Item | Value |
---|---|
geneid | 6341 |
ensemblid | ENSG00000133028.12 |
hgncid | 10603 |
symbol | SCO1 |
name | synthesis of cytochrome C oxidase 1 |
refseq_nuc | NM_004589.4 |
refseq_prot | NP_004580.1 |
ensembl_nuc | ENST00000255390.10 |
ensembl_prot | ENSP00000255390.5 |
mane_status | MANE Select |
chr | chr17 |
start | 10672474 |
end | 10697533 |
strand | - |
ver | v1.2 |
region | chr17:10672474-10697533 |
region5000 | chr17:10667474-10702533 |
regionname0 | SCO1_chr17_10672474_10697533 |
regionname5000 | SCO1_chr17_10667474_10702533 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 301 | 378 | 55 | 75 | 192 | 14 | 40 | 144 | SCO1_chr17_10667474_10702533 | SCO1 | MAMLV others(296): Show |
chr17 | 10667474 | 10702533 |
a0002 | 0/0 | 301 | 36 | 33 | 3 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | MAMLV others(296): Show |
chr17 | 10667474 | 10702533 |
a0003 | 0/0 | 301 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | MAMLV others(296): Show |
chr17 | 10667474 | 10702533 |
a0004 | 0/0 | 301 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | MAMLV others(296): Show |
chr17 | 10667474 | 10702533 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 903 | 370 | 52 | 74 | 189 | 14 | 39 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0001c0004 | 0/0 | 903 | 4 | 3 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0001c0005 | 0/0 | 903 | 3 | 0 | 0 | 2 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0001c0007 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0002c0002 | 0/0 | 903 | 24 | 23 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0002c0003 | 0/0 | 903 | 12 | 10 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0003c0008 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 | ||
a0004c0006 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | ATGGC others(898): Show |
chr17 | 10667474 | 10702533 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9576 | 57 | 2 | 16 | 28 | 5 | 6 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0002 | 0/0 | 9577 | 33 | 3 | 13 | 14 | 1 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0003 | 0/0 | 9577 | 28 | 2 | 8 | 14 | 1 | 3 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0004 | 0/0 | 9578 | 21 | 7 | 7 | 3 | 2 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0005 | 0/0 | 9577 | 17 | 0 | 0 | 16 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0006 | 0/0 | 9578 | 16 | 0 | 1 | 14 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0007 | 0/0 | 9579 | 12 | 1 | 7 | 0 | 1 | 3 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0008 | 0/0 | 9579 | 12 | 0 | 0 | 12 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0009 | 0/0 | 9577 | 9 | 0 | 4 | 5 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0010 | 0/0 | 9578 | 7 | 0 | 1 | 6 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0011 | 0/0 | 9578 | 8 | 0 | 3 | 2 | 0 | 3 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0012 | 0/0 | 9577 | 8 | 0 | 0 | 8 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0013 | 0/0 | 9576 | 8 | 8 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0014 | 1/0 | 9577 | 7 | 5 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0015 | 0/0 | 9578 | 6 | 0 | 0 | 6 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0016 | 0/0 | 9576 | 6 | 0 | 0 | 6 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0017 | 0/0 | 9576 | 5 | 0 | 0 | 3 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0018 | 0/0 | 9577 | 5 | 0 | 0 | 5 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0019 | 0/0 | 9580 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9575): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0022 | 0/0 | 9579 | 4 | 0 | 0 | 4 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0023 | 0/0 | 9579 | 3 | 0 | 0 | 3 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0024 | 0/0 | 9578 | 3 | 0 | 0 | 3 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0026 | 0/0 | 9577 | 3 | 3 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0027 | 0/0 | 9572 | 3 | 3 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9567): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0028 | 0/0 | 9578 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0034 | 0/0 | 9578 | 2 | 0 | 1 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0035 | 0/0 | 9578 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0036 | 0/0 | 9578 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0037 | 0/0 | 9577 | 2 | 0 | 0 | 0 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0038 | 0/0 | 9577 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0039 | 0/0 | 9577 | 2 | 0 | 1 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0040 | 0/0 | 9576 | 2 | 0 | 0 | 0 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0041 | 0/0 | 9576 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0042 | 0/0 | 9577 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0043 | 0/0 | 9578 | 2 | 0 | 1 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0045 | 0/0 | 9577 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0047 | 0/0 | 9576 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0048 | 0/0 | 9577 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0050 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0051 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0052 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0053 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0063 | 0/0 | 9579 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0064 | 0/0 | 9578 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0065 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0066 | 0/0 | 9579 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0067 | 0/0 | 9579 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0068 | 0/0 | 9578 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0069 | 0/0 | 9578 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0070 | 0/0 | 9578 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0071 | 0/0 | 9578 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0072 | 0/0 | 9578 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0073 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0074 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0075 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0076 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0077 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0078 | 0/1 | 9576 | 1 | 0 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0079 | 0/0 | 9577 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0080 | 0/0 | 9578 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0081 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0082 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0083 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0084 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0085 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9574): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0086 | 0/0 | 9578 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0087 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0088 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9576): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0089 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0090 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0091 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0093 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0094 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0095 | 0/0 | 9577 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0096 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0097 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0098 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0099 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0100 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0101 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0102 | 0/0 | 9576 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0104 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0105 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0106 | 0/0 | 9576 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0107 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0108 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0109 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0110 | 0/0 | 9576 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0111 | 0/0 | 9580 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9575): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0112 | 0/0 | 9576 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0113 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0114 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0115 | 0/0 | 9576 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0116 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0117 | 0/0 | 9577 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0118 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9576): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0119 | 0/0 | 9580 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9575): Show |
chr17 | 10667474 | 10702533 |
a0001c0001t0120 | 0/0 | 9577 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0004t0001 | 0/0 | 9576 | 3 | 2 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0001c0004t0092 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0005t0032 | 0/0 | 9578 | 2 | 0 | 0 | 1 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0001c0005t0060 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0001c0007t0010 | 0/0 | 9578 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0020 | 0/0 | 9584 | 4 | 4 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9579): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0021 | 0/0 | 9583 | 4 | 4 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9578): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0029 | 0/0 | 9584 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9579): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0030 | 0/0 | 9583 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9578): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0031 | 0/0 | 9583 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9578): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0033 | 0/0 | 9580 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9575): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0054 | 0/0 | 9586 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9581): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0055 | 0/0 | 9585 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9580): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0056 | 0/0 | 9585 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9580): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0057 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9576): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0058 | 0/0 | 9585 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9580): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0059 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0061 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9576): Show |
chr17 | 10667474 | 10702533 |
a0002c0002t0062 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9576): Show |
chr17 | 10667474 | 10702533 |
a0002c0003t0019 | 0/0 | 9580 | 4 | 3 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9575): Show |
chr17 | 10667474 | 10702533 |
a0002c0003t0025 | 0/0 | 9578 | 3 | 2 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0002c0003t0044 | 0/0 | 9578 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9573): Show |
chr17 | 10667474 | 10702533 |
a0002c0003t0046 | 0/0 | 9577 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
a0002c0003t0049 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0003c0008t0103 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9571): Show |
chr17 | 10667474 | 10702533 |
a0004c0006t0002 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | CAAAG others(9572): Show |
chr17 | 10667474 | 10702533 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 29 | 0 | 3 | 18 | 4 | 4 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0003 | 0/0 | 11 | 2 | 4 | 4 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0012 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0002 | 0/0 | 12 | 1 | 3 | 6 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0006 | 0/0 | 9 | 6 | 1 | 1 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0016 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0005 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0004 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0030 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0009g0010 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0009g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0010g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0010g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0011g0017 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0011g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0012g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0013g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0013g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0013g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0014g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0014g0052 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0015g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0015g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0015g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0016g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0017g0014 