Item | Value |
---|---|
geneid | 54434 |
ensemblid | ENSG00000084112.15 |
hgncid | 30579 |
symbol | SSH1 |
name | slingshot protein phosphatase 1 |
refseq_nuc | NM_018984.4 |
refseq_prot | NP_061857.3 |
ensembl_nuc | ENST00000326495.10 |
ensembl_prot | ENSP00000315713.5 |
mane_status | MANE Select |
chr | chr12 |
start | 108778191 |
end | 108857583 |
strand | - |
ver | v1.2 |
region | chr12:108778191-108857583 |
region5000 | chr12:108773191-108862583 |
regionname0 | SSH1_chr12_108778191_108857583 |
regionname5000 | SSH1_chr12_108773191_108862583 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1049 | 314 | 77 | 65 | 120 | 9 | 41 | 91 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0002 | 0/0 | 1049 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0003 | 0/0 | 1049 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0004 | 0/0 | 1049 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0005 | 0/0 | 1049 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0006 | 0/0 | 1049 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0007 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0008 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0009 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0010 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
a0011 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | MALVT others(1044): Show |
chr12 | 108773191 | 108862583 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3147 | 188 | 51 | 38 | 84 | 4 | 10 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0002 | 1/0 | 3147 | 104 | 15 | 26 | 32 | 5 | 25 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0003 | 0/0 | 3147 | 6 | 6 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0006 | 0/0 | 3147 | 2 | 1 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0007 | 0/0 | 3147 | 2 | 0 | 0 | 0 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0008 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0009 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0010 | 0/0 | 3147 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0013 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0017 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0019 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0023 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0024 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0001c0025 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0002c0005 | 0/0 | 3147 | 4 | 0 | 0 | 4 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0003c0004 | 0/0 | 3147 | 4 | 4 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0004c0011 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0005c0015 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0005c0021 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0006c0022 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0007c0018 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0008c0020 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0009c0014 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0010c0012 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 | ||
a0011c0016 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | ATGGC others(3142): Show |
chr12 | 108773191 | 108862583 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13036 | 5 | 0 | 3 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0002 | 0/0 | 13032 | 31 | 0 | 6 | 24 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0004 | 0/0 | 13034 | 26 | 0 | 4 | 21 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0005 | 0/0 | 13033 | 11 | 2 | 0 | 8 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0006 | 0/1 | 13033 | 10 | 6 | 3 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0007 | 0/0 | 13034 | 9 | 8 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0008 | 0/0 | 13032 | 7 | 1 | 5 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0009 | 0/0 | 13033 | 7 | 7 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0010 | 0/0 | 13038 | 6 | 5 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0011 | 0/0 | 13033 | 4 | 0 | 3 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0012 | 0/0 | 13032 | 5 | 5 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0013 | 0/0 | 13038 | 4 | 0 | 0 | 4 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0014 | 0/0 | 13034 | 3 | 0 | 0 | 1 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0015 | 0/0 | 13033 | 4 | 0 | 0 | 0 | 1 | 3 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0018 | 0/0 | 13033 | 3 | 0 | 0 | 3 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0022 | 0/0 | 13034 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0023 | 0/0 | 13035 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13030): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0024 | 0/0 | 13033 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0025 | 0/0 | 13036 | 2 | 0 | 0 | 0 | 2 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0026 | 0/0 | 13032 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0027 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0028 | 0/0 | 13033 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0029 | 0/0 | 13033 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0030 | 0/0 | 13033 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0031 | 0/0 | 13030 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13025): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0034 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0035 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0038 | 0/0 | 13033 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0053 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0054 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0055 | 0/0 | 13033 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0056 | 0/0 | 13035 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13030): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0057 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0058 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0059 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0060 | 0/0 | 13035 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13030): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0061 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0062 | 0/0 | 13033 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0063 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0064 | 0/0 | 13033 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0066 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0067 | 0/0 | 13033 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0068 | 0/0 | 