Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154075 |
| ensemblid | ENSG00000164483.17 |
| hgncid | 21574 |
| symbol | SAMD3 |
| name | sterile alpha motif domain containing 3 |
| refseq_nuc | NM_001017373.4 |
| refseq_prot | NP_001017373.2 |
| ensembl_nuc | ENST00000439090.7 |
| ensembl_prot | ENSP00000403565.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 130144315 |
| end | 130222951 |
| strand | - |
| ver | v1.2 |
| region | chr6:130144315-130222951 |
| region5000 | chr6:130139315-130227951 |
| regionname0 | SAMD3_chr6_130144315_130222951 |
| regionname5000 | SAMD3_chr6_130139315_130227951 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 328 | 76 | 57 | 138 | 10 | 45 | 102 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0002 | 0/0 | 520 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0003 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0004 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0005 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0006 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0007 | 0/0 | 520 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0008 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| a0009 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | METWS others(515): Show |
chr6 | 130139315 | 130227951 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1560 | 321 | 72 | 57 | 138 | 10 | 42 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0001c0002 | 0/0 | 1560 | 3 | 2 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0001c0004 | 0/0 | 1560 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0001c0007 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0001c0010 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0002c0003 | 0/0 | 1560 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0003c0011 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0004c0008 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0005c0009 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0006c0013 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0007c0012 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0008c0005 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 | ||
| a0009c0006 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | ATGGA others(1555): Show |
chr6 | 130139315 | 130227951 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2093 | 285 | 58 | 47 | 134 | 10 | 34 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0002 | 0/0 | 2093 | 31 | 12 | 9 | 4 | 0 | 6 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0003 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0004 | 0/0 | 2093 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0005 | 0/0 | 2093 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0006 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0001t0007 | 0/0 | 2093 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0002t0001 | 0/0 | 2093 | 3 | 2 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0004t0001 | 0/0 | 2093 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0007t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0001c0010t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0002c0003t0001 | 0/0 | 2093 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0003c0011t0001 | 0/0 | 2093 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0004c0008t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0005c0009t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0006c0013t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0007c0012t0001 | 0/0 | 2093 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0008c0005t0001 | 0/0 | 2093 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| a0009c0006t0001 | 0/0 | 2093 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | AGTCT others(2088): Show |
chr6 | 130139315 | 130227951 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0001c0010t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0003c0011t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0004c0008t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0005c0009t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0006c0013t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0007c0012t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0008c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| a0009c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01433 | hp2 | a0003 | c0011 | t0001 | g0305 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0161 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02258 | hp2 | a0005 | c0009 | t0001 | g0285 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02451 | hp1 | a0006 | c0013 | t0001 | g0253 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02735 | hp2 | a0007 | c0012 | t0001 | g0323 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0201 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03540 | hp2 | a0008 | c0005 | t0001 | g0231 | AFR | GWD | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0298 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18960 | hp1 | a0009 | c0006 | t0001 | g0149 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19043 | hp2 | a0001 | c0010 | t0001 | g0023 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ASW | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | GIH | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0327 | SAS | GIH | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02109 | hp1 | a0004 | c0008 | t0001 | g0280 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | USA | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0115 | REF | REF | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0049 | REF | REF | SAMD3_chr6_130139315_130227951 | SAMD3 | chr6 | 130139315 | 130227951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:130144546 | C | T | 1 | a0005 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1537G>A | p.Val513Ile | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 12/12 | 1862/2093 | 1537/1563 | 513/520 | chr6 | 130144546 | |||
| chr6:130144756 | C | T | 1 | a0004 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1327G>A | p.Glu443Lys | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 12/12 | 1652/2093 | 1327/1563 | 443/520 | chr6 | 130144756 | |||
| chr6:130146093 | G | A | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1112C>T | p.Thr371Ile | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/12 | 1437/2093 | 1112/1563 | 371/520 | chr6 | 130146093 | |||
| chr6:130154862 | A | G | 1 | a0009 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.986T>C | p.Ile329Thr | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/12 | 1311/2093 | 986/1563 | 329/520 | chr6 | 130154862 | |||
| chr6:130154889 | A | G | 1 | a0008 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.959T>C | p.Ile320Thr | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/12 | 1284/2093 | 959/1563 | 320/520 | chr6 | 130154889 | |||
| chr6:130154915 | T | G | 1 | a0007 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.933A>C | p.Gln311His | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/12 | 1258/2093 | 933/1563 | 311/520 | chr6 | 130154915 | |||
| chr6:130184567 | T | C | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.440A>G | p.Tyr147Cys | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/12 | 765/2093 | 440/1563 | 147/520 | chr6 | 130184567 | |||
| chr6:130209580 | C | A | 1 | a0002 | 3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
missense_variant | MODERATE | c.298G>T | p.Ala100Ser | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/12 | 623/2093 | 298/1563 | 100/520 | chr6 | 130209580 | |||
| chr6:130222694 | G | A | 1 | a0001 | 1 | NA20905.hp2 | splice_region_variant | LOW | c.-68C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/12 | chr6 | 130222694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:130145391 | G | C | 1 | a0001c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1227C>G | p.Leu409Leu | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/12 | 1552/2093 | 1227/1563 | 409/520 | chr6 | 130145391 | |||
| chr6:130154837 | C | T | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1011G>A | p.Lys337Lys | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/12 | 1336/2093 | 1011/1563 | 337/520 | chr6 | 130154837 | |||
| chr6:130184139 | C | T | 1 | a0001c0002 | 3 | HG02602.hp1 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.618G>A | p.Gln206Gln | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/12 | 943/2093 | 618/1563 | 206/520 | chr6 | 130184139 | |||
| chr6:130184485 | G | A | 1 | a0001c0004 | 2 | HG03017.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.522C>T | p.Ile174Ile | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/12 | 847/2093 | 522/1563 | 174/520 | chr6 | 130184485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:130144398 | G | A | 1 | a0001c0001t0005 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 12/12 | 122 | chr6 | 130144398 | ||||||
| chr6:130144404 | A | G | 1 | a0001c0001t0002 | 31 | HG00621.hp1 HG01074.hp1 HG01255.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*116T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 12/12 | 116 | chr6 | 130144404 | ||||||
| chr6:130216584 | C | A | 1 | a0001c0001t0006 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/12 | 1311 | chr6 | 130216584 | ||||||
| chr6:130222878 | C | G | 1 | a0001c0001t0004 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-252G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/12 | 7605 | chr6 | 130222878 | ||||||
| chr6:130222942 | C | G | 1 | a0001c0001t0003 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-316G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/12 | 7669 | chr6 | 130222942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:130144949 | A | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0125 others(5): Show |
8 | HG00323.hp1 HG01106.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279-145T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130144949 | |||||||
| chr6:130144977 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1279-173G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130144977 | |||||||
| chr6:130145078 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1278+262G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145078 | |||||||
| chr6:130145089 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(165): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1278+251C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145089 | |||||||
| chr6:130145097 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1278+243A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145097 | |||||||
| chr6:130145174 | G | A | 1 | a0007c0012t0001g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1278+166C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145174 | |||||||
| chr6:130145183 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1278+157T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145183 | |||||||
| chr6:130145268 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1278+72C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 11/11 | chr6 | 130145268 | |||||||
| chr6:130145427 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.1196-5G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/11 | chr6 | 130145427 | |||||||
| chr6:130145531 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1196-109T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/11 | chr6 | 130145531 | |||||||
| chr6:130145805 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1195+205A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/11 | chr6 | 130145805 | |||||||
| chr6:130145811 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1195+199G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/11 | chr6 | 130145811 | |||||||
| chr6:130145927 | T | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195+83A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 10/11 | chr6 | 130145927 | |||||||
| chr6:130146611 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0240 a0001c0001t0001g0252 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-430T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146611 | |||||||
| chr6:130146669 | G | A | 4 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0258 others(1): Show |
4 | HG01891.hp1 HG02257.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-488C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146669 | |||||||
| chr6:130146821 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1024-640T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146821 | |||||||
| chr6:130146839 | A | G | 32 | a0001c0001t0001g0031 a0001c0001t0001g0240 a0001c0001t0001g0252 others(29): Show |
32 | HG00621.hp1 HG01074.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1024-658T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146839 | |||||||
| chr6:130146906 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1024-725G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146906 | |||||||
| chr6:130146973 | CAAAA | C | 29 | a0001c0001t0001g0031 a0001c0001t0002g0020 a0001c0001t0002g0021 others(26): Show |
29 | HG00621.hp1 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024-796_1024-793d others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146973 | |||||||
| chr6:130146997 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1024-816G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130146997 | |||||||
| chr6:130147024 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1024-843A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147024 | |||||||
| chr6:130147053 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0281 |
2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1024-872T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147053 | |||||||
| chr6:130147068 | A | ACT | 5 | a0001c0001t0002g0067 a0001c0001t0002g0070 a0001c0001t0002g0268 others(2): Show |
5 | HG01255.hp1 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-889_1024-888d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147068 | |||||||
| chr6:130147079 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-898G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147079 | |||||||
| chr6:130147142 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1024-961G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147142 | |||||||
| chr6:130147329 | TA | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0178 a0001c0001t0001g0202 |
3 | NA18942.hp2 NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1024-1149delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147329 | |||||||
| chr6:130147347 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-1166A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147347 | |||||||
| chr6:130147612 | T | TA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
111 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1024-1432dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147612 | |||||||
| chr6:130147855 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0306 |
2 | HG02027.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1024-1674A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147855 | |||||||
| chr6:130147922 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1024-1741T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147922 | |||||||
| chr6:130147981 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1024-1800A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130147981 | |||||||
| chr6:130148043 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1024-1862C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148043 | |||||||
| chr6:130148207 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0252 a0001c0001t0001g0259 |
3 | HG02145.hp2 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1024-2026C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148207 | |||||||
| chr6:130148241 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1024-2060G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148241 | |||||||
| chr6:130148303 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1024-2122G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148303 | |||||||
| chr6:130148485 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1024-2304A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148485 | |||||||
| chr6:130148682 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2501C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148682 | |||||||
| chr6:130148780 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1024-2599T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148780 | |||||||
| chr6:130148852 | A | AGT | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1024-2672_1024-267 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130148852 | |||||||
| chr6:130149013 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1024-2832T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149013 | |||||||
| chr6:130149048 | A | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
151 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1024-2867T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149048 | |||||||
| chr6:130149311 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1024-3130C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149311 | |||||||
| chr6:130149361 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1024-3180T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149361 | |||||||
| chr6:130149371 | C | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-3190G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149371 | |||||||
| chr6:130149405 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1024-3224C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149405 | |||||||
| chr6:130149526 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
151 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1024-3345A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149526 | |||||||
| chr6:130149542 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1024-3361A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149542 | |||||||
| chr6:130149566 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024-3385T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149566 | |||||||
| chr6:130149624 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1024-3443A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149624 | |||||||
| chr6:130149649 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1024-3468C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149649 | |||||||
| chr6:130149791 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1024-3610G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149791 | |||||||
| chr6:130149803 | A | T | 1 | a0001c0002t0001g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1024-3622T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149803 | |||||||
| chr6:130149847 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1024-3666C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149847 | |||||||
| chr6:130149918 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
147 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1024-3737T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130149918 | |||||||
| chr6:130150098 | CAT | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0091 others(12): Show |
17 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1024-3919_1024-391 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150098 | |||||||
| chr6:130150099 | ATG | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-3920_1024-391 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150099 | |||||||
| chr6:130150099 | ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0243 others(3): Show |
6 | HG01123.hp2 HG01192.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-3926_1024-391 others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150099 | |||||||
| chr6:130150120 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-3939A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150120 | |||||||
| chr6:130150207 | G | A | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1024-4026C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150207 | |||||||
| chr6:130150427 | T | G | 6 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0258 others(3): Show |
6 | HG01891.hp1 HG02257.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024-4246A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150427 | |||||||
| chr6:130150499 | T | G | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1024-4318A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150499 | |||||||
| chr6:130150568 | A | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+4257T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150568 | |||||||
| chr6:130150692 | T | C | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1023+4133A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150692 | |||||||
| chr6:130150711 | T | A | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1023+4114A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150711 | |||||||
| chr6:130150713 | C | CT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(42): Show |
46 | HG00621.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1023+4111dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150713 | |||||||
| chr6:130150858 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0272 a0002c0003t0001g0086 |
3 | HG02135.hp2 NA19057.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1023+3967A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150858 | |||||||
| chr6:130150936 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0212 a0001c0001t0005g0204 others(1): Show |
4 | HG01074.hp2 HG01981.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+3889A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150936 | |||||||
| chr6:130150991 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0057 others(5): Show |
8 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+3834G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130150991 | |||||||
| chr6:130151091 | C | T | 1 | a0003c0011t0001g0305 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1023+3734G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151091 | |||||||
| chr6:130151117 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1023+3708G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151117 | |||||||
| chr6:130151149 | A | G | 1 | a0001c0001t0001g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1023+3676T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151149 | |||||||
| chr6:130151269 | C | CCT | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1023+3555_1023+355 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151269 | |||||||
| chr6:130151487 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
154 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1023+3338T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151487 | |||||||
| chr6:130151636 | T | C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0252 a0001c0001t0001g0259 |
3 | HG02145.hp2 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1023+3189A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151636 | |||||||
| chr6:130151665 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(151): Show |
158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1023+3160A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151665 | |||||||
| chr6:130151775 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
101 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1023+3050G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151775 | |||||||
| chr6:130151881 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+2944A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151881 | |||||||
| chr6:130151951 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1023+2874C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130151951 | |||||||
| chr6:130152025 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1023+2800G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152025 | |||||||
| chr6:130152026 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1023+2799A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152026 | |||||||
| chr6:130152077 | G | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
96 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1023+2748C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152077 | |||||||
| chr6:130152107 | G | GCCCACCC others(1): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(1): Show |
5 | HG03491.hp2 HG03492.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+2710_1023+271 others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152107 | |||||||
| chr6:130152115 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0313 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1023+2710G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152115 | |||||||
| chr6:130152503 | C | G | 1 | a0001c0001t0001g0273 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1023+2322G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152503 | |||||||
| chr6:130152619 | G | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0010t0001g0023 |
3 | HG02922.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1023+2206C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152619 | |||||||
| chr6:130152655 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG00639.hp1 HG02056.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+2170G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152655 | |||||||
| chr6:130152672 | G | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1023+2153C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152672 | |||||||
| chr6:130152676 | CAATAAAT others(1): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0106 others(5): Show |
11 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1023+2141_1023+214 others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152676 | |||||||
| chr6:130152695 | T | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0132 |
3 | NA18939.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1023+2130A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152695 | |||||||
| chr6:130152699 | T | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(49): Show |
53 | HG00621.hp1 HG00673.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1023+2126A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152699 | |||||||
| chr6:130152959 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0165 |
