Item | Value |
---|---|
geneid | 148418 |
ensemblid | ENSG00000203943.9 |
hgncid | 24582 |
symbol | SAMD13 |
name | sterile alpha motif domain containing 13 |
refseq_nuc | NM_001134663.2 |
refseq_prot | NP_001128135.1 |
ensembl_nuc | ENST00000394834.8 |
ensembl_prot | ENSP00000378311.3 |
mane_status | MANE Select |
chr | chr1 |
start | 84301708 |
end | 84350798 |
strand | + |
ver | v1.2 |
region | chr1:84301708-84350798 |
region5000 | chr1:84296708-84355798 |
regionname0 | SAMD13_chr1_84301708_84350798 |
regionname5000 | SAMD13_chr1_84296708_84355798 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 306 | 297 | 73 | 64 | 122 | 11 | 25 | SAMD13_chr1_84296708_84355798 | SAMD13 | ATGCT others(301): Show |
chr1 | 84296708 | 84355798 | ||
a0001c0002 | 0/0 | 306 | 18 | 8 | 0 | 0 | 3 | 7 | SAMD13_chr1_84296708_84355798 | SAMD13 | ATGCT others(301): Show |
chr1 | 84296708 | 84355798 | ||
a0001c0003 | 0/0 | 306 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | ATGCT others(301): Show |
chr1 | 84296708 | 84355798 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1459 | 283 | 69 | 60 | 118 | 11 | 24 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0002 | 0/0 | 1461 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1456): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0003 | 0/0 | 1459 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0004 | 0/0 | 1459 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0006 | 0/0 | 1459 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0007 | 0/1 | 1459 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0001t0008 | 0/0 | 1459 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0002t0001 | 0/0 | 1459 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
a0001c0002t0002 | 0/0 | 1461 | 10 | 0 | 0 | 0 | 3 | 7 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1456): Show |
chr1 | 84296708 | 84355798 |
a0001c0002t0005 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1456): Show |
chr1 | 84296708 | 84355798 |
a0001c0003t0001 | 0/0 | 1459 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | CCTTT others(1454): Show |
chr1 | 84296708 | 84355798 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0007g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0003 | 0/0 | 6 | 0 | 0 | 0 | 1 | 5 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0179 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0235 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0087 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0088 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03516 | hp1 | a0001 | c0002 | t0005 | g0250 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03540 | hp1 | a0001 | c0002 | t0005 | g0249 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0171 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | TSI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | GIH | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | GIH | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0103 | REF | REF | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0212 | REF | REF | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84325691 | C | T | 1 | a0001c0002 | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.108C>T | p.Val36Val | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/4 | 234/1459 | 108/309 | 36/102 | chr1 | 84325691 | |||
chr1:84325709 | C | T | 1 | a0001c0003 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.126C>T | p.Thr42Thr | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/4 | 252/1459 | 126/309 | 42/102 | chr1 | 84325709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84349785 | T | C | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 |
14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 11 | chr1 | 84349785 | ||||||
chr1:84349879 | G | A | 1 | a0001c0001t0003 | 4 | NA18944.hp1 NA18957.hp1 NA18985.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 105 | chr1 | 84349879 | ||||||
chr1:84349899 | G | A | 1 | a0001c0001t0004 | 4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*125G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 125 | chr1 | 84349899 | ||||||
chr1:84350203 | C | T | 1 | a0001c0001t0008 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 429 | chr1 | 84350203 | ||||||
chr1:84350246 | C | A | 1 | a0001c0002t0005 | 2 | HG03516.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 472 | chr1 | 84350246 | ||||||
chr1:84350388 | G | A | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 |
14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*614G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 614 | chr1 | 84350388 | ||||||
chr1:84350440 | C | T | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(7): Show |
312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*666C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 666 | chr1 | 84350440 | ||||||
chr1:84350565 | A | C | 4 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 others(1): Show |
16 | HG00639.hp1 HG01175.hp2 HG01516.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 791 | chr1 | 84350565 | ||||||
chr1:84350643 | C | CTT | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0005 |
14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*871_*872dupTT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 873 | INFO_REALIGN_3_PRIME | chr1 | 84350643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84302308 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-33+507G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84302308 | |||||||
chr1:84302337 | CT | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-33+554delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | ||||||
chr1:84302337 | CTT | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
13 | HG00099.hp1 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+553_-33+554del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | ||||||
chr1:84302337 | CTTT | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0039 others(9): Show |
15 | HG01081.hp2 HG01169.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+552_-33+554del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | ||||||
chr1:84302541 | T | TAC | 24 | a0001c0001t0001g0017 a0001c0001t0001g0071 a0001c0001t0001g0072 others(21): Show |
25 | HG00323.hp1 HG00544.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32-627_-32-626dup others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | T | TACAC | 14 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 others(11): Show |
15 | HG00741.hp2 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-629_-32-626dup others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TAC | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
57 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-32-627_-32-626del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TACAC | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0050 others(14): Show |
19 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-32-629_-32-626del others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TACACAC | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(18): Show |
29 | HG00099.hp1 HG01081.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32-631_-32-626del others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0199 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-633_-32-626del others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(2): Show |
5 | HG02559.hp1 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-635_-32-626del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302541 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-32-639_-32-626del others(14): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | ||||||
chr1:84302782 | C | A | 4 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0070 others(1): Show |
4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-421C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84302782 | |||||||
chr1:84303072 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-32-131T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84303072 | |||||||
chr1:84303178 | C | T | 9 | a0001c0001t0001g0049 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-25C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84303178 | |||||||
chr1:84303596 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.53+309C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303596 | |||||||
chr1:84303644 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.53+357T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303644 | |||||||
chr1:84303650 | G | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0066 a0001c0001t0001g0067 others(5): Show |
9 | HG01109.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+363G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303650 | |||||||
chr1:84303739 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+452C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303739 | |||||||
chr1:84303847 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0094 |
3 | HG02257.hp2 HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.53+560G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303847 | |||||||
chr1:84304219 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+932C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304219 | |||||||
chr1:84304284 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0173 a0001c0001t0001g0174 |
4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+997A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304284 | |||||||
chr1:84304362 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.53+1075A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304362 | |||||||
chr1:84304666 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.53+1379T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304666 | |||||||
chr1:84304672 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.53+1385G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304672 | |||||||
chr1:84304735 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.53+1448A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304735 | |||||||
chr1:84304785 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.53+1498A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304785 | |||||||
chr1:84304926 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+1639T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304926 | |||||||
chr1:84305315 | A | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 others(3): Show |
6 | HG01175.hp2 HG01981.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+2028A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305315 | |||||||
chr1:84305553 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53+2266T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305553 | |||||||