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0018g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0018g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0019g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0022g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0022g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0022g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0023g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0024g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0024g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0026g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0026g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0027g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0027g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0028g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0034g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0035g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0035g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0036g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0036g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0037g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0037g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0038g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0038g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0039g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0040g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0041g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0042g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0043g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0043g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0045g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0045g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0047g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0048g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0050g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0051g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0052g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0053g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0063g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0064g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0065g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0066g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0067g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0068g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0069g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0070g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0071g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0072g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0073g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0074g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0075g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0076g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0077g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0078g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0079g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0080g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0081g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0082g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0083g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0084g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0085g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0086g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0087g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0088g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0089g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0090g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0091g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0093g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0094g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0095g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0096g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0097g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0098g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0099g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0100g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0101g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0102g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0104g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0105g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0106g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0107g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0108g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0109g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0110g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0111g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0112g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0113g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0114g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0115g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0116g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0117g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0118g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0119g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0001t0120g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0004t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0004t0092g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0005t0032g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0005t0032g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0005t0060g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0001c0007t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0020g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0021g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0029g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0030g0064 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0031g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0033g0062 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0054g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0055g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0056g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0057g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0058g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0059g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0061g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0002t0062g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0019g0061 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0019g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0025g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0025g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0044g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0044g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0046g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0046g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0002c0003t0049g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0003c0008t0103g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
a0004c0006t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00099 | hp2 | a0001 | c0001 | t0110 | g0121 | EUR | GBR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00140 | hp1 | a0001 | c0001 | t0115 | g0111 | EUR | GBR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00140 | hp2 | a0001 | c0001 | t0039 | g0043 | EUR | GBR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0162 | EUR | FIN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0016 | EUR | FIN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00408 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00408 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00438 | hp2 | a0001 | c0001 | t0048 | g0034 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00544 | hp1 | a0001 | c0001 | t0068 | g0184 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00544 | hp2 | a0001 | c0001 | t0024 | g0158 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00558 | hp1 | a0001 | c0001 | t0096 | g0105 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00597 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00597 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00609 | hp1 | a0001 | c0001 | t0116 | g0088 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00621 | hp1 | a0001 | c0001 | t0024 | g0058 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00621 | hp2 | a0001 | c0001 | t0093 | g0128 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00642 | hp1 | a0001 | c0001 | t0043 | g0131 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00673 | hp1 | a0001 | c0001 | t0048 | g0034 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00673 | hp2 | a0001 | c0001 | t0023 | g0020 | EAS | CHS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00738 | hp2 | a0001 | c0001 | t0075 | g0175 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00741 | hp1 | a0001 | c0001 | t0120 | g0113 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG00741 | hp2 | a0002 | c0003 | t0025 | g0215 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01069 | hp1 | a0001 | c0001 | t0034 | g0051 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01070 | hp2 | a0001 | c0001 | t0042 | g0055 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01071 | hp1 | a0001 | c0001 | t0042 | g0055 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01074 | hp2 | a0001 | c0001 | t0039 | g0043 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01081 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0190 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01106 | hp2 | a0002 | c0003 | t0019 | g0061 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01109 | hp1 | a0002 | c0002 | t0057 | g0227 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01109 | hp2 | a0001 | c0001 | t0089 | g0100 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01167 | hp1 | a0001 | c0001 | t0081 | g0160 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01243 | hp1 | a0001 | c0001 | t0074 | g0202 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01243 | hp2 | a0001 | c0001 | t0097 | g0138 | AMR | PUR | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0057 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0028 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0057 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0194 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01496 | hp1 | a0001 | c0001 | t0011 | g0048 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | IBS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0149 | EUR | IBS | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0075 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01891 | hp1 | a0001 | c0001 | t0026 | g0134 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01928 | hp1 | a0001 | c0001 | t0076 | g0176 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01943 | hp2 | a0001 | c0001 | t0082 | g0081 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0004 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0186 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02015 | hp1 | a0001 | c0001 | t0084 | g0083 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02015 | hp2 | a0001 | c0001 | t0035 | g0210 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02040 | hp1 | a0001 | c0001 | t0038 | g0193 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02040 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02055 | hp1 | a0002 | c0003 | t0044 | g0225 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02055 | hp2 | a0001 | c0001 | t0094 | g0065 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02056 | hp1 | a0001 | c0001 | t0051 | g0067 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02056 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02071 | hp2 | a0001 | c0001 | t0015 | g0035 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02074 | hp1 | a0001 | c0001 | t0108 | g0114 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02074 | hp2 | a0001 | c0001 | t0008 | g0089 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02080 | hp1 | a0001 | c0001 | t0035 | g0197 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02080 | hp2 | a0001 | c0001 | t0052 | g0070 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02129 | hp2 | a0001 | c0001 | t0065 | g0167 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02132 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02135 | hp1 | a0001 | c0001 | t0090 | g0107 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02135 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0013 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02155 | hp2 | a0001 | c0001 | t0008 | g0079 | EAS | CDX | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02165 | hp2 | a0001 | c0001 | t0070 | g0171 | EAS | CDX | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02257 | hp1 | a0001 | c0001 | t0098 | g0109 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02257 | hp2 | a0002 | c0003 | t0025 | g0059 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02258 | hp2 | a0003 | c0008 | t0103 | g0232 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0125 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02280 | hp2 | a0002 | c0003 | t0019 | g0223 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02293 | hp1 | a0001 | c0001 | t0009 | g0010 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0133 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02451 | hp2 | a0002 | c0002 | t0031 | g0060 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02523 | hp2 | a0001 | c0001 | t0099 | g0087 | EAS | KHV | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02602 | hp2 | a0001 | c0001 | t0080 | g0178 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02622 | hp1 | a0002 | c0003 | t0019 | g0061 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02622 | hp2 | a0001 | c0001 | t0113 | g0118 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02630 | hp2 | a0002 | c0002 | t0030 | g0064 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02647 | hp1 | a0002 | c0003 | t0025 | g0059 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02647 | hp2 | a0002 | c0002 | t0020 | g0031 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02683 | hp2 | a0001 | c0001 | t0067 | g0169 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02717 | hp1 | a0002 | c0002 | t0055 | g0218 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0074 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02723 | hp1 | a0001 | c0001 | t0109 | g0120 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02735 | hp1 | a0001 | c0001 | t0071 | g0153 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02735 | hp2 | a0001 | c0001 | t0102 | g0110 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02738 | hp1 | a0001 | c0001 | t0034 | g0051 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02809 | hp1 | a0001 | c0001 | t0114 | g0117 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02809 | hp2 | a0001 | c0001 | t0026 | g0124 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0040 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02818 | hp2 | a0002 | c0002 | t0020 | g0031 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02886 | hp1 | a0001 | c0001 | t0027 | g0040 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02895 | hp1 | a0002 | c0002 | t0033 | g0062 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02895 | hp2 | a0001 | c0001 | t0047 | g0041 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02896 | hp1 | a0002 | c0003 | t0046 | g0220 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02896 | hp2 | a0001 | c0001 | t0047 | g0041 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02897 | hp1 | a0002 | c0002 | t0033 | g0062 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02897 | hp2 | a0002 | c0003 | t0044 | g0224 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02922 | hp1 | a0002 | c0003 | t0046 | g0226 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02970 | hp1 | a0002 | c0002 | t0058 | g0231 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02970 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02976 | hp1 | a0001 | c0001 | t0119 | g0142 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02976 | hp2 | a0002 | c0002 | t0030 | g0064 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0025 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03041 | hp2 | a0001 | c0001 | t0026 | g0135 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03098 | hp2 | a0002 | c0002 | t0029 | g0063 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03130 | hp2 | a0002 | c0002 | t0021 | g0019 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03195 | hp1 | a0002 | c0002 | t0031 | g0060 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03195 | hp2 | a0001 | c0001 | t0107 | g0139 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03209 | hp1 | a0002 | c0002 | t0062 | g0229 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03209 | hp2 | a0002 | c0002 | t0029 | g0063 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03225 | hp1 | a0002 | c0002 | t0056 | g0228 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03225 | hp2 | a0002 | c0002 | t0021 | g0019 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03239 | hp1 | a0001 | c0001 | t0117 | g0072 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03239 | hp2 | a0001 | c0001 | t0037 | g0174 