13037 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13032): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0069 | 0/0 | 13033 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0070 | 0/0 | 13033 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0071 | 0/0 | 13033 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0072 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0077 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0079 | 0/0 | 13030 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13025): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0080 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0081 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0082 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0083 | 0/0 | 13032 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0084 | 0/0 | 13034 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0086 | 0/0 | 13035 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13030): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0089 | 0/0 | 13037 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13032): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0090 | 0/0 | 13033 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0091 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0001t0092 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0001 | 0/0 | 13036 | 48 | 1 | 14 | 22 | 1 | 10 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0003 | 1/0 | 13034 | 31 | 11 | 10 | 0 | 2 | 7 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0011 | 0/0 | 13033 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0019 | 0/0 | 13036 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0021 | 0/0 | 13037 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13032): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0027 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0032 | 0/0 | 13038 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0033 | 0/0 | 13036 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0040 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0041 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0042 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0043 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0044 | 0/0 | 13036 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0045 | 0/0 | 13036 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0046 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0047 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0048 | 0/0 | 13037 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13032): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0051 | 0/0 | 13036 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0052 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0073 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0074 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0075 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0076 | 0/0 | 13035 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13030): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0078 | 0/0 | 13034 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0087 | 0/0 | 13034 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0002t0088 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0003t0001 | 0/0 | 13036 | 3 | 3 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0003t0020 | 0/0 | 13036 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0003t0039 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0006t0003 | 0/0 | 13034 | 2 | 1 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0007t0002 | 0/0 | 13032 | 2 | 0 | 0 | 0 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0008t0036 | 0/0 | 13032 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0008t0037 | 0/0 | 13032 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0009t0049 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0009t0050 | 0/0 | 13038 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13033): Show |
chr12 | 108773191 | 108862583 |
a0001c0010t0002 | 0/0 | 13032 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0013t0014 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0001c0017t0001 | 0/0 | 13036 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0019t0002 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0001c0023t0001 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0001c0024t0021 | 0/0 | 13037 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13032): Show |
chr12 | 108773191 | 108862583 |
a0001c0025t0011 | 0/0 | 13033 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0002c0005t0017 | 0/0 | 13033 | 3 | 0 | 0 | 3 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0002c0005t0065 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0003c0004t0016 | 0/0 | 13032 | 4 | 4 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13027): Show |
chr12 | 108773191 | 108862583 |
a0004c0011t0005 | 0/0 | 13033 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13028): Show |
chr12 | 108773191 | 108862583 |
a0005c0015t0085 | 0/0 | 13034 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0005c0021t0004 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0006c0022t0003 | 0/0 | 13034 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0007c0018t0004 | 0/0 | 13034 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0008c0020t0001 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
a0009c0014t0004 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0010c0012t0003 | 0/0 | 13034 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13029): Show |
chr12 | 108773191 | 108862583 |
a0011c0016t0001 | 0/0 | 13036 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | AGGAG others(13031): Show |
