Item | Value |
---|---|
geneid | 142891 |
ensemblid | ENSG00000156671.15 |
hgncid | 26320 |
symbol | SAMD8 |
name | sterile alpha motif domain containing 8 |
refseq_nuc | NM_001174156.2 |
refseq_prot | NP_001167627.1 |
ensembl_nuc | ENST00000542569.6 |
ensembl_prot | ENSP00000438042.1 |
mane_status | MANE Select |
chr | chr10 |
start | 75111656 |
end | 75182123 |
strand | + |
ver | v1.2 |
region | chr10:75111656-75182123 |
region5000 | chr10:75106656-75187123 |
regionname0 | SAMD8_chr10_75111656_75182123 |
regionname5000 | SAMD8_chr10_75106656_75187123 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 415 | 322 | 90 | 54 | 134 | 14 | 28 | 101 | SAMD8_chr10_75106656_75187123 | SAMD8 | MAGPN others(410): Show |
chr10 | 75106656 | 75187123 |
a0002 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | MAGPN others(410): Show |
chr10 | 75106656 | 75187123 |
a0003 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | MAGPN others(410): Show |
chr10 | 75106656 | 75187123 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1245 | 309 | 83 | 52 | 130 | 14 | 28 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0001c0002 | 0/0 | 1245 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0001c0003 | 0/0 | 1245 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0001c0004 | 0/0 | 1245 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0001c0005 | 0/0 | 1245 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0001c0007 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0002c0008 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 | ||
a0003c0006 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | ATGGC others(1240): Show |
chr10 | 75106656 | 75187123 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6760 | 94 | 17 | 9 | 55 | 4 | 9 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0002 | 0/1 | 6761 | 73 | 2 | 15 | 48 | 2 | 5 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0003 | 1/0 | 6761 | 73 | 26 | 19 | 11 | 4 | 12 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0004 | 0/0 | 6761 | 14 | 7 | 2 | 3 | 2 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0005 | 0/0 | 6761 | 11 | 10 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0006 | 0/0 | 6761 | 8 | 7 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0007 | 0/0 | 6761 | 2 | 0 | 0 | 1 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0008 | 0/0 | 6760 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0009 | 0/0 | 6760 | 3 | 0 | 2 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0010 | 0/0 | 6761 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0011 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0012 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0013 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0014 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0015 | 0/0 | 6762 | 2 | 0 | 0 | 1 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6757): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0016 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0017 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0018 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0019 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0020 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0021 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0022 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0023 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0024 | 0/0 | 6760 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0025 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0026 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0027 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0028 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0029 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0001t0030 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0002t0001 | 0/0 | 6760 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6755): Show |
chr10 | 75106656 | 75187123 |
a0001c0003t0007 | 0/0 | 6761 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0004t0012 | 0/0 | 6761 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0005t0003 | 0/0 | 6761 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0001c0007t0011 | 0/0 | 6761 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0002c0008t0002 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
a0003c0006t0002 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | GGACT others(6756): Show |
chr10 | 75106656 | 75187123 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0002 | 1/0 | 4 | 1 | 1 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0009g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0012g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0014g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0014g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0016g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0017g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0018g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0019g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0020g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0022g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0023g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0024g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0025g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0026g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0027g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0028g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0029g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0001t0030g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0003t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0003t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0003t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0003t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0004t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0004t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0005t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0005t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0001c0007t0011g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0002c0008t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
a0003c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0194 | EUR | GBR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0058 | EUR | GBR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | FIN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0277 | EUR | FIN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00609 | hp1 | a0001 | c0001 | t0022 | g0222 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00642 | hp2 | a0001 | c0001 | t0023 | g0303 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00735 | hp2 | a0001 | c0001 | t0018 | g0210 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01069 | hp1 | a0001 | c0004 | t0012 | g0229 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0294 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01070 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01071 | hp2 | a0001 | c0004 | t0012 | g0002 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01255 | hp2 | a0001 | c0001 | t0012 | g0285 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0284 | EUR | IBS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0271 | EUR | IBS | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PEL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02015 | hp2 | a0001 | c0003 | t0007 | g0120 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02083 | hp2 | a0002 | c0008 | t0002 | g0201 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02155 | hp2 | a0001 | c0003 | t0007 | g0121 | EAS | CDX | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CDX | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0283 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0289 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02717 | hp1 | a0001 | c0001 | t0011 | g0302 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02723 | hp1 | a0001 | c0001 | t0027 | g0138 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0281 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02895 | hp2 | a0001 | c0001 | t0013 | g0306 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02896 | hp1 | a0001 | c0005 | t0003 | g0218 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02897 | hp1 | a0001 | c0005 | t0003 | g0217 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02897 | hp2 | a0001 | c0001 | t0013 | g0305 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0295 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03098 | hp1 | a0001 | c0001 | t0029 | g0299 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0296 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03486 | hp1 | a0001 | c0001 | t0025 | g0067 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03486 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | ESN | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03540 | hp1 | a0001 | c0001 | t0020 | g0144 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03579 | hp1 | a0001 | c0001 | t0016 | g0013 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03579 | hp2 | a0001 | c0001 | t0026 | g0304 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0263 | SAS | BEB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03942 | hp2 | a0001 | c0001 | t0015 | g0027 | SAS | BEB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04115 | hp1 | a0001 | c0001 | t0024 | g0023 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18944 | hp1 | a0001 | c0001 | t0017 | g0054 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18947 | hp2 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0223 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18960 | hp2 | a0003 | c0006 | t0002 | g0050 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18973 | hp1 | a0001 | c0001 | t0028 | g0205 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18986 | hp1 | a0001 | c0001 | t0010 | g0267 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18994 | hp2 | a0001 | c0003 | t0007 | g0122 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18998 | hp1 | a0001 | c0001 | t0010 | g0266 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19007 | hp2 | a0001 | c0001 | t0019 | g0114 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | LWK | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19063 | hp1 | a0001 | c0001 | t0008 | g0219 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19068 | hp2 | a0001 | c0003 | t0007 | g0123 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0221 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0268 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | YRI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | ASW | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ASW | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0130 | EUR | TSI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0128 | EUR | TSI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0125 | EUR | TSI | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | CLM | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02486 | hp1 | a0001 | c0007 | t0011 | g0300 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0301 | AFR | ACB | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | USA | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | USA | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA18955 | hp2 | a0001 | c0001 | t0021 | g0169 | EAS | JPT | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | USA | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | USA | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0163 | REF | REF | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0002 | REF | REF | SAMD8_chr10_75106656_75187123 | SAMD8 | chr10 | 75106656 | 75187123 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:75150956 | G | A | 1 | a0003 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.428G>A | p.Arg143Gln | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 510/6761 | 428/1248 | 143/415 | chr10 | 75150956 | |||
chr10:75150959 | G | T | 1 | a0002 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.431G>T | p.Arg144Ile | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 513/6761 | 431/1248 | 144/415 | chr10 | 75150959 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:75150558 | C | T | 1 | a0001c0003 | 4 | HG02015.hp2 HG02155.hp2 NA18994.hp2 others(1): Show |
synonymous_variant | LOW | c.30C>T | p.Arg10Arg | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 112/6761 | 30/1248 | 10/415 | chr10 | 75150558 | |||
chr10:75150975 | C | T | 1 | a0001c0005 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.447C>T | p.Tyr149Tyr | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 529/6761 | 447/1248 | 149/415 | chr10 | 75150975 | |||
chr10:75151062 | T | C | 1 | a0001c0007 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.534T>C | p.Pro178Pro | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 616/6761 | 534/1248 | 178/415 | chr10 | 75151062 | |||
chr10:75164645 | C | T | 1 | a0001c0002 | 4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.579C>T | p.Ser193Ser | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/6 | 661/6761 | 579/1248 | 193/415 | chr10 | 75164645 | |||
chr10:75164714 | C | G | 1 | a0001c0004 | 2 | HG01069.hp1 HG01071.hp2 |
synonymous_variant | LOW | c.648C>G | p.Leu216Leu | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/6 | 730/6761 | 648/1248 | 216/415 | chr10 | 75164714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:75150519 | G | A | 1 | a0001c0001t0017 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/6 | 10 | chr10 | 75150519 | ||||||
chr10:75176745 | G | T | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*53G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 53 | chr10 | 75176745 | ||||||
chr10:75176933 | T | G | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0003t0007 |
20 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 241 | chr10 | 75176933 | ||||||
chr10:75177071 | T | A | 1 | a0001c0001t0018 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 379 | chr10 | 75177071 | ||||||
chr10:75177190 | C | A | 1 | a0001c0001t0013 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*498C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 498 | chr10 | 75177190 | ||||||
chr10:75177340 | G | A | 1 | a0001c0001t0019 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 648 | chr10 | 75177340 | ||||||
chr10:75177465 | C | A | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*773C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 773 | chr10 | 75177465 | ||||||
chr10:75177508 | A | G | 1 | a0001c0001t0028 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 816 | chr10 | 75177508 | ||||||
chr10:75177649 | G | A | 1 | a0001c0001t0020 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*957G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 957 | chr10 | 75177649 | ||||||
chr10:75177817 | T | A | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(8): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1125T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1125 | chr10 | 75177817 | ||||||
chr10:75178010 | T | C | 1 | a0001c0001t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1318T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1318 | chr10 | 75178010 | ||||||
chr10:75178093 | T | G | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1401 | chr10 | 75178093 | ||||||
chr10:75178143 | CT | C | 1 | a0001c0001t0008 | 3 | NA18951.hp1 NA19063.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1452 | chr10 | 75178143 | ||||||
chr10:75178228 | A | G | 1 | a0001c0001t0027 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1536 | chr10 | 75178228 | ||||||
chr10:75178505 | T | A | 11 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(8): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1813 | chr10 | 75178505 | ||||||
chr10:75178521 | G | GA | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(4): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1830dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1831 | INFO_REALIGN_3_PRIME | chr10 | 75178521 | |||||
chr10:75178668 | A | G | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1976A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 1976 | chr10 | 75178668 | ||||||
chr10:75178711 | C | T | 2 | a0001c0001t0012 a0001c0004t0012 |
3 | HG01069.hp1 HG01071.hp2 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2019C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2019 | chr10 | 75178711 | ||||||
chr10:75179058 | T | C | 1 | a0001c0001t0029 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2366 | chr10 | 75179058 | ||||||
chr10:75179089 | C | T | 1 | a0001c0001t0009 | 3 | HG00140.hp2 HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2397C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2397 | chr10 | 75179089 | ||||||
chr10:75179090 | G | A | 1 | a0001c0001t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2398G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2398 | chr10 | 75179090 | ||||||
chr10:75179099 | T | C | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0003t0007 |
20 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2407T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2407 | chr10 | 75179099 | ||||||
chr10:75179139 | A | C | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2447A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2447 | chr10 | 75179139 | ||||||
chr10:75179207 | G | A | 1 | a0001c0001t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2515 | chr10 | 75179207 | ||||||
chr10:75179530 | C | A | 1 | a0001c0001t0021 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2838C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2838 | chr10 | 75179530 | ||||||
chr10:75179584 | T | A | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0019 others(5): Show |
81 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2892T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2892 | chr10 | 75179584 | ||||||
chr10:75179677 | C | A | 1 | a0001c0001t0025 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2985C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 2985 | chr10 | 75179677 | ||||||