chr1:84305816 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+2529T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305816 | |||||||
chr1:84306072 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.53+2785T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306072 | |||||||
chr1:84306312 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.53+3025T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306312 | |||||||
chr1:84306368 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+3081G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306368 | |||||||
chr1:84306381 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53+3094C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306381 | |||||||
chr1:84306523 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.53+3236G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306523 | |||||||
chr1:84306634 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+3347C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306634 | |||||||
chr1:84306644 | C | CA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.53+3376dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306644 | ||||||
chr1:84306661 | AAAG | A | 14 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0197 others(11): Show |
20 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.53+3376_53+3378del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306661 | ||||||
chr1:84306662 | AAG | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(54): Show |
76 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.53+3391_53+3392del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306662 | ||||||
chr1:84306664 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.53+3377G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306664 | |||||||
chr1:84306685 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0244 others(4): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+3398G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306685 | |||||||
chr1:84306830 | A | AAAT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.53+3567_53+3569dup others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | ||||||
chr1:84306830 | A | AAATAATA others(8): Show |
1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+3555_53+3569dup others(15): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | ||||||
chr1:84306830 | AAAT | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(9): Show |
15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+3567_53+3569del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | ||||||
chr1:84306831 | A | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(37): Show |
55 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.53+3544A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306831 | |||||||
chr1:84306834 | A | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(9): Show |
15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+3547A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306834 | |||||||
chr1:84306856 | A | ATAAT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0067 a0001c0001t0001g0068 others(5): Show |
9 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+3569_53+3570ins others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306856 | |||||||
chr1:84306856 | A | ATAATAAT others(3): Show |
1 | a0001c0001t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53+3569_53+3570ins others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306856 | |||||||
chr1:84306859 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0030 others(42): Show |
50 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.53+3572T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306859 | |||||||
chr1:84307159 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02630.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.53+3872G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307159 | |||||||
chr1:84307208 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.53+3921T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307208 | |||||||
chr1:84307235 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53+3948T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307235 | |||||||
chr1:84307414 | A | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
8 | HG01099.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+4127A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307414 | |||||||
chr1:84307454 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.53+4167T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307454 | |||||||
chr1:84307624 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53+4337G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307624 | |||||||
chr1:84307788 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.53+4501A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307788 | |||||||
chr1:84308130 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+4843G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308130 | |||||||
chr1:84308135 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0162 |
2 | NA18965.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.53+4848G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308135 | |||||||
chr1:84308202 | T | G | 13 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0240 others(10): Show |
19 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.53+4915T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308202 | |||||||
chr1:84308292 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.53+5005A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308292 | |||||||
chr1:84308366 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.53+5079T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308366 | |||||||
chr1:84308387 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5100C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308387 | |||||||
chr1:84308650 | GCTTT | G | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5372_53+5375del others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84308650 | ||||||
chr1:84308790 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5503T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308790 | |||||||
chr1:84309017 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5730A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309017 | |||||||
chr1:84309068 | A | G | 13 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0240 others(10): Show |
19 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.53+5781A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309068 | |||||||
chr1:84309121 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.53+5834A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309121 | |||||||
chr1:84309216 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+5929C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309216 | |||||||
chr1:84309274 | G | A | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5987G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309274 | |||||||
chr1:84309378 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.53+6091A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309378 | |||||||
chr1:84309442 | A | C | 11 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 others(8): Show |
12 | HG01175.hp2 HG01891.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+6155A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309442 | |||||||
chr1:84309444 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.53+6157T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309444 | |||||||
chr1:84309585 | A | G | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+6298A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309585 | |||||||
chr1:84309711 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.53+6424A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309711 | |||||||
chr1:84309713 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.53+6426A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309713 | |||||||
chr1:84309860 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.53+6573A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309860 | |||||||
chr1:84309862 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.53+6575G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309862 | |||||||
chr1:84309908 | A | G | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+6621A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309908 | |||||||
chr1:84310241 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.53+6954T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310241 | |||||||
chr1:84310342 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.53+7055T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310342 | |||||||
chr1:84310361 | G | GA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
8 | HG01099.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+7085dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84310361 | ||||||
chr1:84310428 | TC | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0072 |
4 | HG01243.hp2 HG01952.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+7143delC | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84310428 | ||||||
chr1:84310779 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53+7492G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310779 | |||||||
chr1:84310804 | C | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(9): Show |
15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+7517C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310804 | |||||||
chr1:84310858 | T | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.53+7571T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310858 | |||||||
chr1:84310866 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 |
3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.53+7579T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310866 | |||||||
chr1:84310932 | T | C | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+7645T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310932 | |||||||
chr1:84310998 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+7711A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310998 | |||||||
chr1:84311101 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.53+7814C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311101 | |||||||
chr1:84311133 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.53+7846C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311133 | |||||||
chr1:84311157 | GAAATCCC others(10): Show |
G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+7874_53+7890del others(17): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311157 | ||||||