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03486 | hp1 | a0001 | c0001 | t0063 | g0144 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03490 | hp1 | a0001 | c0001 | t0040 | g0053 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03491 | hp1 | a0001 | c0001 | t0095 | g0093 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03491 | hp2 | a0001 | c0001 | t0017 | g0014 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03492 | hp1 | a0001 | c0001 | t0017 | g0014 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03492 | hp2 | a0001 | c0001 | t0040 | g0053 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03516 | hp2 | a0002 | c0002 | t0020 | g0219 | AFR | ESN | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03540 | hp1 | a0002 | c0002 | t0020 | g0031 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03540 | hp2 | a0001 | c0001 | t0104 | g0119 | AFR | GWD | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03579 | hp1 | a0002 | c0002 | t0021 | g0019 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03579 | hp2 | a0002 | c0002 | t0054 | g0217 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0028 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0188 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03688 | hp2 | a0001 | c0001 | t0011 | g0048 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03831 | hp2 | a0001 | c0001 | t0066 | g0168 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03834 | hp1 | a0001 | c0001 | t0037 | g0189 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03834 | hp2 | a0001 | c0001 | t0014 | g0052 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03927 | hp1 | a0001 | c0001 | t0011 | g0017 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03927 | hp2 | a0001 | c0005 | t0032 | g0212 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0152 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0017 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04115 | hp1 | a0001 | c0001 | t0072 | g0173 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04184 | hp2 | a0001 | c0001 | t0007 | g0030 | SAS | BEB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04228 | hp1 | a0001 | c0001 | t0106 | g0130 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG04228 | hp2 | a0001 | c0001 | t0079 | g0177 | SAS | STU | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18522 | hp1 | a0002 | c0003 | t0049 | g0216 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | CHB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18747 | hp2 | a0001 | c0001 | t0015 | g0147 | EAS | CHB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18906 | hp1 | a0001 | c0004 | t0092 | g0123 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18906 | hp2 | a0001 | c0001 | t0019 | g0098 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18940 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18941 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18944 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18946 | hp2 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18947 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18948 | hp2 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18949 | hp1 | a0001 | c0001 | t0028 | g0036 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18949 | hp2 | a0001 | c0001 | t0085 | g0084 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18950 | hp2 | a0001 | c0001 | t0017 | g0014 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18951 | hp1 | a0001 | c0001 | t0028 | g0036 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18951 | hp2 | a0001 | c0001 | t0017 | g0014 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18953 | hp1 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18954 | hp1 | a0001 | c0001 | t0073 | g0157 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18954 | hp2 | a0001 | c0001 | t0105 | g0151 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18956 | hp1 | a0001 | c0005 | t0032 | g0213 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18956 | hp2 | a0001 | c0001 | t0011 | g0179 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18960 | hp1 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18961 | hp1 | a0001 | c0001 | t0015 | g0035 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18961 | hp2 | a0001 | c0007 | t0010 | g0214 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18963 | hp1 | a0001 | c0001 | t0045 | g0096 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18963 | hp2 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18965 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18968 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18970 | hp1 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18974 | hp2 | a0001 | c0001 | t0086 | g0085 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18979 | hp2 | a0001 | c0001 | t0022 | g0050 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18980 | hp2 | a0001 | c0001 | t0053 | g0068 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18981 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18982 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18982 | hp2 | a0001 | c0001 | t0091 | g0108 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18984 | hp1 | a0001 | c0001 | t0045 | g0086 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18984 | hp2 | a0001 | c0001 | t0015 | g0080 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18986 | hp1 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18987 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18987 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18988 | hp1 | a0001 | c0001 | t0041 | g0054 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18990 | hp2 | a0001 | c0001 | t0041 | g0054 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18991 | hp1 | a0001 | c0001 | t0024 | g0058 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18993 | hp1 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18993 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18998 | hp2 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19000 | hp2 | a0001 | c0001 | t0011 | g0163 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19002 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19006 | hp1 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19006 | hp2 | a0001 | c0001 | t0018 | g0115 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19007 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19009 | hp1 | a0001 | c0001 | t0083 | g0082 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19012 | hp1 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19012 | hp2 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19030 | hp1 | a0001 | c0001 | t0118 | g0141 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19030 | hp2 | a0004 | c0006 | t0002 | g0192 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19043 | hp1 | a0001 | c0001 | t0088 | g0077 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19043 | hp2 | a0002 | c0002 | t0021 | g0019 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19054 | hp2 | a0001 | c0001 | t0069 | g0170 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19058 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19058 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19065 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19065 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19070 | hp2 | a0001 | c0001 | t0043 | g0106 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19072 | hp1 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19072 | hp2 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19074 | hp2 | a0001 | c0001 | t0036 | g0156 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19077 | hp1 | a0001 | c0001 | t0022 | g0155 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19078 | hp1 | a0001 | c0001 | t0022 | g0050 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19078 | hp2 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19080 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19080 | hp2 | a0001 | c0001 | t0017 | g0069 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19082 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19084 | hp2 | a0001 | c0001 | t0038 | g0199 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19085 | hp2 | a0001 | c0001 | t0036 | g0172 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19088 | hp1 | a0001 | c0001 | t0022 | g0166 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19088 | hp2 | a0001 | c0001 | t0012 | g0008 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19089 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19089 | hp2 | a0001 | c0005 | t0060 | g0211 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19090 | hp1 | a0001 | c0001 | t0012 | g0097 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19240 | hp1 | a0001 | c0001 | t0014 | g0201 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA19240 | hp2 | a0001 | c0001 | t0101 | g0066 | AFR | YRI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ASW | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20805 | hp2 | a0001 | c0001 | t0064 | g0145 | EUR | TSI | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01123 | hp1 | a0001 | c0001 | t0112 | g0112 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02109 | hp2 | a0002 | c0002 | t0061 | g0221 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02559 | hp1 | a0002 | c0003 | t0019 | g0222 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03471 | hp1 | a0001 | c0001 | t0100 | g0137 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG06807 | hp1 | a0001 | c0001 | t0087 | g0071 | AFR | USA | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18955 | hp1 | a0001 | c0001 | t0050 | g0090 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA18955 | hp2 | a0001 | c0001 | t0077 | g0164 | EAS | JPT | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20300 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | USA | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | USA | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA21309 | hp1 | a0001 | c0001 | t0111 | g0136 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
NA21309 | hp2 | a0002 | c0002 | t0059 | g0230 | AFR | LWK | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
homoSapiens | chm13v2 | a0001 | c0001 | t0078 | g0159 | REF | REF | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0052 | REF | REF | SCO1_chr17_10667474_10702533 | SCO1 | chr17 | 10667474 | 10702533 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10692776 | C | T | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.550G>A | p.Val184Met | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/6 | 576/9577 | 550/906 | 184/301 | chr17 | 10692776 | |||
chr17:10697336 | G | A | 1 | a0002 | 36 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(33): Show |
missense_variant | MODERATE | c.172C>T | p.Pro58Ser | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/6 | 198/9577 | 172/906 | 58/301 | chr17 | 10697336 | |||
chr17:10697467 | G | A | 1 | a0003 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.41C>T | p.Pro14Leu | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/6 | 67/9577 | 41/906 | 14/301 | chr17 | 10697467 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10691933 | T | C | 2 | a0001c0005 a0002c0002 |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
synonymous_variant | LOW | c.594A>G | p.Pro198Pro | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/6 | 620/9577 | 594/906 | 198/301 | chr17 | 10691933 | |||
chr17:10695808 | T | C | 1 | a0001c0004 | 4 | HG00639.hp1 HG02559.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.297A>G | p.Ala99Ala | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/6 | 323/9577 | 297/906 | 99/301 | chr17 | 10695808 | |||
chr17:10697310 | G | A | 1 | a0001c0007 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.198C>T | p.Pro66Pro | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/6 | 224/9577 | 198/906 | 66/301 | chr17 | 10697310 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10672600 | T | C | 2 | a0002c0002t0059 a0002c0003t0025 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8519A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8519 | chr17 | 10672600 | ||||||
chr17:10672677 | A | T | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8442T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8442 | chr17 | 10672677 | ||||||
chr17:10672844 | T | A | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8275A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8275 | chr17 | 10672844 | ||||||
chr17:10672848 | T | A | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8271A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8271 | chr17 | 10672848 | ||||||
chr17:10672908 | T | C | 2 | a0001c0001t0097 a0001c0001t0107 |
2 | HG01243.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8211A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8211 | chr17 | 10672908 | ||||||
chr17:10672947 | T | A | 69 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(66): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*8172A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8172 | chr17 | 10672947 | ||||||
chr17:10673005 | T | C | 69 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(66): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*8114A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8114 | chr17 | 10673005 | ||||||
chr17:10673006 | TC | T | 44 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0013 others(41): Show |
95 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*8112delG | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8112 | chr17 | 10673006 | ||||||
chr17:10673007 | C | T | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0016 others(22): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*8112G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8112 | chr17 | 10673007 | ||||||
chr17:10673007 | CT | C | 50 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(47): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*8111delA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8111 | chr17 | 10673007 | ||||||
chr17:10673008 | T | C | 1 | a0001c0001t0067 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8111A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8111 | chr17 | 10673008 | ||||||
chr17:10673009 | T | C | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0016 others(22): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*8110A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8110 | chr17 | 10673009 | ||||||
chr17:10673010 | T | C | 44 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0013 others(41): Show |
95 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*8109A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8109 | chr17 | 10673010 | ||||||
chr17:10673040 | T | G | 69 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(66): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*8079A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8079 | chr17 | 10673040 | ||||||
chr17:10673058 | C | T | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8061G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8061 | chr17 | 10673058 | ||||||
chr17:10673066 | T | C | 4 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0059 others(1): Show |
7 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8053A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8053 | chr17 | 10673066 | ||||||
chr17:10673107 | G | A | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(37): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*8012C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 8012 | chr17 | 10673107 | ||||||