chr10:75180015 | C | G | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(4): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3323C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3323 | chr10 | 75180015 | ||||||
chr10:75180124 | A | G | 1 | a0001c0001t0026 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3432A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3432 | chr10 | 75180124 | ||||||
chr10:75180313 | C | G | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3621C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3621 | chr10 | 75180313 | ||||||
chr10:75180382 | G | A | 2 | a0001c0001t0007 a0001c0003t0007 |
6 | HG02015.hp2 HG02155.hp2 NA18947.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3690G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3690 | chr10 | 75180382 | ||||||
chr10:75180418 | C | T | 3 | a0001c0001t0011 a0001c0001t0016 a0001c0007t0011 |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3726C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3726 | chr10 | 75180418 | ||||||
chr10:75180458 | A | G | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0015 others(4): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3766A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3766 | chr10 | 75180458 | ||||||
chr10:75180547 | T | C | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3855T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3855 | chr10 | 75180547 | ||||||
chr10:75180675 | T | C | 1 | a0001c0001t0030 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3983T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 3983 | chr10 | 75180675 | ||||||
chr10:75180713 | C | G | 2 | a0001c0001t0011 a0001c0007t0011 |
3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4021C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 4021 | chr10 | 75180713 | ||||||
chr10:75181094 | A | G | 1 | a0001c0001t0023 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4402A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 4402 | chr10 | 75181094 | ||||||
chr10:75181261 | C | T | 1 | a0001c0001t0010 | 3 | NA18986.hp1 NA18998.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4569C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 4569 | chr10 | 75181261 | ||||||
chr10:75181444 | TGC | T | 6 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(3): Show |
104 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*4753_*4754delGC | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 4753 | chr10 | 75181444 | ||||||
chr10:75181719 | A | G | 1 | a0001c0001t0022 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5027A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 5027 | chr10 | 75181719 | ||||||
chr10:75181767 | C | G | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02970.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5075C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 5075 | chr10 | 75181767 | ||||||
chr10:75181773 | C | G | 1 | a0001c0001t0026 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5081C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 5081 | chr10 | 75181773 | ||||||
chr10:75181851 | G | A | 1 | a0001c0001t0005 | 11 | HG01069.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5159G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 6/6 | 5159 | chr10 | 75181851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:75111805 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0012 |
2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-16+83G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75111805 | |||||||
chr10:75111850 | G | A | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-16+128G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75111850 | |||||||
chr10:75112019 | A | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+297A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112019 | |||||||
chr10:75112418 | A | G | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+696A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112418 | |||||||
chr10:75112433 | A | G | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+711A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112433 | |||||||
chr10:75112454 | TTCTCG | T | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0013g0305 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+734_-16+738del others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75112454 | ||||||
chr10:75112743 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-16+1021G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112743 | |||||||
chr10:75112789 | C | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+1067C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112789 | |||||||
chr10:75112832 | A | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+1110A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112832 | |||||||
chr10:75112929 | C | T | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16+1207C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112929 | |||||||
chr10:75112956 | T | C | 3 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0019g0114 |
3 | HG02132.hp1 NA18940.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-16+1234T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75112956 | |||||||
chr10:75113154 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-16+1432T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113154 | |||||||
chr10:75113228 | A | C | 2 | a0001c0001t0002g0297 a0001c0001t0002g0298 |
2 | HG00735.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-16+1506A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113228 | |||||||
chr10:75113390 | C | CT | 8 | a0001c0001t0001g0111 a0001c0001t0003g0296 a0001c0001t0011g0301 others(5): Show |
8 | HG00642.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+1680dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75113390 | ||||||
chr10:75113411 | G | C | 1 | a0001c0001t0001g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-16+1689G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113411 | |||||||
chr10:75113587 | T | TG | 10 | a0001c0001t0005g0010 a0001c0001t0005g0286 a0001c0001t0005g0287 others(7): Show |
11 | HG01069.hp2 HG02451.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+1866dupG | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75113587 | ||||||
chr10:75113608 | C | A | 1 | a0001c0001t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-16+1886C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113608 | |||||||
chr10:75113669 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-16+1947T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113669 | |||||||
chr10:75113789 | C | T | 1 | a0001c0001t0004g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-16+2067C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113789 | |||||||
chr10:75113848 | T | C | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16+2126T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113848 | |||||||
chr10:75113996 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-16+2274T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75113996 | |||||||
chr10:75114194 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-16+2472T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114194 | |||||||
chr10:75114268 | AGCAGAG | A | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02071.hp2 HG02523.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+2548_-16+2553d others(8): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75114268 | ||||||
chr10:75114277 | T | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG02071.hp2 HG02523.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+2555T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114277 | |||||||
chr10:75114290 | C | G | 1 | a0001c0001t0020g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-16+2568C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114290 | |||||||
chr10:75114332 | C | CA | 92 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(89): Show |
98 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-16+2626dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75114332 | ||||||
chr10:75114332 | C | CAA | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-16+2625_-16+2626d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75114332 | ||||||
chr10:75114351 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-16+2629G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114351 | |||||||
chr10:75114363 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+2641G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114363 | |||||||
chr10:75114539 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0098 |
3 | HG00099.hp2 HG01099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-16+2817G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114539 | |||||||
chr10:75114701 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-16+2979C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114701 | |||||||
chr10:75114892 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 |
3 | NA18945.hp2 NA18955.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-16+3170T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114892 | |||||||
chr10:75114940 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16+3218A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75114940 | |||||||
chr10:75115113 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+3391C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115113 | |||||||
chr10:75115129 | A | G | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+3407A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115129 | |||||||
chr10:75115190 | A | G | 1 | a0001c0001t0012g0285 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-16+3468A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115190 | |||||||
chr10:75115471 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-16+3749A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115471 | |||||||
chr10:75115513 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-16+3791G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115513 | |||||||
chr10:75115662 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+3940C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115662 | |||||||
chr10:75115692 | G | A | 1 | a0001c0007t0011g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+3970G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115692 | |||||||
chr10:75115736 | C | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-16+4014C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115736 | |||||||
chr10:75115749 | G | A | 6 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+4027G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115749 | |||||||
chr10:75115834 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-16+4112A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115834 | |||||||
chr10:75115918 | G | A | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16+4196G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75115918 | |||||||
chr10:75115940 | C | CA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0104 a0001c0001t0002g0148 others(4): Show |
7 | HG01891.hp1 HG02723.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+4237dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75115940 | ||||||
chr10:75115940 | CA | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
43 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-16+4237delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75115940 | ||||||
chr10:75116161 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+4439G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116161 | |||||||
chr10:75116187 | C | T | 5 | a0001c0001t0003g0280 a0001c0001t0003g0282 a0001c0001t0003g0296 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+4465C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116187 | |||||||
chr10:75116317 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16+4595G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116317 | |||||||
chr10:75116322 | T | C | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+4600T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116322 | |||||||
chr10:75116339 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-16+4617C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116339 | |||||||
chr10:75116361 | C | A | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | HG02040.hp1 HG02080.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-16+4639C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116361 | |||||||
chr10:75116738 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+5016A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116738 | |||||||
chr10:75116847 | G | A | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+5125G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116847 | |||||||
chr10:75116901 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-16+5179C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116901 | |||||||
chr10:75116903 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-16+5181G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116903 | |||||||
chr10:75116935 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-16+5213C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116935 | |||||||
chr10:75116971 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-16+5249G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116971 | |||||||
chr10:75116975 | A | G | 3 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0007t0011g0300 |
3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-16+5253A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75116975 | |||||||
chr10:75117039 | C | T | 1 | a0001c0001t0005g0294 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-16+5317C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117039 | |||||||
chr10:75117242 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-16+5520G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117242 | |||||||
chr10:75117298 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-16+5576C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117298 | |||||||
chr10:75117379 | G | A | 1 | a0001c0001t0024g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-16+5657G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117379 | |||||||
chr10:75117384 | T | C | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+5662T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117384 | |||||||
chr10:75117424 | A | T | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-16+5702A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117424 | |||||||
chr10:75117441 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+5719G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117441 | |||||||
chr10:75117573 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+5851T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117573 | |||||||
chr10:75117673 | C | T | 12 | a0001c0001t0004g0117 a0001c0001t0004g0125 a0001c0001t0004g0126 others(9): Show |
12 | HG01123.hp2 HG01243.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16+5951C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75117673 | |||||||
chr10:75118084 | A | G | 3 | a0001c0001t0003g0278 a0001c0001t0029g0299 a0001c0001t0030g0295 |
3 | HG01099.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+6362A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118084 | |||||||
chr10:75118095 | C | T | 7 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0001t0005g0290 others(4): Show |
7 | HG01069.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+6373C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118095 | |||||||
chr10:75118139 | A | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+6417A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118139 | |||||||
chr10:75118167 | T | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01192.hp2 HG02015.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+6445T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118167 | |||||||
chr10:75118267 | G | A | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-16+6545G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118267 | |||||||
chr10:75118306 | A | G | 3 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0018g0210 |
3 | HG00735.hp2 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-16+6584A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118306 | |||||||
chr10:75118451 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+6729C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118451 | |||||||
chr10:75118604 | G | A | 1 | a0001c0001t0015g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-16+6882G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118604 | |||||||
chr10:75118804 | A | G | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+7082A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118804 | |||||||
chr10:75118825 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | NA18940.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-16+7103A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118825 | |||||||
chr10:75118946 | A | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+7224A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118946 | |||||||
chr10:75118979 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+7257G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75118979 | |||||||
chr10:75119121 | A | C | 1 | a0001c0001t0002g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-16+7399A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119121 | |||||||
chr10:75119277 | A | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-16+7555A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119277 | |||||||
chr10:75119379 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+7657A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119379 | |||||||
chr10:75119396 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+7674A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119396 | |||||||
chr10:75119403 | C | T | 1 | a0001c0001t0020g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-16+7681C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119403 | |||||||
