Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64092 |
| ensemblid | ENSG00000155307.19 |
| hgncid | 10528 |
| symbol | SAMSN1 |
| name | SAM domain, SH3 domain and nuclear localization signals 1 |
| refseq_nuc | NM_022136.5 |
| refseq_prot | NP_071419.3 |
| ensembl_nuc | ENST00000400566.6 |
| ensembl_prot | ENSP00000383411.2 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 14485228 |
| end | 14546315 |
| strand | - |
| ver | v1.2 |
| region | chr21:14485228-14546315 |
| region5000 | chr21:14480228-14551315 |
| regionname0 | SAMSN1_chr21_14485228_14546315 |
| regionname5000 | SAMSN1_chr21_14480228_14551315 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 373 | 392 | 81 | 67 | 184 | 18 | 40 | 146 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | MLKRK others(368): Show |
chr21 | 14480228 | 14551315 |
| a0002 | 0/0 | 373 | 14 | 11 | 3 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | MLKRK others(368): Show |
chr21 | 14480228 | 14551315 |
| a0003 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | MLKRK others(368): Show |
chr21 | 14480228 | 14551315 |
| a0004 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | MLKRK others(368): Show |
chr21 | 14480228 | 14551315 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1119 | 285 | 57 | 52 | 133 | 15 | 26 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 | ||
| a0001c0002 | 0/0 | 1119 | 107 | 24 | 15 | 51 | 3 | 14 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 | ||
| a0002c0003 | 0/0 | 1119 | 12 | 10 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 | ||
| a0002c0004 | 0/0 | 1119 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 | ||
| a0003c0006 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 | ||
| a0004c0005 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | ATGCT others(1114): Show |
chr21 | 14480228 | 14551315 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1860 | 230 | 47 | 43 | 103 | 14 | 21 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0002 | 0/0 | 1860 | 34 | 5 | 5 | 21 | 0 | 3 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0003 | 0/0 | 1860 | 7 | 0 | 0 | 7 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0004 | 0/0 | 1860 | 4 | 3 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0005 | 0/0 | 1860 | 3 | 0 | 2 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0006 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0007 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0010 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0011 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0012 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0001t0015 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0001 | 0/0 | 1860 | 91 | 20 | 13 | 43 | 3 | 12 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0002 | 0/0 | 1860 | 9 | 2 | 1 | 5 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0003 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0006 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0009 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0013 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0001c0002t0014 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0002c0003t0001 | 0/0 | 1860 | 11 | 9 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0002c0003t0002 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0002c0004t0001 | 0/0 | 1860 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0003c0006t0001 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| a0004c0005t0001 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | AGTTG others(1855): Show |
chr21 | 14480228 | 14551315 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0003 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0004g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0015g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0013g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0014g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0003c0006t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0004c0005t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0030 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00639 | hp2 | a0001 | c0002 | t0009 | g0028 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0088 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0345 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0348 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0347 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0026 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01884 | hp2 | a0003 | c0006 | t0001 | g0351 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0370 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0040 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0372 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0368 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0367 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02280 | hp1 | a0004 | c0005 | t0001 | g0358 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0355 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0343 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0053 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0326 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0354 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0340 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0377 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02970 | hp1 | a0001 | c0002 | t0008 | g0027 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0056 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0308 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0375 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03098 | hp2 | a0001 | c0002 | t0014 | g0342 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0335 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0029 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0352 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03704 | hp2 | a0001 | c0002 | t0013 | g0364 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0328 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0341 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0339 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0322 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0371 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0092 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0374 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0361 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18977 | hp2 | a0001 | c0002 | t0006 | g0296 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0356 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0373 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0349 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ASW | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | ASW | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0346 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0284 | SAS | GIH | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0287 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02486 | hp2 | a0002 | c0003 | t0002 | g0045 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0170 | REF | REF | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0137 | REF | REF | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14486000 | C | T | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1034G>A | p.Gly345Glu | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 1088/1860 | 1034/1122 | 345/373 | chr21 | 14486000 | |||
| chr21:14500543 | T | A | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.754A>T | p.Arg252Trp | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/8 | 808/1860 | 754/1122 | 252/373 | chr21 | 14500543 | |||
| chr21:14516983 | C | G | 1 | a0002 | 14 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
missense_variant | MODERATE | c.188G>C | p.Gly63Ala | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/8 | 242/1860 | 188/1122 | 63/373 | chr21 | 14516983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14546256 | G | C | 4 | a0001c0002 a0002c0004 a0003c0006 others(1): Show |
111 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
synonymous_variant | LOW | c.6C>G | p.Leu2Leu | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 60/1860 | 6/1122 | 2/373 | chr21 | 14546256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14485271 | G | A | 2 | a0001c0001t0004 a0001c0001t0007 |
6 | HG01099.hp2 HG02145.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*641C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 641 | chr21 | 14485271 | ||||||
| chr21:14485430 | T | C | 1 | a0001c0001t0012 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 482 | chr21 | 14485430 | ||||||
| chr21:14485475 | T | C | 2 | a0001c0001t0006 a0001c0002t0006 |
2 | NA18977.hp2 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 437 | chr21 | 14485475 | ||||||
| chr21:14485525 | C | G | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(3): Show |
47 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*387G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 387 | chr21 | 14485525 | ||||||
| chr21:14485639 | T | C | 1 | a0001c0002t0013 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 273 | chr21 | 14485639 | ||||||
| chr21:14485816 | C | G | 1 | a0001c0001t0011 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 96 | chr21 | 14485816 | ||||||
| chr21:14485850 | G | A | 2 | a0001c0001t0007 a0001c0002t0014 |
3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 62 | chr21 | 14485850 | ||||||
| chr21:14485886 | G | A | 1 | a0001c0001t0015 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 26 | chr21 | 14485886 | ||||||
| chr21:14485908 | G | A | 2 | a0001c0001t0003 a0001c0002t0003 |
9 | HG02071.hp1 HG02135.hp1 NA18952.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 4 | chr21 | 14485908 | ||||||
| chr21:14546280 | C | T | 2 | a0001c0001t0005 a0001c0001t0010 |
4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 19 | chr21 | 14546280 | ||||||
| chr21:14546296 | C | T | 2 | a0001c0002t0008 a0001c0002t0009 |
2 | HG00639.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-35G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 35 | chr21 | 14546296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14486159 | A | G | 15 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0076 others(12): Show |
15 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-45T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486159 | |||||||
| chr21:14486238 | G | A | 85 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0065 others(82): Show |
91 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.920-124C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486238 | |||||||
| chr21:14486286 | A | C | 1 | a0001c0002t0001g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-172T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486286 | |||||||
| chr21:14486287 | C | A | 1 | a0001c0002t0001g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-173G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486287 | |||||||
| chr21:14486291 | A | C | 12 | a0001c0001t0001g0081 a0001c0001t0001g0120 a0001c0001t0001g0177 others(9): Show |
14 | NA18942.hp1 NA18944.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-177T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486291 | |||||||
| chr21:14486348 | A | ATTCC | 2 | a0001c0001t0002g0013 a0001c0001t0002g0128 |
3 | NA18943.hp2 NA18949.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.920-235_920-234ins others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486348 | |||||||
| chr21:14486349 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0128 |
3 | NA18943.hp2 NA18949.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.920-235C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486349 | |||||||
| chr21:14486376 | G | A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-262C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486376 | |||||||
| chr21:14486376 | G | T | 59 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0035 others(56): Show |
62 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.920-262C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486376 | |||||||
| chr21:14486563 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-449T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486563 | |||||||
| chr21:14486709 | G | A | 1 | a0001c0002t0002g0300 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.920-595C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486709 | |||||||
| chr21:14486709 | G | T | 1 | a0001c0001t0012g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.920-595C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486709 | |||||||
| chr21:14486768 | G | C | 1 | a0001c0001t0001g0018 | 2 | HG00323.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.920-654C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486768 | |||||||
| chr21:14486778 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-664A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486778 | |||||||
| chr21:14487001 | G | A | 17 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0073 others(14): Show |
17 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.920-887C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487001 | |||||||
| chr21:14487049 | T | C | 93 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(90): Show |
99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-935A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487049 | |||||||
| chr21:14487110 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.920-996C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487110 | |||||||
| chr21:14487129 | C | T | 367 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(364): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.920-1015G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487129 | |||||||
| chr21:14487231 | G | A | 2 | a0001c0002t0001g0283 a0001c0002t0001g0375 |
2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.920-1117C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487231 | |||||||
| chr21:14487253 | TTCAAAGA others(14): Show |
T | 1 | a0001c0002t0014g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920-1160_920-1140d others(23): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487253 | |||||||
| chr21:14487311 | A | T | 90 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(87): Show |
96 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.920-1197T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487311 | |||||||
| chr21:14487345 | T | TTA | 91 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(88): Show |
97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.920-1232_920-1231i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487345 | |||||||
| chr21:14487345 | T | TTATA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0073 others(3): Show |
6 | HG02055.hp1 HG02074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-1232_920-1231i others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487345 | |||||||
| chr21:14487347 | T | A | 127 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0033 others(124): Show |
135 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-1233A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487347 | |||||||
| chr21:14487347 | TTA | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0071 others(17): Show |
23 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.920-1235_920-1234d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487347 | |||||||
| chr21:14487360 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-1246A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487360 | |||||||
| chr21:14487361 | C | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0002t0001g0280 others(4): Show |
8 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-1247G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487361 | |||||||
| chr21:14487367 | T | TG | 196 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(193): Show |
209 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.920-1254_920-1253i others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487367 | |||||||
| chr21:14487375 | A | G | 2 | a0001c0001t0002g0150 a0001c0001t0002g0185 |
2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.920-1261T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487375 | |||||||
| chr21:14487486 | T | G | 14 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
14 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-1372A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487486 | |||||||
| chr21:14487822 | G | A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-1708C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487822 | |||||||
| chr21:14487825 | C | T | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-1711G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487825 | |||||||
| chr21:14487832 | T | C | 42 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0035 others(39): Show |
45 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.920-1718A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487832 | |||||||
| chr21:14487889 | C | CATGGAAG others(8): Show |
1 | a0001c0002t0001g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-1790_920-1776d others(17): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487889 | |||||||
| chr21:14487937 | A | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0074 others(9): Show |
15 | HG01168.hp1 HG01169.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-1823T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487937 | |||||||
| chr21:14487985 | C | G | 1 | a0001c0002t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.920-1871G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487985 | |||||||
| chr21:14487999 | C | T | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0178 others(13): Show |
16 | HG00597.hp2 NA18951.hp2 NA18955.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-1885G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487999 | |||||||
| chr21:14488054 | C | T | 6 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0205 others(3): Show |
6 | HG02015.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-1940G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488054 | |||||||
| chr21:14488079 | A | G | 1 | a0001c0002t0001g0367 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.920-1965T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488079 | |||||||
| chr21:14488334 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2220T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488334 | |||||||
| chr21:14488335 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2221G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488335 | |||||||
| chr21:14488337 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2223T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488337 | |||||||
| chr21:14488567 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.920-2453T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488567 | |||||||
| chr21:14488684 | G | A | 4 | a0001c0001t0001g0158 a0002c0003t0001g0049 a0002c0004t0001g0287 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-2570C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488684 | |||||||
| chr21:14488710 | C | A | 1 | a0001c0001t0002g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.920-2596G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488710 | |||||||
| chr21:14488729 | A | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0057 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-2615T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488729 | |||||||
| chr21:14488806 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0057 others(23): Show |
29 | HG01099.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.920-2692G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488806 | |||||||
| chr21:14488807 | G | A | 5 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0248 others(2): Show |
5 | NA18942.hp2 NA18948.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-2693C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488807 | |||||||
| chr21:14488886 | C | G | 1 | a0001c0001t0003g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.920-2772G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488886 | |||||||
| chr21:14489134 | C | T | 93 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(90): Show |
99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-3020G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489134 | |||||||
| chr21:14489232 | AGTAACAC others(8): Show |
A | 1 | a0001c0002t0001g0318 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-3133_920-3119d others(17): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489232 | |||||||
| chr21:14489274 | T | C | 174 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(171): Show |
184 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.920-3160A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489274 | |||||||
| chr21:14489312 | C | T | 93 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(90): Show |
99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-3198G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489312 | |||||||
| chr21:14489319 | G | A | 3 | a0001c0001t0007g0058 a0001c0001t0007g0174 a0001c0002t0014g0342 |
3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.920-3205C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489319 | |||||||
| chr21:14489332 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.920-3218G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489332 | |||||||
| chr21:14489333 | G | A | 2 | a0001c0001t0001g0031 a0001c0002t0001g0023 |
3 | HG01168.hp1 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3219C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489333 | |||||||
| chr21:14489361 | A | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0002t0001g0281 |
3 | HG02451.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920-3247T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489361 | |||||||
| chr21:14489391 | C | CAT | 172 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0022 others(169): Show |
180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.920-3278_920-3277i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489391 | |||||||
| chr21:14489418 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.920-3304T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489418 | |||||||
| chr21:14489431 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0002t0001g0374 |
3 | NA18906.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.920-3317A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489431 | |||||||
| chr21:14489448 | A | G | 2 | a0001c0001t0001g0183 a0001c0002t0001g0376 |
2 | HG00609.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.920-3334T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489448 | |||||||
| chr21:14489491 | C | T | 193 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(190): Show |