2 | HG01169.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1023+1866T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130152959 | |||||||
| chr6:130153165 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1023+1660G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153165 | |||||||
| chr6:130153194 | CTG | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
86 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1023+1629_1023+163 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153194 | |||||||
| chr6:130153452 | G | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
228 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1023+1373C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153452 | |||||||
| chr6:130153625 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1023+1200C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153625 | |||||||
| chr6:130153636 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1023+1189G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153636 | |||||||
| chr6:130153647 | C | CAT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0001t0001g0277 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1176_1023+117 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATAT | 5 | a0001c0001t0001g0107 a0001c0001t0001g0259 a0001c0001t0001g0283 others(2): Show |
5 | HG02647.hp1 HG03453.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+1174_1023+117 others(8): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(1): Show |
6 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+1170_1023+117 others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1023+1168_1023+117 others(14): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(5): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0266 |
3 | HG00099.hp1 HG02004.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1023+1166_1023+117 others(16): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(7): Show |
6 | a0001c0001t0001g0037 a0001c0001t0001g0078 a0001c0001t0001g0122 others(3): Show |
6 | HG01516.hp1 HG02129.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1023+1164_1023+117 others(18): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(9): Show |
8 | a0001c0001t0001g0033 a0001c0001t0001g0097 a0001c0001t0001g0118 others(5): Show |
8 | HG00639.hp1 HG01099.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+1162_1023+117 others(20): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(11): Show |
20 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0028 others(17): Show |
20 | HG00280.hp2 HG00597.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1023+1160_1023+117 others(22): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(13): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
30 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1023+1177_1023+117 others(24): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(15): Show |
28 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0026 others(25): Show |
28 | HG01106.hp2 HG01261.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1023+1177_1023+117 others(26): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(17): Show |
23 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0039 others(20): Show |
24 | HG00438.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1023+1177_1023+117 others(28): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(19): Show |
11 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
11 | HG00609.hp2 HG00673.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1023+1177_1023+117 others(30): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153647 | C | CATATATA others(21): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0220 a0001c0001t0001g0325 |
3 | HG00544.hp2 HG04115.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1023+1177_1023+117 others(32): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153647 | |||||||
| chr6:130153649 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1023+1176A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153649 | |||||||
| chr6:130153658 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0239 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+1167T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153658 | |||||||
| chr6:130153662 | A | ATATATAT others(5): Show |
1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1023+1162_1023+116 others(16): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153662 | |||||||
| chr6:130153662 | A | ATTTATT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+1162_1023+116 others(10): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153662 | |||||||
| chr6:130153662 | ATATT | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(24): Show |
28 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1023+1159_1023+116 others(8): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153662 | |||||||
| chr6:130153664 | ATT | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
97 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1023+1159_1023+116 others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153664 | |||||||
| chr6:130153665 | T | TATATATA others(20): Show |
1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1023+1159_1023+116 others(31): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153665 | |||||||
| chr6:130153666 | T | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(136): Show |
143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1023+1159A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153666 | |||||||
| chr6:130153669 | T | TATATATA others(6): Show |
1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1023+1155_1023+115 others(17): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153669 | |||||||
| chr6:130153669 | T | TATATATA others(10): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0123 a0001c0001t0001g0318 |
3 | HG01123.hp2 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1023+1155_1023+115 others(21): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153669 | |||||||
| chr6:130153669 | T | TATATATA others(16): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG00642.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+1155_1023+115 others(27): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153669 | |||||||
| chr6:130153670 | T | A | 16 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0038 others(13): Show |
16 | HG00280.hp2 HG00639.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1023+1155A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153670 | |||||||
| chr6:130153679 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1023+1146A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153679 | |||||||
| chr6:130153707 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+1118T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153707 | |||||||
| chr6:130153988 | A | G | 1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1023+837T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130153988 | |||||||
| chr6:130154000 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+825T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154000 | |||||||
| chr6:130154034 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1023+791G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154034 | |||||||
| chr6:130154148 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1023+677C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154148 | |||||||
| chr6:130154235 | CT | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1023+589delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154235 | |||||||
| chr6:130154235 | CTT | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0219 a0001c0001t0001g0315 others(3): Show |
6 | HG02735.hp2 NA18960.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+588_1023+589d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154235 | |||||||
| chr6:130154315 | A | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1023+510T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154315 | |||||||
| chr6:130154648 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1023+177G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154648 | |||||||
| chr6:130154675 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(150): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1023+150C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154675 | |||||||
| chr6:130154695 | G | GA | 11 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0069 others(8): Show |
11 | HG01074.hp1 HG01358.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1023+129dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154695 | GA | G | 6 | a0001c0001t0001g0155 a0001c0001t0001g0232 a0001c0001t0001g0289 others(3): Show |
6 | HG00741.hp2 HG01261.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+129delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154695 | GAAAAAAA others(1): Show |
G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0037 others(44): Show |
50 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1023+122_1023+129d others(10): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154695 | GAAAAAAA others(2): Show |
G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0084 a0001c0001t0001g0158 others(6): Show |
10 | HG02258.hp1 HG03491.hp1 NA18970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1023+121_1023+129d others(11): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154695 | GAAAAAAA others(3): Show |
G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(54): Show |
59 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1023+120_1023+129d others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154695 | GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0113 |
2 | HG01069.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1023+119_1023+129d others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154695 | |||||||
| chr6:130154696 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+129T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154696 | |||||||
| chr6:130154708 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1023+105_1023+116d others(14): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154708 | |||||||
| chr6:130154709 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0193 |
3 | NA18941.hp1 NA18948.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1023+105_1023+115d others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154709 | |||||||
| chr6:130154710 | AAAAAAAA others(3): Show |
A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0102 a0001c0001t0001g0103 others(17): Show |
21 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1023+105_1023+114d others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154710 | |||||||
| chr6:130154711 | AAAAAAAA others(2): Show |
A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0195 others(4): Show |
7 | HG00673.hp1 HG02083.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+105_1023+113d others(11): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154711 | |||||||
| chr6:130154711 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0316 |
3 | NA18906.hp2 NA18977.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1023+103_1023+113d others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154711 | |||||||
| chr6:130154711 | AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+101_1023+113d others(15): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154711 | |||||||
| chr6:130154711 | AAAAAAAA others(10): Show |
A | 1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1023+97_1023+113de others(18): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154711 | |||||||
| chr6:130154712 | AAAAAAAA others(1): Show |
A | 12 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0001g0252 others(9): Show |
12 | HG00544.hp2 HG01123.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+105_1023+112d others(10): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154712 | |||||||
| chr6:130154712 | AAAAAAAA others(3): Show |
A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0074 others(3): Show |
6 | HG02809.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+103_1023+112d others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154712 | |||||||
| chr6:130154713 | AAAAAAAT others(2): Show |
A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0017 others(64): Show |
68 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1023+103_1023+111d others(11): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154713 | |||||||
| chr6:130154713 | AAAAAAAT others(4): Show |
A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0096 a0001c0001t0001g0308 others(1): Show |
4 | NA18968.hp1 NA18985.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+101_1023+111d others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154713 | |||||||
| chr6:130154713 | AAAAAAAT others(8): Show |
A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023+97_1023+111de others(16): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154713 | |||||||
| chr6:130154714 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1023+111T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154714 | |||||||
| chr6:130154714 | AAAAAATA others(3): Show |
A | 1 | a0001c0001t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1023+101_1023+110d others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154714 | |||||||
| chr6:130154716 | A | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0105 a0001c0001t0001g0160 others(6): Show |
9 | HG01981.hp1 HG02258.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1023+109T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154716 | |||||||
| chr6:130154718 | A | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0031 others(50): Show |
56 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1023+107T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154718 | |||||||
| chr6:130154718 | AAT | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0150 a0001c0001t0002g0258 others(3): Show |
6 | HG00673.hp2 HG01255.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023+105_1023+106d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154718 | |||||||
| chr6:130154718 | AATATATA others(5): Show |
A | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1023+95_1023+106de others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154718 | |||||||
| chr6:130154719 | AT | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0077 others(3): Show |
7 | HG03491.hp2 HG03492.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023+105delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154719 | |||||||
| chr6:130154720 | T | A | 11 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0119 others(8): Show |
11 | HG01074.hp1 HG01358.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1023+105A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154720 | |||||||
| chr6:130154722 | T | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(10): Show |
14 | HG00673.hp2 HG03453.hp2 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.1023+103A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154722 | |||||||
| chr6:130154724 | T | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0150 others(3): Show |
7 | HG00673.hp2 HG03453.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023+101A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154724 | |||||||
| chr6:130154802 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1023+23T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154802 | |||||||
| chr6:130154805 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0192 |
2 | NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1023+20A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 9/11 | chr6 | 130154805 | |||||||
| chr6:130155047 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-22A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155047 | |||||||
| chr6:130155050 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-25T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155050 | |||||||
| chr6:130155198 | T | A | 6 | a0001c0001t0001g0056 a0001c0001t0002g0058 a0001c0001t0002g0085 others(3): Show |
6 | HG01074.hp1 HG01358.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-173A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155198 | |||||||
| chr6:130155450 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-425A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155450 | |||||||
| chr6:130155543 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(16): Show |
20 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.823-518C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155543 | |||||||
| chr6:130155555 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.823-530C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155555 | |||||||
| chr6:130155593 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.823-568T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155593 | |||||||
| chr6:130155670 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.823-645G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155670 | |||||||
| chr6:130155847 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.823-822G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155847 | |||||||
| chr6:130155857 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-832C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155857 | |||||||
| chr6:130155923 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-898A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130155923 | |||||||
| chr6:130156118 | C | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0096 |
2 | NA18977.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.823-1093G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156118 | |||||||
| chr6:130156160 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(137): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.823-1135C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156160 | |||||||
| chr6:130156195 | C | T | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823-1170G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156195 | |||||||
| chr6:130156196 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-1171C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156196 | |||||||
| chr6:130156294 | G | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.823-1269C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156294 | |||||||
| chr6:130156373 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.823-1348T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156373 | |||||||
| chr6:130156500 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-1475G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156500 | |||||||
| chr6:130156703 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.823-1678C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130156703 | |||||||
| chr6:130157065 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0281 |
2 | HG01192.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.823-2040C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157065 | |||||||
| chr6:130157072 | A | AAAAT | 10 | a0001c0001t0001g0054 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG01358.hp2 HG01433.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-2051_823-2048d others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157072 | |||||||
| chr6:130157072 | AAAAT | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(70): Show |
77 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.823-2051_823-2048d others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157072 | |||||||
| chr6:130157072 | AAAATAAA others(1): Show |
A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0024 others(118): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.823-2055_823-2048d others(10): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157072 | |||||||
| chr6:130157072 | AAAATAAA others(5): Show |
A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0252 a0001c0001t0001g0259 others(12): Show |
15 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.823-2059_823-2048d others(14): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157072 | |||||||
| chr6:130157072 | AAAATAAA others(9): Show |
A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0034 others(8): Show |
12 | HG01891.hp2 HG02040.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.823-2063_823-2048d others(18): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157072 | |||||||
| chr6:130157114 | A | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.823-2089T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157114 | |||||||
| chr6:130157125 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-2100A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157125 | |||||||
| chr6:130157231 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823-2206C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157231 | |||||||
| chr6:130157318 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823-2293T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157318 | |||||||
| chr6:130157344 | A | AT | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.823-2320dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157344 | |||||||
| chr6:130157390 | G | A | 2 | a0001c0001t0002g0275 a0001c0001t0002g0310 |
2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.823-2365C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157390 | |||||||
| chr6:130157400 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823-2375C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157400 | |||||||
| chr6:130157572 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.823-2547G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157572 | |||||||
| chr6:130157618 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.823-2593G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157618 | |||||||
| chr6:130157689 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.823-2664C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157689 | |||||||
| chr6:130157796 | A | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0239 a0001c0002t0001g0255 |
3 | HG02055.hp1 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.823-2771T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157796 | |||||||
| chr6:130157904 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.823-2879T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157904 | |||||||
| chr6:130157905 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.823-2880G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157905 | |||||||
| chr6:130157906 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0031 others(10): Show |
14 | HG00673.hp2 HG02257.hp2 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.823-2881C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157906 | |||||||
| chr6:130157945 | CA | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.823-2921delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157945 | |||||||
| chr6:130157966 | CA | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.823-2942delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130157966 | |||||||
| chr6:130158160 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-3135G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158160 | |||||||
| chr6:130158196 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-3171A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158196 | |||||||
| chr6:130158423 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.823-3398G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158423 | |||||||
| chr6:130158499 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-3474T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158499 | |||||||
| chr6:130158754 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-3729C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158754 | |||||||
| chr6:130158933 | C | T | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.823-3908G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130158933 | |||||||
| chr6:130159191 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 |
3 | HG01884.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.823-4166C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130159191 | |||||||
| chr6:130159218 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-4193T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130159218 | |||||||
| chr6:130159463 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(16): Show |
20 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.823-4438C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130159463 | |||||||
| chr6:130159698 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG00597.hp2 HG02080.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.823-4673T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130159698 | |||||||
| chr6:130159954 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-4929C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130159954 | |||||||
| chr6:130160076 | A | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-5051T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160076 | |||||||
| chr6:130160175 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(10): Show |
14 | HG00673.hp2 HG02257.hp1 HG03491.hp2 others(11): Show |
intron_variant | MODIFIER | c.823-5150A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160175 | |||||||
| chr6:130160217 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-5192A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160217 | |||||||
| chr6:130160223 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0259 a0001c0001t0002g0235 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-5198G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160223 | |||||||
| chr6:130160280 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-5255T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160280 | |||||||
| chr6:130160421 | A | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0248 others(11): Show |
14 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.823-5396T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160421 | |||||||
| chr6:130160543 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-5518C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160543 | |||||||
| chr6:130160613 | C | T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0001g0254 others(2): Show |
5 | HG01123.hp2 HG01891.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.823-5588G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160613 | |||||||