chr17:10673149 | G | A | 1 | a0002c0002t0059 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7970C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7970 | chr17 | 10673149 | ||||||
chr17:10673153 | G | A | 3 | a0001c0005t0032 a0001c0005t0060 a0002c0003t0025 |
6 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7966C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7966 | chr17 | 10673153 | ||||||
chr17:10673162 | T | C | 1 | a0002c0002t0059 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7957A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7957 | chr17 | 10673162 | ||||||
chr17:10673190 | G | A | 1 | a0001c0001t0051 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7929C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7929 | chr17 | 10673190 | ||||||
chr17:10673237 | C | T | 2 | a0001c0001t0109 a0003c0008t0103 |
2 | HG02258.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7882G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7882 | chr17 | 10673237 | ||||||
chr17:10673294 | G | C | 2 | a0001c0001t0118 a0001c0001t0119 |
2 | HG02976.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7825C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7825 | chr17 | 10673294 | ||||||
chr17:10673354 | CGTCA | C | 1 | a0001c0001t0027 | 3 | HG02717.hp2 HG02818.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7761_*7764delTGAC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7761 | chr17 | 10673354 | ||||||
chr17:10673355 | GTCAA | G | 64 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(61): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*7760_*7763delTTGA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7760 | chr17 | 10673355 | ||||||
chr17:10673383 | T | C | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7736A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7736 | chr17 | 10673383 | ||||||
chr17:10673491 | G | A | 1 | a0001c0001t0106 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7628C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7628 | chr17 | 10673491 | ||||||
chr17:10673518 | T | C | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7601A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7601 | chr17 | 10673518 | ||||||
chr17:10673607 | G | GTC | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7510_*7511dupGA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7511 | chr17 | 10673607 | ||||||
chr17:10673627 | A | G | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7492T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7492 | chr17 | 10673627 | ||||||
chr17:10673659 | A | G | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7460T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7460 | chr17 | 10673659 | ||||||
chr17:10673746 | C | T | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7373G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7373 | chr17 | 10673746 | ||||||
chr17:10673794 | T | C | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7325A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7325 | chr17 | 10673794 | ||||||
chr17:10673849 | G | A | 1 | a0001c0001t0096 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7270C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7270 | chr17 | 10673849 | ||||||
chr17:10673924 | T | C | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7195A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7195 | chr17 | 10673924 | ||||||
chr17:10674008 | A | G | 13 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(10): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*7111T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7111 | chr17 | 10674008 | ||||||
chr17:10674052 | T | TA | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7066dupT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7066 | chr17 | 10674052 | ||||||
chr17:10674106 | G | C | 2 | a0001c0001t0118 a0001c0001t0119 |
2 | HG02976.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7013C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 7013 | chr17 | 10674106 | ||||||
chr17:10674146 | G | A | 1 | a0002c0002t0059 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6973C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6973 | chr17 | 10674146 | ||||||
chr17:10674235 | C | G | 1 | a0001c0001t0073 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6884G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6884 | chr17 | 10674235 | ||||||
chr17:10674238 | G | T | 25 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(22): Show |
58 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6881C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6881 | chr17 | 10674238 | ||||||
chr17:10674256 | A | C | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(41): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6863T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6863 | chr17 | 10674256 | ||||||
chr17:10674306 | A | G | 1 | a0001c0001t0100 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6813T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6813 | chr17 | 10674306 | ||||||
chr17:10674318 | T | C | 2 | a0001c0001t0118 a0001c0001t0119 |
2 | HG02976.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6801A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6801 | chr17 | 10674318 | ||||||
chr17:10674334 | C | T | 1 | a0002c0002t0059 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6785G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6785 | chr17 | 10674334 | ||||||
chr17:10674351 | G | C | 2 | a0001c0001t0097 a0001c0001t0107 |
2 | HG01243.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6768C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6768 | chr17 | 10674351 | ||||||
chr17:10674413 | C | T | 1 | a0001c0001t0098 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6706G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6706 | chr17 | 10674413 | ||||||
chr17:10674414 | G | A | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6705C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6705 | chr17 | 10674414 | ||||||
chr17:10674427 | A | AAAAC | 15 | a0001c0001t0019 a0001c0001t0088 a0001c0001t0111 others(12): Show |
27 | HG01106.hp2 HG02280.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6688_*6691dupGTTT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6691 | chr17 | 10674427 | ||||||
chr17:10674649 | T | C | 2 | a0001c0001t0019 a0002c0003t0019 |
5 | HG01106.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6470A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6470 | chr17 | 10674649 | ||||||
chr17:10674684 | G | A | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6435C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6435 | chr17 | 10674684 | ||||||
chr17:10674717 | G | C | 75 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(72): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*6402C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6402 | chr17 | 10674717 | ||||||
chr17:10674726 | G | T | 1 | a0001c0001t0099 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6393C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6393 | chr17 | 10674726 | ||||||
chr17:10674758 | C | T | 2 | a0002c0002t0029 a0002c0002t0030 |
4 | HG02630.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6361G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6361 | chr17 | 10674758 | ||||||
chr17:10674760 | C | A | 1 | a0001c0001t0079 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6359G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6359 | chr17 | 10674760 | ||||||
chr17:10674929 | A | G | 35 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0010 others(32): Show |
93 | HG00544.hp1 HG01069.hp1 HG01109.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*6190T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6190 | chr17 | 10674929 | ||||||
chr17:10674933 | T | C | 3 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0059 |
4 | HG03927.hp2 NA18956.hp1 NA19089.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6186A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6186 | chr17 | 10674933 | ||||||
chr17:10675005 | C | T | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6114G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 6114 | chr17 | 10675005 | ||||||
chr17:10675133 | T | G | 2 | a0001c0001t0035 a0001c0001t0038 |
4 | HG02015.hp2 HG02040.hp1 HG02080.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5986A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5986 | chr17 | 10675133 | ||||||
chr17:10675139 | G | A | 1 | a0001c0001t0108 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5980C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5980 | chr17 | 10675139 | ||||||
chr17:10675201 | C | T | 3 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0059 |
4 | HG03927.hp2 NA18956.hp1 NA19089.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5918G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5918 | chr17 | 10675201 | ||||||
chr17:10675212 | T | C | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5907A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5907 | chr17 | 10675212 | ||||||
chr17:10675288 | C | T | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5831G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5831 | chr17 | 10675288 | ||||||
chr17:10675475 | T | C | 64 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(61): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*5644A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5644 | chr17 | 10675475 | ||||||
chr17:10675554 | C | T | 1 | a0002c0002t0059 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5565G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5565 | chr17 | 10675554 | ||||||
chr17:10675585 | G | A | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5534C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5534 | chr17 | 10675585 | ||||||
chr17:10675656 | T | C | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5463A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5463 | chr17 | 10675656 | ||||||
chr17:10675659 | A | T | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(79): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*5460T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5460 | chr17 | 10675659 | ||||||
chr17:10675673 | T | C | 2 | a0001c0001t0010 a0001c0007t0010 |
8 | HG02148.hp1 NA18946.hp2 NA18948.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5446A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5446 | chr17 | 10675673 | ||||||
chr17:10675795 | C | A | 2 | a0001c0001t0039 a0001c0001t0071 |
3 | HG00140.hp2 HG01074.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5324G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5324 | chr17 | 10675795 | ||||||
chr17:10675940 | G | A | 1 | a0001c0001t0086 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5179C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5179 | chr17 | 10675940 | ||||||
chr17:10676087 | T | A | 63 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(60): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*5032A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 5032 | chr17 | 10676087 | ||||||
chr17:10676152 | C | T | 1 | a0001c0001t0093 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4967G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4967 | chr17 | 10676152 | ||||||
chr17:10676170 | C | T | 2 | a0001c0001t0065 a0001c0001t0070 |
2 | HG02129.hp2 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4949G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4949 | chr17 | 10676170 | ||||||
chr17:10676188 | T | G | 2 | a0002c0002t0029 a0002c0002t0030 |
4 | HG02630.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4931A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4931 | chr17 | 10676188 | ||||||
chr17:10676193 | A | T | 1 | a0001c0001t0101 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4926T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4926 | chr17 | 10676193 | ||||||
chr17:10676303 | C | T | 1 | a0001c0001t0100 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4816G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4816 | chr17 | 10676303 | ||||||
chr17:10676305 | A | G | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(79): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*4814T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4814 | chr17 | 10676305 | ||||||
chr17:10676334 | A | G | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4785T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4785 | chr17 | 10676334 | ||||||
chr17:10676358 | T | C | 4 | a0002c0002t0021 a0002c0002t0029 a0002c0002t0030 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4761A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4761 | chr17 | 10676358 | ||||||
chr17:10676459 | G | A | 1 | a0001c0001t0098 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4660C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4660 | chr17 | 10676459 | ||||||
chr17:10676498 | T | G | 18 | a0001c0001t0109 a0001c0005t0032 a0001c0005t0060 others(15): Show |
29 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4621A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4621 | chr17 | 10676498 | ||||||
chr17:10676588 | A | G | 14 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(11): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4531T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4531 | chr17 | 10676588 | ||||||
chr17:10676589 | A | C | 1 | a0001c0001t0076 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4530T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4530 | chr17 | 10676589 | ||||||
chr17:10676728 | A | G | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4391T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4391 | chr17 | 10676728 | ||||||
chr17:10676816 | T | C | 3 | a0001c0001t0016 a0001c0001t0018 a0001c0001t0090 |
12 | HG00408.hp2 HG02135.hp1 NA18944.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4303A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4303 | chr17 | 10676816 | ||||||
chr17:10676887 | CT | C | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4231delA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4231 | chr17 | 10676887 | ||||||
chr17:10676969 | T | A | 1 | a0001c0001t0110 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4150A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4150 | chr17 | 10676969 | ||||||
chr17:10677033 | G | A | 1 | a0001c0001t0085 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4086C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4086 | chr17 | 10677033 | ||||||
chr17:10677044 | C | T | 14 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(11): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4075G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 4075 | chr17 | 10677044 | ||||||
chr17:10677136 | T | C | 2 | a0001c0001t0022 a0001c0001t0036 |
6 | NA18979.hp2 NA19074.hp2 NA19077.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3983A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3983 | chr17 | 10677136 | ||||||
chr17:10677199 | C | T | 1 | a0001c0004t0092 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3920G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3920 | chr17 | 10677199 | ||||||
chr17:10677238 | C | T | 5 | a0001c0001t0013 a0001c0001t0026 a0001c0001t0027 others(2): Show |
17 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3881G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3881 | chr17 | 10677238 | ||||||