204 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.920-3377G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489491 | |||||||
| chr21:14489495 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.920-3381T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489495 | |||||||
| chr21:14489689 | A | G | 13 | a0001c0001t0001g0081 a0001c0001t0001g0120 a0001c0001t0001g0177 others(10): Show |
15 | NA18942.hp1 NA18944.hp1 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-3575T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489689 | |||||||
| chr21:14489707 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.920-3593T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489707 | |||||||
| chr21:14489755 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0071 others(19): Show |
25 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.920-3641G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489755 | |||||||
| chr21:14489807 | A | G | 4 | a0001c0001t0001g0249 a0001c0001t0001g0267 a0001c0002t0001g0312 others(1): Show |
4 | NA18986.hp1 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-3693T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489807 | |||||||
| chr21:14489853 | G | C | 2 | a0001c0001t0007g0058 a0001c0001t0007g0174 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.920-3739C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489853 | |||||||
| chr21:14489953 | T | A | 1 | a0001c0002t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.920-3839A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489953 | |||||||
| chr21:14489962 | A | G | 1 | a0001c0002t0001g0307 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.920-3848T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489962 | |||||||
| chr21:14489979 | A | T | 14 | a0001c0001t0001g0032 a0001c0001t0001g0090 a0001c0001t0001g0141 others(11): Show |
14 | HG00140.hp1 HG00741.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-3865T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489979 | |||||||
| chr21:14490029 | A | G | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-3915T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490029 | |||||||
| chr21:14490033 | TA | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0002t0001g0281 |
3 | HG02451.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920-3920delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490033 | |||||||
| chr21:14490170 | A | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(25): Show |
31 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-4056T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490170 | |||||||
| chr21:14490210 | C | T | 4 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0002t0001g0281 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-4096G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490210 | |||||||
| chr21:14490224 | T | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0057 others(18): Show |
22 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-4110A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490224 | |||||||
| chr21:14490263 | G | A | 367 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(364): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.920-4149C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490263 | |||||||
| chr21:14490354 | C | G | 112 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
118 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.920-4240G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490354 | |||||||
| chr21:14490380 | C | T | 93 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0043 others(90): Show |
99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-4266G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490380 | |||||||
| chr21:14490481 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.920-4367T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490481 | |||||||
| chr21:14490609 | A | C | 11 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0076 others(8): Show |
11 | HG00609.hp2 HG00735.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.920-4495T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490609 | |||||||
| chr21:14490622 | A | G | 1 | a0002c0003t0001g0016 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.920-4508T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490622 | |||||||
| chr21:14490683 | C | T | 13 | a0001c0001t0001g0090 a0001c0001t0001g0141 a0001c0001t0003g0187 others(10): Show |
13 | HG00140.hp1 HG00741.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.920-4569G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490683 | |||||||
| chr21:14490806 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.920-4692C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490806 | |||||||
| chr21:14490831 | AAT | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0039 others(11): Show |
15 | HG00639.hp2 HG01081.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-4719_920-4718d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490831 | |||||||
| chr21:14490867 | C | T | 1 | a0001c0002t0001g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.920-4753G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490867 | |||||||
| chr21:14490960 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.920-4846G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490960 | |||||||
| chr21:14491202 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(162): Show |
180 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.920-5088C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491202 | |||||||
| chr21:14491268 | C | CT | 19 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(16): Show |
23 | HG01099.hp2 HG01257.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.920-5155dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491268 | |||||||
| chr21:14491278 | T | C | 18 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0001g0076 others(15): Show |
18 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.920-5164A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491278 | |||||||
| chr21:14491422 | C | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0042 others(83): Show |
92 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.920-5308G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491422 | |||||||
| chr21:14491481 | G | C | 1 | a0001c0002t0014g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920-5367C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491481 | |||||||
| chr21:14491540 | C | G | 1 | a0001c0002t0001g0315 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.920-5426G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491540 | |||||||
| chr21:14491569 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0002t0001g0317 others(1): Show |
4 | NA18948.hp2 NA18972.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-5455G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491569 | |||||||
| chr21:14491634 | A | G | 10 | a0001c0001t0001g0050 a0001c0001t0001g0065 a0001c0001t0001g0072 others(7): Show |
10 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-5520T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491634 | |||||||
| chr21:14491640 | T | C | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.920-5526A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491640 | |||||||
| chr21:14491652 | T | C | 9 | a0001c0001t0001g0060 a0001c0001t0001g0158 a0001c0001t0007g0058 others(6): Show |
9 | HG00639.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-5538A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491652 | |||||||
| chr21:14491653 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(85): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.920-5539T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491653 | |||||||
| chr21:14491662 | T | A | 88 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0034 others(85): Show |
93 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.920-5548A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491662 | |||||||
| chr21:14491671 | A | G | 2 | a0001c0001t0001g0166 a0001c0002t0001g0352 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.920-5557T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491671 | |||||||
| chr21:14491683 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-5569C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491683 | |||||||
| chr21:14491687 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.920-5573G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491687 | |||||||
| chr21:14491753 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.920-5639G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491753 | |||||||
| chr21:14491825 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.920-5711A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491825 | |||||||
| chr21:14491838 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920-5724A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491838 | |||||||
| chr21:14491898 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.920-5784T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491898 | |||||||
| chr21:14491956 | A | T | 3 | a0001c0001t0001g0015 a0001c0001t0007g0058 a0001c0001t0007g0174 |
4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-5842T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491956 | |||||||
| chr21:14491992 | A | AT | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(225): Show |
247 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.920-5879dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491992 | |||||||
| chr21:14491995 | T | C | 6 | a0001c0001t0001g0033 a0001c0002t0008g0027 a0002c0003t0001g0040 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-5881A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491995 | |||||||
| chr21:14492019 | TACTTC | T | 3 | a0001c0001t0001g0192 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.920-5910_920-5906d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492019 | |||||||
| chr21:14492024 | C | T | 235 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(232): Show |
256 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.920-5910G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492024 | |||||||
| chr21:14492095 | T | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-5981A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492095 | |||||||
| chr21:14492205 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.920-6091T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492205 | |||||||
| chr21:14492209 | TTTGA | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0135 a0001c0001t0002g0150 others(2): Show |
6 | HG00544.hp1 HG03209.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-6099_920-6096d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492209 | |||||||
| chr21:14492232 | C | A | 1 | a0001c0002t0001g0346 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920-6118G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492232 | |||||||
| chr21:14492303 | A | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0002t0001g0357 |
3 | HG02647.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.919+6139T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492303 | |||||||
| chr21:14492377 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0014g0342 |
3 | HG02258.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.919+6065A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492377 | |||||||
| chr21:14492516 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.919+5926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492516 | |||||||
| chr21:14492672 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+5770A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492672 | |||||||
| chr21:14492802 | T | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.919+5640A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492802 | |||||||
| chr21:14493026 | T | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG01081.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+5416A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493026 | |||||||
| chr21:14493064 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.919+5378C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493064 | |||||||
| chr21:14493069 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5373G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493069 | |||||||
| chr21:14493070 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0002g0144 others(1): Show |
5 | HG00323.hp1 HG01070.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+5372G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493070 | |||||||
| chr21:14493106 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+5336G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493106 | |||||||
| chr21:14493148 | G | A | 5 | a0001c0001t0001g0050 a0002c0003t0001g0040 a0002c0003t0001g0049 others(2): Show |
5 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+5294C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493148 | |||||||
| chr21:14493240 | C | G | 1 | a0001c0002t0001g0293 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.919+5202G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493240 | |||||||
| chr21:14493411 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5031T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493411 | |||||||
| chr21:14493429 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5013A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493429 | |||||||
| chr21:14493572 | ACAACACA others(7): Show |
A | 1 | a0001c0002t0001g0313 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.919+4856_919+4869d others(16): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | |||||||
| chr21:14493572 | ACAACACA others(9): Show |
A | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.919+4854_919+4869d others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | |||||||
| chr21:14493572 | ACAACACA others(11): Show |
A | 75 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0081 others(72): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.919+4852_919+4869d others(20): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | |||||||
| chr21:14493574 | A | AAC | 55 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0034 others(52): Show |
59 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.919+4866_919+4867d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | A | AACAC | 12 | a0001c0001t0001g0011 a0001c0001t0001g0075 a0001c0001t0001g0077 others(9): Show |
13 | HG00099.hp2 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+4864_919+4867d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | A | AACACAC | 13 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0069 others(10): Show |
13 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+4862_919+4867d others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | A | AACACACA others(1): Show |
11 | a0001c0001t0001g0046 a0001c0001t0001g0189 a0001c0001t0002g0013 others(8): Show |
12 | HG00438.hp1 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+4860_919+4867d others(10): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | A | AACACACA others(3): Show |
3 | a0001c0001t0001g0050 a0002c0004t0001g0287 a0002c0004t0001g0345 |
3 | HG01243.hp2 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+4858_919+4867d others(12): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | A | AACACACA others(5): Show |
2 | a0002c0003t0001g0008 a0002c0003t0001g0040 |
3 | HG01168.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.919+4856_919+4867d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | AAC | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0162 others(11): Show |
15 | HG01099.hp2 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+4866_919+4867d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | AACAC | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0163 a0001c0001t0001g0207 others(8): Show |
12 | HG01978.hp1 HG03209.hp2 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+4864_919+4867d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | AACACAC | A | 14 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0039 others(11): Show |
14 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+4862_919+4867d others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0275 a0001c0002t0008g0027 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4856_919+4867d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493574 | AACACACA others(13): Show |
A | 2 | a0001c0001t0001g0059 a0004c0005t0001g0358 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.919+4848_919+4867d others(22): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | |||||||
| chr21:14493613 | A | ACACACG | 6 | a0001c0001t0001g0012 a0001c0001t0001g0145 a0001c0001t0002g0108 others(3): Show |
7 | HG02056.hp2 HG02129.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | |||||||
| chr21:14493613 | A | ACACG | 4 | a0001c0001t0001g0101 a0001c0001t0001g0166 a0001c0001t0012g0080 others(1): Show |
4 | HG02602.hp1 HG03491.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | |||||||
| chr21:14493613 | A | ACG | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0065 others(7): Show |
10 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | |||||||
| chr21:14493613 | A | G | 2 | a0001c0001t0001g0063 a0004c0005t0001g0358 |
2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+4829T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | |||||||
| chr21:14493635 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919+4807A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493635 | |||||||
| chr21:14493848 | A | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(24): Show |
28 | HG01081.hp1 HG02056.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.919+4594T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493848 | |||||||
| chr21:14493942 | G | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(127): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.919+4500C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493942 | |||||||
| chr21:14493993 | A | G | 130 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0022 others(127): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.919+4449T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493993 | |||||||
| chr21:14494015 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.919+4427T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494015 | |||||||
| chr21:14494092 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.919+4350T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494092 | |||||||
| chr21:14494125 | G | A | 2 | a0001c0001t0001g0035 a0001c0002t0001g0352 |
2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.919+4317C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494125 | |||||||
| chr21:14494142 | G | A | 2 | a0001c0001t0001g0275 a0001c0002t0008g0027 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4300C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494142 | |||||||
| chr21:14494153 | G | A | 2 | a0001c0001t0001g0275 a0001c0002t0008g0027 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4289C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494153 | |||||||
| chr21:14494210 | G | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0166 a0001c0001t0001g0192 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+4232C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494210 | |||||||
| chr21:14494223 | G | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0166 a0001c0001t0001g0192 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+4219C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494223 | |||||||
| chr21:14494346 | C | A | 1 | a0001c0001t0015g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+4096G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494346 | |||||||
| chr21:14494373 | C | T | 1 | a0001c0002t0001g0339 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.919+4069G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494373 | |||||||
| chr21:14494374 | G | A | 2 | a0001c0001t0001g0275 a0001c0002t0008g0027 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4068C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494374 | |||||||
| chr21:14494482 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.919+3960A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494482 | |||||||
| chr21:14494578 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.919+3864C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494578 | |||||||
| chr21:14494708 | C | CA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0171 a0001c0001t0001g0173 others(4): Show |
8 | HG01515.hp1 HG01517.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+3733dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494708 | |||||||
| chr21:14494803 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.919+3639G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494803 | |||||||
| chr21:14494814 | T | A | 80 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0032 others(77): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.919+3628A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494814 | |||||||
| chr21:14495080 | T | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
17 | HG02056.hp2 HG02129.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.919+3362A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495080 | |||||||
| chr21:14495131 | G | C | 3 | a0001c0001t0001g0275 a0001c0002t0008g0027 a0004c0005t0001g0358 |
3 | HG02280.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+3311C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495131 | |||||||
| chr21:14495147 | G | A | 3 | a0001c0001t0001g0275 a0001c0002t0008g0027 a0004c0005t0001g0358 |
3 | HG02280.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+3295C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495147 | |||||||
| chr21:14495239 | T | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(136): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.919+3203A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495239 | |||||||
| chr21:14495416 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0060 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+3026C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495416 | |||||||
| chr21:14495425 | G | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0039 others(22): Show |
27 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+3017C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495425 | |||||||
| chr21:14495505 | C | T | 64 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0032 others(61): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+2937G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495505 | |||||||
| chr21:14495543 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0173 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.919+2899A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495543 | |||||||
| chr21:14495774 | G | T | 25 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0039 others(22): Show |