| chr6:130160637 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-5612A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160637 | |||||||
| chr6:130160652 | C | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.823-5627G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160652 | |||||||
| chr6:130160668 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.823-5643C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160668 | |||||||
| chr6:130160739 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.823-5714T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160739 | |||||||
| chr6:130160831 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.823-5806C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130160831 | |||||||
| chr6:130161015 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-5990G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161015 | |||||||
| chr6:130161237 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(17): Show |
21 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.823-6212C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161237 | |||||||
| chr6:130161365 | A | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823-6340T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161365 | |||||||
| chr6:130161450 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0111 a0001c0001t0001g0223 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.823-6425G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161450 | |||||||
| chr6:130161564 | G | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0072 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.823-6539C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161564 | |||||||
| chr6:130161597 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
101 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.823-6572T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161597 | |||||||
| chr6:130161904 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0273 |
2 | NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.823-6879T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161904 | |||||||
| chr6:130161993 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-6968C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130161993 | |||||||
| chr6:130162077 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.823-7052C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162077 | |||||||
| chr6:130162132 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.823-7107C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162132 | |||||||
| chr6:130162252 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-7227G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162252 | |||||||
| chr6:130162257 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.823-7232A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162257 | |||||||
| chr6:130162299 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-7274T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162299 | |||||||
| chr6:130162500 | AT | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(16): Show |
20 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.823-7476delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162500 | |||||||
| chr6:130162516 | T | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.823-7491A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162516 | |||||||
| chr6:130162617 | A | G | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.823-7592T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162617 | |||||||
| chr6:130162903 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.823-7878G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130162903 | |||||||
| chr6:130163004 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.823-7979G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163004 | |||||||
| chr6:130163060 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0281 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.823-8035C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163060 | |||||||
| chr6:130163137 | C | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0233 others(10): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-8112G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163137 | |||||||
| chr6:130163149 | CA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(10): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.823-8125delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163149 | |||||||
| chr6:130163182 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0050 others(14): Show |
18 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.823-8157T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163182 | |||||||
| chr6:130163349 | A | G | 3 | a0001c0001t0001g0297 a0001c0001t0002g0076 a0001c0001t0002g0175 |
3 | HG02056.hp2 HG02132.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.823-8324T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163349 | |||||||
| chr6:130163477 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.823-8452A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163477 | |||||||
| chr6:130163523 | C | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.823-8498G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163523 | |||||||
| chr6:130163536 | T | C | 2 | a0001c0001t0004g0011 a0001c0004t0001g0201 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.823-8511A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163536 | |||||||
| chr6:130163560 | G | A | 43 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0035 others(40): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.823-8535C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163560 | |||||||
| chr6:130163743 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.823-8718G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163743 | |||||||
| chr6:130163926 | A | C | 1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823-8901T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130163926 | |||||||
| chr6:130164075 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.823-9050T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164075 | |||||||
| chr6:130164085 | G | GA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.823-9061dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164085 | |||||||
| chr6:130164085 | G | GAA | 7 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0259 others(4): Show |
7 | HG02109.hp1 HG02809.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-9062_823-9061d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164085 | |||||||
| chr6:130164179 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.823-9154G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164179 | |||||||
| chr6:130164237 | A | G | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823-9212T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164237 | |||||||
| chr6:130164296 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-9271T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164296 | |||||||
| chr6:130164313 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0184 |
2 | NA19078.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.823-9288T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164313 | |||||||
| chr6:130164317 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823-9292T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164317 | |||||||
| chr6:130164413 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.823-9388G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164413 | |||||||
| chr6:130164414 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.823-9389C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164414 | |||||||
| chr6:130164490 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.823-9465G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164490 | |||||||
| chr6:130164709 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823-9684G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164709 | |||||||
| chr6:130164710 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.823-9685C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164710 | |||||||
| chr6:130164733 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.823-9708C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164733 | |||||||
| chr6:130164822 | C | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.823-9797G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130164822 | |||||||
| chr6:130165292 | A | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0108 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-10267T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165292 | |||||||
| chr6:130165355 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.823-10330T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165355 | |||||||
| chr6:130165368 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0242 |
2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.823-10343T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165368 | |||||||
| chr6:130165408 | C | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
95 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.823-10383G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165408 | |||||||
| chr6:130165538 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.822+10303A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165538 | |||||||
| chr6:130165624 | A | T | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.822+10217T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165624 | |||||||
| chr6:130165660 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.822+10181A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165660 | |||||||
| chr6:130165795 | A | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.822+10046T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165795 | |||||||
| chr6:130165916 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.822+9925C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130165916 | |||||||
| chr6:130166077 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0233 others(9): Show |
13 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+9764G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166077 | |||||||
| chr6:130166137 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.822+9704G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166137 | |||||||
| chr6:130166294 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.822+9547G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166294 | |||||||
| chr6:130166402 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.822+9439T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166402 | |||||||
| chr6:130166413 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.822+9428G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166413 | |||||||
| chr6:130166491 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0050 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+9350A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166491 | |||||||
| chr6:130166544 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.822+9297G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166544 | |||||||
| chr6:130166573 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.822+9268G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166573 | |||||||
| chr6:130166689 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.822+9152C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166689 | |||||||
| chr6:130166765 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822+9076T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166765 | |||||||
| chr6:130166813 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.822+9028C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166813 | |||||||
| chr6:130166814 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.822+9027G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166814 | |||||||
| chr6:130166918 | T | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+8923A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130166918 | |||||||
| chr6:130167224 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+8617G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167224 | |||||||
| chr6:130167251 | C | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.822+8590G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167251 | |||||||
| chr6:130167343 | G | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0242 |
2 | HG01496.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.822+8498C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167343 | |||||||
| chr6:130167481 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.822+8360T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167481 | |||||||
| chr6:130167522 | T | C | 2 | a0001c0001t0001g0022 a0001c0007t0001g0161 |
2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.822+8319A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167522 | |||||||
| chr6:130167523 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.822+8318A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167523 | |||||||
| chr6:130167524 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+8317A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167524 | |||||||
| chr6:130167640 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.822+8201A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167640 | |||||||
| chr6:130167693 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0108 others(6): Show |
9 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+8148G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167693 | |||||||
| chr6:130167767 | A | G | 1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.822+8074T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167767 | |||||||
| chr6:130167815 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+8026T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167815 | |||||||
| chr6:130167892 | A | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0233 a0001c0001t0001g0236 others(4): Show |
8 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.822+7949T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167892 | |||||||
| chr6:130167893 | A | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0108 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+7948T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130167893 | |||||||
| chr6:130168028 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.822+7813C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168028 | |||||||
| chr6:130168044 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.822+7797C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168044 | |||||||
| chr6:130168085 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.822+7756C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168085 | |||||||
| chr6:130168090 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.822+7751T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168090 | |||||||
| chr6:130168099 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0108 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+7742C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168099 | |||||||
| chr6:130168108 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.822+7733A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168108 | |||||||
| chr6:130168122 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.822+7719G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168122 | |||||||
| chr6:130168293 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0108 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+7548C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168293 | |||||||
| chr6:130168413 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.822+7428G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168413 | |||||||
| chr6:130168416 | C | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.822+7425G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168416 | |||||||
| chr6:130168429 | A | AT | 3 | a0001c0001t0001g0015 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+7411_822+7412i others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168429 | |||||||
| chr6:130168430 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.822+7411G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168430 | |||||||
| chr6:130168432 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | HG01884.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+7409G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168432 | |||||||
| chr6:130168530 | A | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.822+7311T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168530 | |||||||
| chr6:130168778 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+7063G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130168778 | |||||||
| chr6:130169013 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.822+6828G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169013 | |||||||
| chr6:130169033 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(31): Show |
35 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.822+6808C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169033 | |||||||
| chr6:130169114 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.822+6727T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169114 | |||||||
| chr6:130169124 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.822+6717G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169124 | |||||||
| chr6:130169198 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.822+6643A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169198 | |||||||
| chr6:130169213 | T | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+6628A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169213 | |||||||
| chr6:130169237 | CA | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0132 others(1): Show |
4 | NA18939.hp1 NA19058.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.822+6603delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169237 | |||||||
| chr6:130169238 | A | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(36): Show |
41 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.822+6603T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169238 | |||||||
| chr6:130169458 | T | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(53): Show |
58 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.822+6383A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169458 | |||||||
| chr6:130169496 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.822+6345T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169496 | |||||||
| chr6:130169504 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.822+6337T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169504 | |||||||
| chr6:130169553 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.822+6288G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169553 | |||||||
| chr6:130169761 | T | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0247 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.822+6080A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169761 | |||||||
| chr6:130169771 | C | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(9): Show |
13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+6070G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169771 | |||||||
| chr6:130169785 | G | A | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.822+6056C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169785 | |||||||
| chr6:130169823 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+6018G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169823 | |||||||
| chr6:130169824 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(44): Show |
49 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.822+6017C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169824 | |||||||
| chr6:130169826 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+6015C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169826 | |||||||
| chr6:130169907 | G | A | 4 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0073 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+5934C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169907 | |||||||
| chr6:130169987 | G | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.822+5854C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169987 | |||||||
| chr6:130169998 | CTT | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0015 others(43): Show |
48 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.822+5841_822+5842d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130169998 | |||||||
| chr6:130170112 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+5729A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170112 | |||||||
| chr6:130170163 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.822+5678C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170163 | |||||||
| chr6:130170345 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(31): Show |
35 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.822+5496C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170345 | |||||||
| chr6:130170406 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(9): Show |
13 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+5435G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170406 | |||||||
| chr6:130170522 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0108 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.822+5319C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170522 | |||||||
| chr6:130170559 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+5282G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170559 | |||||||
| chr6:130170589 | T | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+5252A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170589 | |||||||
| chr6:130170594 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+5247G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170594 | |||||||
| chr6:130170774 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0279 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+5067C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170774 | |||||||
| chr6:130170818 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.822+5023A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170818 | |||||||
| chr6:130170843 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0279 |
3 | HG02280.hp1 NA18965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.822+4998G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170843 | |||||||
| chr6:130170952 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0220 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.822+4889C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130170952 | |||||||
| chr6:130171021 | G | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02145.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.822+4820C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171021 | |||||||
| chr6:130171044 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.822+4797G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171044 | |||||||
| chr6:130171093 | C | CTTA | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+4745_822+4747d others(5): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171093 | |||||||
| chr6:130171549 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.822+4292A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171549 | |||||||
| chr6:130171590 | C | T | 7 | a0001c0001t0001g0057 a0001c0001t0001g0126 a0001c0001t0001g0155 others(4): Show |
7 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.822+4251G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171590 | |||||||
| chr6:130171779 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.822+4062G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171779 | |||||||
| chr6:130171818 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0239 a0001c0002t0001g0255 |
3 | HG02055.hp1 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.822+4023C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171818 | |||||||
| chr6:130171981 | A | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+3860T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130171981 | |||||||
| chr6:130172061 | T | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+3780A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172061 | |||||||
| chr6:130172298 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0233 others(5): Show |
10 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+3543G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172298 | |||||||
| chr6:130172520 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.822+3321C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172520 | |||||||
| chr6:130172621 | C | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+3220G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172621 | |||||||
| chr6:130172649 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+3192G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172649 | |||||||
| chr6:130172821 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.822+3020G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172821 | |||||||
| chr6:130172850 | T | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+2991A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172850 | |||||||
| chr6:130172912 | T | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
13 | HG00673.hp2 HG03491.hp2 HG03492.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+2929A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130172912 | |||||||
| chr6:130173056 | A | C | 1 | a0001c0001t0001g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.822+2785T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173056 | |||||||
| chr6:130173111 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.822+2730C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173111 | |||||||
| chr6:130173145 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0142 a0001c0001t0001g0322 |
4 | HG00639.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.822+2696G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173145 | |||||||
| chr6:130173536 | G | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+2305C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173536 | |||||||