chr1:84311189 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53+7902A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311189 | |||||||
chr1:84311332 | T | TA | 17 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
23 | HG01099.hp2 HG01516.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.53+8063dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311332 | ||||||
chr1:84311332 | TA | T | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+8063delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311332 | ||||||
chr1:84311341 | AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+8059_53+8068del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311341 | ||||||
chr1:84311346 | A | AG | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+8059_53+8060ins others(1): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311346 | |||||||
chr1:84311346 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(60): Show |
71 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.53+8059A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311346 | |||||||
chr1:84311346 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.53+8074_53+8083del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311346 | ||||||
chr1:84311357 | A | G | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+8070A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311357 | |||||||
chr1:84311393 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+8106C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311393 | |||||||
chr1:84311624 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+8337C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311624 | |||||||
chr1:84311694 | C | T | 10 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0240 others(7): Show |
16 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+8407C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311694 | |||||||
chr1:84311823 | T | C | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+8536T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311823 | |||||||
chr1:84311860 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA19082.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.53+8573A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311860 | |||||||
chr1:84311992 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+8705T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311992 | |||||||
chr1:84312008 | G | C | 2 | a0001c0002t0005g0249 a0001c0002t0005g0250 |
2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53+8721G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312008 | |||||||
chr1:84312148 | GT | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.53+8869delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84312148 | ||||||
chr1:84312226 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0006g0179 |
2 | HG00639.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.53+8939T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312226 | |||||||
chr1:84312538 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.53+9251C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312538 | |||||||
chr1:84312548 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0199 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.53+9261A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312548 | |||||||
chr1:84312614 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0002t0002g0003 others(6): Show |
15 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+9327C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312614 | |||||||
chr1:84312615 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(9): Show |
15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+9328G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312615 | |||||||
chr1:84312690 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.53+9403G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312690 | |||||||
chr1:84312743 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.53+9456A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312743 | |||||||
chr1:84312950 | G | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+9663G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312950 | |||||||
chr1:84313187 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+9900T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313187 | |||||||
chr1:84313216 | A | T | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+9929A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313216 | |||||||
chr1:84313339 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+10052T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313339 | |||||||
chr1:84313345 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.53+10058C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313345 | |||||||
chr1:84313446 | T | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
9 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+10159T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313446 | |||||||
chr1:84313816 | G | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+10529G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313816 | |||||||
chr1:84313924 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.53+10637A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313924 | |||||||
chr1:84313958 | T | C | 8 | a0001c0001t0001g0037 a0001c0002t0002g0003 a0001c0002t0002g0086 others(5): Show |
14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+10671T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313958 | |||||||
chr1:84314311 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.53+11024A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314311 | |||||||
chr1:84314333 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
9 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+11046C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314333 | |||||||
chr1:84314335 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.53+11048G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314335 | |||||||
chr1:84314405 | A | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(9): Show |
15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+11118A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314405 | |||||||
chr1:84314592 | C | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-11045C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314592 | |||||||
chr1:84314961 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-10676C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314961 | |||||||
chr1:84315009 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-10628T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315009 | |||||||
chr1:84315145 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.54-10492A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315145 | |||||||
chr1:84315160 | G | T | 1 | a0001c0001t0003g0153 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.54-10477G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315160 | |||||||
chr1:84315169 | A | C | 1 | a0001c0001t0001g0239 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.54-10468A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315169 | |||||||
chr1:84315308 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54-10329A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315308 | |||||||
chr1:84315332 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.54-10305T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315332 | |||||||
chr1:84315542 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0245 |
4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-10095C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315542 | |||||||
chr1:84315700 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0199 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.54-9937G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315700 | |||||||
chr1:84315750 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.54-9887G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315750 | |||||||
chr1:84315875 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-9762A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315875 | |||||||
chr1:84315909 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.54-9728A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315909 | |||||||
chr1:84316039 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.54-9598T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316039 | |||||||
chr1:84316120 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0180 others(1): Show |
4 | HG00639.hp1 HG01884.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-9517C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316120 | |||||||
chr1:84316134 | T | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-9503T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316134 | |||||||
chr1:84316144 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
27 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.54-9493A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316144 | |||||||
chr1:84316263 | CT | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.54-9369delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84316263 | ||||||
chr1:84316309 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.54-9328G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316309 | |||||||
chr1:84316359 | A | T | 1 | a0001c0001t0004g0058 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.54-9278A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316359 | |||||||
chr1:84316400 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.54-9237A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316400 | |||||||
chr1:84316410 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54-9227A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316410 | |||||||
chr1:84316645 | G | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0056 others(11): Show |
17 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.54-8992G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316645 | |||||||
chr1:84316958 | C | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 |
3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-8679C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316958 | |||||||
chr1:84317177 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0004g0057 others(3): Show |
7 | HG01891.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-8460C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317177 | |||||||
chr1:84317232 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.54-8405C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317232 | |||||||
chr1:84317518 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.54-8119A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317518 | |||||||