27 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+2668C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495774 | |||||||
| chr21:14495894 | C | CT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0002g0169 others(7): Show |
11 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+2547dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495894 | |||||||
| chr21:14495894 | CT | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0166 a0001c0001t0001g0192 others(5): Show |
8 | HG02280.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+2547delA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495894 | |||||||
| chr21:14495917 | T | C | 133 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(130): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.919+2525A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495917 | |||||||
| chr21:14496013 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0173 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.919+2429C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496013 | |||||||
| chr21:14496150 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+2292G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496150 | |||||||
| chr21:14496517 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.919+1925G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496517 | |||||||
| chr21:14496625 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.919+1817G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496625 | |||||||
| chr21:14496740 | T | C | 29 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.919+1702A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496740 | |||||||
| chr21:14496851 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.919+1591C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496851 | |||||||
| chr21:14496860 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+1582C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496860 | |||||||
| chr21:14497005 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+1437G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497005 | |||||||
| chr21:14497043 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.919+1399G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497043 | |||||||
| chr21:14497129 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.919+1313C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497129 | |||||||
| chr21:14497168 | T | C | 98 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0034 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.919+1274A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497168 | |||||||
| chr21:14497184 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.919+1258C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497184 | |||||||
| chr21:14497224 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0002g0169 others(7): Show |
11 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+1218C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497224 | |||||||
| chr21:14497272 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.919+1170C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497272 | |||||||
| chr21:14497322 | C | T | 1 | a0001c0002t0002g0338 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.919+1120G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497322 | |||||||
| chr21:14497364 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.919+1078T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497364 | |||||||
| chr21:14497393 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0171 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1049C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497393 | |||||||
| chr21:14497420 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02630.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+1022G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497420 | |||||||
| chr21:14497451 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.919+991G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497451 | |||||||
| chr21:14497485 | C | T | 1 | a0001c0002t0001g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.919+957G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497485 | |||||||
| chr21:14497499 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+943A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497499 | |||||||
| chr21:14497506 | C | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0001g0283 |
3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.919+936G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497506 | |||||||
| chr21:14497534 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.919+908C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497534 | |||||||
| chr21:14497565 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0171 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+877G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497565 | |||||||
| chr21:14497566 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.919+876C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497566 | |||||||
| chr21:14497628 | G | T | 1 | a0001c0001t0003g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.919+814C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497628 | |||||||
| chr21:14497677 | T | A | 29 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0043 others(26): Show |
31 | HG00621.hp1 HG02056.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.919+765A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497677 | |||||||
| chr21:14497850 | C | T | 47 | a0001c0001t0001g0022 a0001c0001t0001g0065 a0001c0001t0001g0113 others(44): Show |
49 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.919+592G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497850 | |||||||
| chr21:14497940 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919+502C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497940 | |||||||
| chr21:14498036 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0166 a0001c0001t0001g0192 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+406C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498036 | |||||||
| chr21:14498046 | G | T | 1 | a0001c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.919+396C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498046 | |||||||
| chr21:14498224 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+218G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498224 | |||||||
| chr21:14498298 | C | G | 2 | a0001c0002t0001g0292 a0001c0002t0001g0293 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.919+144G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498298 | |||||||
| chr21:14498306 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+136A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498306 | |||||||
| chr21:14498317 | C | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.919+125G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498317 | |||||||
| chr21:14498333 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0275 a0001c0002t0008g0027 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+109G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498333 | |||||||
| chr21:14498680 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.769-88G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498680 | |||||||
| chr21:14498703 | T | C | 3 | a0001c0001t0001g0192 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.769-111A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498703 | |||||||
| chr21:14498732 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-140G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498732 | |||||||
| chr21:14498745 | T | G | 14 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0001g0069 others(11): Show |
15 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.769-153A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498745 | |||||||
| chr21:14498772 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.769-180C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498772 | |||||||
| chr21:14498904 | C | G | 1 | a0001c0002t0001g0354 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769-312G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498904 | |||||||
| chr21:14498922 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769-330G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498922 | |||||||
| chr21:14499025 | C | G | 2 | a0001c0001t0001g0035 a0001c0002t0001g0352 |
2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.769-433G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499025 | |||||||
| chr21:14499133 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.769-541T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499133 | |||||||
| chr21:14499255 | A | G | 1 | a0001c0002t0001g0336 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.769-663T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499255 | |||||||
| chr21:14499280 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0166 |
3 | HG02965.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-688C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499280 | |||||||
| chr21:14499309 | C | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0063 a0001c0001t0001g0166 |
3 | HG02965.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-717G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499309 | |||||||
| chr21:14499406 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0255 others(3): Show |
6 | HG02165.hp2 NA18966.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-814A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499406 | |||||||
| chr21:14499467 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0035 others(30): Show |
36 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.769-875C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499467 | |||||||
| chr21:14499491 | CA | C | 63 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(60): Show |
64 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.769-900delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | |||||||
| chr21:14499491 | CAA | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.769-901_769-900del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | |||||||
| chr21:14499491 | CAAA | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(41): Show |
48 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.769-902_769-900del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | |||||||
| chr21:14499518 | G | A | 2 | a0001c0001t0001g0192 a0001c0002t0001g0291 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.769-926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499518 | |||||||
| chr21:14499672 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0275 a0001c0002t0008g0027 |
3 | HG02451.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.768+857A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499672 | |||||||
| chr21:14499688 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.768+841T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499688 | |||||||
| chr21:14499705 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.768+824A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499705 | |||||||
| chr21:14499711 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
87 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.768+818C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499711 | |||||||
| chr21:14499722 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.768+807A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499722 | |||||||
| chr21:14499728 | T | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0035 others(39): Show |
45 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.768+801A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499728 | |||||||
| chr21:14499932 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.768+597C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499932 | |||||||
| chr21:14500006 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.768+523A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500006 | |||||||
| chr21:14500055 | G | A | 1 | a0001c0002t0001g0332 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.768+474C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500055 | |||||||
| chr21:14500070 | G | A | 1 | a0002c0003t0001g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.768+459C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500070 | |||||||
| chr21:14500130 | G | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(22): Show |
27 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.768+399C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500130 | |||||||
| chr21:14500223 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.768+306C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500223 | |||||||
| chr21:14500353 | A | G | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.768+176T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500353 | |||||||
| chr21:14500794 | T | A | 1 | a0001c0001t0012g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.562-59A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500794 | |||||||
| chr21:14500820 | A | T | 4 | a0001c0001t0002g0100 a0001c0002t0001g0024 a0001c0002t0001g0320 others(1): Show |
5 | HG00438.hp1 NA18997.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-85T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500820 | |||||||
| chr21:14500859 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0002t0002g0377 |
3 | HG01081.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.562-124T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500859 | |||||||
| chr21:14500967 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.562-232T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500967 | |||||||
| chr21:14501060 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.562-325C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501060 | |||||||
| chr21:14501064 | TG | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-330delC | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501064 | |||||||
| chr21:14501127 | A | G | 10 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0002c0003t0001g0008 others(7): Show |
11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-392T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501127 | |||||||
| chr21:14501423 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-688T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501423 | |||||||
| chr21:14501462 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(134): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.562-727A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501462 | |||||||
| chr21:14501572 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.562-837C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501572 | |||||||
| chr21:14501577 | T | G | 8 | a0002c0003t0001g0008 a0002c0003t0001g0040 a0002c0003t0001g0049 others(5): Show |
9 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.562-842A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501577 | |||||||
| chr21:14501582 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-847C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501582 | |||||||
| chr21:14501660 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.562-925A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501660 | |||||||
| chr21:14501675 | TAAAGA | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(22): Show |
27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-945_562-941del others(5): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501675 | |||||||
| chr21:14501868 | T | C | 2 | a0001c0001t0001g0065 a0001c0002t0001g0282 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.562-1133A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501868 | |||||||
| chr21:14501913 | G | T | 1 | a0001c0002t0001g0354 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.562-1178C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501913 | |||||||
| chr21:14501999 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.562-1264C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501999 | |||||||
| chr21:14502104 | C | G | 1 | a0001c0001t0002g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.562-1369G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502104 | |||||||
| chr21:14502138 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(135): Show |
143 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.562-1403T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502138 | |||||||
| chr21:14502228 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.562-1493G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502228 | |||||||
| chr21:14502247 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.562-1512T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502247 | |||||||
| chr21:14502256 | G | GCTGGGT | 129 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(126): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.562-1522_562-1521i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502256 | |||||||
| chr21:14502256 | G | GGTGGGT | 8 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG02630.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.562-1522_562-1521i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502256 | |||||||
| chr21:14502518 | C | T | 3 | a0001c0001t0001g0039 a0001c0002t0001g0357 a0001c0002t0014g0342 |
3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.562-1783G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502518 | |||||||
| chr21:14502548 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-1813A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502548 | |||||||
| chr21:14502561 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0003g0241 |
2 | NA18982.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.562-1826C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502561 | |||||||
| chr21:14502621 | C | T | 1 | a0001c0002t0001g0348 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.562-1886G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502621 | |||||||
| chr21:14502710 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-1975G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502710 | |||||||
| chr21:14502784 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2049C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502784 | |||||||
| chr21:14502787 | C | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(22): Show |
27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-2052G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502787 | |||||||
| chr21:14502836 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0001g0283 |
3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.562-2101C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502836 | |||||||
| chr21:14502981 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.562-2246A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502981 | |||||||
| chr21:14503015 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.562-2280A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503015 | |||||||
| chr21:14503021 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0068 others(18): Show |
22 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.562-2286G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503021 | |||||||
| chr21:14503173 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.562-2438C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503173 | |||||||
| chr21:14503189 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-2454T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503189 | |||||||
| chr21:14503255 | T | C | 1 | a0001c0002t0002g0335 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.562-2520A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503255 | |||||||
| chr21:14503258 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0059 |
3 | HG02280.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-2523C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503258 | |||||||
| chr21:14503259 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0119 |
2 | NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.562-2524A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503259 | |||||||
| chr21:14503343 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.562-2608C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503343 | |||||||
| chr21:14503380 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2645A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503380 | |||||||
| chr21:14503523 | C | T | 4 | a0001c0001t0001g0198 a0001c0002t0001g0366 a0001c0002t0001g0367 others(1): Show |
4 | HG00597.hp1 HG01123.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-2788G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503523 | |||||||
| chr21:14503607 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2872C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503607 | |||||||
| chr21:14503659 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0002t0002g0377 |
3 | HG01081.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.562-2924G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503659 | |||||||
| chr21:14503689 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0275 a0001c0002t0008g0027 |
3 | HG02622.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.562-2954C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503689 | |||||||
| chr21:14503736 | C | T | 10 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0002c0003t0001g0008 others(7): Show |
11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-3001G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503736 | |||||||
| chr21:14503806 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-3071T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503806 | |||||||
| chr21:14503928 | G | C | 50 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0032 others(47): Show |
53 | HG00621.hp1 HG01168.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.562-3193C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503928 | |||||||
| chr21:14503947 | T | C | 132 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(129): Show |
137 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.562-3212A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503947 | |||||||
| chr21:14503979 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.562-3244C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503979 | |||||||
| chr21:14504048 | G | A | 135 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(132): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.562-3313C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504048 | |||||||
| chr21:14504077 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.562-3342G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504077 | |||||||
| chr21:14504088 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-3353T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504088 | |||||||