| chr6:130173555 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+2286G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173555 | |||||||
| chr6:130173556 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | HG00544.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+2285C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173556 | |||||||
| chr6:130173595 | C | T | 1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.822+2246G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173595 | |||||||
| chr6:130173614 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.822+2227C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173614 | |||||||
| chr6:130173794 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+2047G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173794 | |||||||
| chr6:130173843 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+1998A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173843 | |||||||
| chr6:130173965 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0107 |
2 | HG01074.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.822+1876G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173965 | |||||||
| chr6:130173987 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.822+1854G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130173987 | |||||||
| chr6:130174064 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.822+1777G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174064 | |||||||
| chr6:130174092 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.822+1749C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174092 | |||||||
| chr6:130174137 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.822+1704G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174137 | |||||||
| chr6:130174166 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+1675A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174166 | |||||||
| chr6:130174338 | T | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0239 a0001c0002t0001g0255 |
3 | HG02055.hp1 HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.822+1503A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174338 | |||||||
| chr6:130174388 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+1453G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174388 | |||||||
| chr6:130174656 | A | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(11): Show |
15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+1185T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174656 | |||||||
| chr6:130174738 | G | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0126 a0001c0001t0001g0155 others(3): Show |
6 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+1103C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174738 | |||||||
| chr6:130174743 | T | G | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0215 |
3 | HG01346.hp2 HG01981.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.822+1098A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174743 | |||||||
| chr6:130174864 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.822+977G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174864 | |||||||
| chr6:130174942 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+899A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130174942 | |||||||
| chr6:130175005 | C | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+836G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175005 | |||||||
| chr6:130175039 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+802T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175039 | |||||||
| chr6:130175175 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.822+666A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175175 | |||||||
| chr6:130175267 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.822+574A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175267 | |||||||
| chr6:130175322 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+519C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175322 | |||||||
| chr6:130175405 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.822+436T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175405 | |||||||
| chr6:130175532 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.822+309G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175532 | |||||||
| chr6:130175576 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0279 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.822+265C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175576 | |||||||
| chr6:130175592 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+249A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175592 | |||||||
| chr6:130175617 | A | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.822+224T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175617 | |||||||
| chr6:130175641 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822+200A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175641 | |||||||
| chr6:130175655 | C | A | 1 | a0008c0005t0001g0231 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.822+186G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175655 | |||||||
| chr6:130175738 | G | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.822+103C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175738 | |||||||
| chr6:130175800 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.822+41T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 8/11 | chr6 | 130175800 | |||||||
| chr6:130176243 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.655-235T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176243 | |||||||
| chr6:130176456 | T | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-448A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176456 | |||||||
| chr6:130176462 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-454C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176462 | |||||||
| chr6:130176506 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655-498C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176506 | |||||||
| chr6:130176516 | A | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-508T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176516 | |||||||
| chr6:130176634 | A | G | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655-626T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176634 | |||||||
| chr6:130176636 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.655-628G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176636 | |||||||
| chr6:130176742 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655-734A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176742 | |||||||
| chr6:130176784 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.655-776C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176784 | |||||||
| chr6:130176883 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-875C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176883 | |||||||
| chr6:130176915 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-907T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176915 | |||||||
| chr6:130176952 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-944A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176952 | |||||||
| chr6:130176953 | G | A | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655-945C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176953 | |||||||
| chr6:130176976 | A | G | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655-968T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130176976 | |||||||
| chr6:130177036 | A | G | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02145.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.655-1028T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177036 | |||||||
| chr6:130177138 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.655-1130G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177138 | |||||||
| chr6:130177139 | T | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1131A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177139 | |||||||
| chr6:130177166 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.655-1158C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177166 | |||||||
| chr6:130177294 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1286C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177294 | |||||||
| chr6:130177404 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.655-1396T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177404 | |||||||
| chr6:130177412 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1404A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177412 | |||||||
| chr6:130177435 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1427A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177435 | |||||||
| chr6:130177438 | A | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1430T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177438 | |||||||
| chr6:130177631 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1623G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177631 | |||||||
| chr6:130177669 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655-1661A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177669 | |||||||
| chr6:130177801 | C | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0233 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-1793G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177801 | |||||||
| chr6:130177824 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.655-1816G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177824 | |||||||
| chr6:130177981 | C | CT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-1974dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177981 | |||||||
| chr6:130177997 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0233 others(7): Show |
11 | HG01891.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-1989C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130177997 | |||||||
| chr6:130178068 | G | T | 1 | a0001c0001t0001g0005 | 2 | NA18941.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.655-2060C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178068 | |||||||
| chr6:130178077 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2069G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178077 | |||||||
| chr6:130178147 | TGTATTTT others(2): Show |
T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0168 others(2): Show |
6 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-2148_655-2140d others(11): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178147 | |||||||
| chr6:130178164 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.655-2156G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178164 | |||||||
| chr6:130178233 | CCCAAAGT others(28): Show |
C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2260_655-2226d others(37): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178233 | |||||||
| chr6:130178331 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(22): Show |
26 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.655-2323G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178331 | |||||||
| chr6:130178334 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.655-2326A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178334 | |||||||
| chr6:130178342 | C | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0126 a0001c0001t0001g0155 others(5): Show |
8 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.655-2334G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178342 | |||||||
| chr6:130178379 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2371T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178379 | |||||||
| chr6:130178381 | G | GA | 6 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.655-2374_655-2373i others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178381 | |||||||
| chr6:130178382 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2374C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178382 | |||||||
| chr6:130178382 | G | GA | 11 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0090 others(8): Show |
11 | HG00597.hp1 HG00597.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.655-2375dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178382 | |||||||
| chr6:130178399 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2391G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178399 | |||||||
| chr6:130178428 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0271 a0001c0001t0001g0317 |
4 | NA18970.hp2 NA18974.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-2420C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178428 | |||||||
| chr6:130178445 | G | C | 1 | a0001c0001t0001g0006 | 2 | HG04204.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.655-2437C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178445 | |||||||
| chr6:130178462 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2454T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178462 | |||||||
| chr6:130178512 | G | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(16): Show |
20 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.655-2504C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178512 | |||||||
| chr6:130178627 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.655-2619C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178627 | |||||||
| chr6:130178677 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.655-2669G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178677 | |||||||
| chr6:130178693 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2685A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178693 | |||||||
| chr6:130178716 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.655-2708T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178716 | |||||||
| chr6:130178752 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.655-2744C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178752 | |||||||
| chr6:130178773 | A | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-2765T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178773 | |||||||
| chr6:130178811 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.655-2803G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130178811 | |||||||
| chr6:130179031 | AT | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(19): Show |
23 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.655-3024delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179031 | |||||||
| chr6:130179050 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.655-3042G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179050 | |||||||
| chr6:130179094 | G | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.655-3086C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179094 | |||||||
| chr6:130179111 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655-3103G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179111 | |||||||
| chr6:130179112 | G | A | 1 | a0004c0008t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.655-3104C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179112 | |||||||
| chr6:130179240 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.655-3232T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179240 | |||||||
| chr6:130179270 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.655-3262G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179270 | |||||||
| chr6:130179286 | C | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.655-3278G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179286 | |||||||
| chr6:130179307 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0007t0001g0161 |
3 | HG01884.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.655-3299C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179307 | |||||||
| chr6:130179308 | A | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.655-3300T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179308 | |||||||
| chr6:130179368 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.655-3360C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179368 | |||||||
| chr6:130179501 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655-3493T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179501 | |||||||
| chr6:130179523 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.655-3515C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179523 | |||||||
| chr6:130179527 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.655-3519A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179527 | |||||||
| chr6:130179605 | C | CA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0108 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-3598dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179605 | |||||||
| chr6:130179605 | CA | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.655-3598delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179605 | |||||||
| chr6:130179627 | G | A | 3 | a0001c0001t0001g0018 a0004c0008t0001g0280 a0008c0005t0001g0231 |
3 | HG02109.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.655-3619C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179627 | |||||||
| chr6:130179732 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.655-3724T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179732 | |||||||
| chr6:130179803 | C | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0126 a0001c0001t0001g0155 others(3): Show |
6 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.655-3795G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179803 | |||||||
| chr6:130179810 | C | CT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.655-3803dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179810 | |||||||
| chr6:130179810 | C | CTT | 19 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0019 others(16): Show |
20 | HG00741.hp1 HG01433.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.655-3804_655-3803d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179810 | |||||||
| chr6:130179871 | C | T | 4 | a0001c0001t0001g0277 a0001c0001t0001g0326 a0001c0002t0001g0027 others(1): Show |
4 | HG02280.hp2 HG02602.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-3863G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179871 | |||||||
| chr6:130179900 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.655-3892A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179900 | |||||||
| chr6:130179907 | T | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.655-3899A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179907 | |||||||
| chr6:130179965 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.655-3957G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130179965 | |||||||
| chr6:130180004 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.655-3996C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180004 | |||||||
| chr6:130180027 | A | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.655-4019T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180027 | |||||||
| chr6:130180061 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.654+4042G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180061 | |||||||
| chr6:130180095 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.654+4008C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180095 | |||||||
| chr6:130180104 | C | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.654+3999G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180104 | |||||||
| chr6:130180110 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.654+3993G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180110 | |||||||
| chr6:130180111 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.654+3992C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180111 | |||||||
| chr6:130180123 | T | A | 1 | a0009c0006t0001g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.654+3980A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180123 | |||||||
| chr6:130180186 | T | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02145.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.654+3917A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180186 | |||||||
| chr6:130180207 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0279 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.654+3896T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180207 | |||||||
| chr6:130180239 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(33): Show |
37 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.654+3864C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180239 | |||||||
| chr6:130180281 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.654+3822A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180281 | |||||||
| chr6:130180287 | A | AT | 14 | a0001c0001t0001g0028 a0001c0001t0001g0056 a0001c0001t0001g0284 others(11): Show |
14 | HG00621.hp1 HG01074.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.654+3815dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180287 | |||||||
| chr6:130180287 | ATTTT | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0057 others(18): Show |
22 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.654+3812_654+3815d others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180287 | |||||||
| chr6:130180287 | ATTTTT | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(34): Show |
38 | HG00438.hp1 HG01123.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.654+3811_654+3815d others(7): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180287 | |||||||
| chr6:130180287 | ATTTTTT | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.654+3810_654+3815d others(8): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180287 | |||||||
| chr6:130180381 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.654+3722G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180381 | |||||||
| chr6:130180382 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.654+3721C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180382 | |||||||
| chr6:130180429 | C | T | 1 | a0001c0002t0001g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.654+3674G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180429 | |||||||
| chr6:130180512 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.654+3591C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180512 | |||||||
| chr6:130180547 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.654+3556T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180547 | |||||||
| chr6:130180588 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0074 a0001c0001t0001g0108 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+3515G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180588 | |||||||
| chr6:130180589 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.654+3514C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180589 | |||||||
| chr6:130180626 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.654+3477A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180626 | |||||||
| chr6:130180680 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0177 others(8): Show |
11 | HG00438.hp1 HG00544.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.654+3423A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180680 | |||||||
| chr6:130180742 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.654+3361A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180742 | |||||||
| chr6:130180759 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.654+3344A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180759 | |||||||
| chr6:130180802 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0132 |
3 | NA18939.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.654+3301G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180802 | |||||||
| chr6:130180825 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.654+3278G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180825 | |||||||
| chr6:130180884 | C | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0233 others(6): Show |
10 | HG01891.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+3219G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180884 | |||||||
| chr6:130180953 | C | CTTTCTTT others(3): Show |
93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
98 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.654+3149_654+3150i others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180953 | |||||||
| chr6:130180953 | C | CTTTCTTT others(4): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0187 |
2 | HG00597.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.654+3149_654+3150i others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180953 | |||||||
| chr6:130180953 | C | CTTTTTTT others(2): Show |
34 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(31): Show |
35 | HG00099.hp2 HG00741.hp2 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.654+3149_654+3150i others(11): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180953 | |||||||
| chr6:130180953 | C | CTTTTTTT others(3): Show |
149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.654+3149_654+3150i others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180953 | |||||||
| chr6:130180953 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0106 a0001c0001t0001g0184 |
3 | HG01243.hp2 HG01261.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.654+3149_654+3150i others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180953 | |||||||
| chr6:130180960 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.654+3143G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180960 | |||||||
| chr6:130180969 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.654+3134G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130180969 | |||||||
| chr6:130181040 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.654+3063G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181040 | |||||||
| chr6:130181073 | A | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.654+3030T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181073 | |||||||
| chr6:130181104 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.654+2999C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181104 | |||||||
| chr6:130181108 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.654+2995C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181108 | |||||||
| chr6:130181221 | A | G | 8 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0246 others(5): Show |
