512 | AAG | A | 5 | a0001c0003t0001g0136 a0001c0006t0001g0140 a0003c0009t0001g0137 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+1535_399+1536d others(4): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586512 | ||||||
| chr17:4586512 | AAGAG | A | 69 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0107 others(66): Show |
91 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.399+1533_399+1536d others(6): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586512 | ||||||
| chr17:4586512 | AAGAGAG | A | 259 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(256): Show |
325 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.399+1531_399+1536d others(8): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586512 | ||||||
| chr17:4586556 | C | T | 1 | a0001c0026t0002g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.399+1552C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586556 | |||||||
| chr17:4586569 | A | G | 2 | a0002c0001t0002g0339 a0002c0001t0002g0340 |
2 | NA18959.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.399+1565A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586569 | |||||||
| chr17:4586770 | G | C | 1 | a0002c0001t0001g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.399+1766G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586770 | |||||||
| chr17:4586812 | A | G | 1 | a0001c0007t0002g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.399+1808A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586812 | |||||||
| chr17:4586864 | G | A | 160 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(157): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.399+1860G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586864 | |||||||
| chr17:4586921 | A | C | 1 | a0002c0001t0002g0340 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.399+1917A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586921 | |||||||
| chr17:4586926 | G | GGGAACTC others(22): Show |
3 | a0002c0001t0001g0333 a0002c0001t0001g0334 a0002c0001t0001g0335 |
3 | NA18950.hp2 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.399+1936_399+1937i others(31): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4586926 | ||||||
| chr17:4586941 | A | C | 160 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(157): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.399+1937A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4586941 | |||||||
| chr17:4587144 | T | C | 334 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(331): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.399+2140T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587144 | |||||||
| chr17:4587153 | G | A | 1 | a0003c0009t0004g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.399+2149G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587153 | |||||||
| chr17:4587173 | A | G | 158 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(155): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.399+2169A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587173 | |||||||
| chr17:4587311 | G | A | 1 | a0002c0001t0001g0108 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.399+2307G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587311 | |||||||
| chr17:4587326 | G | A | 6 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0145 others(3): Show |
6 | HG02559.hp1 HG02630.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+2322G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587326 | |||||||
| chr17:4587366 | G | A | 3 | a0002c0011t0001g0233 a0002c0011t0001g0234 a0003c0009t0001g0235 |
3 | HG03453.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.399+2362G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587366 | |||||||
| chr17:4587575 | T | C | 5 | a0001c0007t0002g0149 a0001c0007t0002g0150 a0001c0007t0002g0151 others(2): Show |
5 | HG01433.hp2 HG01515.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+2571T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587575 | |||||||
| chr17:4587609 | G | A | 1 | a0001c0005t0001g0032 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.399+2605G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587609 | |||||||
| chr17:4587617 | A | G | 161 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(158): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.399+2613A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587617 | |||||||
| chr17:4587733 | C | T | 14 | a0001c0002t0001g0239 a0001c0003t0001g0136 a0001c0003t0002g0135 others(11): Show |
14 | HG01243.hp2 HG02055.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+2729C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587733 | |||||||
| chr17:4587754 | G | A | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | NA18950.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.399+2750G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587754 | |||||||
| chr17:4587764 | T | C | 99 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0161 others(96): Show |
115 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.399+2760T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587764 | |||||||
| chr17:4587859 | C | T | 87 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0161 others(84): Show |
103 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.399+2855C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587859 | |||||||
| chr17:4587981 | G | A | 2 | a0001c0002t0001g0042 a0001c0002t0001g0232 |
3 | HG01099.hp2 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.399+2977G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4587981 | |||||||
| chr17:4588024 | C | G | 3 | a0002c0011t0001g0233 a0002c0011t0001g0234 a0003c0009t0001g0235 |
3 | HG03453.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.399+3020C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588024 | |||||||
| chr17:4588029 | A | T | 1 | a0001c0003t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.399+3025A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588029 | |||||||
| chr17:4588072 | C | T | 1 | a0003c0009t0001g0235 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.399+3068C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588072 | |||||||
| chr17:4588115 | G | C | 1 | a0001c0002t0001g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.399+3111G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588115 | |||||||
| chr17:4588312 | C | T | 1 | a0001c0004t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.399+3308C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588312 | |||||||
| chr17:4588352 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.399+3348C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588352 | |||||||
| chr17:4588360 | C | T | 187 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0042 others(184): Show |
228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.399+3356C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588360 | |||||||
| chr17:4588493 | C | T | 1 | a0001c0013t0001g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.399+3489C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588493 | |||||||
| chr17:4588507 | C | A | 1 | a0001c0002t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.399+3503C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588507 | |||||||
| chr17:4588629 | C | G | 221 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(218): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.399+3625C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588629 | |||||||
| chr17:4588629 | C | T | 3 | a0002c0011t0001g0233 a0002c0011t0001g0234 a0003c0009t0001g0235 |
3 | HG03453.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.399+3625C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588629 | |||||||
| chr17:4588632 | C | T | 221 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(218): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.399+3628C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588632 | |||||||
| chr17:4588661 | T | C | 225 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(222): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.399+3657T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588661 | |||||||
| chr17:4588751 | A | C | 1 | a0002c0001t0001g0337 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.400-3610A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588751 | |||||||
| chr17:4588777 | C | T | 12 | a0001c0006t0001g0033 a0001c0006t0001g0034 a0001c0006t0003g0033 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.400-3584C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588777 | |||||||
| chr17:4588833 | C | T | 160 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(157): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.400-3528C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588833 | |||||||
| chr17:4588902 | A | G | 91 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0207 others(88): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.400-3459A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588902 | |||||||
| chr17:4588976 | A | G | 1 | a0002c0001t0002g0205 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.400-3385A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588976 | |||||||
| chr17:4588983 | G | A | 1 | a0001c0002t0002g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.400-3378G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588983 | |||||||
| chr17:4588986 | C | T | 1 | a0001c0003t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.400-3375C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4588986 | |||||||
| chr17:4589118 | C | T | 11 | a0001c0006t0001g0033 a0001c0006t0001g0034 a0001c0006t0003g0033 others(8): Show |
11 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-3243C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589118 | |||||||
| chr17:4589122 | G | A | 3 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.400-3239G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589122 | |||||||
| chr17:4589138 | G | A | 2 | a0001c0002t0001g0042 a0001c0002t0001g0232 |