chr1:84317563 | A | G | 14 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(11): Show |
16 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-8074A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317563 | |||||||
chr1:84317578 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 |
3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-8059T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317578 | |||||||
chr1:84317687 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.54-7950T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317687 | |||||||
chr1:84317871 | T | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.54-7766T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317871 | |||||||
chr1:84318060 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 |
3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-7577G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318060 | |||||||
chr1:84318079 | T | G | 14 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(11): Show |
16 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-7558T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318079 | |||||||
chr1:84318287 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-7350A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318287 | |||||||
chr1:84318389 | T | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-7248T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318389 | |||||||
chr1:84318430 | C | G | 4 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0070 others(1): Show |
4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-7207C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318430 | |||||||
chr1:84318442 | A | G | 7 | a0001c0002t0002g0003 a0001c0002t0002g0086 a0001c0002t0002g0087 others(4): Show |
12 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-7195A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318442 | |||||||
chr1:84318546 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54-7091A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318546 | |||||||
chr1:84318971 | G | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00741.hp2 HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.54-6666G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318971 | |||||||
chr1:84319111 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-6526A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319111 | |||||||
chr1:84319157 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-6480T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319157 | |||||||
chr1:84319181 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-6456C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319181 | |||||||
chr1:84319549 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0196 |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-6088C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319549 | |||||||
chr1:84319624 | GA | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(45): Show |
63 | HG00544.hp2 HG00673.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.54-5996delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | ||||||
chr1:84319624 | GAA | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
19 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-5997_54-5996del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | ||||||
chr1:84319624 | GAAA | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0067 others(7): Show |
12 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5998_54-5996del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | ||||||
chr1:84319645 | G | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0054 others(7): Show |
12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5992G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319645 | |||||||
chr1:84319723 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.54-5914G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319723 | |||||||
chr1:84319887 | G | A | 3 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0002g0088 |
3 | HG01516.hp2 HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.54-5750G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319887 | |||||||
chr1:84320110 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0004g0057 others(3): Show |
7 | HG01891.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-5527C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320110 | |||||||
chr1:84320211 | T | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0197 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-5426T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320211 | |||||||
chr1:84320243 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0072 |
3 | NA18949.hp2 NA18956.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.54-5394G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320243 | |||||||
chr1:84320273 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.54-5364C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320273 | |||||||
chr1:84320293 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.54-5344G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320293 | |||||||
chr1:84320314 | G | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0045 |
2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.54-5323G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320314 | |||||||
chr1:84320407 | T | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0134 a0001c0001t0003g0153 |
4 | NA18944.hp1 NA18957.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5230T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320407 | |||||||
chr1:84320530 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.54-5107C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320530 | |||||||
chr1:84320540 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-5097G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320540 | |||||||
chr1:84320585 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-5052A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320585 | |||||||
chr1:84320742 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.54-4895A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320742 | |||||||
chr1:84320914 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.54-4723C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320914 | |||||||
chr1:84321135 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-4502G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321135 | |||||||
chr1:84321345 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.54-4292T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321345 | |||||||
chr1:84321351 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.54-4286T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321351 | |||||||
chr1:84321365 | A | AAT | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-4263_54-4262dup others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84321365 | ||||||
chr1:84321518 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54-4119A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321518 | |||||||
chr1:84321566 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.54-4071A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321566 | |||||||
chr1:84321628 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54-4009G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321628 | |||||||
chr1:84321629 | A | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(173): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.54-4008A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321629 | |||||||
chr1:84321657 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0182 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.54-3980A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321657 | |||||||
chr1:84321700 | A | G | 3 | a0001c0001t0001g0083 a0001c0001t0001g0148 a0001c0001t0001g0167 |
3 | NA18971.hp2 NA18988.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.54-3937A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321700 | |||||||
chr1:84321995 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG02027.hp1 HG03704.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.54-3642C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321995 | |||||||
chr1:84322069 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.54-3568G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322069 | |||||||
chr1:84322465 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-3172G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322465 | |||||||
chr1:84322475 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-3162C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322475 | |||||||
chr1:84322521 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-3116A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322521 | |||||||
chr1:84322525 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54-3112T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322525 | |||||||
chr1:84322762 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0234 |
5 | NA18954.hp1 NA18962.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-2875C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322762 | |||||||
chr1:84322773 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.54-2864G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322773 | |||||||
chr1:84322853 | A | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-2784A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322853 | |||||||
chr1:84322853 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-2784A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322853 | |||||||
chr1:84323031 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(209): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.54-2606G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323031 | |||||||
chr1:84323107 | T | C | 12 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(9): Show |
18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-2530T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323107 | |||||||
chr1:84323189 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54-2448A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323189 | |||||||
chr1:84323206 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0056 others(10): Show |
16 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-2431G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323206 | |||||||
chr1:84323307 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.54-2330T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323307 | |||||||
chr1:84323308 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.54-2329A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323308 | |||||||