chr10:75119493 | A | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+7771A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119493 | |||||||
chr10:75119635 | C | T | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+7913C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119635 | |||||||
chr10:75119804 | T | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-16+8082T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119804 | |||||||
chr10:75119929 | G | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+8207G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119929 | |||||||
chr10:75119936 | C | T | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | HG02040.hp1 HG02080.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-16+8214C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119936 | |||||||
chr10:75119989 | A | T | 1 | a0001c0001t0002g0209 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-16+8267A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75119989 | |||||||
chr10:75120040 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-16+8318C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120040 | |||||||
chr10:75120302 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | NA18978.hp1 NA18985.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-16+8580C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120302 | |||||||
chr10:75120503 | T | A | 1 | a0001c0001t0011g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-16+8781T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120503 | |||||||
chr10:75120505 | G | A | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16+8783G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120505 | |||||||
chr10:75120523 | C | G | 21 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(18): Show |
21 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16+8801C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120523 | |||||||
chr10:75120561 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+8839G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120561 | |||||||
chr10:75120564 | C | T | 21 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(18): Show |
21 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16+8842C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120564 | |||||||
chr10:75120565 | G | A | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16+8843G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120565 | |||||||
chr10:75120681 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0095 |
3 | HG03491.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-16+8959C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120681 | |||||||
chr10:75120739 | T | G | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG01257.hp2 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-16+9017T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120739 | |||||||
chr10:75120774 | C | CT | 35 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(32): Show |
36 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16+9076dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75120774 | ||||||
chr10:75120774 | C | CTT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0115 others(62): Show |
70 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-16+9075_-16+9076d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75120774 | ||||||
chr10:75120774 | C | CTTT | 10 | a0001c0001t0002g0112 a0001c0001t0002g0154 a0001c0001t0002g0203 others(7): Show |
10 | HG00609.hp1 HG00621.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+9074_-16+9076d others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75120774 | ||||||
chr10:75120774 | CT | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(16): Show |
19 | HG01123.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-16+9076delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75120774 | ||||||
chr10:75120774 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+9066_-16+9076d others(13): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75120774 | ||||||
chr10:75120802 | A | G | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01433.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+9080A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120802 | |||||||
chr10:75120905 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+9183C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75120905 | |||||||
chr10:75121242 | G | A | 6 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+9520G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121242 | |||||||
chr10:75121584 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-16+9862G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121584 | |||||||
chr10:75121672 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-16+9950A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121672 | |||||||
chr10:75121753 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+10031G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121753 | |||||||
chr10:75121770 | C | T | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+10048C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121770 | |||||||
chr10:75121824 | T | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG01192.hp2 HG02015.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10102T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121824 | |||||||
chr10:75121927 | A | T | 5 | a0001c0001t0003g0224 a0001c0001t0003g0226 a0001c0001t0003g0273 others(2): Show |
5 | HG00639.hp1 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10205A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121927 | |||||||
chr10:75121990 | C | G | 1 | a0001c0001t0003g0272 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-16+10268C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75121990 | |||||||
chr10:75122293 | T | C | 4 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0068 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10571T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122293 | |||||||
chr10:75122316 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG02040.hp2 HG02155.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+10594T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122316 | |||||||
chr10:75122349 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-16+10627C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122349 | |||||||
chr10:75122378 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | NA19055.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-16+10656G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122378 | |||||||
chr10:75122438 | C | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+10716C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122438 | |||||||
chr10:75122599 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0072 others(2): Show |
5 | HG00609.hp2 NA18966.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10877G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122599 | |||||||
chr10:75122612 | C | CA | 6 | a0001c0001t0002g0148 a0001c0001t0002g0161 a0001c0001t0002g0203 others(3): Show |
6 | HG00673.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+10908dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75122612 | ||||||
chr10:75122612 | CA | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
114 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-16+10908delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75122612 | ||||||
chr10:75122633 | C | A | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16+10911C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122633 | |||||||
chr10:75122658 | C | T | 1 | a0001c0001t0016g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-16+10936C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122658 | |||||||
chr10:75122823 | C | T | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+11101C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122823 | |||||||
chr10:75122824 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-16+11102G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122824 | |||||||
chr10:75122904 | C | T | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16+11182C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75122904 | |||||||
chr10:75123051 | T | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG00609.hp2 NA18945.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+11329T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123051 | |||||||
chr10:75123162 | T | TCACCCCA others(8): Show |
3 | a0001c0001t0001g0022 a0001c0005t0003g0217 a0001c0005t0003g0218 |
3 | HG02735.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16+11476_-16+1149 others(19): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123162 | ||||||
chr10:75123162 | TCACCC | T | 109 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(106): Show |
110 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-16+11486_-16+1149 others(9): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123162 | ||||||
chr10:75123162 | TCACCCCA others(3): Show |
T | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+11481_-16+1149 others(14): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123162 | ||||||
chr10:75123162 | TCACCCCA others(8): Show |
T | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0003g0282 others(3): Show |
6 | HG01099.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+11476_-16+1149 others(19): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123162 | ||||||
chr10:75123162 | TCACCCCA others(13): Show |
T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(29): Show |
36 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.-16+11471_-16+1149 others(24): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123162 | ||||||
chr10:75123229 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-16+11507C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123229 | |||||||
chr10:75123230 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+11508G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123230 | |||||||
chr10:75123421 | G | C | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+11699G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123421 | |||||||
chr10:75123422 | G | A | 6 | a0001c0001t0003g0227 a0001c0001t0011g0301 a0001c0001t0011g0302 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+11700G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123422 | |||||||
chr10:75123423 | G | A | 3 | a0001c0001t0026g0304 a0001c0005t0003g0217 a0001c0005t0003g0218 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-16+11701G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123423 | |||||||
chr10:75123428 | A | G | 20 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(17): Show |
20 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+11706A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123428 | |||||||
chr10:75123580 | A | C | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16+11858A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123580 | |||||||
chr10:75123591 | G | A | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16+11869G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123591 | |||||||
chr10:75123789 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-16+12067C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123789 | |||||||
chr10:75123813 | GAGAGTAG others(12): Show |
G | 4 | a0001c0001t0003g0265 a0001c0001t0010g0266 a0001c0001t0010g0267 others(1): Show |
4 | HG02080.hp2 NA18986.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+12120_-16+1213 others(23): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75123813 | ||||||
chr10:75123849 | C | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16+12127C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123849 | |||||||
chr10:75123903 | A | G | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-16+12181A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123903 | |||||||
chr10:75123916 | C | T | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+12194C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123916 | |||||||
chr10:75123970 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-16+12248C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75123970 | |||||||
chr10:75124117 | A | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+12395A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124117 | |||||||
chr10:75124473 | C | T | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16+12751C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124473 | |||||||
chr10:75124474 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-16+12752G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124474 | |||||||
chr10:75124534 | A | T | 1 | a0001c0001t0006g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+12812A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124534 | |||||||
chr10:75124612 | C | CA | 94 | a0001c0001t0001g0079 a0001c0001t0002g0001 a0001c0001t0002g0112 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+12907dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75124612 | ||||||
chr10:75124638 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+12916T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124638 | |||||||
chr10:75124655 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+12933G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124655 | |||||||
chr10:75124778 | C | T | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+13056C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124778 | |||||||
chr10:75124791 | ATTTTTCT others(5): Show |
A | 1 | a0001c0001t0003g0012 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-16+13079_-16+1309 others(16): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75124791 | ||||||
chr10:75124809 | C | CT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(18): Show |
25 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.-16+13099dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75124809 | ||||||
chr10:75124809 | CT | C | 94 | a0001c0001t0001g0104 a0001c0001t0002g0001 a0001c0001t0002g0112 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+13099delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75124809 | ||||||
chr10:75124871 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+13149G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124871 | |||||||
chr10:75124935 | T | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+13213T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124935 | |||||||
chr10:75124938 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-16+13216G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124938 | |||||||
chr10:75124948 | T | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+13226T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124948 | |||||||
chr10:75124970 | A | G | 1 | a0001c0001t0003g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-16+13248A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75124970 | |||||||
chr10:75125202 | A | G | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
78 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-16+13480A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125202 | |||||||
chr10:75125349 | A | C | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+13627A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125349 | |||||||
chr10:75125382 | A | G | 6 | a0001c0001t0003g0009 a0001c0001t0003g0260 a0001c0001t0003g0261 others(3): Show |
7 | HG01123.hp1 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+13660A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125382 | |||||||
chr10:75125668 | A | T | 1 | a0001c0001t0001g0019 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-16+13946A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125668 | |||||||
chr10:75125710 | T | C | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-16+13988T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125710 | |||||||
chr10:75125855 | C | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-16+14133C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125855 | |||||||
chr10:75125865 | C | T | 6 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+14143C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75125865 | |||||||
chr10:75126323 | G | A | 4 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0003g0143 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+14601G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75126323 | |||||||
chr10:75126449 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+14727G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75126449 | |||||||
chr10:75126499 | C | CT | 20 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0063 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+14797dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75126499 | ||||||
chr10:75126499 | CT | C | 10 | a0001c0001t0001g0040 a0001c0001t0002g0164 a0001c0001t0003g0265 others(7): Show |
10 | HG02080.hp2 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+14797delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75126499 | ||||||
chr10:75126620 | G | C | 1 | a0001c0001t0003g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-16+14898G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75126620 | |||||||
chr10:75126958 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+15236C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75126958 | |||||||
chr10:75127187 | C | CA | 228 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(225): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.-16+15483dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75127187 | ||||||
chr10:75127187 | C | CAA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0042 others(10): Show |
13 | HG00609.hp2 HG00642.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16+15482_-16+1548 others(6): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75127187 | ||||||
chr10:75127892 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-16+16170G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75127892 | |||||||
chr10:75128021 | G | A | 4 | a0001c0001t0002g0165 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | NA18960.hp1 NA18980.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+16299G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75128021 | |||||||