3 | HG01099.hp2 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.400-3223G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589138 | |||||||
| chr17:4589234 | AG | A | 16 | a0001c0002t0001g0239 a0001c0003t0004g0237 a0001c0006t0001g0033 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.400-3124delG | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589234 | ||||||
| chr17:4589237 | G | A | 277 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(274): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.400-3124G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589237 | |||||||
| chr17:4589238 | C | A | 16 | a0001c0002t0001g0239 a0001c0003t0004g0237 a0001c0006t0001g0033 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.400-3123C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589238 | |||||||
| chr17:4589239 | C | T | 274 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(271): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.400-3122C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589239 | |||||||
| chr17:4589240 | T | C | 278 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(275): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.400-3121T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589240 | |||||||
| chr17:4589242 | C | T | 4 | a0001c0003t0004g0242 a0002c0011t0001g0229 a0002c0011t0001g0230 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-3119C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589242 | |||||||
| chr17:4589263 | T | C | 52 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(49): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.400-3098T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589263 | |||||||
| chr17:4589303 | C | G | 3 | a0001c0002t0001g0228 a0001c0002t0002g0227 a0001c0007t0002g0231 |
3 | HG00741.hp1 HG01074.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.400-3058C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589303 | |||||||
| chr17:4589306 | A | G | 14 | a0001c0003t0001g0245 a0001c0006t0001g0033 a0001c0006t0001g0034 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.400-3055A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589306 | |||||||
| chr17:4589352 | T | G | 1 | a0001c0002t0002g0338 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.400-3009T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589352 | |||||||
| chr17:4589362 | C | T | 1 | a0001c0002t0001g0087 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.400-2999C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589362 | |||||||
| chr17:4589452 | G | A | 81 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(78): Show |
106 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.400-2909G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589452 | |||||||
| chr17:4589493 | G | A | 1 | a0001c0003t0013g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.400-2868G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589493 | |||||||
| chr17:4589618 | G | T | 2 | a0002c0011t0001g0229 a0002c0011t0001g0230 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.400-2743G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589618 | |||||||
| chr17:4589619 | T | G | 330 | a0001c0002t0001g0009 a0001c0002t0001g0011 a0001c0002t0001g0012 others(327): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.400-2742T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589619 | |||||||
| chr17:4589641 | T | C | 2 | a0001c0017t0009g0166 a0001c0020t0001g0165 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.400-2720T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589641 | |||||||
| chr17:4589675 | C | T | 1 | a0002c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.400-2686C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589675 | |||||||
| chr17:4589796 | A | G | 1 | a0001c0005t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.400-2565A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589796 | |||||||
| chr17:4589824 | C | T | 4 | a0002c0001t0001g0326 a0002c0001t0001g0327 a0002c0001t0001g0328 others(1): Show |
4 | NA18939.hp2 NA18963.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-2537C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589824 | |||||||
| chr17:4589825 | G | C | 1 | a0001c0002t0001g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.400-2536G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589825 | |||||||
| chr17:4589826 | C | G | 1 | a0001c0002t0001g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.400-2535C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589826 | |||||||
| chr17:4589831 | C | T | 66 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0001g0161 others(63): Show |
76 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.400-2530C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589831 | |||||||
| chr17:4589932 | A | G | 69 | a0001c0002t0001g0089 a0001c0002t0001g0154 a0001c0002t0001g0155 others(66): Show |
79 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.400-2429A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589932 | |||||||
| chr17:4589938 | CTTTTTTT others(1): Show |
C | 7 | a0001c0002t0001g0248 a0001c0002t0002g0202 a0001c0002t0002g0203 others(4): Show |
7 | HG00735.hp1 HG01123.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-2384_400-2377d others(10): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(2): Show |
C | 9 | a0001c0002t0001g0247 a0001c0002t0002g0200 a0001c0003t0004g0242 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-2385_400-2377d others(11): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(3): Show |
C | 19 | a0001c0002t0001g0161 a0001c0002t0001g0195 a0001c0002t0001g0199 others(16): Show |
20 | HG00609.hp2 HG01433.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.400-2386_400-2377d others(12): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(4): Show |
C | 15 | a0001c0002t0001g0189 a0001c0002t0001g0239 a0001c0002t0002g0039 others(12): Show |
16 | HG00544.hp2 HG01081.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.400-2387_400-2377d others(13): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(5): Show |
C | 10 | a0001c0002t0001g0155 a0001c0002t0002g0185 a0001c0003t0001g0141 others(7): Show |
10 | HG01515.hp1 HG01515.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.400-2388_400-2377d others(14): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(6): Show |
C | 11 | a0001c0002t0001g0089 a0001c0002t0001g0177 a0001c0003t0001g0143 others(8): Show |
13 | HG02027.hp1 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-2389_400-2377d others(15): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(7): Show |
C | 11 | a0001c0002t0001g0107 a0001c0002t0001g0154 a0001c0002t0006g0173 others(8): Show |
16 | HG00558.hp2 HG00597.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.400-2390_400-2377d others(16): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(8): Show |
C | 3 | a0001c0002t0001g0264 a0001c0003t0002g0170 a0001c0003t0002g0253 |
3 | HG01175.hp1 HG01175.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.400-2391_400-2377d others(17): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(9): Show |
C | 13 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(10): Show |
17 | HG00639.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-2392_400-2377d others(18): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(10): Show |
C | 6 | a0001c0003t0001g0250 a0001c0003t0001g0251 a0001c0003t0002g0017 others(3): Show |
8 | HG00738.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-2393_400-2377d others(19): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(11): Show |
C | 35 | a0001c0002t0001g0207 a0001c0002t0001g0208 a0001c0002t0002g0162 others(32): Show |
37 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.400-2394_400-2377d others(20): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(13): Show |
C | 4 | a0002c0001t0001g0266 a0002c0001t0001g0267 a0002c0001t0001g0268 others(1): Show |
4 | HG01928.hp2 HG02976.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-2396_400-2377d others(22): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(14): Show |
C | 1 | a0002c0001t0001g0035 | 2 | NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.400-2397_400-2377d others(23): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(16): Show |
C | 3 | a0001c0004t0001g0124 a0001c0004t0002g0125 a0002c0001t0002g0265 |
3 | HG03927.hp1 NA18949.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.400-2399_400-2377d others(25): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(17): Show |
C | 43 | a0001c0004t0001g0007 a0001c0004t0001g0030 a0001c0004t0001g0120 others(40): Show |
62 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.400-2400_400-2377d others(26): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(18): Show |
C | 9 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(6): Show |
9 | NA18946.hp1 NA18957.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-2401_400-2377d others(27): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(19): Show |
C | 39 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(36): Show |
46 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.400-2402_400-2377d others(28): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589938 | CTTTTTTT others(20): Show |
C | 2 | a0001c0002t0001g0055 a0001c0002t0002g0168 |
2 | HG00099.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.400-2403_400-2377d others(29): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4589938 | ||||||
| chr17:4589997 | C | T | 11 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0208 others(8): Show |
14 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.400-2364C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4589997 | |||||||
| chr17:4590070 | G | A | 313 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(310): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.400-2291G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590070 | |||||||