chr1:84323309 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-2328A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323309 | |||||||
chr1:84323536 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.54-2101G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323536 | |||||||
chr1:84323583 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.54-2054C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323583 | |||||||
chr1:84323733 | A | G | 36 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(33): Show |
42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.54-1904A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323733 | |||||||
chr1:84323772 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.54-1865T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323772 | |||||||
chr1:84324122 | C | G | 12 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(9): Show |
18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-1515C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324122 | |||||||
chr1:84324435 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.54-1202C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324435 | |||||||
chr1:84324477 | T | G | 1 | a0001c0001t0001g0023 | 2 | NA18978.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.54-1160T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324477 | |||||||
chr1:84324572 | G | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.54-1065G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324572 | |||||||
chr1:84324672 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0199 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.54-965G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324672 | |||||||
chr1:84324742 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.54-895C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324742 | |||||||
chr1:84324743 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-894G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324743 | |||||||
chr1:84325257 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0135 others(1): Show |
5 | HG02071.hp1 NA18974.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-380G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84325257 | |||||||
chr1:84325556 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.54-81T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84325556 | |||||||
chr1:84325918 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+170T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84325918 | |||||||
chr1:84326032 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.165+284G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326032 | |||||||
chr1:84326374 | G | A | 2 | a0001c0001t0001g0175 a0001c0003t0001g0040 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+626G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326374 | |||||||
chr1:84326379 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+631T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326379 | |||||||
chr1:84326420 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+672T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326420 | |||||||
chr1:84326574 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+826G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326574 | |||||||
chr1:84326798 | G | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(8): Show |
14 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+1050G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326798 | |||||||
chr1:84326804 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+1056G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326804 | |||||||
chr1:84326923 | G | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(33): Show |
42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.165+1175G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326923 | |||||||
chr1:84327114 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+1366A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327114 | |||||||
chr1:84327290 | G | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.165+1542G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327290 | |||||||
chr1:84327293 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+1545T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327293 | |||||||
chr1:84327313 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.165+1565C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327313 | |||||||
chr1:84327450 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.165+1702C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327450 | |||||||
chr1:84327506 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0045 |
2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+1758A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327506 | |||||||
chr1:84327579 | TG | T | 12 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(9): Show |
18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+1832delG | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327579 | |||||||
chr1:84327645 | GGTATAAA others(7): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+1900_165+1913d others(16): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84327645 | ||||||
chr1:84327739 | G | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0176 |
3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+1991G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327739 | |||||||
chr1:84327911 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.165+2163C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327911 | |||||||
chr1:84328012 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.165+2264A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328012 | |||||||
chr1:84328060 | C | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+2312C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328060 | |||||||
chr1:84328069 | C | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+2321C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328069 | |||||||
chr1:84328236 | C | A | 9 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0197 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2488C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328236 | |||||||
chr1:84328248 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+2500C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328248 | |||||||
chr1:84328274 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.165+2526C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328274 | |||||||
chr1:84328448 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.165+2700G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328448 | |||||||
chr1:84328587 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+2839C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328587 | |||||||
chr1:84328616 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.165+2868A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328616 | |||||||
chr1:84328661 | A | G | 1 | a0001c0002t0005g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+2913A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328661 | |||||||
chr1:84328721 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.165+2973A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328721 | |||||||
chr1:84329026 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0045 |
2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+3278C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329026 | |||||||
chr1:84329243 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.165+3495A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329243 | |||||||
chr1:84329326 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0176 |
3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+3578A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329326 | |||||||
chr1:84329503 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+3755C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329503 | |||||||
chr1:84329541 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0135 others(1): Show |
5 | HG02071.hp1 NA18974.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+3793A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329541 | |||||||
chr1:84329600 | G | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.165+3852G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329600 | |||||||
chr1:84329823 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+4075G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329823 | |||||||
chr1:84329915 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.165+4167G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329915 | |||||||
chr1:84330085 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.165+4337A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330085 | |||||||
chr1:84330103 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+4355G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330103 | |||||||
chr1:84330154 | T | C | 2 | a0001c0002t0005g0249 a0001c0002t0005g0250 |
2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+4406T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330154 | |||||||
chr1:84330231 | A | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+4483A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330231 | |||||||
chr1:84330362 | A | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.165+4614A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330362 | |||||||
chr1:84330519 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | NA19007.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.165+4771A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330519 | |||||||
chr1:84330524 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+4776G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330524 | |||||||
chr1:84330797 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.165+5049G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330797 | |||||||
chr1:84330819 | G | A | 7 | a0001c0002t0002g0003 a0001c0002t0002g0086 a0001c0002t0002g0087 others(4): Show |
12 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+5071G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330819 | |||||||
chr1:84330965 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+5217T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330965 | |||||||
chr1:84331045 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+5297A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331045 | |||||||
chr1:84331275 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0196 |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+5527A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331275 | |||||||
chr1:84331286 | T | C | 12 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(9): Show |