| chr21:14504126 | C | T | 1 | a0001c0002t0001g0307 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.562-3391G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504126 | |||||||
| chr21:14504142 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0133 |
2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.562-3407G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504142 | |||||||
| chr21:14504210 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.562-3475T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504210 | |||||||
| chr21:14504241 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.562-3506G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504241 | |||||||
| chr21:14504277 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(22): Show |
27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-3542C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504277 | |||||||
| chr21:14504389 | T | C | 2 | a0001c0002t0001g0317 a0001c0002t0001g0318 |
2 | NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.562-3654A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504389 | |||||||
| chr21:14504485 | A | T | 1 | a0001c0002t0001g0306 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.562-3750T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504485 | |||||||
| chr21:14504486 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(22): Show |
27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-3751T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504486 | |||||||
| chr21:14504605 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-3870A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504605 | |||||||
| chr21:14504664 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.562-3929C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504664 | |||||||
| chr21:14504724 | T | G | 1 | a0001c0001t0001g0239 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.562-3989A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504724 | |||||||
| chr21:14504789 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-4054G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504789 | |||||||
| chr21:14504918 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.562-4183G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504918 | |||||||
| chr21:14504936 | C | G | 1 | a0001c0001t0002g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.562-4201G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504936 | |||||||
| chr21:14505067 | C | T | 16 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0059 others(13): Show |
17 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-4332G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505067 | |||||||
| chr21:14505155 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.562-4420G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505155 | |||||||
| chr21:14505194 | C | CA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-4460dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505194 | |||||||
| chr21:14505259 | A | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(24): Show |
29 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.562-4524T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505259 | |||||||
| chr21:14505451 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0039 others(26): Show |
31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-4716A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505451 | |||||||
| chr21:14505555 | C | T | 11 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0002t0001g0352 others(8): Show |
12 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+4755G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505555 | |||||||
| chr21:14505599 | A | G | 1 | a0001c0002t0002g0371 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.561+4711T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505599 | |||||||
| chr21:14505614 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+4696G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505614 | |||||||
| chr21:14505754 | C | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0057 others(21): Show |
25 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.561+4556G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505754 | |||||||
| chr21:14505777 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.561+4533G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505777 | |||||||
| chr21:14505848 | A | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0031 others(136): Show |
143 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.561+4462T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505848 | |||||||
| chr21:14505895 | G | A | 14 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(11): Show |
16 | HG00642.hp2 HG01074.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.561+4415C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505895 | |||||||
| chr21:14505979 | G | A | 1 | a0001c0002t0001g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.561+4331C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505979 | |||||||
| chr21:14506003 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+4307T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506003 | |||||||
| chr21:14506044 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0269 |
2 | HG01106.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.561+4266G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506044 | |||||||
| chr21:14506091 | G | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0063 a0001c0001t0001g0124 others(5): Show |
8 | HG01106.hp1 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+4219C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506091 | |||||||
| chr21:14506118 | G | A | 154 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0031 others(151): Show |
161 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.561+4192C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506118 | |||||||
| chr21:14506267 | T | G | 23 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(20): Show |
23 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+4043A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506267 | |||||||
| chr21:14506293 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+4017T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506293 | |||||||
| chr21:14506344 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3966A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506344 | |||||||
| chr21:14506356 | C | CAG | 22 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(19): Show |
22 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.561+3953_561+3954i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506356 | |||||||
| chr21:14506389 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0002t0001g0357 others(1): Show |
4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3921T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506389 | |||||||
| chr21:14506480 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+3830G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506480 | |||||||
| chr21:14506507 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561+3803G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506507 | |||||||
| chr21:14506518 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+3792G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506518 | |||||||
| chr21:14506571 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.561+3739T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506571 | |||||||
| chr21:14506680 | C | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(24): Show |
28 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.561+3630G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506680 | |||||||
| chr21:14507162 | C | T | 17 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0157 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.561+3148G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507162 | |||||||
| chr21:14507165 | C | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0002t0001g0357 others(1): Show |
4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3145G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507165 | |||||||
| chr21:14507243 | A | T | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.561+3067T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507243 | |||||||
| chr21:14507423 | G | T | 1 | a0001c0002t0008g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561+2887C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507423 | |||||||
| chr21:14507575 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+2735G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507575 | |||||||
| chr21:14507656 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+2654T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507656 | |||||||
| chr21:14507665 | C | T | 3 | a0001c0001t0001g0039 a0001c0002t0001g0357 a0001c0002t0014g0342 |
3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561+2645G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507665 | |||||||
| chr21:14507838 | T | TA | 81 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0072 others(78): Show |
85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.561+2471dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | |||||||
| chr21:14507838 | T | TAA | 8 | a0001c0001t0001g0124 a0001c0001t0002g0036 a0001c0002t0001g0344 others(5): Show |
8 | HG02109.hp2 HG02129.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+2470_561+2471d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | |||||||
| chr21:14507838 | TA | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0041 others(70): Show |
77 | HG00621.hp1 HG01081.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.561+2471delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | |||||||
| chr21:14507853 | T | A | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.561+2457A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507853 | |||||||
| chr21:14507886 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+2424G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507886 | |||||||
| chr21:14507894 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0269 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+2416A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507894 | |||||||
| chr21:14507903 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561+2407T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507903 | |||||||
| chr21:14508016 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.561+2294C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508016 | |||||||
| chr21:14508080 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+2230G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508080 | |||||||
| chr21:14508166 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+2144C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508166 | |||||||
| chr21:14508170 | A | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+2140T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508170 | |||||||
| chr21:14508183 | C | A | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+2127G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508183 | |||||||
| chr21:14508186 | T | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0002t0001g0357 others(1): Show |
4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+2124A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508186 | |||||||
| chr21:14508270 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.561+2040T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508270 | |||||||
| chr21:14508276 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.561+2034G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508276 | |||||||
| chr21:14508357 | G | GA | 31 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(28): Show |
34 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.561+1952dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508357 | |||||||
| chr21:14508363 | A | T | 4 | a0001c0001t0002g0100 a0001c0002t0001g0024 a0001c0002t0001g0320 others(1): Show |
5 | HG00438.hp1 NA18997.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+1947T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508363 | |||||||
| chr21:14508366 | A | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1944T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508366 | |||||||
| chr21:14508367 | C | T | 1 | a0001c0002t0001g0319 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.561+1943G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508367 | |||||||
| chr21:14508427 | C | T | 20 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1883G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508427 | |||||||
| chr21:14508451 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.561+1859T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508451 | |||||||
| chr21:14508602 | C | G | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1708G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508602 | |||||||
| chr21:14508674 | A | G | 20 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1636T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508674 | |||||||
| chr21:14508675 | C | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.561+1635G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508675 | |||||||
| chr21:14508738 | A | G | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1572T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508738 | |||||||
| chr21:14508772 | T | C | 20 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(17): Show |
20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1538A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508772 | |||||||
| chr21:14508855 | C | A | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1455G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508855 | |||||||
| chr21:14508870 | C | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1440G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508870 | |||||||
| chr21:14508914 | G | A | 18 | a0001c0001t0001g0039 a0001c0001t0001g0057 a0001c0001t0001g0068 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1396C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508914 | |||||||
| chr21:14508933 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.561+1377A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508933 | |||||||
| chr21:14508993 | T | A | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.561+1317A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508993 | |||||||
| chr21:14509051 | G | A | 2 | a0001c0001t0001g0041 a0001c0002t0002g0377 |
2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+1259C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509051 | |||||||
| chr21:14509139 | A | AAAAAG | 27 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(24): Show |
29 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+1166_561+1170d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509139 | |||||||
| chr21:14509139 | AAAAAG | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0068 others(12): Show |
15 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.561+1166_561+1170d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509139 | |||||||
| chr21:14509158 | A | AGAAAG | 17 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0206 others(14): Show |
17 | HG01975.hp2 HG02155.hp2 NA18612.hp1 others(14): Show |
intron_variant | MODIFIER | c.561+1147_561+1151d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509158 | |||||||
| chr21:14509319 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+991C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509319 | |||||||
| chr21:14509335 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561+975T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509335 | |||||||
| chr21:14509342 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.561+968T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509342 | |||||||
| chr21:14509834 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0133 |
2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.561+476T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509834 | |||||||
| chr21:14509867 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0269 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+443A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509867 | |||||||
| chr21:14509877 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0269 |
2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+433G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509877 | |||||||
| chr21:14509941 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561+369G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509941 | |||||||
| chr21:14509981 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.561+329A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509981 | |||||||
| chr21:14510023 | C | T | 5 | a0001c0001t0001g0124 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+287G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510023 | |||||||
| chr21:14510032 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.561+278C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510032 | |||||||
| chr21:14510064 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
23 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+246C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510064 | |||||||
| chr21:14510070 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+240A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510070 | |||||||
| chr21:14510093 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+217A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510093 | |||||||
| chr21:14510097 | C | T | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.561+213G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510097 | |||||||
| chr21:14510144 | G | GAA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(5): Show |
9 | HG01106.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+164_561+165dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | |||||||
| chr21:14510144 | G | GAAA | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.561+163_561+165dup others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | |||||||
| chr21:14510144 | GA | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0059 others(24): Show |
29 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+165delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | |||||||
| chr21:14510165 | G | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+145C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510165 | |||||||
| chr21:14510301 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0135 a0001c0001t0001g0249 others(4): Show |
8 | HG02071.hp1 HG02074.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+9A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510301 | |||||||
| chr21:14510528 | CAACT | C | 5 | a0001c0001t0001g0124 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-71_410-68delAG others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510528 | |||||||
| chr21:14510535 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.410-74C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510535 | |||||||
| chr21:14510535 | G | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-74C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510535 | |||||||
| chr21:14510617 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.410-156A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510617 | |||||||
| chr21:14510627 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.410-166A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510627 | |||||||
| chr21:14510677 | A | ACT | 134 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(131): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.410-218_410-217dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510677 | |||||||
| chr21:14510722 | G | A | 1 | a0001c0002t0001g0293 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.410-261C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510722 | |||||||
| chr21:14510761 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.410-300G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510761 | |||||||
| chr21:14510892 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-431C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510892 | |||||||
| chr21:14510910 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0007g0058 a0001c0001t0007g0174 |
4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-449G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510910 | |||||||
| chr21:14510931 | T | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0067 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.410-470A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510931 | |||||||
| chr21:14510961 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.410-500T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510961 | |||||||
| chr21:14510971 | A | G | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.410-510T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510971 | |||||||
| chr21:14511671 | G | C | 1 | a0001c0001t0001g0217 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.409+773C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511671 | |||||||
| chr21:14511777 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0007g0058 a0001c0001t0007g0174 |
4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+667G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511777 | |||||||
| chr21:14511803 | T | A | 1 | a0001c0002t0009g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.409+641A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511803 | |||||||
| chr21:14511834 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+610G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511834 | |||||||
| chr21:14511855 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.409+589T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511855 | |||||||
| chr21:14511884 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+560C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511884 | |||||||
| chr21:14511958 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.409+486C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511958 | |||||||
| chr21:14511960 | G | A | 1 | a0001c0002t0001g0344 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.409+484C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511960 | |||||||
| chr21:14512001 | C | T | 62 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0113 others(59): Show |
64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.409+443G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512001 | |||||||
| chr21:14512023 | A | G | 1 | a0001c0002t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409+421T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512023 | |||||||
| chr21:14512024 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.409+420G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512024 | |||||||
| chr21:14512025 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0136 |