| chr17:4590104 | T | C | 307 | a0001c0002t0001g0009 a0001c0002t0001g0011 a0001c0002t0001g0012 others(304): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.400-2257T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590104 | |||||||
| chr17:4590128 | G | A | 51 | a0001c0004t0001g0007 a0001c0004t0001g0030 a0001c0004t0001g0109 others(48): Show |
70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.400-2233G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590128 | |||||||
| chr17:4590208 | C | G | 117 | a0001c0003t0001g0342 a0001c0007t0001g0054 a0002c0001t0001g0001 others(114): Show |
162 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.400-2153C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590208 | |||||||
| chr17:4590218 | C | T | 13 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(10): Show |
17 | HG00639.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-2143C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590218 | |||||||
| chr17:4590241 | A | G | 2 | a0002c0001t0001g0323 a0002c0001t0001g0324 |
2 | HG01433.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.400-2120A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590241 | |||||||
| chr17:4590253 | C | G | 1 | a0002c0001t0001g0322 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.400-2108C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590253 | |||||||
| chr17:4590263 | G | A | 5 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0084 others(2): Show |
5 | HG00438.hp2 NA18987.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-2098G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590263 | |||||||
| chr17:4590312 | T | G | 1 | a0001c0002t0001g0256 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.400-2049T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590312 | |||||||
| chr17:4590331 | C | T | 41 | a0001c0004t0001g0007 a0001c0004t0001g0030 a0001c0004t0001g0109 others(38): Show |
55 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-2030C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590331 | |||||||
| chr17:4590445 | A | G | 1 | a0001c0003t0002g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.400-1916A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590445 | |||||||
| chr17:4590461 | C | G | 51 | a0001c0004t0001g0007 a0001c0004t0001g0030 a0001c0004t0001g0109 others(48): Show |
70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.400-1900C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590461 | |||||||
| chr17:4590478 | A | G | 111 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(108): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.400-1883A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590478 | |||||||
| chr17:4590532 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.400-1829C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590532 | |||||||
| chr17:4590622 | T | C | 1 | a0001c0002t0001g0092 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.400-1739T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590622 | |||||||
| chr17:4590623 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.400-1738C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590623 | |||||||
| chr17:4590704 | G | A | 1 | a0003c0009t0001g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.400-1657G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590704 | |||||||
| chr17:4590778 | T | C | 124 | a0001c0003t0001g0136 a0001c0003t0001g0342 a0001c0003t0002g0135 others(121): Show |
169 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.400-1583T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590778 | |||||||
| chr17:4590868 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.400-1493C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4590868 | |||||||
| chr17:4591035 | C | T | 7 | a0002c0001t0001g0321 a0002c0001t0002g0051 a0002c0001t0002g0281 others(4): Show |
8 | HG00735.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.400-1326C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591035 | |||||||
| chr17:4591037 | C | G | 10 | a0002c0001t0001g0023 a0002c0001t0001g0280 a0002c0001t0001g0317 others(7): Show |
11 | NA18944.hp1 NA18947.hp1 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.400-1324C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591037 | |||||||
| chr17:4591051 | A | G | 4 | a0001c0002t0001g0214 a0001c0002t0001g0215 a0001c0002t0002g0213 others(1): Show |
4 | HG02280.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-1310A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591051 | |||||||
| chr17:4591133 | C | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-1228C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591133 | |||||||
| chr17:4591135 | T | A | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-1226T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591135 | |||||||
| chr17:4591195 | T | C | 117 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(114): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.400-1166T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591195 | |||||||
| chr17:4591213 | C | T | 25 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(22): Show |
29 | HG00639.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.400-1148C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591213 | |||||||
| chr17:4591341 | C | T | 7 | a0001c0003t0001g0136 a0001c0003t0002g0135 a0001c0006t0001g0140 others(4): Show |
7 | HG02572.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-1020C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591341 | |||||||
| chr17:4591516 | G | T | 345 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(342): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.400-845G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591516 | |||||||
| chr17:4591520 | T | C | 122 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(119): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.400-841T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591520 | |||||||
| chr17:4591539 | C | T | 13 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(10): Show |
17 | HG00639.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.400-822C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591539 | |||||||
| chr17:4591604 | G | A | 12 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0207 others(9): Show |
15 | HG02055.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.400-757G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591604 | |||||||
| chr17:4591713 | G | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-648G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591713 | |||||||
| chr17:4591714 | T | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-647T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591714 | |||||||
| chr17:4591716 | G | C | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-645G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591716 | |||||||
| chr17:4591722 | C | T | 1 | a0002c0001t0001g0278 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.400-639C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591722 | |||||||
| chr17:4591823 | G | A | 1 | a0002c0001t0001g0284 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.400-538G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591823 | |||||||
| chr17:4591831 | C | T | 43 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(40): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.400-530C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591831 | |||||||
| chr17:4591854 | A | G | 1 | a0002c0010t0002g0316 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.400-507A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591854 | |||||||
| chr17:4591915 | C | T | 228 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(225): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.400-446C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4591915 | |||||||
| chr17:4592016 | G | A | 1 | a0001c0012t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.400-345G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4592016 | |||||||
| chr17:4592068 | G | A | 1 | a0002c0001t0002g0265 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.400-293G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4592068 | |||||||
| chr17:4592219 | GTCACTTT others(27): Show |
G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400-140_400-107del others(34): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr17 | 4592219 | ||||||
| chr17:4592326 | C | A | 1 | a0007c0029t0002g0201 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.400-35C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 1/7 | chr17 | 4592326 | |||||||
| chr17:4592538 | C | A | 1 | a0002c0001t0002g0318 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.487+90C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592538 | |||||||
| chr17:4592583 | G | C | 1 | a0001c0004t0002g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.487+135G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592583 | |||||||
| chr17:4592599 | C | T | 1 | a0001c0003t0001g0342 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.487+151C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592599 | |||||||
| chr17:4592629 | G | A | 1 | a0001c0003t0011g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.487+181G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592629 | |||||||
| chr17:4592670 | T | A | 14 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0002t0006g0173 others(11): Show |
18 | HG00558.hp2 HG01167.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.487+222T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592670 | |||||||
| chr17:4592701 | C | T | 32 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0026 others(29): Show |
38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.488-228C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592701 | |||||||
| chr17:4592810 | G | A | 1 | a0002c0001t0001g0269 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.488-119G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 2/7 | chr17 | 4592810 | |||||||