18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+5538T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331286 | |||||||
chr1:84331328 | T | TA | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(9): Show |
16 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+5610dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331328 | ||||||
chr1:84331328 | TA | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0126 others(12): Show |
20 | HG00544.hp2 HG00673.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+5610delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331328 | ||||||
chr1:84331352 | A | AT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0059 others(14): Show |
20 | HG01261.hp2 HG01361.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+5604_165+5605i others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331352 | |||||||
chr1:84331352 | A | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0051 others(3): Show |
8 | HG01106.hp2 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+5604A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331352 | |||||||
chr1:84331354 | A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0189 |
3 | HG02738.hp2 NA18906.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.165+5610_165+5611i others(12): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | ||||||
chr1:84331354 | A | AAAAAAAT others(2): Show |
19 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(16): Show |
27 | HG00099.hp1 HG01081.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.165+5610_165+5611i others(11): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | ||||||
chr1:84331354 | A | AAAAAATA others(1): Show |
97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(94): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.165+5610_165+5611i others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | ||||||
chr1:84331354 | A | AAAAATAC | 50 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0023 others(47): Show |
57 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.165+5611_165+5612i others(9): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | ||||||
chr1:84331354 | A | AAAATAC | 2 | a0001c0002t0002g0003 a0001c0002t0002g0088 |
7 | HG01517.hp2 HG02698.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+5609_165+5610i others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | ||||||
chr1:84331354 | A | C | 25 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
30 | HG01106.hp2 HG01261.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+5606A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331354 | |||||||
chr1:84331512 | G | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+5764G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331512 | |||||||
chr1:84331548 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0219 |
3 | HG01255.hp1 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.165+5800G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331548 | |||||||
chr1:84331633 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.165+5885T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331633 | |||||||
chr1:84332354 | C | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0244 others(4): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6606C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332354 | |||||||
chr1:84332371 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.165+6623C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332371 | |||||||
chr1:84332576 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.165+6828G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332576 | |||||||
chr1:84332780 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.165+7032G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332780 | |||||||
chr1:84332934 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(82): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.165+7186A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332934 | |||||||
chr1:84332959 | C | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(33): Show |
42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.165+7211C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332959 | |||||||
chr1:84333182 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.165+7434C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333182 | |||||||
chr1:84333186 | G | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0075 |
2 | NA18954.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.165+7438G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333186 | |||||||
chr1:84333203 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+7455G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333203 | |||||||
chr1:84333239 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.165+7491T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333239 | |||||||
chr1:84333432 | G | T | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+7684G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333432 | |||||||
chr1:84333471 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+7723A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333471 | |||||||
chr1:84333603 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.165+7855C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333603 | |||||||
chr1:84333734 | C | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+7986C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333734 | |||||||
chr1:84333829 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+8081G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333829 | |||||||
chr1:84333859 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.165+8111T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333859 | |||||||
chr1:84333891 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.165+8143C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333891 | |||||||
chr1:84334002 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+8254G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334002 | |||||||
chr1:84334056 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 |
3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.165+8308T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334056 | |||||||
chr1:84334147 | A | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.165+8399A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334147 | |||||||
chr1:84334158 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+8410A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334158 | |||||||
chr1:84334309 | T | C | 13 | a0001c0001t0001g0049 a0001c0002t0001g0014 a0001c0002t0001g0200 others(10): Show |
19 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+8561T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334309 | |||||||
chr1:84334539 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0176 |
3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+8791T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334539 | |||||||
chr1:84334565 | G | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0244 others(4): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+8817G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334565 | |||||||
chr1:84334570 | G | C | 2 | a0001c0001t0001g0175 a0001c0003t0001g0040 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+8822G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334570 | |||||||
chr1:84334581 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.165+8833T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334581 | |||||||
chr1:84334775 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.165+9027T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334775 | |||||||
chr1:84334882 | T | C | 14 | a0001c0001t0001g0049 a0001c0001t0001g0180 a0001c0002t0001g0014 others(11): Show |
20 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+9134T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334882 | |||||||
chr1:84335250 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.165+9502G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335250 | |||||||
chr1:84335314 | T | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0244 others(4): Show |
9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+9566T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335314 | |||||||
chr1:84335321 | G | A | 1 | a0001c0001t0001g0023 | 2 | NA18978.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.165+9573G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335321 | |||||||
chr1:84335339 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.165+9591G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335339 | |||||||
chr1:84335403 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.165+9655T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335403 | |||||||
chr1:84335411 | T | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.165+9663T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335411 | |||||||
chr1:84335535 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.165+9787C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335535 | |||||||
chr1:84335595 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.165+9847G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335595 | |||||||
chr1:84335745 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0197 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+9997A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335745 | |||||||
chr1:84335879 | A | G | 7 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0112 others(4): Show |
7 | HG00438.hp1 HG00673.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+10131A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335879 | |||||||
chr1:84335987 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.165+10239T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335987 | |||||||
chr1:84336118 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0229 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.165+10370C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336118 | |||||||
chr1:84336249 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+10501A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336249 | |||||||
chr1:84336502 | CCT | C | 5 | a0001c0002t0002g0003 a0001c0002t0002g0086 a0001c0002t0002g0087 others(2): Show |
10 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+10757_165+1075 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84336502 | ||||||
chr1:84336561 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.165+10813T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336561 | |||||||
chr1:84336638 | G | A | 1 | a0001c0002t0005g0249 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+10890G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336638 | |||||||