chr12 | 108773191 | 108862583 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0011g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0011g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0011g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0012g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0012g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0014g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0014g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0014g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0015g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0015g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0018g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0018g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0022g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0022g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0023g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0024g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0025g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0025g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0026g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0026g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0027g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0028g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0028g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0029g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0030g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0031g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0031g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0034g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0035g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0038g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0053g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0054g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0055g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0056g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0057g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0058g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0059g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0060g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0061g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0062g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0063g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0064g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0066g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0067g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0068g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0069g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0070g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0071g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0072g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0077g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0079g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0080g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0081g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0082g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0083g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0084g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0086g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0089g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0090g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0091g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0001t0092g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0011g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0019g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0019g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0021g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0027g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0032g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0033g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0040g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0041g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0042g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0043g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0044g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0045g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0046g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0047g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0048g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0051g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0052g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0073g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0074g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0075g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0076g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0078g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0087g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0002t0088g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0003t0039g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0006t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0006t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0007t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0007t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0008t0036g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0008t0037g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0009t0049g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0009t0050g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0010t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0010t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0013t0014g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0017t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0019t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0023t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0024t0021g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0001c0025t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0002c0005t0017g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0002c0005t0017g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0002c0005t0065g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0003c0004t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0003c0004t0016g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0003c0004t0016g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0003c0004t0016g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0004c0011t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0004c0011t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0005c0015t0085g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0005c0021t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0006c0022t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0007c0018t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0008c0020t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0009c0014t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0010c0012t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