| chr17:4593288 | C | G | 1 | a0001c0002t0001g0084 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.730+117C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593288 | |||||||
| chr17:4593315 | C | T | 1 | a0001c0005t0002g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.730+144C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593315 | |||||||
| chr17:4593327 | C | T | 1 | a0002c0001t0002g0050 | 2 | NA18960.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.730+156C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593327 | |||||||
| chr17:4593367 | G | A | 53 | a0001c0002t0001g0066 a0001c0003t0001g0136 a0001c0004t0001g0007 others(50): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.730+196G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593367 | |||||||
| chr17:4593431 | C | T | 5 | a0001c0003t0001g0143 a0001c0003t0001g0144 a0001c0003t0001g0145 others(2): Show |
5 | HG02630.hp1 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+260C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593431 | |||||||
| chr17:4593452 | T | G | 54 | a0001c0002t0001g0066 a0001c0003t0001g0136 a0001c0004t0001g0007 others(51): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.730+281T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593452 | |||||||
| chr17:4593493 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730+322G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593493 | |||||||
| chr17:4593500 | G | A | 1 | a0001c0007t0002g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.731-322G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593500 | |||||||
| chr17:4593515 | G | A | 3 | a0001c0004t0002g0114 a0001c0004t0002g0116 a0001c0004t0002g0117 |
3 | HG00140.hp1 HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.731-307G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593515 | |||||||
| chr17:4593601 | C | T | 16 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(13): Show |
20 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.731-221C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593601 | |||||||
| chr17:4593749 | C | T | 3 | a0001c0002t0001g0081 a0001c0002t0001g0083 a0001c0002t0001g0256 |
3 | NA19077.hp1 NA19087.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.731-73C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593749 | |||||||
| chr17:4593757 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.731-65G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593757 | |||||||
| chr17:4593766 | T | C | 1 | a0002c0001t0001g0035 | 2 | NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.731-56T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593766 | |||||||
| chr17:4593789 | G | T | 53 | a0001c0003t0001g0136 a0001c0004t0001g0007 a0001c0004t0001g0030 others(50): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.731-33G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 3/7 | chr17 | 4593789 | |||||||
| chr17:4593932 | C | T | 1 | a0001c0006t0003g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.806+35C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4593932 | |||||||
| chr17:4593959 | C | T | 2 | a0001c0007t0002g0231 a0003c0009t0001g0134 |
2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.806+62C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4593959 | |||||||
| chr17:4594028 | A | C | 30 | a0001c0002t0001g0246 a0001c0002t0001g0247 a0001c0002t0001g0248 others(27): Show |
35 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.806+131A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594028 | |||||||
| chr17:4594043 | G | C | 1 | a0001c0003t0004g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.806+146G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594043 | |||||||
| chr17:4594084 | G | C | 2 | a0001c0003t0002g0135 a0001c0003t0010g0172 |
2 | HG01167.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.806+187G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594084 | |||||||
| chr17:4594143 | A | G | 2 | a0001c0003t0001g0036 a0001c0003t0001g0176 |
3 | NA18945.hp2 NA18947.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.806+246A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594143 | |||||||
| chr17:4594171 | G | A | 1 | a0001c0004t0002g0249 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.806+274G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594171 | |||||||
| chr17:4594174 | C | T | 20 | a0001c0003t0001g0036 a0001c0003t0001g0143 a0001c0003t0001g0144 others(17): Show |
24 | HG00558.hp2 HG01167.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.806+277C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594174 | |||||||
| chr17:4594300 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.806+403T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594300 | |||||||
| chr17:4594313 | G | T | 1 | a0001c0003t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.806+416G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594313 | |||||||
| chr17:4594452 | A | AAAAT | 114 | a0001c0002t0001g0089 a0001c0002t0001g0161 a0001c0002t0001g0189 others(111): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.806+580_806+583dup others(4): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr17 | 4594452 | ||||||
| chr17:4594452 | A | AAAATAAA others(1): Show |
2 | a0001c0007t0002g0025 a0001c0007t0002g0149 |
3 | HG01433.hp2 HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.806+576_806+583dup others(8): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr17 | 4594452 | ||||||
| chr17:4594473 | A | AAAT | 15 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(12): Show |
18 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.806+579_806+581dup others(3): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr17 | 4594473 | ||||||
| chr17:4594477 | A | G | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.806+580A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594477 | |||||||
| chr17:4594480 | T | TAAATGAA others(4): Show |
1 | a0001c0002t0002g0069 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.806+583_806+584ins others(11): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594480 | |||||||
| chr17:4594481 | G | A | 6 | a0001c0002t0002g0069 a0003c0009t0001g0315 a0003c0009t0004g0241 others(3): Show |
6 | HG01243.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+584G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594481 | |||||||
| chr17:4594487 | A | C | 70 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(67): Show |
77 | HG00544.hp2 HG00609.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.806+590A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594487 | |||||||
| chr17:4594520 | C | T | 1 | a0001c0004t0001g0030 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.806+623C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594520 | |||||||
| chr17:4594586 | CG | C | 2 | a0002c0001t0001g0020 a0002c0001t0001g0334 |
4 | HG02056.hp2 NA18973.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-557delG | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr17 | 4594586 | ||||||
| chr17:4594658 | C | A | 16 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(13): Show |
20 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.807-487C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594658 | |||||||
| chr17:4594658 | C | T | 5 | a0003c0009t0001g0315 a0003c0009t0004g0241 a0003c0016t0001g0147 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-487C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594658 | |||||||
| chr17:4594674 | C | T | 1 | a0001c0007t0002g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.807-471C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594674 | |||||||
| chr17:4594710 | CT | C | 107 | a0001c0002t0001g0070 a0001c0002t0001g0089 a0001c0002t0001g0154 others(104): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.807-423delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr17 | 4594710 | ||||||
| chr17:4594805 | G | A | 3 | a0001c0013t0001g0028 a0001c0013t0001g0132 a0001c0013t0007g0028 |
3 | HG02257.hp2 HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.807-340G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594805 | |||||||
| chr17:4594813 | G | C | 4 | a0001c0003t0001g0342 a0001c0007t0001g0054 a0001c0017t0009g0166 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-332G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4594813 | |||||||
| chr17:4595130 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.807-15C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 4/7 | chr17 | 4595130 | |||||||
| chr17:4595346 | A | G | 52 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0086 others(49): Show |
59 | HG00544.hp2 HG00609.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.989+19A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595346 | |||||||
| chr17:4595355 | C | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.989+28C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595355 | |||||||
| chr17:4595357 | G | C | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.989+30G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595357 | |||||||
| chr17:4595361 | C | G | 59 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(56): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.989+34C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595361 | |||||||
| chr17:4595387 | C | G | 325 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(322): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.989+60C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595387 | |||||||
| chr17:4595521 | A | G | 1 | a0002c0001t0001g0314 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.989+194A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595521 | |||||||
| chr17:4595687 | C | T | 12 | a0001c0002t0002g0039 a0001c0002t0002g0069 a0001c0002t0002g0162 others(9): Show |
13 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.989+360C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595687 | |||||||
| chr17:4595701 | G | A | 1 | a0001c0002t0002g0068 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.989+374G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595701 | |||||||