8 | HG02280.hp2 HG02602.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+2882T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181221 | |||||||
| chr6:130181222 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
102 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.654+2881A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181222 | |||||||
| chr6:130181236 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0276 |
3 | NA18941.hp2 NA18967.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.654+2867G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181236 | |||||||
| chr6:130181237 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.654+2866C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181237 | |||||||
| chr6:130181238 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.654+2865A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181238 | |||||||
| chr6:130181250 | A | C | 1 | a0001c0001t0001g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.654+2853T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181250 | |||||||
| chr6:130181426 | C | G | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654+2677G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181426 | |||||||
| chr6:130181632 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.654+2471A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181632 | |||||||
| chr6:130181711 | G | C | 18 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0057 others(15): Show |
18 | HG01074.hp1 HG01358.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.654+2392C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181711 | |||||||
| chr6:130181849 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0278 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.654+2254T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181849 | |||||||
| chr6:130181933 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654+2170C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181933 | |||||||
| chr6:130181938 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654+2165T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130181938 | |||||||
| chr6:130182025 | A | C | 3 | a0001c0002t0001g0027 a0001c0002t0001g0131 a0001c0002t0001g0255 |
3 | HG02602.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654+2078T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182025 | |||||||
| chr6:130182064 | C | CA | 22 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0084 others(19): Show |
22 | HG01361.hp1 HG01433.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.654+2038dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182064 | |||||||
| chr6:130182064 | CA | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0196 a0001c0001t0001g0237 others(5): Show |
8 | HG02257.hp2 HG02602.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+2038delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182064 | |||||||
| chr6:130182071 | A | AC | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.654+2031_654+2032i others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182071 | |||||||
| chr6:130182072 | A | C | 16 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0071 others(13): Show |
16 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.654+2031T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182072 | |||||||
| chr6:130182073 | A | C | 3 | a0001c0002t0001g0027 a0001c0002t0001g0131 a0001c0002t0001g0255 |
3 | HG02602.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654+2030T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182073 | |||||||
| chr6:130182075 | A | C | 13 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0065 others(10): Show |
13 | HG01099.hp1 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.654+2028T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182075 | |||||||
| chr6:130182076 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.654+2027T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182076 | |||||||
| chr6:130182077 | A | C | 4 | a0001c0001t0001g0256 a0001c0002t0001g0027 a0001c0002t0001g0131 others(1): Show |
4 | HG02602.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+2026T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182077 | |||||||
| chr6:130182087 | A | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.654+2016T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182087 | |||||||
| chr6:130182161 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.654+1942G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182161 | |||||||
| chr6:130182193 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.654+1910T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182193 | |||||||
| chr6:130182221 | G | T | 28 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
28 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.654+1882C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182221 | |||||||
| chr6:130182261 | TG | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.654+1841delC | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182261 | |||||||
| chr6:130182427 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.654+1676A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182427 | |||||||
| chr6:130182483 | C | A | 1 | a0001c0001t0001g0294 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.654+1620G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182483 | |||||||
| chr6:130182484 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.654+1619A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182484 | |||||||
| chr6:130182499 | C | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0001g0164 others(5): Show |
8 | HG01099.hp1 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+1604G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182499 | |||||||
| chr6:130182527 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1576C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182527 | |||||||
| chr6:130182563 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.654+1540C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182563 | |||||||
| chr6:130182798 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.654+1305C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182798 | |||||||
| chr6:130182808 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.654+1295A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182808 | |||||||
| chr6:130182875 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.654+1228T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182875 | |||||||
| chr6:130182906 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.654+1197C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130182906 | |||||||
| chr6:130183132 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.654+971G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183132 | |||||||
| chr6:130183133 | G | A | 3 | a0001c0002t0001g0027 a0001c0002t0001g0131 a0001c0002t0001g0255 |
3 | HG02602.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654+970C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183133 | |||||||
| chr6:130183181 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.654+922T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183181 | |||||||
| chr6:130183269 | G | A | 3 | a0001c0002t0001g0027 a0001c0002t0001g0131 a0001c0002t0001g0255 |
3 | HG02602.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654+834C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183269 | |||||||
| chr6:130183302 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.654+801T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183302 | |||||||
| chr6:130183307 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0132 others(6): Show |
9 | HG00673.hp2 HG01261.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.654+796T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183307 | |||||||
| chr6:130183323 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.654+780G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183323 | |||||||
| chr6:130183336 | CA | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.654+766delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183336 | |||||||
| chr6:130183349 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0080 others(5): Show |
8 | HG02109.hp1 HG03098.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+754T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183349 | |||||||
| chr6:130183351 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0080 others(5): Show |
8 | HG02109.hp1 HG03098.hp2 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+752C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183351 | |||||||
| chr6:130183403 | A | G | 2 | a0001c0001t0001g0281 a0008c0005t0001g0231 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.654+700T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183403 | |||||||
| chr6:130183408 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.654+695C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183408 | |||||||
| chr6:130183436 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.654+667C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183436 | |||||||
| chr6:130183691 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0273 |
2 | NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.654+412G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183691 | |||||||
| chr6:130183858 | A | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0326 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.654+245T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130183858 | |||||||
| chr6:130184068 | T | C | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654+35A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130184068 | |||||||
| chr6:130184087 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0006c0013t0001g0253 |
3 | HG02451.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.654+16G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130184087 | |||||||
| chr6:130184088 | C | T | 1 | a0001c0001t0006g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.654+15G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 7/11 | chr6 | 130184088 | |||||||
| chr6:130184227 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.570-40T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/11 | chr6 | 130184227 | |||||||
| chr6:130184229 | A | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.570-42T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/11 | chr6 | 130184229 | |||||||
| chr6:130184258 | A | G | 2 | a0001c0001t0001g0284 a0005c0009t0001g0285 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.570-71T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/11 | chr6 | 130184258 | |||||||
| chr6:130184308 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0279 |
3 | HG02280.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.570-121T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/11 | chr6 | 130184308 | |||||||
| chr6:130184326 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.569+112G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 6/11 | chr6 | 130184326 | |||||||
| chr6:130184860 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.384-237T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130184860 | |||||||
| chr6:130185019 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.384-396G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185019 | |||||||
| chr6:130185158 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.384-535G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185158 | |||||||
| chr6:130185237 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(101): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.384-614T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185237 | |||||||
| chr6:130185248 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-625A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185248 | |||||||
| chr6:130185447 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02145.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-824C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185447 | |||||||
| chr6:130185520 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0106 others(26): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.384-897T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185520 | |||||||
| chr6:130185534 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0018 |
2 | HG02074.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.384-911C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185534 | |||||||
| chr6:130185569 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.384-946A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185569 | |||||||
| chr6:130185574 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.384-951T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185574 | |||||||
| chr6:130185599 | C | T | 51 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0028 others(48): Show |
51 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.384-976G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185599 | |||||||
| chr6:130185607 | C | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(128): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.384-984G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185607 | |||||||
| chr6:130185611 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(128): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.384-988C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185611 | |||||||
| chr6:130185619 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.384-996T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185619 | |||||||
| chr6:130185627 | A | AG | 3 | a0001c0001t0001g0050 a0001c0001t0001g0164 a0001c0001t0001g0263 |
3 | HG01099.hp1 HG01175.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.384-1005_384-1004i others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185627 | |||||||
| chr6:130185628 | A | AT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0043 others(13): Show |
17 | HG00597.hp2 HG00741.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.384-1006dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185628 | |||||||
| chr6:130185628 | A | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0164 a0001c0001t0001g0263 |
3 | HG01099.hp1 HG01175.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.384-1005T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185628 | |||||||
| chr6:130185628 | AT | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(10): Show |
14 | HG01993.hp2 HG03491.hp2 HG03492.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-1006delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185628 | |||||||
| chr6:130185628 | ATT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0277 others(5): Show |
9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-1007_384-1006d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185628 | |||||||
| chr6:130185681 | TGTGCAGT others(1133): Show |
T | 2 | a0001c0001t0002g0138 a0001c0001t0002g0227 |
2 | HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.384-2198_384-1059d others(2): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185681 | |||||||
| chr6:130185777 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0282 others(2): Show |
5 | HG02145.hp1 HG02257.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-1154G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185777 | |||||||
| chr6:130185788 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.384-1165C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185788 | |||||||
| chr6:130185856 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.384-1233A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185856 | |||||||
| chr6:130185894 | G | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.384-1271C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185894 | |||||||
| chr6:130185899 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0164 others(4): Show |
7 | HG01099.hp1 HG01175.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-1276C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130185899 | |||||||
| chr6:130186129 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(127): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.384-1506T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186129 | |||||||
| chr6:130186300 | A | G | 1 | a0001c0007t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.384-1677T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186300 | |||||||
| chr6:130186329 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
8 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.384-1706C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186329 | |||||||
| chr6:130186394 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.384-1771A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186394 | |||||||
| chr6:130186397 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(89): Show |
93 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.384-1774C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186397 | |||||||
| chr6:130186425 | G | A | 7 | a0001c0001t0001g0150 a0001c0001t0001g0185 a0001c0001t0001g0289 others(4): Show |
7 | HG00673.hp2 HG01261.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-1802C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186425 | |||||||
| chr6:130186506 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.384-1883G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186506 | |||||||
| chr6:130186547 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0164 others(1): Show |
4 | HG01099.hp1 HG01175.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-1924T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186547 | |||||||
| chr6:130186767 | A | AT | 37 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0031 others(34): Show |
37 | HG00621.hp2 HG00673.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.384-2145dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186767 | |||||||
| chr6:130186767 | A | ATT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.384-2146_384-2145d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186767 | |||||||
| chr6:130186767 | A | ATTT | 34 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0024 others(31): Show |
35 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.384-2147_384-2145d others(5): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186767 | |||||||
| chr6:130186767 | A | ATTTT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0132 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-2148_384-2145d others(6): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186767 | |||||||
| chr6:130186839 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.384-2216G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186839 | |||||||
| chr6:130186856 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(10): Show |
15 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(12): Show |
intron_variant | MODIFIER | c.384-2233G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186856 | |||||||
| chr6:130186873 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384-2250G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186873 | |||||||
| chr6:130186938 | T | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(78): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.384-2315A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186938 | |||||||
| chr6:130186977 | G | A | 2 | a0001c0001t0001g0015 a0001c0010t0001g0023 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.384-2354C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130186977 | |||||||
| chr6:130187276 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-2653T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187276 | |||||||
| chr6:130187332 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.384-2709G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187332 | |||||||
| chr6:130187376 | T | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.384-2753A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187376 | |||||||
| chr6:130187412 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(90): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.384-2789T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187412 | |||||||
| chr6:130187457 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.384-2834A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187457 | |||||||
| chr6:130187663 | TA | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0150 a0001c0001t0001g0185 others(4): Show |
7 | HG00673.hp2 HG02602.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-3041delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187663 | |||||||
| chr6:130187831 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.384-3208G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187831 | |||||||
| chr6:130187945 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18946.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.384-3322C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130187945 | |||||||
| chr6:130188250 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.384-3627C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130188250 | |||||||
| chr6:130188253 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0239 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.384-3630G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130188253 | |||||||
| chr6:130188639 | C | A | 1 | a0001c0004t0001g0298 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.384-4016G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130188639 | |||||||
| chr6:130188859 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.384-4236A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130188859 | |||||||
| chr6:130188885 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.384-4262C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130188885 | |||||||
| chr6:130189103 | C | CA | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
120 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.384-4481dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189103 | |||||||
| chr6:130189103 | C | CAA | 8 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0187 others(5): Show |
8 | HG00597.hp2 HG00673.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.384-4482_384-4481d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189103 | |||||||
| chr6:130189103 | CA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(67): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.384-4481delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189103 | |||||||
| chr6:130189120 | C | G | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(105): Show |
111 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.384-4497G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189120 | |||||||
| chr6:130189150 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0038 others(23): Show |
27 | HG00609.hp2 HG00639.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.384-4527T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189150 | |||||||
| chr6:130189316 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384-4693C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189316 | |||||||
| chr6:130189373 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.384-4750A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189373 | |||||||
| chr6:130189388 | C | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-4765G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189388 | |||||||
| chr6:130189492 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-4869T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189492 | |||||||
| chr6:130189632 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.384-5009G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189632 | |||||||
| chr6:130189779 | A | G | 1 | a0001c0001t0002g0268 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.384-5156T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130189779 | |||||||
| chr6:130190062 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0002t0001g0131 |
3 | HG02257.hp2 HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.384-5439C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190062 | |||||||
| chr6:130190082 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384-5459C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190082 | |||||||
| chr6:130190136 | AC | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-5514delG | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190136 | |||||||
| chr6:130190139 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-5516T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190139 | |||||||
| chr6:130190168 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.384-5545A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190168 | |||||||
| chr6:130190175 | A | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-5552T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190175 | |||||||
| chr6:130190193 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.384-5570G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190193 | |||||||
| chr6:130190203 | A | T | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384-5580T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190203 | |||||||
| chr6:130190238 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.384-5615C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190238 | |||||||
| chr6:130190248 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-5625G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190248 | |||||||
| chr6:130190276 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384-5653T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190276 | |||||||
| chr6:130190315 | C | CA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.384-5693dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190315 | |||||||
| chr6:130190315 | C | CAA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0186 others(6): Show |
10 | HG00597.hp2 HG02027.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.384-5694_384-5693d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190315 | |||||||
| chr6:130190415 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(47): Show |
52 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.384-5792C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190415 | |||||||
| chr6:130190437 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-5814C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190437 | |||||||