chr10:75128073 | A | AT | 13 | a0001c0001t0001g0092 a0001c0001t0002g0112 a0001c0001t0002g0208 others(10): Show |
13 | HG00642.hp2 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16+16372dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75128073 | ||||||
chr10:75128073 | AT | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-16+16372delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75128073 | ||||||
chr10:75128125 | T | G | 68 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(65): Show |
69 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-16+16403T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75128125 | |||||||
chr10:75128136 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+16414G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75128136 | |||||||
chr10:75128928 | C | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+17206C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75128928 | |||||||
chr10:75129045 | A | C | 1 | a0001c0001t0002g0198 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-16+17323A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129045 | |||||||
chr10:75129137 | T | TC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-16+17415_-16+1741 others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129137 | |||||||
chr10:75129138 | A | AT | 93 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(90): Show |
99 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.-16+17429dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75129138 | ||||||
chr10:75129138 | A | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0098 a0001c0001t0001g0107 others(1): Show |
4 | HG01099.hp1 HG02523.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+17416A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129138 | |||||||
chr10:75129138 | A | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.-16+17416A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129138 | |||||||
chr10:75129226 | C | T | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16+17504C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129226 | |||||||
chr10:75129309 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16+17587C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129309 | |||||||
chr10:75129360 | T | C | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-16+17638T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129360 | |||||||
chr10:75129400 | C | G | 1 | a0001c0001t0003g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-16+17678C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129400 | |||||||
chr10:75129533 | C | T | 1 | a0001c0001t0003g0278 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-16+17811C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75129533 | |||||||
chr10:75130031 | T | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-16+18309T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130031 | |||||||
chr10:75130239 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+18517C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130239 | |||||||
chr10:75130268 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-16+18546G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130268 | |||||||
chr10:75130434 | A | T | 1 | a0001c0001t0015g0060 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-16+18712A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130434 | |||||||
chr10:75130455 | G | A | 95 | a0001c0001t0001g0084 a0001c0001t0002g0001 a0001c0001t0002g0112 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+18733G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130455 | |||||||
chr10:75130616 | A | AC | 3 | a0001c0001t0003g0226 a0001c0001t0003g0273 a0001c0001t0003g0274 |
3 | HG00639.hp1 HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-16+18894_-16+1889 others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130616 | |||||||
chr10:75130913 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-16+19191A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75130913 | |||||||
chr10:75131282 | G | T | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15-19232G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131282 | |||||||
chr10:75131284 | A | G | 1 | a0001c0001t0005g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-15-19230A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131284 | |||||||
chr10:75131338 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-15-19176T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131338 | |||||||
chr10:75131366 | A | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG00558.hp2 HG00621.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-19148A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131366 | |||||||
chr10:75131525 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15-18989G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131525 | |||||||
chr10:75131648 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-15-18866A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131648 | |||||||
chr10:75131669 | T | A | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-18845T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131669 | |||||||
chr10:75131944 | G | T | 1 | a0001c0001t0005g0010 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-15-18570G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75131944 | |||||||
chr10:75132169 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-15-18345C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132169 | |||||||
chr10:75132175 | T | G | 1 | a0001c0001t0015g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15-18339T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132175 | |||||||
chr10:75132234 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-15-18280C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132234 | |||||||
chr10:75132272 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-15-18242G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132272 | |||||||
chr10:75132447 | G | A | 3 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0007t0011g0300 |
3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-15-18067G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132447 | |||||||
chr10:75132453 | C | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(90): Show |
99 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.-15-18061C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132453 | |||||||
chr10:75132657 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15-17857C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132657 | |||||||
chr10:75132696 | AT | A | 233 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-15-17807delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75132696 | ||||||
chr10:75132726 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-15-17788C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132726 | |||||||
chr10:75132800 | G | C | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-17714G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132800 | |||||||
chr10:75132937 | C | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(90): Show |
99 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.-15-17577C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75132937 | |||||||
chr10:75133097 | G | A | 1 | a0001c0001t0004g0133 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-15-17417G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133097 | |||||||
chr10:75133139 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-15-17375G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133139 | |||||||
chr10:75133237 | CA | C | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-15-17269delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75133237 | ||||||
chr10:75133281 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-15-17233T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133281 | |||||||
chr10:75133336 | G | T | 1 | a0001c0001t0003g0271 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-15-17178G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133336 | |||||||
chr10:75133361 | C | T | 2 | a0001c0001t0003g0011 a0001c0001t0003g0012 |
2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-15-17153C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133361 | |||||||
chr10:75133362 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-15-17152C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133362 | |||||||
chr10:75133432 | C | T | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-17082C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133432 | |||||||
chr10:75133433 | G | A | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15-17081G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133433 | |||||||
chr10:75133768 | G | C | 1 | a0001c0001t0002g0172 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-15-16746G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133768 | |||||||
chr10:75133887 | A | C | 1 | a0001c0001t0002g0203 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-15-16627A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133887 | |||||||
chr10:75133929 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-16585C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75133929 | |||||||
chr10:75134042 | C | T | 6 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-16472C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134042 | |||||||
chr10:75134224 | T | G | 1 | a0001c0001t0003g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-15-16290T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134224 | |||||||
chr10:75134270 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15-16244G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134270 | |||||||
chr10:75134495 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-16019C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134495 | |||||||
chr10:75134615 | G | A | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-15-15899G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134615 | |||||||
chr10:75134626 | CT | C | 29 | a0001c0001t0002g0149 a0001c0001t0003g0139 a0001c0001t0003g0140 others(26): Show |
29 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-15885delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75134626 | ||||||
chr10:75134628 | T | A | 27 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(24): Show |
27 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15-15886T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134628 | |||||||
chr10:75134639 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-15-15875A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134639 | |||||||
chr10:75134783 | G | A | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-15731G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134783 | |||||||
chr10:75134873 | A | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-15641A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134873 | |||||||
chr10:75134941 | G | C | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-15573G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134941 | |||||||
chr10:75134956 | G | A | 7 | a0001c0001t0005g0288 a0001c0001t0005g0289 a0001c0001t0005g0290 others(4): Show |
7 | HG01069.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-15558G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75134956 | |||||||
chr10:75135067 | A | G | 1 | a0001c0001t0010g0268 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-15-15447A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135067 | |||||||
chr10:75135122 | C | T | 4 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0192 others(1): Show |
4 | HG02132.hp1 NA18940.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-15392C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135122 | |||||||
chr10:75135220 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG01891.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-15-15294A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135220 | |||||||
chr10:75135223 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-15291C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135223 | |||||||
chr10:75135308 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15-15206T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135308 | |||||||
chr10:75135440 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-15-15074C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135440 | |||||||
chr10:75135453 | CA | C | 122 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0075 others(119): Show |
128 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-15-15045delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75135453 | ||||||
chr10:75135475 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-15039C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135475 | |||||||
chr10:75135621 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01433.hp2 HG02451.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-14893C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135621 | |||||||
chr10:75135656 | T | G | 2 | a0001c0001t0004g0125 a0001c0001t0004g0127 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15-14858T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135656 | |||||||
chr10:75135657 | C | A | 1 | a0001c0001t0007g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-14857C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135657 | |||||||
chr10:75135860 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA18939.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-15-14654T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135860 | |||||||
chr10:75135970 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-15-14544C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75135970 | |||||||
chr10:75136453 | T | C | 3 | a0001c0001t0003g0227 a0001c0001t0003g0232 a0001c0001t0003g0233 |
3 | HG03491.hp2 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-15-14061T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75136453 | |||||||
chr10:75136804 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.-15-13710T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75136804 | |||||||
chr10:75136815 | T | A | 4 | a0001c0003t0007g0120 a0001c0003t0007g0121 a0001c0003t0007g0122 others(1): Show |
4 | HG02015.hp2 HG02155.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-13699T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75136815 | |||||||
chr10:75136841 | A | G | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15-13673A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75136841 | |||||||
chr10:75137015 | A | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-13499A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137015 | |||||||
chr10:75137109 | G | A | 5 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-13405G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137109 | |||||||
chr10:75137229 | T | C | 4 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0068 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-13285T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137229 | |||||||
chr10:75137231 | T | C | 1 | a0001c0001t0005g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-15-13283T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137231 | |||||||
chr10:75137265 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-13249C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137265 | |||||||
chr10:75137325 | A | C | 1 | a0001c0001t0002g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15-13189A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137325 | |||||||
chr10:75137384 | AC | A | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG00558.hp2 HG00621.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-13129delC | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137384 | |||||||
chr10:75137465 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-15-13049G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137465 | |||||||
chr10:75137505 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15-13009A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137505 | |||||||
chr10:75137539 | C | CA | 51 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
51 | HG00609.hp2 HG00639.hp2 HG02040.hp2 others(48): Show |
intron_variant | MODIFIER | c.-15-12961dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75137539 | ||||||
chr10:75137615 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-15-12899C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137615 | |||||||
chr10:75137778 | A | G | 2 | a0001c0001t0002g0192 a0001c0001t0019g0114 |
2 | NA19007.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-15-12736A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137778 | |||||||
chr10:75137813 | C | T | 2 | a0001c0001t0003g0253 a0001c0001t0003g0258 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-15-12701C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137813 | |||||||
chr10:75137999 | C | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-12515C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75137999 | |||||||
chr10:75138452 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15-12062C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138452 | |||||||
chr10:75138633 | A | C | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-11881A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138633 | |||||||
chr10:75138694 | T | G | 1 | a0001c0001t0007g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-11820T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138694 | |||||||
chr10:75138749 | T | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-11765T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138749 | |||||||
chr10:75138786 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-15-11728C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138786 | |||||||
chr10:75138895 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15-11619C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138895 | |||||||
chr10:75138930 | T | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-11584T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138930 | |||||||