3 | HG01255.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.409+419C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512025 | |||||||
| chr21:14512103 | C | T | 63 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0113 others(60): Show |
65 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.409+341G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512103 | |||||||
| chr21:14512133 | G | C | 88 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0065 others(85): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.409+311C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512133 | |||||||
| chr21:14512154 | G | T | 88 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0065 others(85): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.409+290C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512154 | |||||||
| chr21:14512260 | T | A | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.409+184A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512260 | |||||||
| chr21:14512302 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.409+142T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512302 | |||||||
| chr21:14512304 | A | C | 1 | a0001c0002t0003g0372 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.409+140T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512304 | |||||||
| chr21:14512428 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.409+16C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512428 | |||||||
| chr21:14512437 | G | A | 3 | a0001c0001t0001g0039 a0001c0002t0001g0357 a0001c0002t0014g0342 |
3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.409+7C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512437 | |||||||
| chr21:14512578 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.280-5T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512578 | |||||||
| chr21:14512628 | A | T | 228 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(225): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.280-55T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512628 | |||||||
| chr21:14512634 | A | T | 94 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0066 others(91): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.280-61T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512634 | |||||||
| chr21:14512653 | C | CAAG | 94 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0066 others(91): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.280-81_280-80insCT others(1): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512653 | |||||||
| chr21:14512713 | T | A | 16 | a0001c0001t0001g0065 a0001c0001t0001g0171 a0001c0001t0001g0173 others(13): Show |
18 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-140A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512713 | |||||||
| chr21:14512744 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-171G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512744 | |||||||
| chr21:14512783 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.280-210G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512783 | |||||||
| chr21:14512868 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0002g0044 |
3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.280-295C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512868 | |||||||
| chr21:14512917 | T | C | 18 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0171 others(15): Show |
20 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.280-344A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512917 | |||||||
| chr21:14512953 | C | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-380G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512953 | |||||||
| chr21:14513195 | T | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-622A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513195 | |||||||
| chr21:14513262 | G | A | 2 | a0002c0003t0001g0049 a0002c0004t0001g0287 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.280-689C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513262 | |||||||
| chr21:14513327 | A | T | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-754T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513327 | |||||||
| chr21:14513428 | T | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-855A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513428 | |||||||
| chr21:14513484 | A | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-911T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513484 | |||||||
| chr21:14513498 | T | C | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-925A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513498 | |||||||
| chr21:14513520 | CGT | C | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(102): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.280-949_280-948del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513520 | |||||||
| chr21:14513747 | A | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-1174T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513747 | |||||||
| chr21:14514295 | T | C | 218 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(215): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.280-1722A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514295 | |||||||
| chr21:14514545 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-1972T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514545 | |||||||
| chr21:14514552 | G | T | 2 | a0001c0001t0004g0001 a0001c0001t0004g0048 |
4 | HG01099.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1979C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514552 | |||||||
| chr21:14514598 | T | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-2025A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514598 | |||||||
| chr21:14514611 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.280-2038C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514611 | |||||||
| chr21:14514629 | A | G | 19 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0066 others(16): Show |
21 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.280-2056T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514629 | |||||||
| chr21:14514670 | A | C | 226 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(223): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.280-2097T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514670 | |||||||
| chr21:14514793 | A | G | 1 | a0001c0002t0009g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.279+2099T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514793 | |||||||
| chr21:14514819 | C | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0258 a0001c0001t0001g0260 others(4): Show |
7 | HG02129.hp2 NA18974.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2073G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514819 | |||||||
| chr21:14514902 | T | C | 16 | a0001c0001t0001g0065 a0001c0001t0001g0171 a0001c0001t0001g0173 others(13): Show |
18 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+1990A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514902 | |||||||
| chr21:14514908 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.279+1984T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514908 | |||||||
| chr21:14514958 | A | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.279+1934T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514958 | |||||||
| chr21:14514977 | G | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.279+1915C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514977 | |||||||
| chr21:14515198 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+1694G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515198 | |||||||
| chr21:14515224 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+1668T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515224 | |||||||
| chr21:14515424 | G | A | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+1468C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515424 | |||||||
| chr21:14515426 | A | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+1466T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515426 | |||||||
| chr21:14515481 | T | A | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+1411A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515481 | |||||||
| chr21:14515515 | C | T | 5 | a0001c0001t0002g0100 a0001c0002t0001g0024 a0001c0002t0001g0320 others(2): Show |
6 | HG00438.hp1 HG04115.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1377G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515515 | |||||||
| chr21:14515575 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+1317A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515575 | |||||||
| chr21:14515638 | T | A | 1 | a0001c0002t0001g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.279+1254A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515638 | |||||||
| chr21:14515660 | C | T | 2 | a0001c0001t0001g0041 a0001c0002t0002g0377 |
2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.279+1232G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515660 | |||||||
| chr21:14515915 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+977C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515915 | |||||||
| chr21:14516054 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0179 a0001c0001t0001g0186 others(7): Show |
12 | HG00597.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+838C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516054 | |||||||
| chr21:14516207 | C | A | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+685G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516207 | |||||||
| chr21:14516274 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0166 a0001c0002t0009g0028 |
3 | HG00639.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+618A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516274 | |||||||
| chr21:14516374 | T | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0219 |
2 | HG00597.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.279+518A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516374 | |||||||
| chr21:14516396 | T | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+496A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516396 | |||||||
| chr21:14516415 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+477G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516415 | |||||||
| chr21:14516440 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+452C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516440 | |||||||
| chr21:14516536 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+356G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516536 | |||||||
| chr21:14516581 | G | A | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+311C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516581 | |||||||
| chr21:14516641 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.279+251G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516641 | |||||||
| chr21:14516643 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.279+249G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516643 | |||||||
| chr21:14516719 | C | A | 11 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(8): Show |
11 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+173G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516719 | |||||||
| chr21:14516805 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0001g0283 |
3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+87A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516805 | |||||||
| chr21:14517213 | C | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130-172G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517213 | |||||||
| chr21:14517232 | G | A | 133 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130-191C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517232 | |||||||
| chr21:14517450 | C | A | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-409G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517450 | |||||||
| chr21:14517503 | G | A | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-462C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517503 | |||||||
| chr21:14517562 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130-521C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517562 | |||||||
| chr21:14517747 | T | A | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(355): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.130-706A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517747 | |||||||
| chr21:14517750 | G | C | 1 | a0001c0002t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130-709C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517750 | |||||||
| chr21:14517821 | GA | G | 62 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0113 others(59): Show |
64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.130-781delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517821 | |||||||
| chr21:14517899 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
151 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.130-858A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517899 | |||||||
| chr21:14517912 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.130-871G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517912 | |||||||
| chr21:14517921 | T | C | 1 | a0001c0002t0001g0365 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130-880A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517921 | |||||||
| chr21:14518119 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.130-1078G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518119 | |||||||
| chr21:14518150 | C | T | 69 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0113 others(66): Show |
71 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.130-1109G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518150 | |||||||
| chr21:14518222 | AC | A | 12 | a0002c0003t0001g0008 a0002c0003t0001g0016 a0002c0003t0001g0040 others(9): Show |
14 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-1182delG | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518222 | |||||||
| chr21:14518256 | C | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0115 others(1): Show |
4 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1215G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518256 | |||||||
| chr21:14518320 | T | C | 2 | a0002c0003t0001g0049 a0002c0004t0001g0287 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.130-1279A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518320 | |||||||
| chr21:14518355 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130-1314A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518355 | |||||||
| chr21:14518438 | G | A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-1397C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518438 | |||||||
| chr21:14518445 | A | AT | 221 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(218): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.130-1405dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518445 | |||||||
| chr21:14518551 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0255 |
3 | HG02165.hp2 NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.130-1510A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518551 | |||||||
| chr21:14518553 | G | A | 221 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(218): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.130-1512C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518553 | |||||||
| chr21:14518570 | CATTCACT others(5): Show |
C | 1 | a0001c0002t0001g0324 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.130-1541_130-1530d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518570 | |||||||
| chr21:14518659 | T | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1618A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518659 | |||||||
| chr21:14518695 | C | A | 1 | a0001c0002t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1654G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518695 | |||||||
| chr21:14518879 | A | C | 1 | a0001c0002t0001g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.130-1838T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518879 | |||||||
| chr21:14518882 | T | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1841A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518882 | |||||||
| chr21:14518885 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.130-1844G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518885 | |||||||
| chr21:14518895 | A | G | 6 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0131 others(3): Show |
6 | HG00323.hp2 HG01515.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-1854T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518895 | |||||||
| chr21:14518938 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(110): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.130-1897G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518938 | |||||||
| chr21:14519019 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.130-1978C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519019 | |||||||
| chr21:14519077 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 others(1): Show |
4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2036G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519077 | |||||||
| chr21:14519093 | A | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-2052T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519093 | |||||||
| chr21:14519101 | A | G | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.129+2049T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519101 | |||||||
| chr21:14519265 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG00280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.129+1885A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519265 | |||||||
| chr21:14519416 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.129+1734A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519416 | |||||||
| chr21:14519472 | T | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1678A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519472 | |||||||
| chr21:14519488 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1662G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519488 | |||||||
| chr21:14519555 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1595A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519555 | |||||||
| chr21:14519602 | A | G | 14 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0002g0169 others(11): Show |
14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+1548T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519602 | |||||||
| chr21:14519695 | GAT | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1453_129+1454d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519695 | |||||||
| chr21:14519721 | GGATCTAA others(9): Show |
G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | NA18974.hp2 NA19000.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.129+1413_129+1428d others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519721 | |||||||
| chr21:14519759 | A | G | 2 | a0001c0001t0001g0041 a0001c0002t0002g0377 |
2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.129+1391T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519759 | |||||||
| chr21:14519818 | A | G | 15 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0202 others(12): Show |
17 | HG00642.hp2 HG01074.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+1332T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519818 | |||||||
| chr21:14519919 | A | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1231T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519919 | |||||||
| chr21:14519923 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1227G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519923 | |||||||
| chr21:14519932 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0161 others(2): Show |
6 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1218C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519932 | |||||||
| chr21:14520094 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+1056G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520094 | |||||||
| chr21:14520189 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(23): Show |
27 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+961G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520189 | |||||||
| chr21:14520233 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.129+917G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520233 | |||||||
| chr21:14520238 | G | C | 3 | a0001c0001t0001g0192 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.129+912C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520238 | |||||||
| chr21:14520255 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+895A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520255 | |||||||
| chr21:14520478 | C | G | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.129+672G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520478 | |||||||
| chr21:14520499 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.129+651C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520499 | |||||||
| chr21:14520616 | C | A | 1 | a0001c0001t0001g0014 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+534G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520616 | |||||||
| chr21:14520659 | A | C | 2 | a0001c0001t0001g0041 a0001c0002t0002g0377 |
2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.129+491T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520659 | |||||||
| chr21:14520669 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129+481A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520669 | |||||||
| chr21:14520703 | T | G | 1 | a0001c0002t0001g0347 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.129+447A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520703 | |||||||
| chr21:14520760 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+390C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520760 | |||||||
| chr21:14520763 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+387C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520763 | |||||||
| chr21:14520805 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.129+345T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520805 | |||||||
| chr21:14520813 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
106 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.129+337C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520813 | |||||||
| chr21:14520865 | T | C | 356 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(353): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.129+285A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520865 | |||||||
| chr21:14520883 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129+267A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520883 | |||||||
| chr21:14520907 | C | T | 84 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(81): Show |