| chr6:130190496 | G | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-5873C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190496 | |||||||
| chr6:130190644 | A | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(36): Show |
41 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.384-6021T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190644 | |||||||
| chr6:130190737 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.384-6114A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190737 | |||||||
| chr6:130190784 | A | T | 1 | a0001c0001t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.384-6161T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190784 | |||||||
| chr6:130190789 | C | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-6166G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190789 | |||||||
| chr6:130190804 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(35): Show |
40 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.384-6181C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190804 | |||||||
| chr6:130190887 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-6264T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190887 | |||||||
| chr6:130190938 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.384-6315A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190938 | |||||||
| chr6:130190991 | A | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
115 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.384-6368T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190991 | |||||||
| chr6:130190998 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.384-6375G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130190998 | |||||||
| chr6:130191123 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.384-6500A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191123 | |||||||
| chr6:130191284 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.384-6661C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191284 | |||||||
| chr6:130191292 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.384-6669G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191292 | |||||||
| chr6:130191345 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-6722A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191345 | |||||||
| chr6:130191446 | T | A | 1 | a0001c0001t0002g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.384-6823A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191446 | |||||||
| chr6:130191509 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-6886T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191509 | |||||||
| chr6:130191558 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0002t0001g0131 |
3 | HG02257.hp2 HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.384-6935A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191558 | |||||||
| chr6:130191624 | CT | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.384-7002delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191624 | |||||||
| chr6:130191648 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG01978.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-7025C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191648 | |||||||
| chr6:130191787 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.384-7164C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191787 | |||||||
| chr6:130191834 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-7211T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191834 | |||||||
| chr6:130191850 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-7227T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191850 | |||||||
| chr6:130191962 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0002t0001g0131 |
3 | HG02257.hp2 HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.384-7339A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130191962 | |||||||
| chr6:130192097 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384-7474G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192097 | |||||||
| chr6:130192110 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0002g0020 others(1): Show |
4 | HG02809.hp2 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-7487G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192110 | |||||||
| chr6:130192170 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-7547T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192170 | |||||||
| chr6:130192305 | G | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-7682C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192305 | |||||||
| chr6:130192428 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384-7805A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192428 | |||||||
| chr6:130192598 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384-7975A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192598 | |||||||
| chr6:130192698 | C | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-8075G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192698 | |||||||
| chr6:130192699 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG01109.hp1 HG01517.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-8076C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192699 | |||||||
| chr6:130192721 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0135 |
2 | HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.384-8098G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192721 | |||||||
| chr6:130192764 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0071 |
2 | HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.384-8141C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192764 | |||||||
| chr6:130192783 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.384-8160G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192783 | |||||||
| chr6:130192784 | G | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(40): Show |
45 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.384-8161C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192784 | |||||||
| chr6:130192892 | T | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-8269A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192892 | |||||||
| chr6:130192897 | C | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18965.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.384-8274G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130192897 | |||||||
| chr6:130193004 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-8381C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193004 | |||||||
| chr6:130193086 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.384-8463G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193086 | |||||||
| chr6:130193133 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.384-8510C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193133 | |||||||
| chr6:130193278 | A | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.384-8655T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193278 | |||||||
| chr6:130193333 | C | G | 2 | a0001c0001t0001g0284 a0005c0009t0001g0285 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.384-8710G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193333 | |||||||
| chr6:130193364 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
162 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.384-8741A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193364 | |||||||
| chr6:130193402 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-8779C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193402 | |||||||
| chr6:130193445 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(72): Show |
76 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.384-8822G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193445 | |||||||
| chr6:130193496 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-8873G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193496 | |||||||
| chr6:130193706 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0005g0204 |
2 | HG01981.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.384-9083G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193706 | |||||||
| chr6:130193794 | T | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-9171A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193794 | |||||||
| chr6:130193834 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-9211A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193834 | |||||||
| chr6:130193889 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.384-9266A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193889 | |||||||
| chr6:130193945 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.384-9322C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193945 | |||||||
| chr6:130193951 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.384-9328C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130193951 | |||||||
| chr6:130194018 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0160 others(1): Show |
4 | HG03139.hp1 HG03239.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-9395C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194018 | |||||||
| chr6:130194066 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-9443A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194066 | |||||||
| chr6:130194086 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.384-9463T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194086 | |||||||
| chr6:130194087 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.384-9464G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194087 | |||||||
| chr6:130194101 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-9478G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194101 | |||||||
| chr6:130194102 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-9479T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194102 | |||||||
| chr6:130194144 | C | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.384-9521G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194144 | |||||||
| chr6:130194193 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(44): Show |
49 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.384-9570G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194193 | |||||||
| chr6:130194220 | C | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-9597G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194220 | |||||||
| chr6:130194278 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0106 a0001c0001t0001g0108 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.384-9655C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194278 | |||||||
| chr6:130194349 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(70): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.384-9726G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194349 | |||||||
| chr6:130194436 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.384-9813G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194436 | |||||||
| chr6:130194437 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.384-9814A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194437 | |||||||
| chr6:130194464 | T | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | NA18975.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.384-9841A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194464 | |||||||
| chr6:130194480 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.384-9857A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194480 | |||||||
| chr6:130194496 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0002t0001g0131 |
3 | HG02257.hp2 HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.384-9873A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194496 | |||||||
| chr6:130194599 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.384-9976A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194599 | |||||||
| chr6:130194650 | G | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-10027C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194650 | |||||||
| chr6:130194652 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0106 a0001c0001t0001g0108 others(8): Show |
14 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-10029A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194652 | |||||||
| chr6:130194654 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0106 a0001c0001t0001g0108 others(8): Show |
14 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.384-10031T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194654 | |||||||
| chr6:130194680 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.384-10057C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194680 | |||||||
| chr6:130194727 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.384-10104A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194727 | |||||||
| chr6:130194733 | A | G | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(101): Show |
106 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.384-10110T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194733 | |||||||
| chr6:130194780 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0279 |
3 | HG02280.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.384-10157C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194780 | |||||||
| chr6:130194827 | T | C | 1 | a0001c0001t0001g0311 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.384-10204A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194827 | |||||||
| chr6:130194863 | C | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
161 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.384-10240G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194863 | |||||||
| chr6:130194922 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-10299A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194922 | |||||||
| chr6:130194930 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.384-10307C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194930 | |||||||
| chr6:130194937 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.384-10314T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194937 | |||||||
| chr6:130194957 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-10334A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194957 | |||||||
| chr6:130194992 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-10369C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130194992 | |||||||
| chr6:130195016 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.384-10393T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195016 | |||||||
| chr6:130195059 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.384-10436T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195059 | |||||||
| chr6:130195061 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.384-10438G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195061 | |||||||
| chr6:130195070 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.384-10447T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195070 | |||||||
| chr6:130195107 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-10484C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195107 | |||||||
| chr6:130195267 | C | T | 69 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.384-10644G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195267 | |||||||
| chr6:130195273 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.384-10650A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195273 | |||||||
| chr6:130195280 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.384-10657G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195280 | |||||||
| chr6:130195306 | C | A | 1 | a0001c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.384-10683G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195306 | |||||||
| chr6:130195308 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.384-10685A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195308 | |||||||
| chr6:130195368 | A | T | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.384-10745T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195368 | |||||||
| chr6:130195447 | A | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.384-10824T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195447 | |||||||
| chr6:130195535 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-10912A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195535 | |||||||
| chr6:130195548 | A | G | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-10925T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195548 | |||||||
| chr6:130195613 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.384-10990C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195613 | |||||||
| chr6:130195614 | C | A | 1 | a0001c0002t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.384-10991G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195614 | |||||||
| chr6:130195705 | G | C | 10 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0088 others(7): Show |
10 | HG00673.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.384-11082C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195705 | |||||||
| chr6:130195808 | G | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-11185C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195808 | |||||||
| chr6:130195834 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0257 a0001c0001t0002g0036 |
3 | HG02451.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.384-11211G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195834 | |||||||
| chr6:130195915 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0326 a0001c0010t0001g0023 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-11292A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130195915 | |||||||
| chr6:130196011 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384-11388G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196011 | |||||||
| chr6:130196012 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.384-11389T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196012 | |||||||
| chr6:130196017 | C | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-11394G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196017 | |||||||
| chr6:130196100 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(45): Show |
50 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.384-11477C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196100 | |||||||
| chr6:130196498 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.384-11875T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196498 | |||||||
| chr6:130196583 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-11960G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196583 | |||||||
| chr6:130196718 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.384-12095A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196718 | |||||||
| chr6:130196760 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.384-12137G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196760 | |||||||
| chr6:130196798 | T | G | 2 | a0001c0001t0001g0018 a0001c0002t0001g0027 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.384-12175A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196798 | |||||||
| chr6:130196860 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(18): Show |
22 | HG01099.hp1 HG01175.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.384-12237C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196860 | |||||||
| chr6:130196977 | C | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.384-12354G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196977 | |||||||
| chr6:130196995 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.384-12372G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130196995 | |||||||
| chr6:130197009 | C | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.384-12386G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197009 | |||||||
| chr6:130197014 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384-12391G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197014 | |||||||
| chr6:130197037 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.384-12414G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197037 | |||||||
| chr6:130197121 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+12374G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197121 | |||||||
| chr6:130197193 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.383+12302C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197193 | |||||||
| chr6:130197262 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.383+12233G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197262 | |||||||
| chr6:130197322 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.383+12173A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197322 | |||||||
| chr6:130197351 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+12144C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197351 | |||||||
| chr6:130197357 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.383+12138G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197357 | |||||||
| chr6:130197523 | C | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+11972G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197523 | |||||||
| chr6:130197696 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.383+11799G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197696 | |||||||
| chr6:130197708 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.383+11787G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197708 | |||||||
| chr6:130197764 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+11731G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197764 | |||||||
| chr6:130197930 | G | A | 4 | a0001c0001t0001g0239 a0001c0001t0001g0252 a0001c0001t0001g0254 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+11565C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130197930 | |||||||
| chr6:130198117 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.383+11378G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198117 | |||||||
| chr6:130198118 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+11377C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198118 | |||||||
| chr6:130198162 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.383+11333A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198162 | |||||||
| chr6:130198214 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0273 |
2 | NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.383+11281G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198214 | |||||||
| chr6:130198298 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+11197C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198298 | |||||||
| chr6:130198304 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.383+11191T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198304 | |||||||
| chr6:130198317 | C | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.383+11178G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198317 | |||||||
| chr6:130198457 | C | T | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+11038G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198457 | |||||||
| chr6:130198495 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.383+11000G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198495 | |||||||
| chr6:130198822 | T | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+10673A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198822 | |||||||
| chr6:130198849 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0002g0020 others(3): Show |
6 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+10646G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198849 | |||||||
| chr6:130198959 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0293 a0001c0001t0001g0322 |
3 | HG04184.hp2 NA19065.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.383+10536G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130198959 | |||||||
| chr6:130199053 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0279 |
3 | HG02280.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.383+10442A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199053 | |||||||
| chr6:130199254 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18946.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.383+10241G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199254 | |||||||
| chr6:130199317 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+10178A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199317 | |||||||
| chr6:130199322 | A | T | 3 | a0002c0003t0001g0086 a0002c0003t0001g0087 a0002c0003t0001g0159 |
3 | NA18981.hp2 NA18983.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.383+10173T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199322 | |||||||
| chr6:130199417 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.383+10078C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199417 | |||||||
| chr6:130199498 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.383+9997A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199498 | |||||||
| chr6:130199527 | A | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.383+9968T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199527 | |||||||
| chr6:130199575 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.383+9920A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199575 | |||||||
| chr6:130199684 | T | A | 1 | a0001c0001t0002g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.383+9811A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199684 | |||||||
| chr6:130199726 | C | G | 1 | a0001c0001t0001g0293 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.383+9769G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199726 | |||||||
| chr6:130199730 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.383+9765C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199730 | |||||||
| chr6:130199798 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+9697C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199798 | |||||||
| chr6:130199798 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.383+9697C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199798 | |||||||
| chr6:130199817 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.383+9678A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199817 | |||||||
| chr6:130199875 | C | A | 2 | a0001c0001t0001g0284 a0005c0009t0001g0285 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.383+9620G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199875 | |||||||