chr1:84336640 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+10892T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336640 | |||||||
chr1:84336747 | C | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+10999C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336747 | |||||||
chr1:84336838 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0196 |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+11090G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336838 | |||||||
chr1:84337069 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0199 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.165+11321C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337069 | |||||||
chr1:84337193 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165+11445A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337193 | |||||||
chr1:84337428 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+11680C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337428 | |||||||
chr1:84337471 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.165+11723C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337471 | |||||||
chr1:84337489 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.165+11741G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337489 | |||||||
chr1:84337837 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.166-11794A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337837 | |||||||
chr1:84337859 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0071 others(4): Show |
9 | HG01243.hp2 HG01952.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-11772A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337859 | |||||||
chr1:84337885 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-11746C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337885 | |||||||
chr1:84337930 | C | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.166-11701C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337930 | |||||||
chr1:84337965 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0239 |
3 | HG01515.hp1 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.166-11666A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337965 | |||||||
chr1:84337994 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-11637C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337994 | |||||||
chr1:84338036 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-11595C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338036 | |||||||
chr1:84338216 | G | T | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-11415G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338216 | |||||||
chr1:84338432 | C | CT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.166-11176dupT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | ||||||
chr1:84338432 | C | CTT | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0056 others(4): Show |
7 | HG01099.hp2 HG02055.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-11177_166-1117 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | ||||||
chr1:84338432 | CTT | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0037 others(12): Show |
18 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-11177_166-1117 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | ||||||
chr1:84338432 | CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0028 others(16): Show |
29 | HG00733.hp2 HG01192.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.166-11184_166-1117 others(13): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | ||||||
chr1:84338452 | T | TTTTC | 9 | a0001c0001t0001g0032 a0001c0001t0001g0144 a0001c0001t0001g0155 others(6): Show |
10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-11176_166-1117 others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338452 | ||||||
chr1:84338531 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.166-11100G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338531 | |||||||
chr1:84338693 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-10938C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338693 | |||||||
chr1:84338760 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.166-10871A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338760 | |||||||
chr1:84338795 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0176 |
3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.166-10836A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338795 | |||||||
chr1:84338872 | C | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0177 |
3 | HG01884.hp2 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.166-10759C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338872 | |||||||
chr1:84338901 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.166-10730A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338901 | |||||||
chr1:84339249 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.166-10382G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339249 | |||||||
chr1:84339560 | G | A | 2 | a0001c0001t0001g0175 a0001c0003t0001g0040 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-10071G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339560 | |||||||
chr1:84339626 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.166-10005C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339626 | |||||||
chr1:84339829 | TACTC | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0051 |
3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.166-9799_166-9796d others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84339829 | ||||||
chr1:84339893 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0196 |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-9738G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339893 | |||||||
chr1:84339932 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0196 |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-9699G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339932 | |||||||
chr1:84340175 | T | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-9456T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340175 | |||||||
chr1:84340200 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0037 others(15): Show |
21 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-9431T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340200 | |||||||
chr1:84340279 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.166-9352C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340279 | |||||||
chr1:84340374 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-9257A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340374 | |||||||
chr1:84340545 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0193 a0001c0003t0001g0040 |
3 | HG03195.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-9086G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340545 | |||||||
chr1:84340549 | A | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.166-9082A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340549 | |||||||
chr1:84340632 | A | G | 5 | a0001c0002t0001g0014 a0001c0002t0001g0200 a0001c0002t0001g0201 others(2): Show |
6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-8999A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340632 | |||||||
chr1:84340837 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-8794G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340837 | |||||||
chr1:84341017 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.166-8614C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341017 | |||||||
chr1:84341129 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.166-8502C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341129 | |||||||
chr1:84341209 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.166-8422C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341209 | |||||||
chr1:84341451 | C | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(165): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.166-8180C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341451 | |||||||
chr1:84341532 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.166-8099G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341532 | |||||||
chr1:84341563 | G | T | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-8068G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341563 | |||||||
chr1:84341740 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.166-7891A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341740 | |||||||
chr1:84341950 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.166-7681A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341950 | |||||||
chr1:84342094 | A | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0143 |
2 | NA18950.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.166-7537A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342094 | |||||||
chr1:84342315 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.166-7316A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342315 | |||||||
chr1:84342476 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-7155C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342476 | |||||||
chr1:84342495 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7136G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342495 | |||||||
chr1:84342500 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.166-7131A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342500 | |||||||
chr1:84342500 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-7131A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342500 | |||||||
chr1:84342501 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7130A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342501 | |||||||
chr1:84342502 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7129A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342502 | |||||||
chr1:84342503 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7128A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342503 | |||||||
chr1:84342504 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0186 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7127C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342504 | |||||||
chr1:84342742 | C | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.166-6889C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342742 | |||||||
chr1:84342888 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-6743G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342888 | |||||||
chr1:84342891 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0061 |
2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.166-6740A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342891 | |||||||
chr1:84342916 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.166-6715G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342916 | |||||||