chr17:10677324 | T | C | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3795A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3795 | chr17 | 10677324 | ||||||
chr17:10677468 | G | C | 1 | a0001c0001t0047 | 2 | HG02895.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3651C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3651 | chr17 | 10677468 | ||||||
chr17:10677521 | T | C | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3598A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3598 | chr17 | 10677521 | ||||||
chr17:10677526 | G | C | 1 | a0001c0001t0072 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3593 | chr17 | 10677526 | ||||||
chr17:10677562 | C | T | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3557G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3557 | chr17 | 10677562 | ||||||
chr17:10677644 | T | C | 1 | a0001c0001t0111 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3475A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3475 | chr17 | 10677644 | ||||||
chr17:10677657 | A | G | 1 | a0001c0001t0113 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3462T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3462 | chr17 | 10677657 | ||||||
chr17:10677711 | A | G | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3408T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3408 | chr17 | 10677711 | ||||||
chr17:10677891 | G | A | 1 | a0001c0001t0042 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3228C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3228 | chr17 | 10677891 | ||||||
chr17:10677933 | T | C | 1 | a0002c0002t0031 | 2 | HG02451.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3186A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3186 | chr17 | 10677933 | ||||||
chr17:10677978 | G | T | 1 | a0001c0001t0091 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3141C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3141 | chr17 | 10677978 | ||||||
chr17:10678028 | T | C | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3091A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 3091 | chr17 | 10678028 | ||||||
chr17:10678127 | GA | G | 5 | a0001c0001t0077 a0002c0002t0021 a0002c0002t0029 others(2): Show |
11 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2991delT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2991 | chr17 | 10678127 | ||||||
chr17:10678242 | G | A | 1 | a0002c0002t0058 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2877C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2877 | chr17 | 10678242 | ||||||
chr17:10678319 | C | T | 1 | a0001c0001t0069 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2800 | chr17 | 10678319 | ||||||
chr17:10678498 | G | A | 2 | a0001c0001t0098 a0001c0001t0112 |
2 | HG01123.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2621C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2621 | chr17 | 10678498 | ||||||
chr17:10678511 | A | C | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2608T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2608 | chr17 | 10678511 | ||||||
chr17:10678513 | C | T | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2606G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2606 | chr17 | 10678513 | ||||||
chr17:10678578 | T | C | 2 | a0001c0001t0113 a0001c0001t0114 |
2 | HG02622.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2541A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2541 | chr17 | 10678578 | ||||||
chr17:10678621 | G | C | 64 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(61): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2498C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2498 | chr17 | 10678621 | ||||||
chr17:10678641 | T | C | 1 | a0001c0001t0074 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2478A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2478 | chr17 | 10678641 | ||||||
chr17:10678652 | T | G | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2467A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2467 | chr17 | 10678652 | ||||||
chr17:10678683 | T | C | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(79): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*2436A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2436 | chr17 | 10678683 | ||||||
chr17:10678698 | C | T | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2421G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2421 | chr17 | 10678698 | ||||||
chr17:10678810 | T | C | 9 | a0002c0002t0020 a0002c0002t0033 a0002c0002t0054 others(6): Show |
13 | HG01109.hp1 HG02109.hp2 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2309A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2309 | chr17 | 10678810 | ||||||
chr17:10678863 | TG | T | 12 | a0001c0001t0016 a0002c0002t0020 a0002c0002t0021 others(9): Show |
21 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2255delC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2255 | chr17 | 10678863 | ||||||
chr17:10678864 | G | GT | 4 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0017 others(1): Show |
7 | HG00323.hp2 HG02074.hp1 HG02683.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2254dupA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2254 | chr17 | 10678864 | ||||||
chr17:10678864 | G | T | 7 | a0001c0001t0005 a0001c0001t0073 a0002c0002t0020 others(4): Show |
7 | HG01109.hp1 HG02970.hp1 HG03225.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2255C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2255 | chr17 | 10678864 | ||||||
chr17:10678864 | GT | G | 9 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(6): Show |
24 | HG00741.hp2 HG01070.hp1 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2254delA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2254 | chr17 | 10678864 | ||||||
chr17:10678960 | T | C | 14 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(11): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2159A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2159 | chr17 | 10678960 | ||||||
chr17:10678969 | G | A | 14 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(11): Show |
41 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2150C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2150 | chr17 | 10678969 | ||||||
chr17:10678984 | C | T | 4 | a0002c0002t0021 a0002c0002t0029 a0002c0002t0030 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2135G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2135 | chr17 | 10678984 | ||||||
chr17:10679001 | G | A | 2 | a0001c0001t0052 a0001c0001t0053 |
2 | HG02080.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2118C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2118 | chr17 | 10679001 | ||||||
chr17:10679006 | C | T | 3 | a0001c0001t0009 a0001c0001t0024 a0001c0001t0076 |
13 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2113G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2113 | chr17 | 10679006 | ||||||
chr17:10679089 | G | A | 21 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(18): Show |
54 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2030C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2030 | chr17 | 10679089 | ||||||
chr17:10679094 | C | T | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2025G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2025 | chr17 | 10679094 | ||||||
chr17:10679102 | T | C | 1 | a0001c0001t0115 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2017A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 2017 | chr17 | 10679102 | ||||||
chr17:10679140 | G | C | 21 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(18): Show |
54 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1979C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1979 | chr17 | 10679140 | ||||||
chr17:10679221 | T | C | 1 | a0001c0001t0079 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1898A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1898 | chr17 | 10679221 | ||||||
chr17:10679232 | G | T | 1 | a0002c0003t0025 | 3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1887C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1887 | chr17 | 10679232 | ||||||
chr17:10679346 | C | T | 2 | a0002c0002t0056 a0002c0002t0057 |
2 | HG01109.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1773G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1773 | chr17 | 10679346 | ||||||
chr17:10679396 | G | A | 7 | a0001c0001t0017 a0001c0001t0051 a0001c0001t0052 others(4): Show |
13 | HG02055.hp1 HG02056.hp1 HG02080.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1723C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1723 | chr17 | 10679396 | ||||||
chr17:10679399 | A | G | 1 | a0001c0001t0075 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1720T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1720 | chr17 | 10679399 | ||||||
chr17:10679425 | G | GT | 5 | a0001c0001t0117 a0002c0002t0021 a0002c0002t0029 others(2): Show |
11 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1693dupA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1693 | chr17 | 10679425 | ||||||
chr17:10679434 | C | A | 1 | a0001c0001t0117 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1685 | chr17 | 10679434 | ||||||
chr17:10679531 | G | C | 1 | a0001c0001t0088 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1588 | chr17 | 10679531 | ||||||
chr17:10679531 | G | T | 3 | a0002c0002t0020 a0002c0002t0054 a0002c0002t0055 |
6 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1588C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1588 | chr17 | 10679531 | ||||||
chr17:10679555 | A | G | 2 | a0001c0001t0068 a0001c0001t0083 |
2 | HG00544.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1564T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1564 | chr17 | 10679555 | ||||||
chr17:10679691 | A | G | 1 | a0001c0001t0090 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1428T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1428 | chr17 | 10679691 | ||||||
chr17:10679743 | A | AG | 14 | a0002c0002t0020 a0002c0002t0021 a0002c0002t0029 others(11): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1375_*1376insC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1375 | chr17 | 10679743 | ||||||
chr17:10679791 | A | G | 1 | a0001c0001t0089 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1328 | chr17 | 10679791 | ||||||
chr17:10679856 | G | A | 60 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(57): Show |
202 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1263C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1263 | chr17 | 10679856 | ||||||
chr17:10679946 | C | T | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1173G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1173 | chr17 | 10679946 | ||||||
chr17:10679961 | C | CG | 29 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(26): Show |
84 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1157dupC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1157 | chr17 | 10679961 | ||||||
chr17:10679961 | C | CGG | 13 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0022 others(10): Show |
40 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1156_*1157dupCC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1157 | chr17 | 10679961 | ||||||
chr17:10679961 | CG | C | 35 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0016 others(32): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1157delC | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1157 | chr17 | 10679961 | ||||||
chr17:10679963 | G | A | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1156C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1156 | chr17 | 10679963 | ||||||
chr17:10679970 | G | C | 9 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0042 others(6): Show |
51 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1149C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1149 | chr17 | 10679970 | ||||||
chr17:10679970 | G | GC | 3 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0075 |
12 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1148_*1149insG | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1148 | chr17 | 10679970 | ||||||
chr17:10680017 | G | A | 1 | a0001c0001t0080 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1102 | chr17 | 10680017 | ||||||
chr17:10680082 | G | A | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1037 | chr17 | 10680082 | ||||||
chr17:10680106 | T | C | 2 | a0001c0005t0032 a0001c0005t0060 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1013A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 1013 | chr17 | 10680106 | ||||||
chr17:10680126 | G | A | 2 | a0001c0001t0118 a0001c0001t0119 |
2 | HG02976.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*993C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 993 | chr17 | 10680126 | ||||||
chr17:10680148 | G | T | 1 | a0001c0001t0082 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*971C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 971 | chr17 | 10680148 | ||||||
chr17:10680251 | G | A | 1 | a0001c0001t0081 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*868C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 868 | chr17 | 10680251 | ||||||
chr17:10680272 | T | C | 83 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(80): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*847A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 847 | chr17 | 10680272 | ||||||
chr17:10680329 | C | T | 2 | a0001c0001t0063 a0001c0001t0064 |
2 | HG03486.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*790G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 790 | chr17 | 10680329 | ||||||
chr17:10680397 | G | C | 65 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(62): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*722C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 722 | chr17 | 10680397 | ||||||
chr17:10680467 | C | A | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 652 | chr17 | 10680467 | ||||||
chr17:10680575 | T | G | 3 | a0002c0002t0033 a0002c0002t0061 a0002c0002t0062 |
4 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*544A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 544 | chr17 | 10680575 | ||||||
chr17:10680809 | G | A | 17 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(14): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*310C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 310 | chr17 | 10680809 | ||||||
chr17:10680847 | A | G | 16 | a0001c0005t0032 a0001c0005t0060 a0002c0002t0020 others(13): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*272T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 272 | chr17 | 10680847 | ||||||
chr17:10680849 | A | T | 7 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0028 others(4): Show |
14 | HG00673.hp2 HG02056.hp1 HG02080.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*270T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 270 | chr17 | 10680849 | ||||||
chr17:10681063 | G | A | 1 | a0001c0001t0120 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 56 | chr17 | 10681063 | ||||||
chr17:10681101 | C | T | 1 | a0002c0003t0049 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 6/6 | 18 | chr17 | 10681101 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10681403 | C | T | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-150G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10681403 | |||||||
chr17:10681436 | C | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-183G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10681436 | |||||||
chr17:10681647 | T | C | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.772-394A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10681647 | |||||||