a0011c0016t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0015 | g0124 | EUR | GBR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00099 | hp2 | a0001 | c0002 | t0088 | g0280 | EUR | GBR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00140 | hp1 | a0001 | c0002 | t0003 | g0273 | EUR | GBR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00140 | hp2 | a0001 | c0001 | t0011 | g0250 | EUR | GBR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00438 | hp1 | a0001 | c0001 | t0092 | g0189 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0291 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00673 | hp1 | a0001 | c0001 | t0058 | g0178 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00673 | hp2 | a0001 | c0002 | t0047 | g0074 | EAS | CHS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0239 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0284 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00738 | hp1 | a0001 | c0002 | t0045 | g0053 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0266 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0287 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0253 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0021 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01070 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0021 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01074 | hp1 | a0001 | c0001 | t0072 | g0025 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0272 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01081 | hp2 | a0001 | c0001 | t0067 | g0209 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0180 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01167 | hp1 | a0001 | c0001 | t0086 | g0114 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01167 | hp2 | a0001 | c0001 | t0062 | g0133 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01168 | hp1 | a0001 | c0001 | t0081 | g0121 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01168 | hp2 | a0001 | c0001 | t0028 | g0113 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01169 | hp2 | a0001 | c0001 | t0028 | g0115 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0278 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0028 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01243 | hp2 | a0001 | c0006 | t0003 | g0254 | AMR | PUR | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0027 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01255 | hp2 | a0006 | c0022 | t0003 | g0265 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01256 | hp1 | a0001 | c0001 | t0077 | g0279 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01261 | hp1 | a0001 | c0001 | t0070 | g0249 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0274 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01346 | hp1 | a0001 | c0001 | t0027 | g0276 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01358 | hp1 | a0001 | c0002 | t0027 | g0275 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01433 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0181 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0070 | EUR | IBS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01517 | hp2 | a0001 | c0002 | t0076 | g0271 | EUR | IBS | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0293 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01884 | hp2 | a0001 | c0009 | t0049 | g0302 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01891 | hp2 | a0001 | c0001 | t0056 | g0211 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01943 | hp2 | a0001 | c0001 | t0038 | g0126 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01952 | hp2 | a0001 | c0001 | t0071 | g0251 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01978 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02015 | hp1 | a0002 | c0005 | t0017 | g0141 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02040 | hp2 | a0001 | c0002 | t0019 | g0038 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0104 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0234 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02071 | hp1 | a0007 | c0018 | t0004 | g0164 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02071 | hp2 | a0001 | c0001 | t0054 | g0080 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02074 | hp1 | a0001 | c0001 | t0023 | g0185 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02129 | hp1 | a0001 | c0002 | t0046 | g0037 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02132 | hp1 | a0002 | c0005 | t0017 | g0010 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02145 | hp1 | a0001 | c0002 | t0040 | g0055 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02145 | hp2 | a0003 | c0004 | t0016 | g0227 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02165 | hp2 | a0001 | c0002 | t0052 | g0077 | EAS | CDX | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02257 | hp1 | a0001 | c0001 | t0010 | g0244 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02257 | hp2 | a0001 | c0008 | t0036 | g0308 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0224 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02280 | hp1 | a0001 | c0003 | t0020 | g0231 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02280 | hp2 | a0004 | c0011 | t0005 | g0218 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0283 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02451 | hp2 | a0003 | c0004 | t0016 | g0230 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02523 | hp2 | a0001 | c0001 | t0080 | g0223 | EAS | KHV | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02572 | hp1 | a0001 | c0002 | t0078 | g0258 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0296 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02602 | hp1 | a0001 | c0025 | t0011 | g0252 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02602 | hp2 | a0001 | c0002 | t0032 | g0049 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02622 | hp1 | a0008 | c0020 | t0001 | g0157 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0130 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0286 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0210 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0158 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02735 | hp2 | a0001 | c0017 | t0001 | g0076 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02818 | hp1 | a0001 | c0001 | t0035 | g0304 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02886 | hp1 | a0001 | c0001 | t0089 | g0306 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02886 | hp2 | a0003 | c0004 | t0016 | g0229 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02896 | hp1 | a0001 | c0001 | t0030 | g0016 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0277 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02897 | hp2 | a0001 | c0001 | t0030 | g0016 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02922 | hp2 | a0001 | c0001 | t0010 | g0241 