88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.129+243G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520907 | |||||||
| chr21:14521034 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+116G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14521034 | |||||||
| chr21:14521088 | G | A | 1 | a0001c0002t0009g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129+62C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14521088 | |||||||
| chr21:14521224 | A | T | 3 | a0001c0001t0001g0192 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.58-3T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521224 | |||||||
| chr21:14521246 | A | T | 85 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(82): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-25T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521246 | |||||||
| chr21:14521262 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58-41A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521262 | |||||||
| chr21:14521273 | T | C | 197 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.58-52A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521273 | |||||||
| chr21:14521323 | C | A | 1 | a0001c0002t0001g0303 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.58-102G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521323 | |||||||
| chr21:14521420 | T | C | 1 | a0002c0003t0001g0008 | 2 | HG01168.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.58-199A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521420 | |||||||
| chr21:14521709 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 |
3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-488C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521709 | |||||||
| chr21:14521859 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0173 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.58-638C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521859 | |||||||
| chr21:14521900 | T | TA | 112 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(109): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.58-680dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521900 | |||||||
| chr21:14521900 | TA | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0136 others(6): Show |
10 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-680delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521900 | |||||||
| chr21:14521957 | G | A | 206 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(203): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.58-736C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521957 | |||||||
| chr21:14522042 | G | A | 85 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0072 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-821C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522042 | |||||||
| chr21:14522043 | G | A | 85 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0072 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-822C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522043 | |||||||
| chr21:14522052 | A | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(112): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.58-831T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522052 | |||||||
| chr21:14522197 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0275 |
2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58-976C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522197 | |||||||
| chr21:14522205 | A | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0188 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.58-984T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522205 | |||||||
| chr21:14522253 | G | A | 14 | a0001c0001t0001g0135 a0001c0001t0001g0177 a0001c0001t0001g0206 others(11): Show |
14 | HG02155.hp2 NA18612.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-1032C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522253 | |||||||
| chr21:14522262 | A | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(95): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-1041T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522262 | |||||||
| chr21:14522517 | T | C | 225 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(222): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.58-1296A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522517 | |||||||
| chr21:14522659 | T | C | 206 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(203): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.58-1438A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522659 | |||||||
| chr21:14522666 | C | T | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(3): Show |
7 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1445G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522666 | |||||||
| chr21:14522667 | A | C | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(3): Show |
7 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1446T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522667 | |||||||
| chr21:14522733 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 |
4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1512C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522733 | |||||||
| chr21:14522776 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-1555T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522776 | |||||||
| chr21:14522983 | G | T | 1 | a0001c0002t0003g0294 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.58-1762C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522983 | |||||||
| chr21:14523007 | G | A | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-1786C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523007 | |||||||
| chr21:14523199 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(4): Show |
7 | HG02165.hp2 NA18948.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1978T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523199 | |||||||
| chr21:14523257 | A | C | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2036T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523257 | |||||||
| chr21:14523361 | TGACTTGC others(11): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.58-2158_58-2141del others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523361 | |||||||
| chr21:14523364 | C | T | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2143G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523364 | |||||||
| chr21:14523370 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-2149T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523370 | |||||||
| chr21:14523428 | C | A | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2207G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523428 | |||||||
| chr21:14523574 | C | A | 1 | a0001c0002t0001g0341 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.58-2353G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523574 | |||||||
| chr21:14523575 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0002g0132 |
2 | HG01515.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.58-2354C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523575 | |||||||
| chr21:14523690 | A | G | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58-2469T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523690 | |||||||
| chr21:14523691 | T | C | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2470A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523691 | |||||||
| chr21:14523694 | A | G | 93 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(90): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.58-2473T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523694 | |||||||
| chr21:14523718 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 |
3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-2497C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523718 | |||||||
| chr21:14523728 | G | T | 86 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0072 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-2507C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523728 | |||||||
| chr21:14523804 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0173 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.58-2583T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523804 | |||||||
| chr21:14523839 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.58-2618A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523839 | |||||||
| chr21:14523890 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.58-2669T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523890 | |||||||
| chr21:14523915 | A | C | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.58-2694T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523915 | |||||||
| chr21:14523960 | A | G | 86 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0072 others(83): Show |
89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-2739T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523960 | |||||||
| chr21:14524101 | A | G | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2880T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524101 | |||||||
| chr21:14524186 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0166 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58-2965C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524186 | |||||||
| chr21:14524195 | T | C | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2974A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524195 | |||||||
| chr21:14524226 | A | T | 1 | a0001c0001t0001g0022 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.58-3005T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524226 | |||||||
| chr21:14524243 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58-3022T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524243 | |||||||
| chr21:14524263 | A | G | 1 | a0001c0002t0001g0299 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58-3042T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524263 | |||||||
| chr21:14524274 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG00639.hp2 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-3053A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524274 | |||||||
| chr21:14524375 | G | GC | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-3155_58-3154ins others(1): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524375 | |||||||
| chr21:14524389 | A | T | 1 | a0001c0002t0001g0026 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58-3168T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524389 | |||||||
| chr21:14524390 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 |
3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-3169A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524390 | |||||||
| chr21:14524463 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0269 |
3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-3242A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524463 | |||||||
| chr21:14524676 | T | C | 2 | a0001c0001t0001g0186 a0001c0002t0001g0323 |
2 | NA18950.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.58-3455A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524676 | |||||||
| chr21:14524705 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.58-3484C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524705 | |||||||
| chr21:14524761 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0002g0044 |
3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-3540A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524761 | |||||||
| chr21:14525036 | T | A | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58-3815A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525036 | |||||||
| chr21:14525047 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.58-3826T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525047 | |||||||
| chr21:14525123 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.58-3902A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525123 | |||||||
| chr21:14525152 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.58-3931A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525152 | |||||||
| chr21:14525252 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-4031A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525252 | |||||||
| chr21:14525369 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58-4148G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525369 | |||||||
| chr21:14525486 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.58-4265T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525486 | |||||||
| chr21:14525536 | A | G | 85 | a0001c0001t0001g0057 a0001c0001t0001g0072 a0001c0001t0001g0074 others(82): Show |
88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-4315T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525536 | |||||||
| chr21:14525550 | C | G | 1 | a0001c0001t0002g0117 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.58-4329G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525550 | |||||||
| chr21:14525608 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
140 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.58-4387C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525608 | |||||||
| chr21:14525651 | C | T | 3 | a0001c0001t0001g0192 a0001c0002t0001g0290 a0001c0002t0001g0291 |
3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58-4430G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525651 | |||||||
| chr21:14525670 | G | A | 10 | a0001c0001t0001g0065 a0001c0001t0001g0171 a0001c0001t0001g0173 others(7): Show |
10 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-4449C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525670 | |||||||
| chr21:14525718 | T | C | 112 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(109): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.58-4497A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525718 | |||||||
| chr21:14525745 | T | C | 1 | a0001c0002t0001g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-4524A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525745 | |||||||
| chr21:14525776 | T | C | 1 | a0001c0001t0007g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-4555A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525776 | |||||||
| chr21:14525779 | A | T | 1 | a0001c0002t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.58-4558T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525779 | |||||||
| chr21:14525821 | T | C | 17 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0175 others(14): Show |
19 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-4600A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525821 | |||||||
| chr21:14525831 | T | G | 110 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(107): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-4610A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525831 | |||||||
| chr21:14525853 | C | T | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.58-4632G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525853 | |||||||
| chr21:14525863 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 |
4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4642A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525863 | |||||||
| chr21:14525933 | C | T | 109 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(106): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.58-4712G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525933 | |||||||
| chr21:14525934 | G | C | 2 | a0001c0001t0001g0059 a0001c0002t0001g0352 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58-4713C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525934 | |||||||
| chr21:14525963 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(95): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.58-4742C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525963 | |||||||
| chr21:14525985 | C | A | 2 | a0001c0001t0001g0041 a0001c0002t0002g0377 |
2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.58-4764G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525985 | |||||||
| chr21:14526077 | AG | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 |
4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4857delC | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526077 | |||||||
| chr21:14526114 | C | G | 106 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(103): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.58-4893G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526114 | |||||||
| chr21:14526133 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.58-4912C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526133 | |||||||
| chr21:14526146 | G | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0002t0014g0342 |
3 | HG02647.hp2 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58-4925C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526146 | |||||||
| chr21:14526156 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58-4935G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526156 | |||||||
| chr21:14526270 | C | T | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(94): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.58-5049G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526270 | |||||||
| chr21:14526271 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58-5050C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526271 | |||||||
| chr21:14526271 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58-5050C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526271 | |||||||
| chr21:14526295 | T | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.58-5074A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526295 | |||||||
| chr21:14526360 | C | G | 98 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.58-5139G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526360 | |||||||
| chr21:14526388 | C | T | 4 | a0001c0002t0001g0332 a0001c0002t0001g0362 a0001c0002t0001g0363 others(1): Show |
4 | HG02129.hp1 NA18953.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-5167G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526388 | |||||||
| chr21:14526454 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-5233C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526454 | |||||||
| chr21:14526470 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.58-5249A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526470 | |||||||
| chr21:14526499 | C | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.58-5278G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526499 | |||||||
| chr21:14526505 | T | G | 1 | a0001c0001t0002g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.58-5284A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526505 | |||||||
| chr21:14526540 | A | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.58-5319T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526540 | |||||||
| chr21:14526543 | T | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(92): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.58-5322A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526543 | |||||||
| chr21:14526599 | G | A | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.58-5378C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526599 | |||||||
| chr21:14526764 | G | A | 110 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0103 others(107): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-5543C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526764 | |||||||
| chr21:14526852 | C | G | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5631G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526852 | |||||||
| chr21:14526885 | G | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
127 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.58-5664C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526885 | |||||||
| chr21:14526902 | A | T | 119 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0051 others(116): Show |
125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.58-5681T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526902 | |||||||
| chr21:14526931 | A | G | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.58-5710T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526931 | |||||||
| chr21:14526954 | G | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5733C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526954 | |||||||
| chr21:14527000 | G | A | 1 | a0001c0001t0003g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.58-5779C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527000 | |||||||
| chr21:14527043 | T | A | 96 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(93): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5822A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527043 | |||||||
| chr21:14527053 | C | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0157 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-5832G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527053 | |||||||
| chr21:14527076 | T | C | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(92): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.58-5855A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527076 | |||||||
| chr21:14527147 | G | A | 1 | a0001c0002t0001g0328 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.58-5926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527147 | |||||||
| chr21:14527184 | T | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5963A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527184 | |||||||
| chr21:14527185 | C | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5964G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527185 | |||||||
| chr21:14527250 | T | C | 1 | a0001c0002t0001g0376 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.58-6029A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527250 | |||||||
| chr21:14527291 | G | A | 56 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0037 others(53): Show |
59 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.58-6070C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527291 | |||||||
| chr21:14527399 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.58-6178C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527399 | |||||||
| chr21:14527420 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58-6199T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527420 | |||||||
| chr21:14527443 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.58-6222G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527443 | |||||||
| chr21:14527549 | G | T | 1 | a0002c0003t0001g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-6328C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527549 | |||||||
| chr21:14527625 | T | C | 3 | a0001c0001t0001g0065 a0001c0002t0001g0282 a0001c0002t0001g0283 |
3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.58-6404A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527625 | |||||||