chr10:75138958 | C | CT | 9 | a0001c0001t0002g0148 a0001c0001t0002g0161 a0001c0001t0002g0165 others(6): Show |
9 | HG00642.hp2 HG00673.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-11537dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75138958 | ||||||
chr10:75138958 | CTTTTTTT others(4): Show |
C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-11547_-15-1153 others(15): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75138958 | ||||||
chr10:75138962 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-15-11552T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138962 | |||||||
chr10:75138963 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-15-11551T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75138963 | |||||||
chr10:75139000 | G | A | 2 | a0001c0001t0003g0228 a0001c0001t0003g0270 |
2 | NA18951.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-15-11514G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139000 | |||||||
chr10:75139101 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0002g0204 |
2 | NA18947.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-15-11413C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139101 | |||||||
chr10:75139118 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15-11396G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139118 | |||||||
chr10:75139203 | A | G | 1 | a0001c0003t0007g0123 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-15-11311A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139203 | |||||||
chr10:75139220 | C | T | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-15-11294C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139220 | |||||||
chr10:75139253 | G | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-15-11261G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139253 | |||||||
chr10:75139360 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-15-11154T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139360 | |||||||
chr10:75139507 | T | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15-11007T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139507 | |||||||
chr10:75139735 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-15-10779T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75139735 | |||||||
chr10:75140009 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.-15-10505G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75140009 | |||||||
chr10:75140009 | G | T | 5 | a0001c0001t0003g0225 a0001c0001t0003g0249 a0001c0001t0003g0250 others(2): Show |
5 | NA18953.hp2 NA18970.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-10505G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75140009 | |||||||
chr10:75140429 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-10085C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75140429 | |||||||
chr10:75140475 | C | G | 3 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0018g0210 |
3 | HG00735.hp2 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-15-10039C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75140475 | |||||||
chr10:75140792 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-15-9722C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75140792 | |||||||
chr10:75141056 | A | G | 4 | a0001c0001t0002g0162 a0001c0001t0002g0188 a0001c0001t0002g0189 others(1): Show |
4 | HG01175.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-9458A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141056 | |||||||
chr10:75141091 | C | G | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15-9423C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141091 | |||||||
chr10:75141101 | G | A | 1 | a0001c0001t0004g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15-9413G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141101 | |||||||
chr10:75141211 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0059 |
2 | HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-15-9303A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141211 | |||||||
chr10:75141227 | A | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15-9287A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141227 | |||||||
chr10:75141308 | C | T | 2 | a0001c0001t0005g0286 a0001c0001t0005g0287 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-15-9206C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141308 | |||||||
chr10:75141538 | C | CT | 12 | a0001c0001t0001g0038 a0001c0001t0002g0162 a0001c0001t0002g0187 others(9): Show |
12 | HG01175.hp2 HG02056.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-8959dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75141538 | ||||||
chr10:75141538 | CT | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
33 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.-15-8959delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75141538 | ||||||
chr10:75141615 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-15-8899C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141615 | |||||||
chr10:75141743 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-8771G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141743 | |||||||
chr10:75141777 | A | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-8737A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141777 | |||||||
chr10:75141807 | C | T | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15-8707C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141807 | |||||||
chr10:75141830 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01192.hp2 HG02015.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-8684C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141830 | |||||||
chr10:75141870 | A | G | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-8644A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75141870 | |||||||
chr10:75142341 | A | G | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15-8173A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142341 | |||||||
chr10:75142514 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-8000G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142514 | |||||||
chr10:75142678 | G | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15-7836G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142678 | |||||||
chr10:75142724 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0090 others(2): Show |
6 | HG00099.hp2 HG01099.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-7790C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142724 | |||||||
chr10:75142775 | C | G | 4 | a0001c0001t0003g0265 a0001c0001t0010g0266 a0001c0001t0010g0267 others(1): Show |
4 | HG02080.hp2 NA18986.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-7739C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142775 | |||||||
chr10:75142892 | A | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-7622A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75142892 | |||||||
chr10:75143060 | G | A | 1 | a0001c0001t0018g0210 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-15-7454G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143060 | |||||||
chr10:75143183 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15-7331C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143183 | |||||||
chr10:75143309 | A | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-7205A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143309 | |||||||
chr10:75143415 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-15-7099G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143415 | |||||||
chr10:75143632 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15-6882A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143632 | |||||||
chr10:75143732 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-15-6782G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143732 | |||||||
chr10:75143808 | A | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-15-6706A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143808 | |||||||
chr10:75143892 | C | T | 1 | a0001c0001t0003g0260 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-15-6622C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143892 | |||||||
chr10:75143966 | C | CT | 15 | a0001c0001t0001g0057 a0001c0001t0001g0074 a0001c0001t0001g0075 others(12): Show |
15 | HG01361.hp2 HG02056.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15-6530dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75143966 | ||||||
chr10:75143997 | T | C | 2 | a0001c0002t0001g0068 a0001c0002t0001g0136 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-15-6517T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75143997 | |||||||
chr10:75144160 | G | A | 3 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0007t0011g0300 |
3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-15-6354G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75144160 | |||||||
chr10:75144207 | A | AT | 288 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-15-6307_-15-6306i others(3): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75144207 | |||||||
chr10:75144296 | ATTAAGTA others(224): Show |
A | 6 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-6216_-15-5986d others(2): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75144296 | ||||||
chr10:75144379 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.-15-6135G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75144379 | |||||||
chr10:75145243 | A | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-5271A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145243 | |||||||
chr10:75145500 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG00639.hp2 NA18961.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-5014T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145500 | |||||||
chr10:75145749 | A | G | 6 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-4765A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145749 | |||||||
chr10:75145764 | A | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15-4750A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145764 | |||||||
chr10:75145821 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-15-4693T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145821 | |||||||
chr10:75145905 | A | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-4609A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145905 | |||||||
chr10:75145940 | A | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-15-4574A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75145940 | |||||||
chr10:75146272 | C | CT | 20 | a0001c0001t0003g0012 a0001c0001t0003g0139 a0001c0001t0003g0140 others(17): Show |
20 | HG00280.hp2 HG00642.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-4214dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75146272 | ||||||
chr10:75146272 | CT | C | 38 | a0001c0001t0002g0112 a0001c0001t0002g0146 a0001c0001t0002g0148 others(35): Show |
38 | HG00735.hp1 HG00735.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.-15-4214delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75146272 | ||||||
chr10:75146272 | CTT | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0042 others(80): Show |
90 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-15-4215_-15-4214d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75146272 | ||||||
chr10:75146272 | CTTT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(87): Show |
94 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15-4216_-15-4214d others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75146272 | ||||||
chr10:75146295 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG00639.hp2 NA18961.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-4219T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146295 | |||||||
chr10:75146811 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15-3703C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146811 | |||||||
chr10:75146894 | G | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-3620G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146894 | |||||||
chr10:75146915 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15-3599G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146915 | |||||||
chr10:75146949 | A | G | 1 | a0001c0001t0010g0267 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-15-3565A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146949 | |||||||
chr10:75146969 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-15-3545C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75146969 | |||||||
chr10:75147080 | C | T | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-3434C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147080 | |||||||
chr10:75147113 | T | C | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-3401T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147113 | |||||||
chr10:75147145 | A | T | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02165.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-15-3369A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147145 | |||||||
chr10:75147572 | C | T | 7 | a0001c0001t0003g0008 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
8 | HG00642.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-2942C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147572 | |||||||
chr10:75147603 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-15-2911G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147603 | |||||||
chr10:75147755 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-15-2759A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147755 | |||||||
chr10:75147792 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0022g0222 |
2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-15-2722C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147792 | |||||||
chr10:75147827 | G | A | 5 | a0001c0001t0007g0124 a0001c0003t0007g0120 a0001c0003t0007g0121 others(2): Show |
5 | HG02015.hp2 HG02155.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-2687G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75147827 | |||||||
chr10:75148336 | G | C | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
78 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-15-2178G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75148336 | |||||||
chr10:75148346 | C | CT | 14 | a0001c0001t0003g0007 a0001c0001t0003g0011 a0001c0001t0003g0230 others(11): Show |
15 | HG00642.hp2 HG01123.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15-2143dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT | 6 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2149_-15-2143d others(9): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(3): Show |
21 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0028 others(18): Show |
22 | HG00140.hp2 HG00639.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.-15-2152_-15-2143d others(12): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0022 others(23): Show |
26 | HG01433.hp2 HG02015.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-15-2153_-15-2143d others(13): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0048 others(13): Show |
16 | HG00558.hp2 HG01192.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15-2154_-15-2143d others(14): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0041 others(3): Show |
6 | HG02300.hp1 HG03492.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-2155_-15-2143d others(15): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-15-2156_-15-2143d others(16): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0004g0134 a0001c0001t0004g0137 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15-2157_-15-2143d others(17): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0104 a0001c0001t0004g0117 a0001c0001t0004g0133 |
3 | HG01243.hp2 NA19082.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-15-2159_-15-2143d others(19): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(11): Show |
4 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0135 others(1): Show |
4 | HG02717.hp2 HG03540.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2160_-15-2143d others(20): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0013g0305 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-2161_-15-2143d others(21): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0003g0139 a0001c0001t0013g0306 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-15-2162_-15-2143d others(22): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0004g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-15-2164_-15-2143d others(24): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0003g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-2165_-15-2143d others(25): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0004g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15-2166_-15-2143d others(26): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0001c0001t0004g0129 |
3 | HG01123.hp2 HG03130.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15-2143_-15-2142i others(30): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0004g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15-2143_-15-2142i others(31): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(23): Show |
2 | a0001c0001t0003g0143 a0001c0001t0004g0128 |
2 | HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-15-2143_-15-2142i others(32): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0007g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-2143_-15-2142i others(36): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTT | C | 7 | a0001c0001t0005g0010 a0001c0001t0005g0288 a0001c0001t0005g0289 others(4): Show |
8 | HG01069.hp2 HG02451.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-2144_-15-2143d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTTTT | C | 8 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0096 others(5): Show |
8 | HG00423.hp2 HG00741.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-2146_-15-2143d others(6): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTTTTT | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-15-2147_-15-2143d others(7): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG00609.hp2 NA18945.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-2151_-15-2143d others(11): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTTTTTTT others(3): Show |