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02965 | hp1 | a0001 | c0008 | t0037 | g0307 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02965 | hp2 | a0001 | c0009 | t0050 | g0303 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02970 | hp1 | a0001 | c0003 | t0020 | g0232 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0247 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02976 | hp1 | a0001 | c0001 | t0031 | g0294 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02976 | hp2 | a0001 | c0001 | t0055 | g0116 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03017 | hp1 | a0001 | c0001 | t0014 | g0219 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03041 | hp2 | a0001 | c0001 | t0083 | g0112 | AFR | GWD | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0215 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0305 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03195 | hp2 | a0001 | c0001 | t0031 | g0245 | AFR | ESN | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03209 | hp1 | a0001 | c0002 | t0087 | g0235 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03209 | hp2 | a0001 | c0001 | t0029 | g0015 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0289 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03239 | hp2 | a0001 | c0013 | t0014 | g0023 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0295 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03453 | hp2 | a0001 | c0001 | t0024 | g0261 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03490 | hp1 | a0001 | c0024 | t0021 | g0091 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0020 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0020 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03579 | hp1 | a0001 | c0001 | t0079 | g0246 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03669 | hp1 | a0001 | c0002 | t0011 | g0290 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03688 | hp1 | a0001 | c0001 | t0014 | g0221 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03688 | hp2 | a0001 | c0002 | t0044 | g0087 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0007 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03831 | hp2 | a0001 | c0002 | t0075 | g0268 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0184 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0269 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03927 | hp1 | a0001 | c0007 | t0002 | g0142 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03942 | hp1 | a0009 | c0014 | t0004 | g0163 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0281 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04115 | hp1 | a0001 | c0002 | t0033 | g0050 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04115 | hp2 | a0001 | c0002 | t0074 | g0264 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04184 | hp1 | a0001 | c0001 | t0064 | g0125 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04184 | hp2 | a0001 | c0002 | t0051 | g0062 | SAS | BEB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0248 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04199 | hp2 | a0001 | c0001 | t0015 | g0007 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04204 | hp1 | a0001 | c0007 | t0002 | g0143 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | STU | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0243 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18522 | hp2 | a0001 | c0001 | t0084 | g0106 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18612 | hp1 | a0001 | c0001 | t0063 | g0155 | EAS | CHB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0267 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18941 | hp1 | a0001 | c0001 | t0014 | g0220 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18942 | hp2 | a0001 | c0001 | t0018 | g0030 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18945 | hp1 | a0001 | c0001 | t0026 | g0160 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18945 | hp2 | a0002 | c0005 | t0017 | g0010 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18947 | hp2 | a0001 | c0002 | t0019 | g0064 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18948 | hp2 | a0001 | c0001 | t0026 | g0139 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18949 | hp2 | a0001 | c0002 | t0048 | g0096 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18950 | hp1 | a0001 | c0001 | t0091 | g0109 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18951 | hp2 | a0001 | c0002 | t0041 | g0073 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18960 | hp1 | a0001 | c0001 | t0022 | g0200 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18960 | hp2 | a0001 | c0001 | t0018 | g0026 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18963 | hp1 | a0001 | c0001 | t0018 | g0029 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18966 | hp2 | a0001 | c0001 | t0013 | g0177 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18968 | hp1 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18970 | hp2 | a0001 | c0001 | t0068 | g0146 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18971 | hp1 | a0001 | c0010 | t0002 | g0135 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18971 | hp2 | a0001 | c0001 | t0066 | g0086 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18986 | hp2 | a0001 | c0002 | t0042 | g0095 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18994 | hp1 | a0001 | c0002 | t0021 | g0083 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18994 | hp2 | a0001 | c0001 | t0023 | g0167 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19000 | hp1 | a0001 | c0010 | t0002 | g0108 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19000 | hp2 | a0005 | c0021 | t0004 | g0166 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19002 | hp2 | a0001 | c0001 | t0059 | g0165 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19003 | hp2 | a0001 | c0001 | t0034 | g0204 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19005 | hp2 | a0001 | c0019 | t0002 | g0147 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19030 | hp2 | a0001 | c0006 | t0003 | g0255 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0288 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19055 | hp1 | a0001 | c0001 | t0057 | g0190 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19055 | hp2 | a0001 | c0002 | t0043 | g0059 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19057 | hp2 | a0001 | c0001 | t0060 | g0201 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19064 | hp1 | a0001 | c0023 | t0001 | g0093 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19065 | hp2 | a0001 | c0001 | t0082 | g0034 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19082 | hp1 | a0001 | c0001 | t0022 | g0199 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19086 | hp1 | a0001 | c0001 | t0061 | g0195 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19086 | hp2 | a0001 | c0001 | t0053 | g0203 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19088 | hp1 | a0002 | c0005 | t0065 | g0140 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19088 | hp2 | a0001 | c0001 | t0013 | g0170 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19091 | hp1 | a0001 | c0001 | t0013 | g0172 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19240 | hp1 | a0001 | c0001 | t0029 | g0015 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0257 | AFR | YRI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20129 | hp1 | a0001 | c0001 | t0090 | g0297 | AFR | ASW | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20129 | hp2 | a0003 | c0004 | t0016 | g0228 | AFR | ASW | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20752 | hp1 | a0001 | c0001 | t0025 | g0300 | EUR | TSI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20752 | hp2 | a0010 | c0012 | t0003 | g0022 | EUR | TSI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0285 | EUR | TSI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20805 | hp2 | a0001 | c0001 | t0025 | g0299 | EUR | TSI | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20905 | hp1 | a0001 | c0002 | t0073 | g0270 | SAS | GIH | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0120 | SAS | GIH | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01123 | hp1 | a0001 | c0002 | t0003 | g0282 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02486 | hp1 | a0004 | c0011 | t0005 | g0217 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0242 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02559 | hp1 | a0001 | c0001 | t0069 | g0024 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG02559 | hp2 | a0005 | c0015 | t0085 | g0129 | AFR | ACB | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0240 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0260 | AFR | MSL | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | USA | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
HG06807 | hp2 | a0001 | c0001 | t0024 | g0262 | AFR | USA | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20300 | hp1 | a0001 | c0003 | t0039 | g0301 | AFR | USA | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0174 | AFR | USA | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0105 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
NA21309 | hp2 | a0011 | c0016 | t0001 | g0072 | AFR | LWK | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0236 | REF | REF | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0263 | REF | REF | SSH1_chr12_108773191_108862583 | SSH1 | chr12 | 108773191 | 108862583 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108778193 | A | C | 1 | a0001 | 2 | NA20752.hp1 NA20805.hp2 |
splice_region_variant | LOW | c.*9795T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | chr12 | 108778193 | |||||||
chr12:108788233 | C | T | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2905G>A | p.Val969Ile | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2992/13034 | 2905/3150 | 969/1049 | chr12 | 108788233 | |||
chr12:108788995 | G | C | 1 | a0003 | 4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.2143C>G | p.Leu715Val | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2230/13034 | 2143/3150 | 715/1049 | chr12 | 108788995 | |||
chr12:108789123 | T | C | 1 | a0008 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2015A>G | p.Asn672Ser | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2102/13034 | 2015/3150 | 672/1049 | chr12 | 108789123 | |||
chr12:108789163 | C | T | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1975G>A | p.Gly659Arg | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2062/13034 | 1975/3150 | 659/1049 | chr12 | 108789163 | |||
chr12:108792317 | T | C | 1 | a0002 | 4 | HG02015.hp1 HG02132.hp1 NA18945.hp2 others(1): Show |
missense_variant | MODERATE | c.1862A>G | p.Asn621Ser | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/15 | 1949/13034 | 1862/3150 | 621/1049 | chr12 | 108792317 | |||
chr12:108792644 | C | T | 1 | a0005 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1535G>A | p.Arg512Gln | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/15 | 1622/13034 | 1535/3150 | 512/1049 | chr12 | 108792644 | |||
chr12:108792645 | G | A | 1 | a0005 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.1534C>T | p.Arg512Trp | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/15 | 1621/13034 | 1534/3150 | 512/1049 | chr12 | 108792645 | |||
chr12:108792729 | G | A | 1 | a0006 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1450C>T | p.Pro484Ser | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/15 | 1537/13034 | 1450/3150 | 484/1049 | chr12 | 108792729 | |||
chr12:108807658 | C | T | 1 | a0009 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.706G>A | p.Asp236Asn | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/15 | 793/13034 | 706/3150 | 236/1049 | chr12 | 108807658 | |||
chr12:108817153 | G | A | 1 | a0004 | 2 | HG02280.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.286C>T | p.Arg96Cys | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/15 | 373/13034 | 286/3150 | 96/1049 | chr12 | 108817153 | |||
chr12:108857462 | G | C | 1 | a0010 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.35C>G | p.Pro12Arg | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/15 | 122/13034 | 35/3150 | 12/1049 | chr12 | 108857462 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108788006 | C | G | 1 | a0001c0008 | 2 | HG02257.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.3132G>C | p.Ser1044Ser | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3219/13034 | 3132/3150 | 1044/1049 | chr12 | 108788006 | |||
chr12:108788138 | G | A | 2 | a0001c0003 a0001c0009 |
8 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.3000C>T | p.Thr1000Thr | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3087/13034 | 3000/3150 | 1000/1049 | chr12 | 108788138 | |||
chr12:108788234 | G | A | 2 | a0001c0017 a0001c0019 |
2 | HG02735.hp2 NA19005.hp2 |
synonymous_variant | LOW | c.2904C>T | p.Thr968Thr | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2991/13034 | 2904/3150 | 968/1049 | chr12 | 108788234 | |||
chr12:108788273 | T | C | 14 | a0001c0001 a0001c0007 a0001c0009 others(11): Show |
210 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