| chr21:14527634 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.58-6413C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527634 | |||||||
| chr21:14527760 | TA | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0066 others(3): Show |
6 | HG01081.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-6540delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | |||||||
| chr21:14527760 | TAAA | T | 97 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0035 others(94): Show |
102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-6542_58-6540del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | |||||||
| chr21:14527760 | TAAAA | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
111 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.58-6543_58-6540del others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | |||||||
| chr21:14527799 | A | G | 7 | a0001c0001t0001g0195 a0001c0002t0001g0005 a0001c0002t0001g0295 others(4): Show |
9 | HG00408.hp2 HG00438.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-6578T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527799 | |||||||
| chr21:14527806 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58-6585T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527806 | |||||||
| chr21:14527876 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58-6655G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527876 | |||||||
| chr21:14527877 | A | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.58-6656T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527877 | |||||||
| chr21:14527901 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.58-6680A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527901 | |||||||
| chr21:14528101 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0002g0112 |
2 | HG00621.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-6880G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528101 | |||||||
| chr21:14528203 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-6982C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528203 | |||||||
| chr21:14528380 | T | C | 1 | a0001c0002t0001g0324 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.58-7159A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528380 | |||||||
| chr21:14528549 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58-7328A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528549 | |||||||
| chr21:14528633 | C | G | 1 | a0001c0002t0002g0371 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58-7412G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528633 | |||||||
| chr21:14528839 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.58-7618C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528839 | |||||||
| chr21:14528883 | C | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0133 |
2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.58-7662G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528883 | |||||||
| chr21:14528896 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-7675G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528896 | |||||||
| chr21:14528939 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-7718C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528939 | |||||||
| chr21:14529023 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-7802G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529023 | |||||||
| chr21:14529271 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.58-8050G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529271 | |||||||
| chr21:14529346 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0002g0044 |
3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-8125C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529346 | |||||||
| chr21:14529415 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-8194T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529415 | |||||||
| chr21:14529471 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58-8250T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529471 | |||||||
| chr21:14529594 | A | C | 1 | a0001c0002t0001g0348 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.58-8373T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529594 | |||||||
| chr21:14529656 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 |
5 | HG01256.hp2 HG01258.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-8435T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529656 | |||||||
| chr21:14529689 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-8468T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529689 | |||||||
| chr21:14529694 | T | C | 1 | a0001c0002t0003g0372 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.58-8473A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529694 | |||||||
| chr21:14529814 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-8593A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529814 | |||||||
| chr21:14529965 | C | A | 98 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(95): Show |
104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.58-8744G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529965 | |||||||
| chr21:14529966 | C | T | 111 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0135 others(108): Show |
117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.58-8745G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529966 | |||||||
| chr21:14530034 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0002g0044 |
3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-8813A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530034 | |||||||
| chr21:14530057 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58-8836G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530057 | |||||||
| chr21:14530071 | C | T | 1 | a0001c0002t0001g0025 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.58-8850G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530071 | |||||||
| chr21:14530098 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.58-8877G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530098 | |||||||
| chr21:14530174 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
102 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-8953C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530174 | |||||||
| chr21:14530181 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-8960C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530181 | |||||||
| chr21:14530188 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-8967C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530188 | |||||||
| chr21:14530189 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-8968A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530189 | |||||||
| chr21:14530241 | T | C | 5 | a0001c0002t0001g0280 a0001c0002t0001g0348 a0001c0002t0001g0349 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-9020A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530241 | |||||||
| chr21:14530300 | G | C | 6 | a0001c0002t0001g0365 a0001c0002t0001g0366 a0001c0002t0001g0367 others(3): Show |
6 | HG00597.hp1 HG02135.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-9079C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530300 | |||||||
| chr21:14530311 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58-9090G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530311 | |||||||
| chr21:14530312 | G | A | 1 | a0001c0002t0001g0352 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58-9091C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530312 | |||||||
| chr21:14530316 | C | CA | 15 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0062 others(12): Show |
15 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-9096dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530316 | |||||||
| chr21:14530333 | A | AAAAAAG | 12 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0134 others(9): Show |
13 | HG00438.hp1 HG01081.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-9113_58-9112ins others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | |||||||
| chr21:14530333 | A | AAAAAG | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.58-9113_58-9112ins others(5): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | |||||||
| chr21:14530333 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-9112T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | |||||||
| chr21:14530337 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0173 a0001c0001t0007g0174 |
4 | HG02895.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9116C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530337 | |||||||
| chr21:14530339 | A | AAGAAATA others(3): Show |
34 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0078 others(31): Show |
37 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.58-9128_58-9119dup others(10): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | |||||||
| chr21:14530339 | A | AATAATC | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.58-9119_58-9118ins others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | |||||||
| chr21:14530339 | A | AGAAAGAA others(6): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0173 a0001c0001t0007g0174 |
4 | HG02895.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9119_58-9118ins others(13): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | |||||||
| chr21:14530358 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.58-9137G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530358 | |||||||
| chr21:14530378 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.58-9157C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530378 | |||||||
| chr21:14530522 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-9301G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530522 | |||||||
| chr21:14530657 | G | T | 213 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(210): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.58-9436C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530657 | |||||||
| chr21:14530764 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0270 a0001c0001t0001g0271 |
4 | HG00639.hp1 HG01433.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9543A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530764 | |||||||
| chr21:14530922 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0003g0262 |
2 | NA18979.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.58-9701A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530922 | |||||||
| chr21:14530994 | T | A | 2 | a0001c0002t0001g0327 a0001c0002t0001g0328 |
2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.58-9773A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530994 | |||||||
| chr21:14531073 | T | C | 1 | a0001c0002t0002g0371 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58-9852A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531073 | |||||||
| chr21:14531287 | T | C | 1 | a0001c0002t0001g0329 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-10066A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531287 | |||||||
| chr21:14531521 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-10300A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531521 | |||||||
| chr21:14531528 | T | C | 1 | a0001c0002t0003g0372 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.58-10307A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531528 | |||||||
| chr21:14531897 | C | A | 34 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0051 others(31): Show |
38 | HG00639.hp2 HG01099.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.58-10676G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531897 | |||||||
| chr21:14531907 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-10686C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531907 | |||||||
| chr21:14531999 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-10778C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531999 | |||||||
| chr21:14532071 | G | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.58-10850C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532071 | |||||||
| chr21:14532099 | G | A | 1 | a0001c0002t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58-10878C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532099 | |||||||
| chr21:14532182 | G | A | 3 | a0001c0001t0001g0065 a0001c0002t0001g0282 a0001c0002t0001g0283 |
3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.58-10961C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532182 | |||||||
| chr21:14532263 | T | C | 1 | a0001c0002t0002g0330 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.58-11042A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532263 | |||||||
| chr21:14532295 | C | A | 1 | a0001c0002t0001g0331 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.58-11074G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532295 | |||||||
| chr21:14532674 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.58-11453A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532674 | |||||||
| chr21:14532901 | ATTAT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
8 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-11684_58-11681d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532901 | |||||||
| chr21:14532921 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-11700A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532921 | |||||||
| chr21:14532936 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.58-11715A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532936 | |||||||
| chr21:14533138 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.58-11917A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533138 | |||||||
| chr21:14533194 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
8 | HG01256.hp2 HG01258.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-11973C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533194 | |||||||
| chr21:14533232 | A | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0002g0105 |
3 | NA18945.hp2 NA18962.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.58-12011T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533232 | |||||||
| chr21:14533259 | C | T | 54 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0154 others(51): Show |
58 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.58-12038G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533259 | |||||||
| chr21:14533887 | A | C | 2 | a0001c0002t0001g0292 a0001c0002t0001g0293 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.57+12318T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533887 | |||||||
| chr21:14533959 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+12246C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533959 | |||||||
| chr21:14534015 | A | C | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.57+12190T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534015 | |||||||
| chr21:14534214 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.57+11991T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534214 | |||||||
| chr21:14534253 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+11952G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534253 | |||||||
| chr21:14534269 | G | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(242): Show |
265 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+11936C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534269 | |||||||
| chr21:14534326 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.57+11879G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534326 | |||||||
| chr21:14534378 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0063 |
2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.57+11827T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534378 | |||||||
| chr21:14534399 | G | C | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+11806C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534399 | |||||||
| chr21:14534477 | T | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0269 |
2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+11728A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534477 | |||||||
| chr21:14534523 | TC | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG02258.hp1 HG02647.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+11681delG | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534523 | |||||||
| chr21:14534524 | C | CT | 236 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(233): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.57+11680dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534524 | |||||||
| chr21:14534524 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
9 | HG01106.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+11681G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534524 | |||||||
| chr21:14534594 | C | A | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.57+11611G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534594 | |||||||
| chr21:14534608 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0067 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57+11597G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534608 | |||||||
| chr21:14534665 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.57+11540C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534665 | |||||||
| chr21:14534728 | A | C | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+11477T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534728 | |||||||
| chr21:14534974 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+11231G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534974 | |||||||
| chr21:14534986 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+11219G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534986 | |||||||
| chr21:14535134 | C | T | 9 | a0001c0001t0002g0169 a0001c0001t0002g0176 a0001c0002t0001g0290 others(6): Show |
9 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+11071G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535134 | |||||||
| chr21:14535198 | C | A | 1 | a0001c0002t0001g0346 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.57+11007G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535198 | |||||||
| chr21:14535224 | T | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0269 a0001c0002t0002g0377 |
3 | HG01106.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.57+10981A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535224 | |||||||
| chr21:14535590 | T | A | 2 | a0002c0003t0001g0049 a0002c0004t0001g0287 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.57+10615A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535590 | |||||||
| chr21:14535759 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.57+10446A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535759 | |||||||
| chr21:14535998 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+10207G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535998 | |||||||
| chr21:14536054 | C | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(94): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.57+10151G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536054 | |||||||
| chr21:14536088 | A | G | 1 | a0002c0003t0002g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.57+10117T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536088 | |||||||
| chr21:14536141 | T | C | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+10064A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536141 | |||||||
| chr21:14536158 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+10047C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536158 | |||||||
| chr21:14536243 | A | C | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+9962T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536243 | |||||||
| chr21:14536318 | T | C | 1 | a0001c0002t0001g0347 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.57+9887A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536318 | |||||||
| chr21:14536321 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(102): Show |
118 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.57+9884G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536321 | |||||||
| chr21:14536407 | C | G | 10 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0157 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+9798G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536407 | |||||||
| chr21:14536570 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+9635C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536570 | |||||||
| chr21:14536649 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.57+9556A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536649 | |||||||
| chr21:14536685 | AAAG | A | 4 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0001t0002g0164 others(1): Show |
5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+9517_57+9519del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536685 | |||||||
| chr21:14536702 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+9503G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536702 | |||||||
| chr21:14536702 | C | T | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+9503G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536702 | |||||||
| chr21:14536707 | C | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(261): Show |
286 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.57+9498G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536707 | |||||||
| chr21:14536752 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.57+9453G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536752 | |||||||
| chr21:14536777 | G | A | 1 | a0002c0003t0001g0016 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.57+9428C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536777 | |||||||
| chr21:14536888 | G | A | 5 | a0001c0002t0001g0280 a0001c0002t0001g0348 a0001c0002t0001g0349 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+9317C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536888 | |||||||
| chr21:14536930 | A | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(110): Show |
127 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.57+9275T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536930 | |||||||
| chr21:14536947 | T | A | 1 | a0001c0001t0001g0097 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.57+9258A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536947 | |||||||
| chr21:14536969 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+9236A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536969 | |||||||
| chr21:14536970 | C | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(81): Show |
93 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.57+9235G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536970 | |||||||
| chr21:14537042 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(106): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.57+9163T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537042 | |||||||
| chr21:14537128 | C | T | 1 | a0001c0002t0001g0288 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.57+9077G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537128 | |||||||