| chr17:4595826 | A | G | 283 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(280): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.989+499A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595826 | |||||||
| chr17:4595837 | C | G | 8 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(5): Show |
8 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.989+510C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595837 | |||||||
| chr17:4595874 | T | A | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.989+547T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4595874 | |||||||
| chr17:4595899 | AGTGTGGC others(273): Show |
A | 3 | a0003c0009t0001g0137 a0003c0009t0001g0138 a0003c0009t0001g0139 |
3 | HG02572.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.989+598_990-656del | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4595899 | ||||||
| chr17:4595925 | TCTGCTGT others(73): Show |
T | 57 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(54): Show |
68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.989+743_990-711del others(80): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4595925 | ||||||
| chr17:4595990 | CGCGTGGT others(113): Show |
C | 17 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(14): Show |
21 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.989+678_990-736del | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4595990 | ||||||
| chr17:4596019 | G | C | 1 | a0002c0001t0001g0337 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.989+692G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596019 | |||||||
| chr17:4596033 | G | A | 4 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0044 others(1): Show |
7 | HG01258.hp1 HG01928.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.989+706G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596033 | |||||||
| chr17:4596085 | C | T | 42 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(39): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.989+758C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596085 | |||||||
| chr17:4596085 | CCTGCTGT others(33): Show |
C | 4 | a0003c0009t0001g0315 a0003c0016t0001g0147 a0003c0016t0001g0216 others(1): Show |
4 | HG02717.hp2 HG02970.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.990-735_990-696del others(40): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4596085 | ||||||
| chr17:4596123 | T | A | 8 | a0001c0003t0001g0036 a0001c0003t0001g0176 a0002c0001t0001g0001 others(5): Show |
11 | HG01346.hp1 HG02523.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.990-737T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596123 | |||||||
| chr17:4596140 | G | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-720G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596140 | |||||||
| chr17:4596141 | T | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-719T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596141 | |||||||
| chr17:4596142 | G | A | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-718G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596142 | |||||||
| chr17:4596150 | A | C | 107 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(104): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.990-710A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596150 | |||||||
| chr17:4596156 | G | T | 52 | a0001c0004t0001g0007 a0001c0004t0001g0030 a0001c0004t0001g0109 others(49): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.990-704G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596156 | |||||||
| chr17:4596173 | G | A | 1 | a0001c0004t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.990-687G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596173 | |||||||
| chr17:4596179 | GGTGTGGC others(33): Show |
G | 22 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(19): Show |
22 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.990-641_990-602del others(40): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4596179 | ||||||
| chr17:4596219 | A | G | 7 | a0003c0009t0001g0137 a0003c0009t0001g0138 a0003c0009t0001g0139 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.990-641A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596219 | |||||||
| chr17:4596233 | G | A | 1 | a0001c0002t0001g0084 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.990-627G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596233 | |||||||
| chr17:4596243 | T | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-617T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596243 | |||||||
| chr17:4596244 | G | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-616G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596244 | |||||||
| chr17:4596245 | C | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-615C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596245 | |||||||
| chr17:4596247 | T | A | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-613T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596247 | |||||||
| chr17:4596436 | T | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-424T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596436 | |||||||
| chr17:4596456 | T | C | 15 | a0001c0002t0001g0089 a0002c0001t0001g0014 a0002c0001t0001g0015 others(12): Show |
20 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.990-404T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596456 | |||||||
| chr17:4596467 | G | T | 41 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(38): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.990-393G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596467 | |||||||
| chr17:4596535 | C | A | 1 | a0002c0001t0001g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.990-325C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596535 | |||||||
| chr17:4596593 | G | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-267G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596593 | |||||||
| chr17:4596603 | AG | A | 8 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(5): Show |
8 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.990-253delG | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr17 | 4596603 | ||||||
| chr17:4596777 | A | G | 281 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(278): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.990-83A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596777 | |||||||
| chr17:4596802 | C | T | 3 | a0001c0004t0002g0117 a0001c0006t0003g0156 a0002c0001t0001g0327 |
3 | HG00140.hp1 HG03225.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.990-58C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596802 | |||||||
| chr17:4596813 | A | T | 17 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(14): Show |
21 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.990-47A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596813 | |||||||
| chr17:4596829 | C | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.990-31C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 5/7 | chr17 | 4596829 | |||||||
| chr17:4597009 | C | T | 105 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(102): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1107+32C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 6/7 | chr17 | 4597009 | |||||||
| chr17:4597092 | G | A | 3 | a0001c0002t0001g0055 a0001c0002t0001g0071 a0001c0002t0002g0072 |
3 | HG00099.hp1 HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1108-80G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 6/7 | chr17 | 4597092 | |||||||
| chr17:4597405 | G | A | 4 | a0001c0008t0001g0123 a0002c0001t0001g0005 a0002c0001t0001g0045 others(1): Show |
9 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.1259+82G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597405 | |||||||
| chr17:4597444 | C | T | 8 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(5): Show |
8 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259+121C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597444 | |||||||
| chr17:4597693 | C | T | 2 | a0003c0009t0001g0315 a0011c0022t0008g0236 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1259+370C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597693 | |||||||
| chr17:4597720 | G | A | 16 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(13): Show |
19 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1259+397G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597720 | |||||||
| chr17:4597872 | T | C | 8 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(5): Show |
8 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259+549T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597872 | |||||||
| chr17:4597889 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1259+566T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597889 | |||||||
| chr17:4597962 | G | C | 1 | a0001c0002t0002g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1259+639G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4597962 | |||||||
| chr17:4598049 | G | A | 1 | a0002c0011t0001g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1259+726G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598049 | |||||||
| chr17:4598082 | G | C | 2 | a0001c0002t0001g0042 a0002c0001t0001g0310 |
3 | HG01928.hp1 HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1259+759G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598082 | |||||||
| chr17:4598159 | A | G | 2 | a0001c0008t0001g0127 a0001c0008t0001g0130 |
2 | NA18968.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1259+836A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598159 | |||||||
| chr17:4598232 | C | T | 2 | a0001c0002t0001g0024 a0001c0002t0001g0062 |
3 | HG02886.hp2 HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1259+909C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598232 | |||||||
| chr17:4598241 | C | T | 109 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(106): Show |