| chr6:130199925 | T | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+9570A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199925 | |||||||
| chr6:130199976 | C | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
115 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.383+9519G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130199976 | |||||||
| chr6:130200005 | A | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.383+9490T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200005 | |||||||
| chr6:130200067 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0002g0020 others(3): Show |
6 | HG02717.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+9428C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200067 | |||||||
| chr6:130200279 | C | T | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+9216G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200279 | |||||||
| chr6:130200280 | G | A | 4 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0254 others(1): Show |
4 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+9215C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200280 | |||||||
| chr6:130200385 | C | CA | 183 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(180): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.383+9109dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200385 | |||||||
| chr6:130200422 | A | C | 1 | a0001c0001t0003g0010 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.383+9073T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200422 | |||||||
| chr6:130200513 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.383+8982G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200513 | |||||||
| chr6:130200517 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.383+8978G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200517 | |||||||
| chr6:130200549 | C | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+8946G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200549 | |||||||
| chr6:130200551 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+8944C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200551 | |||||||
| chr6:130200551 | G | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.383+8944C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200551 | |||||||
| chr6:130200557 | C | CA | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.383+8937dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200557 | |||||||
| chr6:130200557 | C | CAA | 31 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0099 others(28): Show |
31 | HG00621.hp2 HG00642.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.383+8936_383+8937d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200557 | |||||||
| chr6:130200557 | CA | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+8937delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200557 | |||||||
| chr6:130200623 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0002t0001g0131 |
3 | HG02257.hp2 HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.383+8872A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200623 | |||||||
| chr6:130200649 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.383+8846C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200649 | |||||||
| chr6:130200757 | C | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0171 others(21): Show |
25 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.383+8738G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200757 | |||||||
| chr6:130200884 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.383+8611G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200884 | |||||||
| chr6:130200943 | C | T | 2 | a0001c0001t0001g0284 a0005c0009t0001g0285 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.383+8552G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130200943 | |||||||
| chr6:130201049 | A | T | 1 | a0001c0001t0003g0010 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.383+8446T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201049 | |||||||
| chr6:130201274 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0315 |
3 | NA19056.hp2 NA19082.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.383+8221T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201274 | |||||||
| chr6:130201319 | T | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(36): Show |
41 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.383+8176A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201319 | |||||||
| chr6:130201377 | A | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | NA18975.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.383+8118T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201377 | |||||||
| chr6:130201397 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.383+8098T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201397 | |||||||
| chr6:130201914 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+7581G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201914 | |||||||
| chr6:130201991 | A | G | 2 | a0001c0001t0001g0313 a0001c0001t0002g0314 |
2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.383+7504T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130201991 | |||||||
| chr6:130202059 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0257 a0001c0001t0002g0036 |
3 | HG02451.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.383+7436T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202059 | |||||||
| chr6:130202410 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.383+7085A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202410 | |||||||
| chr6:130202572 | ATAAGTAT others(4): Show |
A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.383+6912_383+6922d others(13): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202572 | |||||||
| chr6:130202585 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.383+6910T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202585 | |||||||
| chr6:130202655 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.383+6840T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202655 | |||||||
| chr6:130202905 | GC | G | 168 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(165): Show |
174 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.383+6589delG | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202905 | |||||||
| chr6:130202918 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.383+6577G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130202918 | |||||||
| chr6:130203150 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.383+6345G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203150 | |||||||
| chr6:130203227 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.383+6268T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203227 | |||||||
| chr6:130203268 | AT | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.383+6226delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203268 | |||||||
| chr6:130203295 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.383+6200G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203295 | |||||||
| chr6:130203577 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+5918T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203577 | |||||||
| chr6:130203800 | C | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0243 |
3 | HG02717.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.383+5695G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130203800 | |||||||
| chr6:130204034 | A | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.383+5461T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204034 | |||||||
| chr6:130204051 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.383+5444C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204051 | |||||||
| chr6:130204230 | T | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+5265A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204230 | |||||||
| chr6:130204342 | A | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(39): Show |
44 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.383+5153T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204342 | |||||||
| chr6:130204344 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.383+5151G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204344 | |||||||
| chr6:130204463 | A | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.383+5032T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204463 | |||||||
| chr6:130204465 | T | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.383+5030A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204465 | |||||||
| chr6:130204472 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0162 a0001c0001t0002g0296 |
3 | HG01243.hp1 HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.383+5023G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204472 | |||||||
| chr6:130204480 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0160 others(1): Show |
4 | HG03139.hp1 HG03239.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+5015C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204480 | |||||||
| chr6:130204520 | C | G | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.383+4975G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204520 | |||||||
| chr6:130204584 | G | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.383+4911C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204584 | |||||||
| chr6:130204596 | C | CA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(63): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.383+4898dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204596 | |||||||
| chr6:130204596 | C | CAA | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(42): Show |
47 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.383+4897_383+4898d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204596 | |||||||
| chr6:130204596 | C | CAAA | 5 | a0001c0001t0001g0040 a0001c0001t0001g0164 a0001c0001t0002g0166 others(2): Show |
5 | HG01175.hp1 HG04199.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.383+4896_383+4898d others(5): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204596 | |||||||
| chr6:130204604 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.383+4891C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204604 | |||||||
| chr6:130204662 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0273 |
2 | NA19076.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.383+4833A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204662 | |||||||
| chr6:130204672 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.383+4823G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204672 | |||||||
| chr6:130204741 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383+4754G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204741 | |||||||
| chr6:130204765 | CT | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
150 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.383+4729delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204765 | |||||||
| chr6:130204765 | CTT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(73): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.383+4728_383+4729d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204765 | |||||||
| chr6:130204998 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.383+4497C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130204998 | |||||||
| chr6:130205042 | C | T | 102 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(99): Show |
104 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.383+4453G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205042 | |||||||
| chr6:130205154 | T | TA | 87 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.383+4340dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205154 | |||||||
| chr6:130205154 | T | TAA | 101 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
104 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.383+4339_383+4340d others(4): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205154 | |||||||
| chr6:130205154 | T | TAAAAAA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+4335_383+4340d others(8): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205154 | |||||||
| chr6:130205154 | TA | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(38): Show |
43 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.383+4340delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205154 | |||||||
| chr6:130205191 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.383+4304A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205191 | |||||||
| chr6:130205292 | ATATTT | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0029 others(40): Show |
45 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.383+4198_383+4202d others(7): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205292 | |||||||
| chr6:130205292 | ATATTTTA others(3): Show |
A | 1 | a0001c0001t0001g0266 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.383+4193_383+4202d others(12): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205292 | |||||||
| chr6:130205297 | T | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.383+4198A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205297 | |||||||
| chr6:130205352 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG04204.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383+4143C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205352 | |||||||
| chr6:130205361 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.383+4134A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205361 | |||||||
| chr6:130205552 | C | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
7 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+3943G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205552 | |||||||
| chr6:130205552 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3943G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205552 | |||||||
| chr6:130205553 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3942G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205553 | |||||||
| chr6:130205555 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3940G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205555 | |||||||
| chr6:130205556 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3939T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205556 | |||||||
| chr6:130205558 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3937G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205558 | |||||||
| chr6:130205559 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3936G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205559 | |||||||
| chr6:130205561 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3934G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205561 | |||||||
| chr6:130205564 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383+3931T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205564 | |||||||
| chr6:130205601 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383+3894C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205601 | |||||||
| chr6:130205817 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(5): Show |
9 | HG01255.hp2 HG01884.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+3678G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205817 | |||||||
| chr6:130205906 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0005g0204 |
2 | HG01981.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.383+3589G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130205906 | |||||||
| chr6:130206443 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.383+3052G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206443 | |||||||
| chr6:130206455 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.383+3040A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206455 | |||||||
| chr6:130206532 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.383+2963G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206532 | |||||||
| chr6:130206703 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.383+2792A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206703 | |||||||
| chr6:130206722 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+2773C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206722 | |||||||
| chr6:130206778 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0002g0085 |
3 | HG03239.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.383+2717G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206778 | |||||||
| chr6:130206807 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.383+2688G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206807 | |||||||
| chr6:130206828 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.383+2667T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130206828 | |||||||
| chr6:130207042 | C | T | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.383+2453G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207042 | |||||||
| chr6:130207043 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.383+2452T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207043 | |||||||
| chr6:130207046 | G | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG02040.hp2 HG02074.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+2449C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207046 | |||||||
| chr6:130207054 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0147 others(44): Show |
48 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.383+2441G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207054 | |||||||
| chr6:130207105 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(4): Show |
7 | HG02257.hp2 HG02602.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+2390G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207105 | |||||||
| chr6:130207159 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(4): Show |
8 | HG01255.hp2 HG03225.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.383+2328_383+2335d others(10): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207159 | |||||||
| chr6:130207159 | CA | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(37): Show |
42 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.383+2335delT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207159 | |||||||
| chr6:130207163 | A | AT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(4): Show |
7 | HG02257.hp2 HG02602.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+2331_383+2332i others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207163 | |||||||
| chr6:130207169 | A | AAAAAAAG | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.383+2325_383+2326i others(9): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207169 | |||||||
| chr6:130207216 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.383+2279C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207216 | |||||||
| chr6:130207519 | T | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | NA18939.hp1 NA18956.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+1976A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207519 | |||||||
| chr6:130207521 | TG | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0032 others(3): Show |
7 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+1973delC | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207521 | |||||||
| chr6:130207557 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383+1938C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207557 | |||||||
| chr6:130207637 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.383+1858C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207637 | |||||||
| chr6:130207864 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0132 others(13): Show |
17 | HG00609.hp2 HG02040.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.383+1631G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207864 | |||||||
| chr6:130207931 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.383+1564C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130207931 | |||||||
| chr6:130208042 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.383+1453G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208042 | |||||||
| chr6:130208088 | G | A | 2 | a0001c0001t0001g0018 a0001c0002t0001g0027 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.383+1407C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208088 | |||||||
| chr6:130208131 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.383+1364G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208131 | |||||||
| chr6:130208216 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+1279C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208216 | |||||||
| chr6:130208444 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.383+1051G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208444 | |||||||
| chr6:130208514 | G | A | 2 | a0001c0001t0001g0326 a0008c0005t0001g0231 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.383+981C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208514 | |||||||
| chr6:130208764 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383+731A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208764 | |||||||
| chr6:130208794 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.383+701G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208794 | |||||||
| chr6:130208899 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+596G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208899 | |||||||
| chr6:130208987 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383+508T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130208987 | |||||||
| chr6:130209019 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383+476C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130209019 | |||||||
| chr6:130209241 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383+254G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130209241 | |||||||
| chr6:130209272 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383+223T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130209272 | |||||||
| chr6:130209305 | A | C | 1 | a0009c0006t0001g0149 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.383+190T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130209305 | |||||||
| chr6:130209487 | A | AC | 8 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0106 others(5): Show |
8 | HG01099.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.383+7dupG | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 5/11 | chr6 | 130209487 | |||||||
| chr6:130209670 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.270-62G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130209670 | |||||||
| chr6:130209829 | A | G | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270-221T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130209829 | |||||||
| chr6:130209849 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.270-241G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130209849 | |||||||
| chr6:130209890 | A | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270-282T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130209890 | |||||||
| chr6:130210021 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.270-413G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210021 | |||||||
| chr6:130210106 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270-498A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210106 | |||||||
| chr6:130210175 | A | C | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270-567T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210175 | |||||||
| chr6:130210232 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.270-624G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210232 | |||||||
| chr6:130210296 | C | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.270-688G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210296 | |||||||
| chr6:130210327 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.270-719C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210327 | |||||||
| chr6:130210336 | C | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0162 a0001c0001t0002g0296 |
3 | HG01243.hp1 HG01516.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.270-728G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210336 | |||||||
| chr6:130210441 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.270-833T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210441 | |||||||
| chr6:130210460 | A | G | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0215 others(3): Show |
6 | HG00741.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-852T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210460 | |||||||
| chr6:130210470 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270-862C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210470 | |||||||
| chr6:130210545 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.270-937C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210545 | |||||||
| chr6:130210577 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0172 others(7): Show |
11 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.270-969G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210577 | |||||||
| chr6:130210597 | C | CA | 7 | a0001c0001t0001g0014 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02074.hp1 NA18963.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.270-990dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210597 | |||||||
| chr6:130210619 | G | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.270-1011C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210619 | |||||||
| chr6:130210750 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.270-1142G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210750 | |||||||
| chr6:130210760 | T | G | 1 | a0001c0007t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.270-1152A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210760 | |||||||
| chr6:130210902 | C | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0031 others(37): Show |
42 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.270-1294G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210902 | |||||||
| chr6:130210905 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.270-1297C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130210905 | |||||||
| chr6:130211234 | C | CT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0165 a0001c0001t0001g0168 others(2): Show |