chr17:10681651 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-398G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10681651 | |||||||
chr17:10681844 | A | C | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.772-591T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10681844 | |||||||
chr17:10682129 | C | G | 1 | a0001c0001t0004g0187 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.772-876G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682129 | |||||||
chr17:10682235 | T | C | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.772-982A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682235 | |||||||
chr17:10682385 | A | G | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-1132T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682385 | |||||||
chr17:10682390 | A | C | 4 | a0002c0002t0021g0019 a0002c0002t0029g0063 a0002c0002t0030g0064 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-1137T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682390 | |||||||
chr17:10682414 | A | G | 2 | a0002c0003t0044g0224 a0002c0003t0046g0220 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.772-1161T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682414 | |||||||
chr17:10682636 | A | G | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-1383T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682636 | |||||||
chr17:10682653 | C | T | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.772-1400G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682653 | |||||||
chr17:10682706 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(113): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.772-1453A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682706 | |||||||
chr17:10682752 | T | C | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.772-1499A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682752 | |||||||
chr17:10682868 | G | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-1615C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682868 | |||||||
chr17:10682896 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-1643G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10682896 | |||||||
chr17:10683009 | G | A | 1 | a0001c0001t0011g0179 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.772-1756C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683009 | |||||||
chr17:10683181 | G | A | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-1928C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683181 | |||||||
chr17:10683201 | C | G | 4 | a0002c0002t0021g0019 a0002c0002t0029g0063 a0002c0002t0030g0064 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.772-1948G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683201 | |||||||
chr17:10683305 | G | A | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-2052C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683305 | |||||||
chr17:10683566 | C | T | 1 | a0001c0001t0022g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.772-2313G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683566 | |||||||
chr17:10683625 | T | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.772-2372A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683625 | |||||||
chr17:10683723 | T | C | 1 | a0001c0001t0112g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.772-2470A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683723 | |||||||
chr17:10683747 | T | A | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.772-2494A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683747 | |||||||
chr17:10683809 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.772-2556C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683809 | |||||||
chr17:10683844 | T | A | 1 | a0001c0001t0004g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.772-2591A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683844 | |||||||
chr17:10683861 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.772-2608G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683861 | |||||||
chr17:10683890 | T | C | 5 | a0001c0001t0017g0014 a0001c0001t0017g0069 a0001c0001t0051g0067 others(2): Show |
8 | HG02056.hp1 HG02080.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.772-2637A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683890 | |||||||
chr17:10683925 | C | T | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.772-2672G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10683925 | |||||||
chr17:10684088 | T | C | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+2639A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684088 | |||||||
chr17:10684089 | C | T | 35 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(32): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.771+2638G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684089 | |||||||
chr17:10684110 | T | C | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+2617A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684110 | |||||||
chr17:10684116 | T | C | 1 | a0002c0003t0025g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.771+2611A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684116 | |||||||
chr17:10684189 | T | C | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.771+2538A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684189 | |||||||
chr17:10684200 | T | C | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+2527A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684200 | |||||||
chr17:10684574 | G | C | 14 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(11): Show |
23 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.771+2153C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684574 | |||||||
chr17:10684692 | T | C | 4 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0054g0217 others(1): Show |
6 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+2035A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684692 | |||||||
chr17:10684799 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+1928G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684799 | |||||||
chr17:10684800 | G | A | 1 | a0001c0001t0111g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.771+1927C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684800 | |||||||
chr17:10684807 | C | T | 1 | a0001c0001t0006g0165 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.771+1920G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684807 | |||||||
chr17:10684915 | C | T | 2 | a0001c0001t0008g0079 a0001c0001t0015g0080 |
2 | HG02155.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.771+1812G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10684915 | |||||||
chr17:10685042 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.771+1685T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685042 | |||||||
chr17:10685051 | C | G | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.771+1676G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685051 | |||||||
chr17:10685118 | T | C | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+1609A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685118 | |||||||
chr17:10685238 | C | G | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.771+1489G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685238 | |||||||
chr17:10685289 | C | T | 3 | a0002c0003t0019g0061 a0002c0003t0019g0222 a0002c0003t0019g0223 |
4 | HG01106.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1438G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685289 | |||||||
chr17:10685361 | C | T | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.771+1366G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685361 | |||||||
chr17:10685388 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.771+1339C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685388 | |||||||
chr17:10685396 | T | G | 4 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(1): Show |
4 | HG03927.hp2 NA18522.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1331A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685396 | |||||||
chr17:10685421 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.771+1306A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685421 | |||||||
chr17:10685461 | A | C | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.771+1266T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685461 | |||||||
chr17:10685549 | C | T | 1 | a0001c0001t0008g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.771+1178G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685549 | |||||||
chr17:10685558 | A | C | 1 | a0001c0001t0002g0049 | 2 | HG00642.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.771+1169T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685558 | |||||||
chr17:10685645 | C | T | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+1082G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685645 | |||||||
chr17:10685832 | T | C | 1 | a0001c0001t0111g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.771+895A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685832 | |||||||
chr17:10685888 | T | C | 2 | a0001c0005t0032g0213 a0001c0005t0060g0211 |
2 | NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.771+839A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685888 | |||||||
chr17:10685939 | T | C | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+788A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685939 | |||||||
chr17:10685972 | A | C | 1 | a0001c0001t0088g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.771+755T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10685972 | |||||||
chr17:10686044 | C | G | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+683G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686044 | |||||||
chr17:10686093 | C | T | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.771+634G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686093 | |||||||
chr17:10686180 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+547G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686180 | |||||||
chr17:10686193 | GATCGCAC others(6): Show |
G | 1 | a0001c0001t0026g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.771+521_771+533del others(13): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686193 | |||||||
chr17:10686200 | C | G | 1 | a0001c0001t0006g0004 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.771+527G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686200 | |||||||
chr17:10686236 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+491G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686236 | |||||||
chr17:10686272 | C | T | 4 | a0001c0001t0002g0029 a0001c0001t0002g0206 a0001c0001t0011g0163 others(1): Show |
6 | NA18955.hp2 NA18997.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.771+455G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686272 | |||||||
chr17:10686317 | G | A | 1 | a0001c0001t0120g0113 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.771+410C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686317 | |||||||
chr17:10686452 | C | T | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.771+275G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686452 | |||||||
chr17:10686513 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.771+214G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686513 | |||||||
chr17:10686554 | C | T | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.771+173G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686554 | |||||||
chr17:10686581 | CA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(108): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.771+145delT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686581 | |||||||
chr17:10686581 | CAA | C | 25 | a0001c0001t0013g0133 a0001c0001t0015g0147 a0001c0001t0017g0014 others(22): Show |
37 | HG00741.hp2 HG01109.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.771+144_771+145del others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686581 | |||||||
chr17:10686622 | T | C | 4 | a0002c0002t0021g0019 a0002c0002t0029g0063 a0002c0002t0030g0064 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.771+105A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686622 | |||||||
chr17:10686626 | A | G | 1 | a0001c0001t0007g0186 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.771+101T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686626 | |||||||
chr17:10686654 | A | G | 1 | a0001c0001t0004g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.771+73T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 5/5 | chr17 | 10686654 | |||||||
chr17:10687016 | G | A | 5 | a0001c0001t0087g0071 a0002c0003t0044g0224 a0002c0003t0044g0225 others(2): Show |
5 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-174C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687016 | |||||||
chr17:10687065 | G | A | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-223C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687065 | |||||||
chr17:10687126 | G | A | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.656-284C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687126 | |||||||
chr17:10687126 | G | C | 1 | a0001c0001t0088g0077 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.656-284C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687126 | |||||||
chr17:10687146 | C | G | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.656-304G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687146 | |||||||
chr17:10687335 | G | GTTAA | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.656-497_656-494dup others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687335 | |||||||
chr17:10687415 | G | A | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-573C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687415 | |||||||
chr17:10687541 | C | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0101 others(3): Show |
9 | HG00733.hp1 HG01070.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-699G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687541 | |||||||
chr17:10687562 | A | G | 1 | a0001c0001t0096g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.656-720T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10687562 | |||||||
chr17:10688017 | T | C | 1 | a0002c0003t0019g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.656-1175A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688017 | |||||||
chr17:10688033 | T | G | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.656-1191A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688033 | |||||||
chr17:10688042 | C | T | 2 | a0001c0001t0063g0144 a0001c0001t0064g0145 |
2 | HG03486.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.656-1200G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688042 | |||||||
chr17:10688057 | A | G | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-1215T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688057 | |||||||
chr17:10688100 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.656-1258A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688100 | |||||||
chr17:10688111 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0103 |
3 | HG00639.hp2 HG01934.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.656-1269A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688111 | |||||||
chr17:10688135 | T | C | 1 | a0001c0001t0004g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.656-1293A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688135 | |||||||
chr17:10688220 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.656-1378C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688220 | |||||||