161 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1259+918C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598241 | |||||||
| chr17:4598258 | G | A | 42 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(39): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1259+935G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598258 | |||||||
| chr17:4598345 | C | T | 15 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(12): Show |
18 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1259+1022C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598345 | |||||||
| chr17:4598602 | T | A | 112 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(109): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1259+1279T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598602 | |||||||
| chr17:4598635 | G | C | 112 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(109): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1259+1312G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598635 | |||||||
| chr17:4598644 | C | T | 112 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(109): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1259+1321C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598644 | |||||||
| chr17:4598645 | G | A | 1 | a0001c0007t0001g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1259+1322G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598645 | |||||||
| chr17:4598781 | A | C | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1458A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598781 | |||||||
| chr17:4598782 | C | A | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1459C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598782 | |||||||
| chr17:4598788 | T | C | 269 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0012 others(266): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1259+1465T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598788 | |||||||
| chr17:4598824 | TA | T | 58 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(55): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1259+1516delA | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4598824 | ||||||
| chr17:4598842 | G | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1519G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598842 | |||||||
| chr17:4598883 | G | C | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1560G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598883 | |||||||
| chr17:4598884 | C | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1561C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598884 | |||||||
| chr17:4598938 | G | A | 1 | a0001c0008t0002g0031 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1259+1615G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598938 | |||||||
| chr17:4598949 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1259+1626C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598949 | |||||||
| chr17:4598950 | G | A | 54 | a0001c0004t0001g0030 a0001c0004t0001g0109 a0001c0004t0001g0111 others(51): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1259+1627G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598950 | |||||||
| chr17:4598968 | C | G | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1645C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598968 | |||||||
| chr17:4598969 | G | A | 1 | a0002c0010t0002g0285 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1259+1646G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598969 | |||||||
| chr17:4598970 | G | C | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1647G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598970 | |||||||
| chr17:4598976 | G | C | 11 | a0001c0003t0002g0008 a0001c0003t0002g0164 a0001c0003t0002g0169 others(8): Show |
14 | HG00558.hp2 HG01346.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1259+1653G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4598976 | |||||||
| chr17:4599014 | G | C | 1 | a0002c0001t0001g0100 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1259+1691G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599014 | |||||||
| chr17:4599015 | T | G | 55 | a0001c0004t0001g0030 a0001c0004t0001g0109 a0001c0004t0001g0111 others(52): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1259+1692T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599015 | |||||||
| chr17:4599017 | A | T | 1 | a0001c0008t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1259+1694A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599017 | |||||||
| chr17:4599049 | C | A | 2 | a0001c0003t0002g0178 a0001c0003t0002g0179 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1259+1726C>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599049 | |||||||
| chr17:4599075 | C | T | 1 | a0001c0003t0013g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1259+1752C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599075 | |||||||
| chr17:4599091 | G | A | 1 | a0001c0002t0001g0026 | 2 | HG01255.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1259+1768G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599091 | |||||||
| chr17:4599092 | A | G | 5 | a0001c0004t0002g0129 a0003c0009t0001g0315 a0003c0016t0001g0147 others(2): Show |
5 | HG02717.hp2 HG02970.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+1769A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599092 | |||||||
| chr17:4599290 | G | A | 3 | a0001c0008t0001g0131 a0001c0026t0002g0223 a0002c0001t0001g0292 |
3 | HG00408.hp1 HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1259+1967G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599290 | |||||||
| chr17:4599400 | C | T | 2 | a0003c0016t0001g0147 a0003c0016t0001g0216 |
2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1259+2077C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599400 | |||||||
| chr17:4599410 | G | A | 8 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(5): Show |
8 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259+2087G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599410 | |||||||
| chr17:4599419 | A | G | 1 | a0001c0004t0002g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1259+2096A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599419 | |||||||
| chr17:4599425 | A | C | 28 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(25): Show |
31 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.1259+2102A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599425 | |||||||
| chr17:4599542 | G | C | 18 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(15): Show |
22 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1259+2219G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599542 | |||||||
| chr17:4599580 | T | C | 2 | a0001c0002t0001g0264 a0002c0021t0001g0275 |
2 | HG01175.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1259+2257T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599580 | |||||||
| chr17:4599588 | G | C | 3 | a0001c0017t0003g0240 a0001c0017t0009g0166 a0001c0020t0001g0165 |
3 | HG02055.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1259+2265G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599588 | |||||||
| chr17:4599666 | A | G | 18 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(15): Show |
22 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1259+2343A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599666 | |||||||
| chr17:4599738 | C | T | 17 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(14): Show |
21 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1259+2415C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599738 | |||||||
| chr17:4599900 | G | A | 103 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(100): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1259+2577G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599900 | |||||||
| chr17:4599935 | A | C | 2 | a0001c0002t0001g0042 a0002c0001t0001g0310 |
3 | HG01928.hp1 HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1259+2612A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4599935 | |||||||
| chr17:4600011 | C | T | 7 | a0001c0002t0001g0232 a0001c0007t0002g0151 a0001c0007t0002g0152 others(4): Show |
10 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259+2688C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600011 | |||||||
| chr17:4600044 | G | A | 1 | a0003c0009t0001g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1259+2721G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600044 | |||||||
| chr17:4600069 | G | A | 3 | a0003c0009t0001g0137 a0003c0009t0001g0138 a0003c0009t0001g0139 |
3 | HG02572.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1259+2746G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600069 | |||||||
| chr17:4600102 | GT | G | 7 | a0001c0004t0001g0030 a0001c0007t0001g0186 a0001c0007t0001g0243 others(4): Show |
8 | HG01099.hp1 HG01952.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1259+2780delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600102 | |||||||
| chr17:4600262 | C | G | 1 | a0001c0002t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1259+2939C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600262 | |||||||
| chr17:4600488 | G | A | 4 | a0001c0004t0001g0030 a0001c0007t0001g0186 a0001c0007t0001g0243 others(1): Show |
5 | HG01099.hp1 HG01952.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+3165G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600488 | |||||||
| chr17:4600723 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1259+3400C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600723 | |||||||
| chr17:4600724 | G | C | 1 | a0001c0003t0002g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1259+3401G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600724 | |||||||
| chr17:4600751 | G | A | 1 | a0002c0001t0001g0293 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1259+3428G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600751 | |||||||
| chr17:4600805 | G | A | 2 | a0001c0002t0005g0040 a0001c0002t0005g0188 |
3 | NA18956.hp2 NA19082.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1259+3482G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600805 | |||||||