synonymous_variant | LOW | c.2865A>G | p.Thr955Thr | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2952/13034 | 2865/3150 | 955/1049 | chr12 | 108788273 | |||
chr12:108788470 | A | G | 1 | a0001c0007 | 2 | HG03927.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.2668T>C | p.Leu890Leu | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2755/13034 | 2668/3150 | 890/1049 | chr12 | 108788470 | |||
chr12:108789227 | C | G | 2 | a0001c0006 a0010c0012 |
3 | HG01243.hp2 NA19030.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.1911G>C | p.Gly637Gly | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1998/13034 | 1911/3150 | 637/1049 | chr12 | 108789227 | |||
chr12:108792466 | T | C | 1 | a0001c0010 | 2 | NA18971.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.1713A>G | p.Lys571Lys | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/15 | 1800/13034 | 1713/3150 | 571/1049 | chr12 | 108792466 | |||
chr12:108800848 | G | A | 1 | a0001c0023 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.1080C>T | p.Val360Val | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/15 | 1167/13034 | 1080/3150 | 360/1049 | chr12 | 108800848 | |||
chr12:108805056 | G | A | 1 | a0001c0024 | 1 | HG03490.hp1 | splice_region_variant&synonymous_variant | LOW | c.954C>T | p.Leu318Leu | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/15 | 1041/13034 | 954/3150 | 318/1049 | chr12 | 108805056 | |||
chr12:108805071 | G | A | 1 | a0001c0025 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.939C>T | p.Phe313Phe | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/15 | 1026/13034 | 939/3150 | 313/1049 | chr12 | 108805071 | |||
chr12:108857452 | G | T | 1 | a0001c0013 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.45C>A | p.Ala15Ala | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/15 | 132/13034 | 45/3150 | 15/1049 | chr12 | 108857452 | |||
chr12:108857464 | C | T | 1 | a0010c0012 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.33G>A | p.Thr11Thr | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/15 | 120/13034 | 33/3150 | 11/1049 | chr12 | 108857464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108778256 | C | A | 1 | a0001c0003t0020 | 2 | HG02280.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9732G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 9732 | chr12 | 108778256 | ||||||
chr12:108778261 | G | A | 1 | a0001c0001t0025 | 2 | NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9727C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 9727 | chr12 | 108778261 | ||||||
chr12:108778701 | A | G | 1 | a0001c0001t0080 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9287T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 9287 | chr12 | 108778701 | ||||||
chr12:108778769 | T | G | 1 | a0001c0001t0010 | 6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9219A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 9219 | chr12 | 108778769 | ||||||
chr12:108778804 | C | A | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9184G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 9184 | chr12 | 108778804 | ||||||
chr12:108779067 | G | A | 1 | a0001c0001t0089 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8921C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8921 | chr12 | 108779067 | ||||||
chr12:108779075 | A | G | 1 | a0001c0001t0069 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8913T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8913 | chr12 | 108779075 | ||||||
chr12:108779099 | C | CCAGA | 36 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0012 others(33): Show |
104 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*8888_*8889insTCTG | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8888 | chr12 | 108779099 | ||||||
chr12:108779133 | T | A | 1 | a0001c0002t0073 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8855A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8855 | chr12 | 108779133 | ||||||
chr12:108779167 | G | A | 1 | a0001c0002t0045 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8821C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8821 | chr12 | 108779167 | ||||||
chr12:108779411 | G | T | 1 | a0001c0001t0090 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8577C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8577 | chr12 | 108779411 | ||||||
chr12:108779509 | G | A | 1 | a0001c0002t0046 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8479C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8479 | chr12 | 108779509 | ||||||
chr12:108779882 | C | A | 1 | a0001c0001t0059 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8106G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 8106 | chr12 | 108779882 | ||||||
chr12:108780054 | C | G | 2 | a0001c0001t0010 a0001c0001t0035 |
7 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7934G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7934 | chr12 | 108780054 | ||||||
chr12:108780187 | G | A | 1 | a0001c0001t0010 | 6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7801C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7801 | chr12 | 108780187 | ||||||
chr12:108780333 | A | G | 34 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0013 others(31): Show |
97 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*7655T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7655 | chr12 | 108780333 | ||||||
chr12:108780364 | C | A | 2 | a0001c0001t0027 a0001c0002t0027 |
2 | HG01346.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7624G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7624 | chr12 | 108780364 | ||||||
chr12:108780588 | G | A | 1 | a0001c0001t0029 | 2 | HG03209.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7400C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7400 | chr12 | 108780588 | ||||||
chr12:108780622 | A | T | 1 | a0003c0004t0016 | 4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7366T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7366 | chr12 | 108780622 | ||||||
chr12:108780679 | C | A | 28 | a0001c0001t0001 a0001c0001t0013 a0001c0002t0001 others(25): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*7309G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7309 | chr12 | 108780679 | ||||||
chr12:108780777 | G | A | 1 | a0001c0001t0010 | 6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7211C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7211 | chr12 | 108780777 | ||||||
chr12:108780845 | C | T | 13 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0024 others(10): Show |
32 | HG00733.hp2 HG01081.hp2 HG01167.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7143G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7143 | chr12 | 108780845 | ||||||