C | 1 | a0001c0005t0003g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-2152_-15-2143d others(12): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148346 | CTTTTTTT others(4): Show |
C | 1 | a0001c0005t0003g0217 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-15-2153_-15-2143d others(13): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148346 | ||||||
chr10:75148514 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-15-2000C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75148514 | |||||||
chr10:75148515 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15-1999G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75148515 | |||||||
chr10:75148623 | G | A | 1 | a0001c0001t0007g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-1891G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75148623 | |||||||
chr10:75148714 | A | G | 2 | a0001c0001t0004g0134 a0001c0001t0004g0135 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-15-1800A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75148714 | |||||||
chr10:75148891 | GA | G | 5 | a0001c0001t0003g0280 a0001c0001t0003g0282 a0001c0001t0003g0296 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1619delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75148891 | ||||||
chr10:75149038 | C | T | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15-1476C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149038 | |||||||
chr10:75149247 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-15-1267G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149247 | |||||||
chr10:75149444 | C | T | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-15-1070C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149444 | |||||||
chr10:75149600 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-15-914C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149600 | |||||||
chr10:75149686 | T | C | 1 | a0001c0001t0007g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-15-828T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149686 | |||||||
chr10:75149804 | T | G | 12 | a0001c0001t0004g0117 a0001c0001t0004g0125 a0001c0001t0004g0126 others(9): Show |
12 | HG01123.hp2 HG01243.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-15-710T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75149804 | |||||||
chr10:75150059 | CGT | C | 29 | a0001c0001t0002g0179 a0001c0001t0003g0139 a0001c0001t0003g0140 others(26): Show |
29 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-442_-15-441del others(2): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75150059 | ||||||
chr10:75150086 | C | T | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-428C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75150086 | |||||||
chr10:75150095 | C | CAT | 6 | a0001c0001t0003g0007 a0001c0001t0003g0255 a0001c0001t0003g0272 others(3): Show |
7 | HG00642.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-405_-15-404dup others(2): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75150095 | ||||||
chr10:75150118 | GT | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-387delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75150118 | ||||||
chr10:75150119 | T | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-395T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75150119 | |||||||
chr10:75150194 | T | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-15-320T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | chr10 | 75150194 | |||||||
chr10:75150279 | AT | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-15-214delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr10 | 75150279 | ||||||
chr10:75151550 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.578+444C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151550 | |||||||
chr10:75151614 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.578+508A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151614 | |||||||
chr10:75151649 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.578+543G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151649 | |||||||
chr10:75151768 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+662C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151768 | |||||||
chr10:75151771 | C | T | 1 | a0001c0001t0020g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.578+665C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151771 | |||||||
chr10:75151941 | G | A | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+835G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75151941 | |||||||
chr10:75152047 | C | T | 3 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | HG02040.hp1 HG02080.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.578+941C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152047 | |||||||
chr10:75152058 | TA | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.578+953delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152058 | |||||||
chr10:75152059 | A | T | 115 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
115 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.578+953A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152059 | |||||||
chr10:75152114 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.578+1008A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152114 | |||||||
chr10:75152173 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.578+1067C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152173 | |||||||
chr10:75152251 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+1145G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152251 | |||||||
chr10:75152261 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+1155G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152261 | |||||||
chr10:75152378 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.578+1272C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152378 | |||||||
chr10:75152516 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.578+1410C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152516 | |||||||
chr10:75152523 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.578+1417A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152523 | |||||||
chr10:75152536 | GA | G | 22 | a0001c0001t0002g0181 a0001c0001t0004g0117 a0001c0001t0004g0118 others(19): Show |
22 | HG00642.hp2 HG01123.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.578+1442delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75152536 | ||||||
chr10:75152540 | A | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.578+1434A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152540 | |||||||
chr10:75152586 | C | A | 1 | a0001c0001t0003g0236 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.578+1480C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152586 | |||||||
chr10:75152642 | C | T | 1 | a0001c0001t0015g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.578+1536C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152642 | |||||||
chr10:75152768 | A | G | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.578+1662A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152768 | |||||||
chr10:75152853 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.578+1747G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152853 | |||||||
chr10:75152875 | A | T | 1 | a0001c0001t0002g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.578+1769A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75152875 | |||||||
chr10:75153003 | A | G | 1 | a0001c0001t0003g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.578+1897A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153003 | |||||||
chr10:75153139 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.578+2033G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153139 | |||||||
chr10:75153163 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+2057G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153163 | |||||||
chr10:75153171 | G | A | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.578+2065G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153171 | |||||||
chr10:75153188 | G | T | 1 | a0001c0001t0003g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.578+2082G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153188 | |||||||
chr10:75153271 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.578+2165T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153271 | |||||||
chr10:75153367 | C | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.578+2261C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153367 | |||||||
chr10:75153455 | A | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.578+2349A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153455 | |||||||
chr10:75153588 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+2482C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153588 | |||||||
chr10:75153589 | G | C | 2 | a0001c0001t0002g0145 a0001c0001t0002g0155 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.578+2483G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153589 | |||||||
chr10:75153690 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.578+2584G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153690 | |||||||
chr10:75153760 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.578+2654A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153760 | |||||||
chr10:75153762 | GA | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.578+2657delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153762 | |||||||
chr10:75153765 | G | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.578+2659G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75153765 | |||||||
chr10:75154120 | G | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.578+3014G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154120 | |||||||
chr10:75154301 | T | C | 2 | a0001c0001t0003g0253 a0001c0001t0003g0258 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.578+3195T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154301 | |||||||
chr10:75154552 | A | G | 4 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0158 others(1): Show |
4 | HG01081.hp2 HG01891.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+3446A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154552 | |||||||
chr10:75154590 | A | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+3484A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154590 | |||||||
chr10:75154677 | T | TG | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.578+3575dupG | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75154677 | ||||||
chr10:75154691 | G | A | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.578+3585G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154691 | |||||||
chr10:75154836 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.578+3730T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154836 | |||||||
chr10:75154838 | A | G | 1 | a0001c0001t0003g0250 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.578+3732A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154838 | |||||||
chr10:75154865 | G | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.578+3759G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154865 | |||||||
chr10:75154941 | G | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.578+3835G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154941 | |||||||
chr10:75154947 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.578+3841T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75154947 | |||||||
chr10:75155049 | A | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.578+3943A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155049 | |||||||
chr10:75155125 | C | G | 1 | a0001c0001t0028g0205 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.578+4019C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155125 | |||||||
chr10:75155257 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.578+4151C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155257 | |||||||
chr10:75155274 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0061 a0001c0001t0001g0063 others(6): Show |
9 | HG00558.hp2 HG00621.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.578+4168T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155274 | |||||||
chr10:75155448 | G | T | 20 | a0001c0001t0004g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(17): Show |
20 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.578+4342G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155448 | |||||||
chr10:75155503 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.578+4397T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155503 | |||||||
chr10:75155533 | T | G | 3 | a0001c0001t0002g0162 a0001c0001t0002g0188 a0001c0001t0002g0189 |
3 | HG01433.hp1 HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.578+4427T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155533 | |||||||
chr10:75155619 | A | G | 1 | a0001c0001t0003g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.578+4513A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155619 | |||||||
chr10:75155765 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.578+4659A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155765 | |||||||
chr10:75155766 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.578+4660G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155766 | |||||||
chr10:75155832 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0085 others(4): Show |
9 | HG00544.hp1 NA18939.hp1 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.578+4726A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75155832 | |||||||
chr10:75156232 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.578+5126A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156232 | |||||||
chr10:75156258 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.578+5152C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156258 | |||||||
chr10:75156259 | GA | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.578+5157delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75156259 | ||||||
chr10:75156598 | G | C | 6 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.578+5492G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156598 | |||||||
chr10:75156600 | C | T | 1 | a0001c0001t0004g0117 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.578+5494C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156600 | |||||||
chr10:75156613 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.578+5507G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156613 | |||||||
chr10:75156638 | C | CA | 31 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(28): Show |
31 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.578+5545dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75156638 | ||||||
chr10:75156672 | C | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0069 others(6): Show |
9 | HG00558.hp2 HG00621.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.578+5566C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156672 | |||||||
chr10:75156674 | A | T | 1 | a0001c0001t0002g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.578+5568A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156674 | |||||||
chr10:75156833 | C | G | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.578+5727C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156833 | |||||||
chr10:75156934 | T | C | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.578+5828T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156934 | |||||||
chr10:75156944 | G | A | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.578+5838G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75156944 | |||||||
chr10:75157136 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.578+6030G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157136 | |||||||
chr10:75157234 | G | GGA | 6 | a0001c0001t0007g0124 a0001c0001t0007g0130 a0001c0003t0007g0120 others(3): Show |
6 | HG02015.hp2 HG02155.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+6149_578+6150d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75157234 | ||||||
chr10:75157482 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0017g0054 |
2 | NA18944.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.578+6376G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157482 | |||||||
chr10:75157668 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.578+6562C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157668 | |||||||
chr10:75157690 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.578+6584G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157690 | |||||||
chr10:75157881 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.579-6764C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157881 | |||||||
chr10:75157975 | C | G | 2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.579-6670C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75157975 | |||||||
chr10:75158122 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.579-6523G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158122 | |||||||
chr10:75158185 | G | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.579-6460G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158185 | |||||||
chr10:75158341 | C | T | 1 | a0001c0001t0009g0058 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.579-6304C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158341 | |||||||
chr10:75158656 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.579-5989A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158656 | |||||||
chr10:75158799 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-5846C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158799 | |||||||
chr10:75158882 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.579-5763A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158882 | |||||||
chr10:75158940 | T | A | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-5705T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75158940 | |||||||
chr10:75159015 | G | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0255 a0001c0001t0003g0272 |
4 | HG02257.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-5630G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159015 | |||||||