chr17:10688256 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.656-1414G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688256 | |||||||
chr17:10688328 | G | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-1486C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688328 | |||||||
chr17:10688475 | A | G | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-1633T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688475 | |||||||
chr17:10688679 | T | C | 1 | a0001c0001t0005g0056 | 2 | NA18972.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.656-1837A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688679 | |||||||
chr17:10688684 | A | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0127 others(2): Show |
9 | HG00423.hp1 HG01975.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-1842T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688684 | |||||||
chr17:10688709 | G | A | 1 | a0001c0001t0068g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.656-1867C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688709 | |||||||
chr17:10688799 | G | A | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.656-1957C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688799 | |||||||
chr17:10688809 | C | G | 7 | a0001c0001t0004g0006 a0001c0001t0004g0187 a0001c0001t0004g0209 others(4): Show |
18 | HG01257.hp2 HG01516.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.656-1967G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688809 | |||||||
chr17:10688818 | TAGAAAGC others(309): Show |
T | 16 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(13): Show |
25 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-2292_656-1977d others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688818 | |||||||
chr17:10688912 | C | T | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.656-2070G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688912 | |||||||
chr17:10688932 | C | T | 4 | a0001c0001t0002g0181 a0001c0005t0032g0212 a0001c0005t0032g0213 others(1): Show |
4 | HG01175.hp1 HG03927.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-2090G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688932 | |||||||
chr17:10688943 | C | T | 2 | a0001c0001t0113g0118 a0001c0001t0114g0117 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.656-2101G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688943 | |||||||
chr17:10688972 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.656-2130G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688972 | |||||||
chr17:10688973 | G | A | 1 | a0001c0001t0112g0112 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.656-2131C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688973 | |||||||
chr17:10688979 | G | A | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.656-2137C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688979 | |||||||
chr17:10688982 | A | G | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.656-2140T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688982 | |||||||
chr17:10688985 | G | C | 2 | a0002c0003t0025g0059 a0002c0003t0025g0215 |
3 | HG00741.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.656-2143C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10688985 | |||||||
chr17:10689019 | G | C | 2 | a0001c0001t0004g0047 a0001c0001t0007g0028 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.656-2177C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689019 | |||||||
chr17:10689115 | C | CA | 5 | a0001c0001t0002g0003 a0001c0001t0004g0016 a0001c0001t0006g0165 others(2): Show |
6 | HG03516.hp1 HG06807.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-2274dupT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689115 | |||||||
chr17:10689115 | C | CAAAA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0012g0008 others(4): Show |
10 | HG00639.hp2 HG02129.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-2277_656-2274d others(6): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689115 | |||||||
chr17:10689115 | C | CAAAAA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(101): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.656-2278_656-2274d others(7): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689115 | |||||||
chr17:10689115 | C | CAAAAAA | 18 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0032 others(15): Show |
24 | HG00621.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.656-2279_656-2274d others(8): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689115 | |||||||
chr17:10689143 | G | A | 1 | a0001c0001t0108g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.656-2301C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689143 | |||||||
chr17:10689257 | C | T | 4 | a0002c0002t0021g0019 a0002c0002t0029g0063 a0002c0002t0030g0064 others(1): Show |
10 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-2415G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689257 | |||||||
chr17:10689350 | C | G | 1 | a0002c0003t0025g0215 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.656-2508G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689350 | |||||||
chr17:10689409 | ATG | A | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+2461_655+2462d others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689409 | |||||||
chr17:10689419 | T | TAATA | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.655+2449_655+2452d others(6): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689419 | |||||||
chr17:10689528 | T | A | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+2344A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689528 | |||||||
chr17:10689557 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.655+2315A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689557 | |||||||
chr17:10689676 | G | C | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655+2196C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689676 | |||||||
chr17:10689851 | C | G | 2 | a0001c0001t0094g0065 a0001c0001t0101g0066 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655+2021G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689851 | |||||||
chr17:10689970 | G | A | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655+1902C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10689970 | |||||||
chr17:10690093 | T | C | 1 | a0001c0001t0009g0057 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.655+1779A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690093 | |||||||
chr17:10690149 | G | C | 2 | a0001c0001t0094g0065 a0001c0001t0101g0066 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.655+1723C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690149 | |||||||
chr17:10690229 | A | G | 1 | a0001c0001t0114g0117 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.655+1643T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690229 | |||||||
chr17:10690325 | A | C | 4 | a0001c0001t0002g0012 a0001c0001t0002g0161 a0001c0001t0011g0048 others(1): Show |
9 | HG01074.hp1 HG01167.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+1547T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690325 | |||||||
chr17:10690339 | A | G | 1 | a0001c0001t0043g0131 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.655+1533T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690339 | |||||||
chr17:10690428 | T | A | 16 | a0001c0001t0018g0115 a0002c0002t0020g0031 a0002c0002t0020g0219 others(13): Show |
25 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.655+1444A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690428 | |||||||
chr17:10690443 | A | G | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+1429T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690443 | |||||||
chr17:10690510 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.655+1362T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690510 | |||||||
chr17:10690562 | A | C | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+1310T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690562 | |||||||
chr17:10690829 | ATACGTCA others(8): Show |
A | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+1028_655+1042d others(17): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690829 | |||||||
chr17:10690838 | G | A | 1 | a0001c0001t0018g0015 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.655+1034C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690838 | |||||||
chr17:10690907 | T | A | 1 | a0001c0001t0002g0185 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.655+965A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690907 | |||||||
chr17:10690969 | G | A | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+903C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690969 | |||||||
chr17:10690987 | G | A | 2 | a0001c0001t0118g0141 a0001c0001t0119g0142 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.655+885C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10690987 | |||||||
chr17:10691000 | T | C | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+872A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691000 | |||||||
chr17:10691012 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(147): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.655+860A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691012 | |||||||
chr17:10691059 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.655+813A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691059 | |||||||
chr17:10691134 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.655+738G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691134 | |||||||
chr17:10691161 | C | T | 2 | a0001c0001t0004g0047 a0001c0001t0007g0028 |
5 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+711G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691161 | |||||||
chr17:10691220 | C | T | 3 | a0002c0003t0019g0061 a0002c0003t0019g0222 a0002c0003t0019g0223 |
4 | HG01106.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+652G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691220 | |||||||
chr17:10691310 | G | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+562C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691310 | |||||||
chr17:10691357 | GTGATCCA others(8): Show |
G | 1 | a0002c0002t0056g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.655+500_655+514del others(15): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691357 | |||||||
chr17:10691373 | G | A | 1 | a0002c0002t0056g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.655+499C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691373 | |||||||
chr17:10691402 | C | T | 1 | a0001c0001t0038g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+470G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691402 | |||||||
chr17:10691471 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.655+401C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691471 | |||||||
chr17:10691472 | T | C | 1 | a0002c0002t0058g0231 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.655+400A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691472 | |||||||
chr17:10691562 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.655+310C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691562 | |||||||
chr17:10691605 | C | G | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+267G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691605 | |||||||
chr17:10691700 | T | A | 1 | a0002c0003t0049g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+172A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691700 | |||||||
chr17:10691707 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(132): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.655+165G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691707 | |||||||
chr17:10691740 | C | T | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.655+132G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691740 | |||||||
chr17:10691835 | A | C | 3 | a0001c0001t0010g0013 a0001c0001t0010g0045 a0001c0007t0010g0214 |
8 | HG02148.hp1 NA18946.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.655+37T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691835 | |||||||
chr17:10691862 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.655+10T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 4/5 | chr17 | 10691862 | |||||||
chr17:10692074 | G | A | 19 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(16): Show |
28 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.563-110C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692074 | |||||||
chr17:10692081 | G | A | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.563-117C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692081 | |||||||
chr17:10692105 | G | A | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.563-141C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692105 | |||||||
chr17:10692126 | T | C | 1 | a0002c0002t0062g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.563-162A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692126 | |||||||
chr17:10692603 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.562+161C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692603 | |||||||
chr17:10692638 | C | T | 1 | a0002c0002t0058g0231 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.562+126G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 3/5 | chr17 | 10692638 | |||||||
chr17:10692983 | C | T | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.365-22G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10692983 | |||||||
chr17:10693063 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0091 others(8): Show |
16 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.365-102C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693063 | |||||||
chr17:10693096 | C | T | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-135G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693096 | |||||||
chr17:10693104 | T | A | 1 | a0001c0001t0006g0204 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.365-143A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693104 | |||||||
chr17:10693110 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.365-149T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693110 | |||||||
chr17:10693113 | C | A | 6 | a0001c0001t0104g0119 a0001c0001t0109g0120 a0002c0003t0025g0059 others(3): Show |
7 | HG00741.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-152G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693113 | |||||||
chr17:10693166 | G | T | 1 | a0001c0001t0024g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.365-205C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693166 | |||||||
chr17:10693216 | A | G | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.365-255T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693216 | |||||||
chr17:10693261 | T | C | 25 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(22): Show |
35 | HG00741.hp2 HG01109.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.365-300A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693261 | |||||||
chr17:10693289 | C | CAA | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-330_365-329dup others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693289 | |||||||
chr17:10693346 | A | C | 18 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(15): Show |
27 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.365-385T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693346 | |||||||
chr17:10693366 | T | C | 36 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(33): Show |
57 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.365-405A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693366 | |||||||