| chr17:4600843 | G | C | 1 | a0002c0001t0001g0021 | 3 | NA19064.hp1 NA19084.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1259+3520G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600843 | |||||||
| chr17:4600981 | G | A | 1 | a0002c0001t0001g0266 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1259+3658G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4600981 | |||||||
| chr17:4601002 | C | T | 1 | a0011c0022t0008g0236 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1259+3679C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601002 | |||||||
| chr17:4601007 | C | T | 14 | a0001c0006t0001g0033 a0001c0006t0001g0034 a0001c0006t0001g0140 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1259+3684C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601007 | |||||||
| chr17:4601085 | C | T | 52 | a0001c0003t0001g0251 a0001c0003t0002g0017 a0001c0003t0002g0180 others(49): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1259+3762C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601085 | |||||||
| chr17:4601377 | T | C | 7 | a0001c0003t0001g0182 a0001c0005t0001g0004 a0001c0005t0001g0032 others(4): Show |
12 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1259+4054T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601377 | |||||||
| chr17:4601380 | A | G | 1 | a0001c0003t0001g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1259+4057A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601380 | |||||||
| chr17:4601414 | C | CA | 278 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(275): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1259+4102dupA | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4601414 | ||||||
| chr17:4601414 | C | CAA | 13 | a0001c0002t0001g0161 a0001c0002t0001g0189 a0001c0003t0001g0036 others(10): Show |
15 | HG01099.hp1 HG01952.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1259+4101_1259+410 others(6): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4601414 | ||||||
| chr17:4601512 | A | ATGAT | 28 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(25): Show |
34 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1259+4217_1259+422 others(8): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4601512 | ||||||
| chr17:4601512 | ATGAT | A | 25 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0080 others(22): Show |
32 | HG01167.hp2 HG01934.hp1 HG01993.hp1 others(29): Show |
intron_variant | MODIFIER | c.1259+4217_1259+422 others(8): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4601512 | ||||||
| chr17:4601542 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1259+4219G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601542 | |||||||
| chr17:4601673 | A | C | 23 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(20): Show |
23 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1259+4350A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601673 | |||||||
| chr17:4601689 | AT | A | 157 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(154): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1259+4379delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4601689 | ||||||
| chr17:4601703 | A | G | 4 | a0001c0002t0002g0079 a0001c0002t0002g0213 a0001c0003t0002g0178 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259+4380A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601703 | |||||||
| chr17:4601716 | A | C | 291 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(288): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1259+4393A>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601716 | |||||||
| chr17:4601731 | G | C | 106 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(103): Show |
157 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1259+4408G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601731 | |||||||
| chr17:4601809 | C | T | 14 | a0001c0006t0001g0033 a0001c0006t0001g0034 a0001c0006t0001g0140 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1259+4486C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601809 | |||||||
| chr17:4601810 | G | A | 5 | a0001c0004t0002g0016 a0001c0004t0002g0115 a0001c0005t0002g0016 others(2): Show |
6 | HG00621.hp2 NA18946.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1259+4487G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601810 | |||||||
| chr17:4601813 | C | T | 1 | a0001c0006t0003g0156 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1259+4490C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601813 | |||||||
| chr17:4601942 | A | G | 1 | a0006c0024t0001g0309 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1259+4619A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601942 | |||||||
| chr17:4601976 | C | T | 1 | a0002c0001t0001g0301 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1259+4653C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4601976 | |||||||
| chr17:4602070 | T | A | 1 | a0002c0001t0001g0101 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1259+4747T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602070 | |||||||
| chr17:4602166 | T | C | 1 | a0001c0002t0001g0084 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1259+4843T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602166 | |||||||
| chr17:4602213 | T | C | 1 | a0001c0007t0001g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1259+4890T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602213 | |||||||
| chr17:4602276 | C | G | 1 | a0001c0003t0002g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1259+4953C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602276 | |||||||
| chr17:4602311 | C | CT | 22 | a0001c0002t0001g0009 a0001c0002t0001g0080 a0001c0002t0001g0208 others(19): Show |
24 | HG01243.hp2 HG01978.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1259+5016dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CT | C | 110 | a0001c0002t0001g0056 a0001c0002t0001g0060 a0001c0002t0001g0070 others(107): Show |
161 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1259+5016delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CTT | C | 115 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0018 others(112): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1259+5015_1259+501 others(6): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CTTT | C | 17 | a0001c0003t0004g0237 a0001c0006t0001g0033 a0001c0006t0001g0034 others(14): Show |
17 | HG01243.hp1 HG01891.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1259+5014_1259+501 others(7): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CTTTT | C | 7 | a0001c0003t0001g0250 a0001c0003t0004g0242 a0001c0005t0001g0219 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259+5013_1259+501 others(8): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CTTTTTTT others(4): Show |
C | 1 | a0001c0004t0002g0128 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1259+5006_1259+501 others(15): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602311 | CTTTTTTT others(10): Show |
C | 1 | a0002c0001t0001g0302 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1259+5000_1259+501 others(21): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4602311 | ||||||
| chr17:4602509 | G | T | 13 | a0001c0006t0001g0033 a0001c0006t0001g0034 a0001c0006t0001g0140 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1260-4852G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602509 | |||||||
| chr17:4602569 | C | T | 4 | a0001c0003t0001g0036 a0001c0003t0001g0176 a0002c0001t0001g0294 others(1): Show |
5 | NA18747.hp2 NA18945.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260-4792C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602569 | |||||||
| chr17:4602701 | G | A | 51 | a0001c0002t0002g0075 a0001c0003t0001g0251 a0001c0003t0002g0017 others(48): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1260-4660G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602701 | |||||||
| chr17:4602789 | C | T | 9 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(6): Show |
9 | HG02572.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260-4572C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602789 | |||||||
| chr17:4602854 | C | T | 1 | a0001c0019t0001g0221 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1260-4507C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4602854 | |||||||
| chr17:4603259 | G | T | 51 | a0001c0002t0002g0075 a0001c0003t0001g0251 a0001c0003t0002g0017 others(48): Show |
64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1260-4102G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4603259 | |||||||
| chr17:4603374 | A | AGAATAAG others(10): Show |
1 | a0001c0003t0011g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1260-3985_1260-396 others(21): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4603374 | ||||||
| chr17:4603482 | T | G | 2 | a0001c0002t0001g0262 a0001c0002t0001g0263 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1260-3879T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4603482 | |||||||
| chr17:4603578 | G | A | 18 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(15): Show |
22 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1260-3783G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4603578 | |||||||
| chr17:4603883 | C | T | 103 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(100): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1260-3478C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4603883 | |||||||
| chr17:4604002 | A | G | 3 | a0001c0002t0001g0018 a0004c0014t0001g0018 a0004c0014t0001g0261 |
4 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260-3359A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604002 | |||||||
| chr17:4604033 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1260-3328C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604033 | |||||||
| chr17:4604136 | C | T | 3 | a0001c0003t0002g0253 a0002c0001t0002g0303 a0002c0011t0002g0277 |