chr10:75159063 | C | CTTTTTTT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
121 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.579-5575_579-5569d others(9): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75159063 | ||||||
chr10:75159063 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0061 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.579-5576_579-5569d others(10): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75159063 | ||||||
chr10:75159063 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-5578_579-5569d others(12): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75159063 | ||||||
chr10:75159132 | C | T | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.579-5513C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159132 | |||||||
chr10:75159172 | C | T | 2 | a0001c0001t0003g0228 a0001c0001t0003g0270 |
2 | NA18951.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.579-5473C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159172 | |||||||
chr10:75159301 | G | A | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-5344G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159301 | |||||||
chr10:75159347 | C | T | 6 | a0001c0001t0003g0009 a0001c0001t0003g0260 a0001c0001t0003g0261 others(3): Show |
7 | HG01123.hp1 HG01255.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.579-5298C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159347 | |||||||
chr10:75159515 | C | T | 68 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(65): Show |
69 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.579-5130C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159515 | |||||||
chr10:75159554 | C | T | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579-5091C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159554 | |||||||
chr10:75159743 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.579-4902C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159743 | |||||||
chr10:75159776 | C | T | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.579-4869C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159776 | |||||||
chr10:75159777 | T | A | 3 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0018g0210 |
3 | HG00735.hp2 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.579-4868T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75159777 | |||||||
chr10:75160051 | A | AG | 231 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.579-4594_579-4593i others(3): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160051 | |||||||
chr10:75160051 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.579-4594A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160051 | |||||||
chr10:75160190 | T | C | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.579-4455T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160190 | |||||||
chr10:75160335 | T | C | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-4310T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160335 | |||||||
chr10:75160354 | G | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.579-4291G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160354 | |||||||
chr10:75160363 | A | AT | 8 | a0001c0001t0003g0008 a0001c0001t0003g0242 a0001c0001t0003g0243 others(5): Show |
9 | HG00642.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.579-4267dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75160363 | ||||||
chr10:75160363 | AT | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.579-4267delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75160363 | ||||||
chr10:75160441 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.579-4204T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160441 | |||||||
chr10:75160590 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.579-4055G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75160590 | |||||||
chr10:75161102 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.579-3543C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161102 | |||||||
chr10:75161208 | A | C | 7 | a0001c0001t0003g0008 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
8 | HG00642.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.579-3437A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161208 | |||||||
chr10:75161310 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.579-3335C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161310 | |||||||
chr10:75161436 | A | T | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
78 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.579-3209A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161436 | |||||||
chr10:75161483 | A | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-3162A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161483 | |||||||
chr10:75161584 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.579-3061A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161584 | |||||||
chr10:75161705 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0004g0118 |
2 | HG02258.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.579-2940A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75161705 | |||||||
chr10:75162163 | G | A | 1 | a0001c0001t0005g0010 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.579-2482G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162163 | |||||||
chr10:75162253 | G | C | 1 | a0001c0001t0005g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.579-2392G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162253 | |||||||
chr10:75162345 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.579-2300C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162345 | |||||||
chr10:75162369 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.579-2276G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162369 | |||||||
chr10:75162393 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.579-2252T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162393 | |||||||
chr10:75162495 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.579-2150C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162495 | |||||||
chr10:75162603 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-2042C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162603 | |||||||
chr10:75162649 | CA | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
138 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.579-1975delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75162649 | ||||||
chr10:75162649 | CAA | C | 92 | a0001c0001t0001g0089 a0001c0001t0002g0001 a0001c0001t0002g0113 others(89): Show |
98 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.579-1976_579-1975d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75162649 | ||||||
chr10:75162690 | G | C | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.579-1955G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162690 | |||||||
chr10:75162858 | A | G | 2 | a0001c0001t0004g0134 a0001c0001t0004g0135 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.579-1787A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75162858 | |||||||
chr10:75163189 | T | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579-1456T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163189 | |||||||
chr10:75163278 | A | G | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.579-1367A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163278 | |||||||
chr10:75163362 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-1283A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163362 | |||||||
chr10:75163530 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.579-1115C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163530 | |||||||
chr10:75163679 | T | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.579-966T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163679 | |||||||
chr10:75163779 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.579-866T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75163779 | |||||||
chr10:75164153 | G | A | 2 | a0001c0001t0005g0286 a0001c0001t0005g0287 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.579-492G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164153 | |||||||
chr10:75164166 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.579-479T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164166 | |||||||
chr10:75164167 | G | A | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-478G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164167 | |||||||
chr10:75164189 | A | G | 1 | a0001c0001t0003g0244 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.579-456A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164189 | |||||||
chr10:75164251 | A | G | 4 | a0001c0001t0002g0207 a0001c0001t0008g0219 a0001c0001t0008g0221 others(1): Show |
4 | NA18951.hp1 NA19063.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-394A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164251 | |||||||
chr10:75164282 | A | G | 6 | a0001c0001t0006g0147 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01081.hp2 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-363A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164282 | |||||||
chr10:75164362 | G | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(72): Show |
80 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.579-283G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164362 | |||||||
chr10:75164386 | C | CT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.579-244dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr10 | 75164386 | ||||||
chr10:75164401 | T | C | 1 | a0001c0001t0005g0010 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.579-244T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 2/5 | chr10 | 75164401 | |||||||
chr10:75164745 | C | T | 6 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(3): Show |
6 | HG01167.hp2 HG01257.hp2 HG01346.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.674+5C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75164745 | |||||||
chr10:75164751 | A | C | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.674+11A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75164751 | |||||||
chr10:75164952 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.674+212G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75164952 | |||||||
chr10:75165065 | C | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0155 a0001c0001t0002g0194 |
3 | HG00099.hp1 HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.674+325C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165065 | |||||||
chr10:75165251 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.674+511C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165251 | |||||||
chr10:75165273 | A | C | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.674+533A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165273 | |||||||
chr10:75165425 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.674+685C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165425 | |||||||
chr10:75165539 | G | A | 2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.674+799G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165539 | |||||||
chr10:75165670 | C | CA | 8 | a0001c0001t0001g0109 a0001c0001t0003g0246 a0001c0001t0006g0212 others(5): Show |
8 | HG00642.hp1 HG02071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.674+946dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr10 | 75165670 | ||||||
chr10:75165908 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.674+1168C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75165908 | |||||||
chr10:75165977 | C | CA | 41 | a0001c0001t0001g0040 a0001c0001t0001g0073 a0001c0001t0001g0085 others(38): Show |
41 | HG00621.hp2 HG00673.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.674+1258dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr10 | 75165977 | ||||||
chr10:75166013 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.674+1273T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166013 | |||||||
chr10:75166063 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.674+1323T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166063 | |||||||
chr10:75166304 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.674+1564C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166304 | |||||||
chr10:75166318 | A | G | 94 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.674+1578A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166318 | |||||||
chr10:75166331 | A | C | 6 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(3): Show |
6 | HG01167.hp2 HG01257.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.674+1591A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166331 | |||||||
chr10:75166397 | T | TA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
108 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.674+1671dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr10 | 75166397 | ||||||
chr10:75166397 | TA | T | 9 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0209 others(6): Show |
9 | HG00639.hp1 HG00733.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.674+1671delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr10 | 75166397 | ||||||
chr10:75166502 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.674+1762G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166502 | |||||||
chr10:75166525 | T | C | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.674+1785T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166525 | |||||||
chr10:75166786 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.675-1755T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166786 | |||||||
chr10:75166855 | G | A | 2 | a0001c0005t0003g0217 a0001c0005t0003g0218 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.675-1686G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166855 | |||||||
chr10:75166945 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.675-1596T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75166945 | |||||||
chr10:75167038 | T | A | 30 | a0001c0001t0003g0008 a0001c0001t0003g0011 a0001c0001t0003g0012 others(27): Show |
31 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.675-1503T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167038 | |||||||
chr10:75167170 | A | T | 1 | a0001c0001t0002g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.675-1371A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167170 | |||||||
chr10:75167179 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675-1362T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167179 | |||||||
chr10:75167202 | TAA | T | 3 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 |
3 | NA18990.hp1 NA19074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.675-1338_675-1337d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167202 | |||||||
chr10:75167460 | G | A | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.675-1081G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167460 | |||||||
chr10:75167836 | T | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0255 |
3 | HG02257.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.675-705T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167836 | |||||||
chr10:75167849 | T | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.675-692T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167849 | |||||||
chr10:75167898 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.675-643T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167898 | |||||||
chr10:75167907 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.675-634T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167907 | |||||||
chr10:75167921 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.675-620G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167921 | |||||||
chr10:75167938 | G | A | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.675-603G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167938 | |||||||
chr10:75167999 | A | G | 1 | a0001c0001t0003g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.675-542A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75167999 | |||||||
chr10:75168153 | C | T | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
78 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.675-388C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168153 | |||||||
chr10:75168310 | T | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-231T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168310 | |||||||
chr10:75168362 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-179C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168362 | |||||||
chr10:75168391 | G | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.675-150G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168391 | |||||||
chr10:75168393 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.675-148T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168393 | |||||||
chr10:75168428 | A | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.675-113A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 3/5 | chr10 | 75168428 | |||||||
chr10:75168809 | G | C | 1 | a0001c0001t0029g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.792+151G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75168809 | |||||||
chr10:75168819 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.792+161A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75168819 | |||||||
chr10:75168882 | G | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0255 |
3 | HG02257.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.792+224G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75168882 | |||||||
chr10:75168933 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.792+275G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75168933 | |||||||
chr10:75168934 | A | G | 1 | a0001c0001t0002g0176 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.792+276A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75168934 | |||||||
chr10:75169153 | G | C | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.792+495G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169153 | |||||||
chr10:75169169 | C | CA | 61 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0073 others(58): Show |