chr1:84342924 | A | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0026 others(6): Show |
13 | HG00099.hp1 HG01081.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6707A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342924 | |||||||
chr1:84342990 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.166-6641G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342990 | |||||||
chr1:84343086 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.166-6545G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343086 | |||||||
chr1:84343144 | C | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6487C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343144 | |||||||
chr1:84343174 | G | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0021 others(63): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.166-6457G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343174 | |||||||
chr1:84343302 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-6329C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343302 | |||||||
chr1:84343384 | A | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6247A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343384 | |||||||
chr1:84343524 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0028 others(12): Show |
24 | HG00733.hp2 HG01192.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-6107C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343524 | |||||||
chr1:84343873 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.166-5758A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343873 | |||||||
chr1:84343879 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0197 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-5752A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343879 | |||||||
chr1:84343897 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0175 a0001c0001t0001g0193 others(1): Show |
4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-5734G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343897 | |||||||
chr1:84343945 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.166-5686T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343945 | |||||||
chr1:84344015 | TG | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0184 others(9): Show |
17 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-5613delG | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84344015 | ||||||
chr1:84344067 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0199 |
3 | HG02257.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.166-5564T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344067 | |||||||
chr1:84344078 | CT | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
56 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.166-5541delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84344078 | ||||||
chr1:84344084 | T | C | 10 | a0001c0001t0001g0021 a0001c0001t0001g0048 a0001c0001t0001g0073 others(7): Show |
11 | HG00621.hp2 NA18612.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-5547T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344084 | |||||||
chr1:84344213 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0197 a0001c0001t0001g0204 others(1): Show |
4 | HG02109.hp2 HG03688.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-5418G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344213 | |||||||
chr1:84344466 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.166-5165A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344466 | |||||||
chr1:84344479 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-5152G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344479 | |||||||
chr1:84344615 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02559.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-5016C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344615 | |||||||
chr1:84344653 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-4978G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344653 | |||||||
chr1:84344662 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.166-4969G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344662 | |||||||
chr1:84344713 | A | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.166-4918A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344713 | |||||||
chr1:84344911 | A | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0076 |
2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.166-4720A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344911 | |||||||
chr1:84345088 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.166-4543C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345088 | |||||||
chr1:84345132 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.166-4499A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345132 | |||||||
chr1:84345534 | G | A | 9 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0002t0002g0003 others(6): Show |
14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-4097G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345534 | |||||||
chr1:84345577 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-4054C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345577 | |||||||
chr1:84345586 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.166-4045C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345586 | |||||||
chr1:84345617 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0241 |
2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.166-4014A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345617 | |||||||
chr1:84345919 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-3712G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345919 | |||||||
chr1:84345979 | C | G | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3652C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345979 | |||||||
chr1:84346219 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.166-3412A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346219 | |||||||
chr1:84346257 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.166-3374T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346257 | |||||||
chr1:84346304 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-3327C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346304 | |||||||
chr1:84346379 | C | A | 11 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0066 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3252C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346379 | |||||||
chr1:84346419 | T | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.166-3212T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346419 | |||||||
chr1:84346543 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-3088G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346543 | |||||||
chr1:84346558 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
8 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-3073G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346558 | |||||||
chr1:84346638 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-2993G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346638 | |||||||
chr1:84346724 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.166-2907A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346724 | |||||||
chr1:84346751 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.166-2880T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346751 | |||||||
chr1:84346913 | GA | G | 9 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0002t0002g0003 others(6): Show |
14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-2716delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84346913 | ||||||
chr1:84346955 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0154 a0001c0001t0001g0158 |
3 | HG02523.hp1 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.166-2676G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346955 | |||||||
chr1:84346981 | T | C | 33 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0029 others(30): Show |
43 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.166-2650T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346981 | |||||||
chr1:84346989 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-2642C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346989 | |||||||
chr1:84347070 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.166-2561C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347070 | |||||||
chr1:84347135 | G | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.166-2496G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347135 | |||||||
chr1:84347402 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.166-2229A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347402 | |||||||
chr1:84347676 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.166-1955G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347676 | |||||||
chr1:84347744 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-1887C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347744 | |||||||
chr1:84347747 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0108 a0001c0001t0001g0154 others(1): Show |
4 | HG02080.hp1 HG02523.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1884C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347747 | |||||||
chr1:84347754 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.166-1877G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347754 | |||||||
chr1:84347788 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-1843C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347788 | |||||||
chr1:84347852 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.166-1779A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347852 | |||||||
chr1:84347979 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.166-1652G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347979 | |||||||
chr1:84348181 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0208 |
3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-1450C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348181 | |||||||
chr1:84348283 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.166-1348A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348283 | |||||||
chr1:84348396 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-1235C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348396 | |||||||
chr1:84348506 | G | GCA | 10 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0001t0006g0102 others(7): Show |
15 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-1122_166-1121d others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84348506 | ||||||
chr1:84348747 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.166-884T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348747 |