| chr21:14537155 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+9050G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537155 | |||||||
| chr21:14537208 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.57+8997T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537208 | |||||||
| chr21:14537247 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0001t0002g0164 others(1): Show |
5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+8958G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537247 | |||||||
| chr21:14537282 | A | C | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+8923T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537282 | |||||||
| chr21:14537355 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(102): Show |
118 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.57+8850G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537355 | |||||||
| chr21:14537375 | A | AT | 29 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(26): Show |
31 | HG01081.hp1 HG01099.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+8829dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537375 | |||||||
| chr21:14537460 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
235 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.57+8745G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537460 | |||||||
| chr21:14537492 | G | A | 1 | a0001c0002t0002g0373 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.57+8713C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537492 | |||||||
| chr21:14537499 | T | C | 2 | a0001c0001t0001g0063 a0001c0002t0001g0352 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+8706A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537499 | |||||||
| chr21:14537536 | G | A | 1 | a0001c0002t0001g0353 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+8669C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537536 | |||||||
| chr21:14537557 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(101): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.57+8648G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537557 | |||||||
| chr21:14537715 | T | A | 107 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0154 others(104): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+8490A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537715 | |||||||
| chr21:14537854 | G | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+8351C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537854 | |||||||
| chr21:14537952 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.57+8253G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537952 | |||||||
| chr21:14538034 | T | A | 1 | a0001c0001t0001g0263 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.57+8171A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538034 | |||||||
| chr21:14538072 | G | A | 7 | a0001c0001t0002g0169 a0001c0001t0002g0176 a0001c0002t0001g0354 others(4): Show |
7 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+8133C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538072 | |||||||
| chr21:14538158 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0099 |
3 | HG00099.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.57+8047G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538158 | |||||||
| chr21:14538194 | T | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+8011A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538194 | |||||||
| chr21:14538233 | ACATTTTA others(6): Show |
A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7959_57+7971del others(13): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538233 | |||||||
| chr21:14538246 | T | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(277): Show |
303 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.57+7959A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538246 | |||||||
| chr21:14538247 | G | A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7958C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538247 | |||||||
| chr21:14538248 | T | C | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7957A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538248 | |||||||
| chr21:14538251 | T | A | 1 | a0004c0005t0001g0358 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7954A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538251 | |||||||
| chr21:14538606 | T | G | 10 | a0001c0001t0001g0167 a0001c0001t0001g0255 a0001c0001t0001g0256 others(7): Show |
10 | HG02129.hp2 NA18943.hp1 NA18974.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+7599A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538606 | |||||||
| chr21:14538916 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+7289C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538916 | |||||||
| chr21:14539008 | A | C | 1 | a0001c0001t0003g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.57+7197T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539008 | |||||||
| chr21:14539015 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 |
4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+7190A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539015 | |||||||
| chr21:14539112 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG02615.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+7093C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539112 | |||||||
| chr21:14539149 | C | A | 107 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0154 others(104): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+7056G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539149 | |||||||
| chr21:14539286 | T | G | 1 | a0001c0001t0004g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.57+6919A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539286 | |||||||
| chr21:14539412 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.57+6793T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539412 | |||||||
| chr21:14539463 | G | A | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+6742C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539463 | |||||||
| chr21:14539566 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+6639T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539566 | |||||||
| chr21:14539567 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+6638T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539567 | |||||||
| chr21:14539624 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+6581A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539624 | |||||||
| chr21:14539641 | A | T | 3 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0002c0003t0001g0008 |
4 | HG01168.hp2 HG02004.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+6564T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539641 | |||||||
| chr21:14539686 | A | G | 1 | a0001c0002t0001g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.57+6519T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539686 | |||||||
| chr21:14539698 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.57+6507G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539698 | |||||||
| chr21:14539712 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
8 | HG00423.hp1 HG00609.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+6493G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539712 | |||||||
| chr21:14539746 | A | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+6459T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539746 | |||||||
| chr21:14539781 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
8 | HG01106.hp1 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+6424G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539781 | |||||||
| chr21:14539835 | A | G | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(10): Show |
14 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+6370T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539835 | |||||||
| chr21:14539890 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | NA18942.hp1 NA19010.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.57+6315T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539890 | |||||||
| chr21:14540233 | C | G | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+5972G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540233 | |||||||
| chr21:14540404 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.57+5801C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540404 | |||||||
| chr21:14540475 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+5730C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540475 | |||||||
| chr21:14540479 | A | G | 3 | a0001c0001t0001g0065 a0001c0002t0001g0282 a0001c0002t0001g0283 |
3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.57+5726T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540479 | |||||||
| chr21:14540538 | A | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0171 a0001c0001t0001g0172 others(5): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+5667T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540538 | |||||||
| chr21:14540743 | G | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
260 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.57+5462C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540743 | |||||||
| chr21:14540750 | T | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
260 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.57+5455A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540750 | |||||||
| chr21:14540807 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57+5398G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540807 | |||||||
| chr21:14540832 | A | G | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+5373T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540832 | |||||||
| chr21:14540853 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
260 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.57+5352C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540853 | |||||||
| chr21:14541024 | T | C | 2 | a0002c0003t0001g0040 a0002c0003t0001g0049 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.57+5181A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541024 | |||||||
| chr21:14541025 | G | T | 2 | a0002c0003t0001g0040 a0002c0003t0001g0049 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.57+5180C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541025 | |||||||
| chr21:14541074 | T | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.57+5131A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541074 | |||||||
| chr21:14541116 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5089G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541116 | |||||||
| chr21:14541145 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+5060C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541145 | |||||||
| chr21:14541147 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5058C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541147 | |||||||
| chr21:14541187 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5018C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541187 | |||||||
| chr21:14541239 | C | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+4966G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541239 | |||||||
| chr21:14541323 | T | TA | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+4881dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541323 | |||||||
| chr21:14541323 | TAA | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
263 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.57+4880_57+4881del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541323 | |||||||
| chr21:14541372 | C | A | 3 | a0001c0002t0001g0359 a0001c0002t0001g0360 a0001c0002t0002g0361 |
3 | NA18944.hp1 NA18953.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.57+4833G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541372 | |||||||
| chr21:14541380 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+4825T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541380 | |||||||
| chr21:14541448 | C | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+4757G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541448 | |||||||
| chr21:14541458 | C | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0004g0001 others(2): Show |
7 | HG01099.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+4747G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541458 | |||||||
| chr21:14541515 | G | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+4690C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541515 | |||||||
| chr21:14541520 | T | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
263 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.57+4685A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541520 | |||||||
| chr21:14541603 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+4602A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541603 | |||||||
| chr21:14541649 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0001t0002g0164 others(1): Show |
5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+4556T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541649 | |||||||
| chr21:14541699 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
13 | HG02683.hp1 HG04184.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+4506G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541699 | |||||||
| chr21:14541918 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.57+4287T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541918 | |||||||
| chr21:14541958 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+4247G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541958 | |||||||
| chr21:14541965 | CTGGGTAA others(5): Show |
C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+4228_57+4239del others(12): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541965 | |||||||
| chr21:14541987 | G | GAA | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(216): Show |
239 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.57+4216_57+4217dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541987 | |||||||
| chr21:14541987 | G | GAAA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
22 | HG00597.hp1 HG01981.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+4215_57+4217dup others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541987 | |||||||
| chr21:14542059 | G | C | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.57+4146C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542059 | |||||||
| chr21:14542077 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.57+4128C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542077 | |||||||
| chr21:14542154 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.57+4051G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542154 | |||||||
| chr21:14542565 | T | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+3640A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542565 | |||||||
| chr21:14542619 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.57+3586T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542619 | |||||||
| chr21:14542690 | T | C | 1 | a0001c0002t0001g0374 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.57+3515A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542690 | |||||||
| chr21:14542990 | C | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | HG02615.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.57+3215G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542990 | |||||||
| chr21:14543153 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | NA18962.hp2 NA18982.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.57+3052G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543153 | |||||||
| chr21:14543159 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+3046C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543159 | |||||||
| chr21:14543185 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(130): Show |
147 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.57+3020T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543185 | |||||||
| chr21:14543278 | T | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
263 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.57+2927A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543278 | |||||||
| chr21:14543402 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(234): Show |
258 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.57+2803G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543402 | |||||||
| chr21:14543417 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+2788A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543417 | |||||||
| chr21:14543480 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.57+2725T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543480 | |||||||
| chr21:14543533 | C | T | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+2672G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543533 | |||||||
| chr21:14543732 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.57+2473A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543732 | |||||||
| chr21:14543751 | A | C | 108 | a0001c0001t0001g0035 a0001c0001t0001g0167 a0001c0001t0002g0036 others(105): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.57+2454T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543751 | |||||||
| chr21:14543813 | A | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(277): Show |
303 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.57+2392T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543813 | |||||||
| chr21:14543905 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+2300G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543905 | |||||||
| chr21:14544015 | T | C | 1 | a0001c0002t0001g0375 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+2190A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544015 | |||||||
| chr21:14544044 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+2161G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544044 | |||||||
| chr21:14544231 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0270 a0001c0001t0001g0271 |
4 | HG00639.hp1 HG01433.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+1974A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544231 | |||||||
| chr21:14544270 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(239): Show |
263 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.57+1935C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544270 | |||||||
| chr21:14544285 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+1920T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544285 | |||||||
| chr21:14544302 | C | T | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+1903G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544302 | |||||||
| chr21:14544303 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+1902C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544303 | |||||||
| chr21:14544309 | GCAAAGTG others(28): Show |
G | 1 | a0002c0003t0001g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.57+1861_57+1895del others(35): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544309 | |||||||
| chr21:14544394 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0001t0002g0164 others(1): Show |
5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+1811T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544394 | |||||||
| chr21:14544660 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+1545T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544660 | |||||||
| chr21:14544738 | A | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18941.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.57+1467T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544738 | |||||||
| chr21:14545091 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02165.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.57+1114G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545091 | |||||||
| chr21:14545240 | A | T | 108 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0002t0001g0005 others(105): Show |
115 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.57+965T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545240 | |||||||
| chr21:14545254 | C | T | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0277 others(2): Show |
5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+951G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545254 | |||||||
| chr21:14545499 | G | A | 1 | a0001c0002t0001g0376 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.57+706C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545499 | |||||||
| chr21:14545536 | CT | C | 8 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(5): Show |
8 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+668delA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545536 | |||||||
| chr21:14545536 | CTT | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(126): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.57+667_57+668delAA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545536 | |||||||
| chr21:14545547 | TA | T | 107 | a0001c0001t0001g0035 a0001c0001t0002g0036 a0001c0002t0001g0005 others(104): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+657delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545547 | |||||||
| chr21:14545548 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0275 |
2 | HG02886.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.57+657T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545548 | |||||||
| chr21:14545626 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00735.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.57+579C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545626 | |||||||
| chr21:14545627 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.57+578C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545627 | |||||||
| chr21:14545629 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.57+576C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545629 | |||||||
| chr21:14545655 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+550G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545655 | |||||||
| chr21:14545714 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 |
4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+491G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545714 | |||||||
| chr21:14545808 | G | A | 1 | a0001c0002t0002g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+397C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545808 | |||||||
| chr21:14545820 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.57+385A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545820 | |||||||
| chr21:14545887 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.57+318C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545887 | |||||||
| chr21:14546046 | CTT | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+157_57+158delAA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14546046 |