6 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.270-1627dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211234 | |||||||
| chr6:130211275 | A | T | 1 | a0001c0001t0002g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270-1667T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211275 | |||||||
| chr6:130211275 | AATTTTTT | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(66): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.270-1674_270-1668d others(9): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211275 | |||||||
| chr6:130211276 | A | AT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0071 others(4): Show |
7 | HG01361.hp2 HG03831.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.270-1669dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211276 | |||||||
| chr6:130211276 | A | T | 1 | a0001c0001t0002g0275 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.270-1668T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211276 | |||||||
| chr6:130211276 | AT | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0069 others(6): Show |
9 | HG02897.hp1 NA18747.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.270-1669delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211276 | |||||||
| chr6:130211276 | ATTTTTT | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0260 a0001c0001t0001g0278 others(5): Show |
9 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.270-1674_270-1669d others(8): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211276 | |||||||
| chr6:130211276 | ATTTTTTT | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
162 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.270-1675_270-1669d others(9): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211276 | |||||||
| chr6:130211430 | C | A | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270-1822G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211430 | |||||||
| chr6:130211432 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.270-1824G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211432 | |||||||
| chr6:130211531 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.270-1923C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211531 | |||||||
| chr6:130211751 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(36): Show |
41 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.270-2143C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211751 | |||||||
| chr6:130211944 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.270-2336G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130211944 | |||||||
| chr6:130212054 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.269+2283C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212054 | |||||||
| chr6:130212209 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.269+2128G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212209 | |||||||
| chr6:130212223 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(105): Show |
111 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.269+2114T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212223 | |||||||
| chr6:130212302 | G | A | 101 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(98): Show |
103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+2035C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212302 | |||||||
| chr6:130212577 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.269+1760A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212577 | |||||||
| chr6:130212589 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.269+1748G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212589 | |||||||
| chr6:130212674 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.269+1663A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212674 | |||||||
| chr6:130212759 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.269+1578C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212759 | |||||||
| chr6:130212803 | C | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.269+1534G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212803 | |||||||
| chr6:130212816 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.269+1521G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212816 | |||||||
| chr6:130212849 | G | A | 1 | a0001c0007t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.269+1488C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212849 | |||||||
| chr6:130212939 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.269+1398C>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130212939 | |||||||
| chr6:130213005 | G | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
151 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.269+1332C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213005 | |||||||
| chr6:130213231 | G | C | 6 | a0001c0001t0001g0164 a0001c0001t0001g0260 a0001c0001t0001g0263 others(3): Show |
6 | HG01099.hp1 HG01175.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.269+1106C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213231 | |||||||
| chr6:130213239 | C | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.269+1098G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213239 | |||||||
| chr6:130213259 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.269+1078G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213259 | |||||||
| chr6:130213315 | T | C | 101 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(98): Show |
103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+1022A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213315 | |||||||
| chr6:130213322 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.269+1015A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213322 | |||||||
| chr6:130213323 | T | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(46): Show |
51 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.269+1014A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213323 | |||||||
| chr6:130213324 | T | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.269+1013A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213324 | |||||||
| chr6:130213325 | T | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.269+1012A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213325 | |||||||
| chr6:130213446 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.269+891G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213446 | |||||||
| chr6:130213568 | C | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.269+769G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213568 | |||||||
| chr6:130213691 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.269+646G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213691 | |||||||
| chr6:130213784 | T | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | NA18612.hp2 NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.269+553A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213784 | |||||||
| chr6:130213838 | T | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 |
4 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+499A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213838 | |||||||
| chr6:130213847 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.269+490A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213847 | |||||||
| chr6:130213929 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0042 others(3): Show |
6 | HG00438.hp2 NA18946.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+408T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130213929 | |||||||
| chr6:130214194 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.269+143C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130214194 | |||||||
| chr6:130214275 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.269+62C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130214275 | |||||||
| chr6:130214288 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.269+49A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 4/11 | chr6 | 130214288 | |||||||
| chr6:130214537 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.80-11C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 3/11 | chr6 | 130214537 | |||||||
| chr6:130214867 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.79+328A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 3/11 | chr6 | 130214867 | |||||||
| chr6:130214896 | T | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+299A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 3/11 | chr6 | 130214896 | |||||||
| chr6:130214962 | G | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0002c0003t0001g0086 others(2): Show |
5 | HG01099.hp1 HG01175.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+233C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 3/11 | chr6 | 130214962 | |||||||
| chr6:130215349 | AT | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.-21-56delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215349 | |||||||
| chr6:130215595 | C | T | 1 | a0001c0004t0001g0298 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-21-301G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215595 | |||||||
| chr6:130215627 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0002g0234 a0001c0001t0002g0235 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-333T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215627 | |||||||
| chr6:130215739 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 |
4 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-445T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215739 | |||||||
| chr6:130215769 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-475A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215769 | |||||||
| chr6:130215860 | G | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(100): Show |
105 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-21-566C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215860 | |||||||
| chr6:130215893 | G | C | 1 | a0001c0001t0001g0001 | 4 | HG01069.hp2 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-599C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215893 | |||||||
| chr6:130215963 | T | C | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-22+608A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130215963 | |||||||
| chr6:130216062 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-22+509A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216062 | |||||||
| chr6:130216079 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-22+492G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216079 | |||||||
| chr6:130216096 | C | CA | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-22+474dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216096 | |||||||
| chr6:130216123 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-22+448T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216123 | |||||||
| chr6:130216156 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-22+415T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216156 | |||||||
| chr6:130216221 | A | G | 2 | a0001c0001t0001g0260 a0001c0010t0001g0023 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-22+350T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216221 | |||||||
| chr6:130216254 | G | A | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-22+317C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216254 | |||||||
| chr6:130216285 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-22+286C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216285 | |||||||
| chr6:130216458 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-22+113A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216458 | |||||||
| chr6:130216542 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG02040.hp2 HG02074.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+29C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 2/11 | chr6 | 130216542 | |||||||
| chr6:130216843 | T | C | 1 | a0007c0012t0001g0323 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-67-227A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130216843 | |||||||
| chr6:130216902 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-67-286T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130216902 | |||||||
| chr6:130216980 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-67-364G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130216980 | |||||||
| chr6:130217247 | A | C | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-67-631T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217247 | |||||||
| chr6:130217326 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | NA18967.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-67-710C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217326 | |||||||
| chr6:130217352 | C | T | 101 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(98): Show |
103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-67-736G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217352 | |||||||
| chr6:130217407 | T | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0260 others(10): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-67-791A>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217407 | |||||||
| chr6:130217413 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-67-797A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217413 | |||||||
| chr6:130217434 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-67-818G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217434 | |||||||
| chr6:130217596 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-67-980A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217596 | |||||||
| chr6:130217781 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-67-1165C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217781 | |||||||
| chr6:130217842 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-67-1226C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130217842 | |||||||
| chr6:130218049 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-67-1433A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218049 | |||||||
| chr6:130218053 | A | C | 1 | a0001c0001t0001g0266 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-67-1437T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218053 | |||||||
| chr6:130218161 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0091 others(6): Show |
10 | HG01255.hp2 HG02135.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67-1545C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218161 | |||||||
| chr6:130218235 | T | C | 1 | a0001c0001t0002g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-67-1619A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218235 | |||||||
| chr6:130218262 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-67-1646G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218262 | |||||||
| chr6:130218271 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-67-1655G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218271 | |||||||
| chr6:130218314 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-67-1698A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218314 | |||||||
| chr6:130218361 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-67-1745C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218361 | |||||||
| chr6:130218714 | G | A | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-67-2098C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218714 | |||||||
| chr6:130218747 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-67-2131G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218747 | |||||||
| chr6:130218749 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-67-2133A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218749 | |||||||
| chr6:130218789 | AT | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0278 others(8): Show |
12 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-67-2174delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218789 | |||||||
| chr6:130218804 | T | TA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0091 others(7): Show |
11 | HG01255.hp2 HG02135.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.-67-2189dupT | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218804 | |||||||
| chr6:130218813 | C | A | 2 | a0001c0001t0001g0022 a0001c0010t0001g0023 |
2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-67-2197G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130218813 | |||||||
| chr6:130219040 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0326 a0008c0005t0001g0231 |
3 | HG02280.hp2 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-67-2424C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219040 | |||||||
| chr6:130219123 | G | A | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-67-2507C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219123 | |||||||
| chr6:130219238 | A | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(20): Show |
25 | HG00609.hp2 HG00639.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-67-2622T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219238 | |||||||
| chr6:130219244 | C | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-67-2628G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219244 | |||||||
| chr6:130219303 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-67-2687G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219303 | |||||||
| chr6:130219305 | A | AT | 9 | a0001c0001t0001g0008 a0001c0001t0001g0278 a0001c0001t0001g0279 others(6): Show |
10 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67-2690dupA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219305 | |||||||
| chr6:130219306 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0263 |
2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-67-2690A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219306 | |||||||
| chr6:130219329 | AT | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
151 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-67-2714delA | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219329 | |||||||
| chr6:130219374 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-67-2758C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219374 | |||||||
| chr6:130219558 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-67-2942G>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219558 | |||||||
| chr6:130219581 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-67-2965C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219581 | |||||||
| chr6:130219696 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0091 others(5): Show |
9 | HG01255.hp2 HG03491.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.-68+2998G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219696 | |||||||
| chr6:130219702 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-68+2992A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219702 | |||||||
| chr6:130219744 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-68+2950C>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130219744 | |||||||
| chr6:130220065 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-68+2629A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220065 | |||||||
| chr6:130220094 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0002g0036 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-68+2600G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220094 | |||||||
| chr6:130220254 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(33): Show |
38 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-68+2440G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220254 | |||||||
| chr6:130220343 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-68+2351C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220343 | |||||||
| chr6:130220371 | G | A | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-68+2323C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220371 | |||||||
| chr6:130220460 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-68+2234A>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220460 | |||||||
| chr6:130220477 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-68+2217G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220477 | |||||||
| chr6:130220544 | T | C | 2 | a0001c0001t0001g0130 a0001c0002t0001g0131 |
2 | HG02602.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-68+2150A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220544 | |||||||
| chr6:130220785 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-68+1909C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220785 | |||||||
| chr6:130220947 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-68+1747C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130220947 | |||||||
| chr6:130221010 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-68+1684G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221010 | |||||||
| chr6:130221015 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0230 |
2 | HG00323.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-68+1679T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221015 | |||||||
| chr6:130221026 | T | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
150 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.-68+1668A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221026 | |||||||
| chr6:130221030 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-68+1664C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221030 | |||||||
| chr6:130221045 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-68+1649C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221045 | |||||||
| chr6:130221055 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0229 |
5 | HG01069.hp2 HG01071.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+1639A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221055 | |||||||
| chr6:130221076 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-68+1618C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221076 | |||||||
| chr6:130221089 | T | C | 36 | a0001c0001t0001g0230 a0001c0001t0001g0232 a0001c0001t0001g0233 others(33): Show |
36 | HG00323.hp1 HG01106.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.-68+1605A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221089 | |||||||
| chr6:130221096 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-68+1598A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221096 | |||||||
| chr6:130221097 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-68+1597C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221097 | |||||||
| chr6:130221101 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-68+1593T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221101 | |||||||
| chr6:130221105 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-68+1589A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221105 | |||||||
| chr6:130221134 | A | G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0029 others(9): Show |
12 | HG01192.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-68+1560T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221134 | |||||||
| chr6:130221143 | C | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-68+1551G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221143 | |||||||
| chr6:130221144 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(2): Show |
5 | HG01192.hp1 HG03471.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+1550T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221144 | |||||||
| chr6:130221145 | C | T | 1 | a0001c0010t0001g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-68+1549G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221145 | |||||||
| chr6:130221224 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-68+1470A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221224 | |||||||
| chr6:130221352 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0002g0020 others(1): Show |
4 | HG02717.hp1 HG02809.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+1342G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221352 | |||||||
| chr6:130221442 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
5 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+1252T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221442 | |||||||
| chr6:130221507 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-68+1187G>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221507 | |||||||
| chr6:130221622 | T | C | 1 | a0001c0001t0006g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-68+1072A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221622 | |||||||
| chr6:130221670 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0286 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+1024G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221670 | |||||||
| chr6:130221729 | T | TGTC | 11 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0269 others(8): Show |
11 | HG00438.hp2 HG01496.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+962_-68+964dup others(3): Show |
SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221729 | |||||||
| chr6:130221979 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+715C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221979 | |||||||
| chr6:130221996 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0277 others(12): Show |
16 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-68+698C>T | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130221996 | |||||||
| chr6:130222246 | A | T | 1 | a0001c0001t0001g0016 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-68+448T>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130222246 | |||||||
| chr6:130222302 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-68+392T>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130222302 | |||||||
| chr6:130222542 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0289 a0001c0001t0001g0290 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-68+152A>G | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130222542 | |||||||
| chr6:130222624 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | NA19078.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-68+70T>C | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130222624 | |||||||
| chr6:130222693 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02074.hp2 | splice_donor_variant&intron_variant | HIGH | c.-68+1G>A | SAMD3 | ENSG00000164483.17 | transcript | ENST00000439090.7 | protein_coding | 1/11 | chr6 | 130222693 |