3 | HG01081.hp1 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1260-3225C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604136 | |||||||
| chr17:4604212 | C | T | 16 | a0001c0002t0001g0010 a0001c0002t0001g0018 a0001c0002t0001g0042 others(13): Show |
20 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1260-3149C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604212 | |||||||
| chr17:4604259 | A | G | 1 | a0001c0005t0002g0110 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1260-3102A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604259 | |||||||
| chr17:4604363 | T | C | 1 | a0002c0010t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1260-2998T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604363 | |||||||
| chr17:4604409 | G | A | 1 | a0001c0003t0010g0172 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260-2952G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604409 | |||||||
| chr17:4604442 | G | C | 1 | a0001c0003t0010g0172 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260-2919G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604442 | |||||||
| chr17:4604517 | G | A | 1 | a0001c0004t0001g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1260-2844G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604517 | |||||||
| chr17:4604534 | T | C | 1 | a0001c0003t0010g0172 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260-2827T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604534 | |||||||
| chr17:4604559 | G | A | 1 | a0001c0003t0010g0172 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260-2802G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604559 | |||||||
| chr17:4604681 | C | CT | 24 | a0001c0002t0001g0161 a0001c0002t0001g0189 a0001c0003t0007g0244 others(21): Show |
25 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260-2671dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4604681 | ||||||
| chr17:4604749 | G | A | 1 | a0002c0001t0001g0297 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1260-2612G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604749 | |||||||
| chr17:4604817 | G | A | 2 | a0001c0002t0001g0086 a0002c0010t0001g0270 |
2 | HG00280.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1260-2544G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604817 | |||||||
| chr17:4604846 | T | C | 61 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0024 others(58): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1260-2515T>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604846 | |||||||
| chr17:4604946 | C | G | 3 | a0001c0017t0003g0240 a0001c0017t0009g0166 a0001c0020t0001g0165 |
3 | HG02055.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1260-2415C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604946 | |||||||
| chr17:4604961 | G | A | 1 | a0002c0001t0014g0288 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1260-2400G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604961 | |||||||
| chr17:4604981 | T | G | 85 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(82): Show |
128 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1260-2380T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4604981 | |||||||
| chr17:4605030 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1260-2331G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605030 | |||||||
| chr17:4605153 | G | GT | 87 | a0001c0002t0001g0009 a0001c0002t0001g0041 a0001c0002t0001g0070 others(84): Show |
110 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1260-2182dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4605153 | ||||||
| chr17:4605153 | G | GTT | 63 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0026 others(60): Show |
74 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1260-2183_1260-218 others(6): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4605153 | ||||||
| chr17:4605153 | G | GTTT | 16 | a0001c0002t0001g0067 a0001c0002t0001g0077 a0001c0002t0001g0078 others(13): Show |
19 | HG00280.hp2 HG00597.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1260-2184_1260-218 others(7): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4605153 | ||||||
| chr17:4605153 | GT | G | 12 | a0001c0002t0002g0191 a0001c0002t0002g0194 a0001c0003t0001g0144 others(9): Show |
17 | HG01109.hp1 HG01256.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1260-2182delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4605153 | ||||||
| chr17:4605158 | T | G | 1 | a0001c0003t0010g0172 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1260-2203T>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605158 | |||||||
| chr17:4605269 | C | T | 8 | a0001c0005t0002g0260 a0002c0001t0002g0051 a0002c0001t0002g0099 others(5): Show |
9 | HG00735.hp2 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260-2092C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605269 | |||||||
| chr17:4605335 | A | T | 2 | a0001c0004t0002g0259 a0002c0010t0002g0272 |
2 | HG02523.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1260-2026A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605335 | |||||||
| chr17:4605608 | C | T | 2 | a0001c0002t0002g0185 a0001c0002t0002g0198 |
2 | NA18967.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1260-1753C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605608 | |||||||
| chr17:4605624 | G | A | 224 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0011 others(221): Show |
293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1260-1737G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605624 | |||||||
| chr17:4605678 | A | G | 1 | a0001c0003t0002g0180 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260-1683A>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605678 | |||||||
| chr17:4605714 | T | A | 9 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0001g0182 others(6): Show |
14 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1260-1647T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605714 | |||||||
| chr17:4605757 | T | A | 1 | a0001c0002t0002g0162 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1260-1604T>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605757 | |||||||
| chr17:4605771 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1260-1590C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605771 | |||||||
| chr17:4605801 | C | T | 4 | a0001c0003t0001g0143 a0001c0003t0001g0146 a0001c0003t0001g0342 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260-1560C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605801 | |||||||
| chr17:4605818 | CA | C | 24 | a0001c0002t0001g0161 a0001c0002t0001g0189 a0001c0003t0007g0244 others(21): Show |
25 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260-1542delA | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605818 | |||||||
| chr17:4605865 | G | T | 2 | a0003c0016t0001g0147 a0003c0016t0001g0216 |
2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1260-1496G>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4605865 | |||||||
| chr17:4606086 | G | C | 35 | a0001c0002t0001g0161 a0001c0002t0001g0189 a0001c0003t0001g0250 others(32): Show |
36 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260-1275G>C | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606086 | |||||||
| chr17:4606125 | CT | C | 12 | a0001c0002t0001g0210 a0001c0003t0001g0144 a0001c0003t0001g0145 others(9): Show |
17 | HG01109.hp1 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1260-1225delT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4606125 | ||||||
| chr17:4606163 | C | CCAGGCTG others(11): Show |
1 | a0001c0002t0001g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1260-1195_1260-117 others(22): Show |
SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4606163 | ||||||
| chr17:4606204 | C | G | 1 | a0001c0002t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1260-1157C>G | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606204 | |||||||
| chr17:4606365 | G | A | 9 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0001g0182 others(6): Show |
14 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1260-996G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606365 | |||||||
| chr17:4606424 | C | CT | 10 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0084 others(7): Show |
10 | HG00438.hp2 HG02145.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260-924dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4606424 | ||||||
| chr17:4606555 | G | A | 11 | a0001c0003t0001g0250 a0001c0003t0004g0237 a0001c0003t0004g0242 others(8): Show |
11 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1260-806G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606555 | |||||||
| chr17:4606706 | A | T | 1 | a0002c0001t0002g0049 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1260-655A>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606706 | |||||||
| chr17:4606875 | G | A | 4 | a0001c0003t0001g0143 a0001c0003t0001g0146 a0001c0003t0001g0342 others(1): Show |
4 | HG01243.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260-486G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4606875 | |||||||
| chr17:4607214 | G | A | 10 | a0001c0002t0001g0009 a0001c0002t0001g0080 a0001c0002t0001g0208 others(7): Show |
12 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1260-147G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4607214 | |||||||
| chr17:4607231 | C | T | 4 | a0001c0003t0002g0180 a0001c0003t0002g0253 a0002c0001t0002g0303 others(1): Show |
4 | HG01081.hp1 HG01175.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260-130C>T | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4607231 | |||||||
| chr17:4607284 | G | A | 1 | a0001c0002t0001g0024 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1260-77G>A | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | chr17 | 4607284 | |||||||
| chr17:4607305 | C | CT | 92 | a0001c0002t0001g0060 a0001c0002t0001g0061 a0001c0002t0001g0070 others(89): Show |
136 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.1260-55dupT | SMTNL2 | ENSG00000188176.12 | transcript | ENST00000389313.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr17 | 4607305 |