chr17:10693396 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(49): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.365-435G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693396 | |||||||
chr17:10693503 | C | G | 21 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(18): Show |
31 | HG00741.hp2 HG01109.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.365-542G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693503 | |||||||
chr17:10693513 | G | C | 1 | a0001c0001t0110g0121 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.365-552C>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693513 | |||||||
chr17:10693546 | T | C | 3 | a0001c0001t0023g0020 a0001c0001t0028g0036 a0001c0001t0050g0090 |
6 | HG00673.hp2 NA18949.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.365-585A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693546 | |||||||
chr17:10693567 | A | G | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.365-606T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693567 | |||||||
chr17:10693599 | G | A | 1 | a0001c0001t0037g0189 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.365-638C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693599 | |||||||
chr17:10693716 | G | A | 15 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(12): Show |
24 | HG01109.hp1 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-755C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693716 | |||||||
chr17:10693740 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(76): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.365-779A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693740 | |||||||
chr17:10693741 | G | A | 12 | a0001c0001t0013g0026 a0001c0001t0013g0042 a0001c0001t0013g0075 others(9): Show |
17 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.365-780C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693741 | |||||||
chr17:10693997 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0003g0126 a0001c0001t0089g0100 |
3 | HG01109.hp2 HG01175.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.365-1036G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10693997 | |||||||
chr17:10694118 | C | T | 21 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(18): Show |
31 | HG00741.hp2 HG01109.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.365-1157G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694118 | |||||||
chr17:10694168 | C | T | 2 | a0001c0001t0013g0125 a0001c0001t0026g0124 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.365-1207G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694168 | |||||||
chr17:10694225 | A | G | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-1264T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694225 | |||||||
chr17:10694340 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.365-1379G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694340 | |||||||
chr17:10694350 | T | A | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.365-1389A>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694350 | |||||||
chr17:10694352 | C | G | 2 | a0001c0005t0032g0213 a0001c0005t0060g0211 |
2 | NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.364+1389G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694352 | |||||||
chr17:10694356 | T | C | 3 | a0001c0001t0007g0190 a0001c0001t0063g0144 a0001c0001t0064g0145 |
3 | HG01099.hp1 HG03486.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.364+1385A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694356 | |||||||
chr17:10694447 | CAAAT | C | 19 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(16): Show |
28 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.364+1290_364+1293d others(6): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694447 | |||||||
chr17:10694577 | A | G | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+1164T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694577 | |||||||
chr17:10694694 | C | T | 19 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(16): Show |
28 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.364+1047G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694694 | |||||||
chr17:10694766 | TTTTG | T | 14 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0033g0062 others(11): Show |
17 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.364+971_364+974del others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694766 | |||||||
chr17:10694842 | C | A | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.364+899G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694842 | |||||||
chr17:10694858 | ATATG | A | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+879_364+882del others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10694858 | |||||||
chr17:10695015 | C | A | 2 | a0001c0001t0118g0141 a0001c0001t0119g0142 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.364+726G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695015 | |||||||
chr17:10695141 | C | G | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.364+600G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695141 | |||||||
chr17:10695173 | C | T | 1 | a0001c0001t0019g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.364+568G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695173 | |||||||
chr17:10695266 | C | A | 1 | a0001c0001t0016g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.364+475G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695266 | |||||||
chr17:10695292 | A | C | 28 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(25): Show |
39 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.364+449T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695292 | |||||||
chr17:10695317 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(135): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.364+424A>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695317 | |||||||
chr17:10695497 | A | G | 5 | a0002c0002t0021g0019 a0002c0002t0031g0060 a0002c0003t0019g0061 others(2): Show |
10 | HG01106.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.364+244T>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695497 | |||||||
chr17:10695535 | T | C | 31 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(28): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.364+206A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695535 | |||||||
chr17:10695541 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.364+200A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695541 | |||||||
chr17:10695598 | T | C | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364+143A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695598 | |||||||
chr17:10695609 | T | C | 2 | a0001c0001t0118g0141 a0001c0001t0119g0142 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.364+132A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695609 | |||||||
chr17:10695624 | A | AT | 25 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(22): Show |
35 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.364+116dupA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695624 | |||||||
chr17:10695631 | G | A | 1 | a0001c0001t0005g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.364+110C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695631 | |||||||
chr17:10695699 | GAAGA | G | 31 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(28): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.364+38_364+41delTC others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695699 | |||||||
chr17:10695704 | C | G | 31 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(28): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.364+37G>C | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695704 | |||||||
chr17:10695706 | TTTATAC | T | 31 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(28): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.364+29_364+34delGT others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695706 | |||||||
chr17:10695714 | G | T | 31 | a0001c0001t0008g0007 a0001c0001t0008g0076 a0001c0001t0008g0078 others(28): Show |
52 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.364+27C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 2/5 | chr17 | 10695714 | |||||||
chr17:10695977 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.274-146T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10695977 | |||||||
chr17:10695987 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(107): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.274-156A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10695987 | |||||||
chr17:10696066 | G | A | 2 | a0001c0001t0097g0138 a0001c0001t0107g0139 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.274-235C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696066 | |||||||
chr17:10696071 | T | TA | 17 | a0001c0001t0002g0146 a0001c0001t0002g0203 a0001c0001t0004g0196 others(14): Show |
17 | HG00609.hp2 HG01243.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-241dupT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696071 | T | TAA | 7 | a0001c0001t0008g0076 a0001c0001t0015g0033 a0001c0001t0017g0014 others(4): Show |
11 | HG02056.hp1 HG03491.hp2 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-242_274-241dup others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696071 | T | TAAA | 27 | a0001c0001t0001g0037 a0001c0001t0001g0091 a0001c0001t0001g0092 others(24): Show |
45 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.274-243_274-241dup others(3): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696071 | T | TAAAA | 52 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(49): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.274-244_274-241dup others(4): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696071 | T | TAAAAA | 18 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0003g0009 others(15): Show |
28 | HG00438.hp1 HG00621.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-245_274-241dup others(5): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696071 | TA | T | 10 | a0001c0001t0002g0027 a0001c0001t0002g0154 a0001c0001t0005g0046 others(7): Show |
15 | HG00099.hp1 HG02109.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-241delT | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696071 | |||||||
chr17:10696075 | A | T | 19 | a0002c0002t0020g0031 a0002c0002t0021g0019 a0002c0002t0029g0063 others(16): Show |
29 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.274-244T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696075 | |||||||
chr17:10696076 | A | T | 2 | a0002c0002t0061g0221 a0002c0003t0046g0220 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.274-245T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696076 | |||||||
chr17:10696080 | A | T | 2 | a0001c0001t0039g0043 a0001c0001t0071g0153 |
3 | HG00140.hp2 HG01074.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.274-249T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696080 | |||||||
chr17:10696087 | A | T | 1 | a0003c0008t0103g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-256T>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696087 | |||||||
chr17:10696167 | G | A | 2 | a0001c0001t0009g0205 a0001c0001t0024g0058 |
3 | HG00621.hp1 NA18960.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.274-336C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696167 | |||||||
chr17:10696167 | G | T | 1 | a0001c0001t0004g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.274-336C>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696167 | |||||||
chr17:10696172 | C | T | 2 | a0001c0001t0118g0141 a0001c0001t0119g0142 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.274-341G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696172 | |||||||
chr17:10696322 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.274-491G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696322 | |||||||
chr17:10696377 | G | A | 1 | a0001c0001t0100g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.274-546C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696377 | |||||||
chr17:10696479 | A | C | 3 | a0002c0003t0025g0059 a0002c0003t0025g0215 a0002c0003t0049g0216 |
4 | HG00741.hp2 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-648T>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696479 | |||||||
chr17:10696633 | T | C | 2 | a0001c0001t0097g0138 a0001c0001t0107g0139 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.273+602A>G | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696633 | |||||||
chr17:10696672 | AACTAG | A | 28 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 others(25): Show |
39 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.273+558_273+562del others(5): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696672 | |||||||
chr17:10696743 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.273+492C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696743 | |||||||
chr17:10696821 | C | A | 1 | a0002c0002t0059g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+414G>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696821 | |||||||
chr17:10696821 | C | T | 21 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(18): Show |
31 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+414G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696821 | |||||||
chr17:10696952 | A | AT | 13 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0002g0143 others(10): Show |
14 | HG00609.hp2 HG01516.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+282dupA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696952 | |||||||
chr17:10696952 | A | ATT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(90): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.273+281_273+282dup others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696952 | |||||||
chr17:10696952 | A | ATTT | 8 | a0001c0001t0001g0032 a0001c0001t0017g0014 a0001c0001t0017g0069 others(5): Show |
12 | HG01952.hp2 HG02056.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+280_273+282dup others(3): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696952 | |||||||
chr17:10696952 | AT | A | 11 | a0001c0001t0002g0206 a0001c0001t0004g0209 a0001c0001t0005g0208 others(8): Show |
13 | HG02015.hp2 HG02647.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+282delA | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696952 | |||||||
chr17:10696952 | ATT | A | 22 | a0001c0005t0032g0213 a0002c0002t0021g0019 a0002c0002t0029g0063 others(19): Show |
31 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+281_273+282del others(2): Show |
SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10696952 | |||||||
chr17:10697116 | G | A | 22 | a0002c0002t0020g0031 a0002c0002t0020g0219 a0002c0002t0021g0019 others(19): Show |
32 | HG01106.hp2 HG01109.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.273+119C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10697116 | |||||||
chr17:10697148 | G | A | 1 | a0002c0002t0058g0231 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.273+87C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10697148 | |||||||
chr17:10697162 | C | T | 2 | a0001c0001t0094g0065 a0001c0001t0101g0066 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.273+73G>A | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10697162 | |||||||
chr17:10697179 | G | A | 3 | a0001c0005t0032g0212 a0001c0005t0032g0213 a0001c0005t0060g0211 |
3 | HG03927.hp2 NA18956.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.273+56C>T | SCO1 | ENSG00000133028.12 | transcript | ENST00000255390.10 | protein_coding | 1/5 | chr17 | 10697179 |