62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.792+535dupA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75169169 | ||||||
chr10:75169169 | C | CAA | 54 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0115 others(51): Show |
59 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.792+534_792+535dup others(2): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75169169 | ||||||
chr10:75169169 | C | CAAA | 20 | a0001c0001t0002g0112 a0001c0001t0002g0146 a0001c0001t0002g0148 others(17): Show |
20 | HG00673.hp1 HG00735.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.792+533_792+535dup others(3): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75169169 | ||||||
chr10:75169169 | CA | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(19): Show |
24 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.792+535delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75169169 | ||||||
chr10:75169199 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.792+541T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169199 | |||||||
chr10:75169385 | T | C | 2 | a0001c0001t0016g0013 a0001c0001t0016g0014 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.792+727T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169385 | |||||||
chr10:75169418 | G | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.792+760G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169418 | |||||||
chr10:75169463 | C | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.792+805C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169463 | |||||||
chr10:75169487 | CAAAGAAA others(1): Show |
C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.792+849_792+856del others(8): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75169487 | ||||||
chr10:75169651 | C | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.792+993C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169651 | |||||||
chr10:75169690 | G | A | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.792+1032G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169690 | |||||||
chr10:75169801 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.792+1143C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75169801 | |||||||
chr10:75170122 | G | A | 1 | a0001c0001t0005g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.792+1464G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170122 | |||||||
chr10:75170254 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.792+1596C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170254 | |||||||
chr10:75170341 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
107 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.792+1683A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170341 | |||||||
chr10:75170412 | T | C | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.792+1754T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170412 | |||||||
chr10:75170416 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.792+1758C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170416 | |||||||
chr10:75170591 | A | C | 3 | a0001c0001t0004g0125 a0001c0001t0004g0127 a0001c0001t0004g0128 |
3 | HG01123.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.792+1933A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170591 | |||||||
chr10:75170770 | G | GT | 27 | a0001c0001t0003g0012 a0001c0001t0003g0225 a0001c0001t0003g0227 others(24): Show |
27 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.792+2133dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75170770 | ||||||
chr10:75170770 | G | T | 1 | a0001c0001t0002g0164 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.792+2112G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170770 | |||||||
chr10:75170770 | GT | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.792+2133delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75170770 | ||||||
chr10:75170783 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.792+2125T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170783 | |||||||
chr10:75170786 | T | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
8 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2128T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170786 | |||||||
chr10:75170789 | T | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.792+2131T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170789 | |||||||
chr10:75170842 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.792+2184T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170842 | |||||||
chr10:75170864 | C | A | 2 | a0001c0001t0005g0286 a0001c0001t0005g0287 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.792+2206C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170864 | |||||||
chr10:75170990 | A | C | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.792+2332A>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75170990 | |||||||
chr10:75171151 | TTTC | T | 5 | a0001c0001t0005g0293 a0001c0001t0006g0147 a0001c0001t0006g0156 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2496_792+2498d others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171151 | ||||||
chr10:75171154 | CTTTTTCT others(6): Show |
C | 4 | a0001c0001t0003g0265 a0001c0001t0010g0266 a0001c0001t0010g0267 others(1): Show |
4 | HG02080.hp2 NA18986.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2502_792+2514d others(15): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171154 | ||||||
chr10:75171158 | T | C | 2 | a0001c0001t0006g0159 a0001c0001t0006g0160 |
2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.792+2500T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171158 | |||||||
chr10:75171159 | T | C | 5 | a0001c0001t0005g0293 a0001c0001t0006g0147 a0001c0001t0006g0156 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2501T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171159 | |||||||
chr10:75171160 | C | CT | 81 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0055 others(78): Show |
87 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.792+2526dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | C | CTT | 37 | a0001c0001t0002g0145 a0001c0001t0002g0148 a0001c0001t0002g0176 others(34): Show |
37 | HG00741.hp1 HG01123.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.792+2525_792+2526d others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | C | CTTT | 7 | a0001c0001t0003g0139 a0001c0001t0004g0117 a0001c0001t0004g0118 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2524_792+2526d others(5): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | C | T | 8 | a0001c0001t0002g0215 a0001c0001t0005g0293 a0001c0001t0006g0147 others(5): Show |
8 | HG01081.hp2 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2502C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171160 | |||||||
chr10:75171160 | CT | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0087 a0001c0001t0001g0094 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2526delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
7 | HG01433.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2518_792+2526d others(11): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0071 a0001c0001t0025g0067 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.792+2517_792+2526d others(12): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171160 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.792+2515_792+2526d others(14): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75171160 | ||||||
chr10:75171177 | T | C | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.792+2519T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171177 | |||||||
chr10:75171236 | G | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.792+2578G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171236 | |||||||
chr10:75171358 | G | A | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.792+2700G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171358 | |||||||
chr10:75171414 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.792+2756G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171414 | |||||||
chr10:75171547 | C | A | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.792+2889C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171547 | |||||||
chr10:75171799 | C | T | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+3141C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171799 | |||||||
chr10:75171963 | C | T | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.792+3305C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75171963 | |||||||
chr10:75172011 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
29 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.792+3353G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172011 | |||||||
chr10:75172021 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.792+3363A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172021 | |||||||
chr10:75172025 | CA | C | 30 | a0001c0001t0001g0042 a0001c0001t0003g0139 a0001c0001t0003g0140 others(27): Show |
30 | HG00609.hp2 HG01123.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.792+3383delA | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75172025 | ||||||
chr10:75172144 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.792+3486C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172144 | |||||||
chr10:75172251 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.792+3593T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172251 | |||||||
chr10:75172363 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.793-3703G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172363 | |||||||
chr10:75172483 | C | T | 1 | a0001c0001t0007g0124 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.793-3583C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172483 | |||||||
chr10:75172501 | AT | A | 6 | a0001c0001t0003g0270 a0001c0001t0003g0271 a0001c0001t0004g0137 others(3): Show |
6 | HG01517.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-3550delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75172501 | ||||||
chr10:75172561 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-3505G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172561 | |||||||
chr10:75172627 | A | G | 12 | a0001c0001t0004g0117 a0001c0001t0004g0125 a0001c0001t0004g0126 others(9): Show |
12 | HG01123.hp2 HG01243.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.793-3439A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172627 | |||||||
chr10:75172643 | G | A | 4 | a0001c0001t0002g0165 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | NA18960.hp1 NA18980.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-3423G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172643 | |||||||
chr10:75172708 | G | T | 2 | a0001c0002t0001g0068 a0001c0002t0001g0136 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.793-3358G>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172708 | |||||||
chr10:75172746 | T | C | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.793-3320T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172746 | |||||||
chr10:75172762 | C | T | 7 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-3304C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172762 | |||||||
chr10:75172822 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793-3244C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75172822 | |||||||
chr10:75173023 | A | G | 1 | a0001c0001t0023g0303 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.793-3043A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75173023 | |||||||
chr10:75173313 | T | A | 1 | a0001c0001t0026g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.793-2753T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75173313 | |||||||
chr10:75173442 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.793-2624C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75173442 | |||||||
chr10:75173510 | T | G | 2 | a0001c0001t0003g0227 a0001c0001t0003g0233 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.793-2556T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75173510 | |||||||
chr10:75173554 | A | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-2512A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75173554 | |||||||
chr10:75174048 | ATTATG | A | 6 | a0001c0001t0003g0008 a0001c0001t0003g0242 a0001c0001t0003g0243 others(3): Show |
7 | HG00642.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-2013_793-2009d others(7): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75174048 | ||||||
chr10:75174127 | T | G | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793-1939T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174127 | |||||||
chr10:75174212 | C | A | 1 | a0001c0001t0003g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.793-1854C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174212 | |||||||
chr10:75174264 | G | A | 1 | a0001c0001t0005g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793-1802G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174264 | |||||||
chr10:75174308 | T | G | 5 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0001t0016g0013 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-1758T>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174308 | |||||||
chr10:75174343 | A | G | 1 | a0001c0001t0030g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.793-1723A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174343 | |||||||
chr10:75174343 | A | T | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.793-1723A>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174343 | |||||||
chr10:75174430 | C | CT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0069 a0001c0001t0001g0110 others(5): Show |
8 | HG02080.hp1 HG02145.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-1615dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75174430 | ||||||
chr10:75174430 | CT | C | 17 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0056 others(14): Show |
17 | HG01069.hp2 HG01099.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-1615delT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75174430 | ||||||
chr10:75174626 | G | GT | 235 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.793-1436dupT | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75174626 | ||||||
chr10:75174670 | T | A | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793-1396T>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174670 | |||||||
chr10:75174684 | C | T | 28 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(25): Show |
28 | HG01123.hp2 HG01243.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.793-1382C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174684 | |||||||
chr10:75174737 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.793-1329G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174737 | |||||||
chr10:75174819 | GC | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
106 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.793-1246delC | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174819 | |||||||
chr10:75174820 | C | T | 2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.793-1246C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174820 | |||||||
chr10:75174831 | G | C | 6 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(3): Show |
6 | HG02145.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-1235G>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174831 | |||||||
chr10:75174944 | G | A | 5 | a0001c0001t0003g0225 a0001c0001t0003g0249 a0001c0001t0003g0250 others(2): Show |
5 | NA18953.hp2 NA18970.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-1122G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75174944 | |||||||
chr10:75175156 | C | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793-910C>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175156 | |||||||
chr10:75175186 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.793-880A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175186 | |||||||
chr10:75175226 | A | G | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793-840A>G | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175226 | |||||||
chr10:75175367 | G | A | 3 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0018g0210 |
3 | HG00735.hp2 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.793-699G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175367 | |||||||
chr10:75175515 | C | CATTT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0059 a0001c0001t0001g0061 others(17): Show |
20 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.793-526_793-523dup others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75175515 | ||||||
chr10:75175515 | CATTT | C | 7 | a0001c0001t0003g0235 a0001c0001t0011g0301 a0001c0001t0011g0302 others(4): Show |
7 | HG01496.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-526_793-523del others(4): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75175515 | ||||||
chr10:75175588 | G | A | 2 | a0001c0001t0029g0299 a0001c0001t0030g0295 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793-478G>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175588 | |||||||
chr10:75175699 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-367C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175699 | |||||||
chr10:75175753 | T | C | 95 | a0001c0001t0002g0001 a0001c0001t0002g0112 a0001c0001t0002g0113 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.793-313T>C | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75175753 | |||||||
chr10:75175932 | A | ACTG | 3 | a0001c0001t0011g0301 a0001c0001t0011g0302 a0001c0007t0011g0300 |
3 | HG02486.hp1 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.793-133_793-131dup others(3): Show |
SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr10 | 75175932 | ||||||
chr10:75176021 | C | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | NA18978.hp1 NA18985.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.793-45C>A | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75176021 | |||||||
chr10:75176024 | C | T | 2 | a0001c0001t0013g0305 a0001c0001t0013g0306 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793-42C>T | SAMD8 | ENSG00000156671.15 | transcript | ENST00000542569.6 | protein_coding | 4/5 | chr10 | 75176024 |