chr12:108780865 | C | A | 1 | a0001c0001t0018 | 3 | NA18942.hp2 NA18960.hp2 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7123G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7123 | chr12 | 108780865 | ||||||
chr12:108780873 | G | A | 1 | a0001c0001t0063 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7115C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7115 | chr12 | 108780873 | ||||||
chr12:108780899 | G | A | 1 | a0001c0002t0047 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7089C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7089 | chr12 | 108780899 | ||||||
chr12:108780941 | G | A | 2 | a0001c0001t0022 a0001c0001t0060 |
3 | NA18960.hp1 NA19057.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7047C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7047 | chr12 | 108780941 | ||||||
chr12:108780984 | G | A | 1 | a0001c0001t0070 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7004C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 7004 | chr12 | 108780984 | ||||||
chr12:108781043 | G | GA | 2 | a0001c0001t0010 a0001c0001t0035 |
7 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6944dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6944 | chr12 | 108781043 | ||||||
chr12:108781044 | A | G | 8 | a0001c0001t0009 a0001c0001t0028 a0001c0001t0031 others(5): Show |
16 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6944T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6944 | chr12 | 108781044 | ||||||
chr12:108781117 | A | G | 1 | a0001c0001t0025 | 2 | NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6871T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6871 | chr12 | 108781117 | ||||||
chr12:108781137 | G | C | 1 | a0001c0002t0074 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6851C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6851 | chr12 | 108781137 | ||||||
chr12:108781143 | G | T | 2 | a0001c0001t0015 a0001c0001t0081 |
5 | HG00099.hp1 HG01168.hp1 HG03704.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6845C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6845 | chr12 | 108781143 | ||||||
chr12:108781416 | C | A | 1 | a0001c0001t0069 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6572G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6572 | chr12 | 108781416 | ||||||
chr12:108781453 | A | G | 1 | a0001c0001t0072 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6535T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6535 | chr12 | 108781453 | ||||||
chr12:108781483 | T | C | 1 | a0001c0002t0075 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6505A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6505 | chr12 | 108781483 | ||||||
chr12:108781814 | G | A | 1 | a0001c0001t0071 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6174C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 6174 | chr12 | 108781814 | ||||||
chr12:108782127 | A | G | 1 | a0001c0002t0044 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5861T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5861 | chr12 | 108782127 | ||||||
chr12:108782132 | C | CA | 5 | a0001c0001t0023 a0001c0001t0056 a0001c0001t0060 others(2): Show |
6 | HG01167.hp1 HG01517.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5855dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5855 | chr12 | 108782132 | ||||||
chr12:108782132 | CA | C | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(43): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*5855delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5855 | chr12 | 108782132 | ||||||
chr12:108782132 | CAA | C | 22 | a0001c0001t0001 a0001c0001t0025 a0001c0001t0083 others(19): Show |
78 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5854_*5855delTT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5854 | chr12 | 108782132 | ||||||
chr12:108782145 | A | T | 1 | a0001c0002t0043 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5843T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5843 | chr12 | 108782145 | ||||||
chr12:108782146 | A | T | 1 | a0001c0002t0043 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5842T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5842 | chr12 | 108782146 | ||||||
chr12:108782151 | A | T | 5 | a0001c0001t0012 a0001c0001t0035 a0001c0002t0048 others(2): Show |
11 | HG01884.hp1 HG02015.hp1 HG02132.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5837T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5837 | chr12 | 108782151 | ||||||
chr12:108782153 | T | A | 6 | a0001c0001t0012 a0001c0001t0035 a0001c0001t0061 others(3): Show |
12 | HG01884.hp1 HG02015.hp1 HG02132.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5835A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5835 | chr12 | 108782153 | ||||||
chr12:108782154 | A | T | 6 | a0001c0001t0057 a0001c0001t0062 a0001c0001t0081 others(3): Show |
6 | HG01167.hp2 HG01168.hp1 HG02602.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5834T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5834 | chr12 | 108782154 | ||||||
chr12:108782363 | T | C | 1 | a0002c0005t0065 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5625A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5625 | chr12 | 108782363 | ||||||
chr12:108782369 | G | A | 1 | a0001c0001t0066 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5619C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5619 | chr12 | 108782369 | ||||||
chr12:108782414 | C | CT | 4 | a0001c0001t0014 a0001c0001t0080 a0001c0002t0041 others(1): Show |
6 | HG02523.hp2 HG03017.hp1 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5573dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5573 | chr12 | 108782414 | ||||||
chr12:108782439 | C | A | 2 | a0001c0001t0010 a0001c0001t0035 |
7 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5549G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5549 | chr12 | 108782439 | ||||||
chr12:108782624 | T | C | 1 | a0001c0001t0030 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5364A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5364 | chr12 | 108782624 | ||||||
chr12:108782655 | TG | T | 15 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0026 others(12): Show |
56 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5332delC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 5332 | chr12 | 108782655 | ||||||
chr12:108783472 | G | C | 1 | a0001c0002t0087 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4516C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 4516 | chr12 | 108783472 | ||||||
chr12:108783764 | T | A | 1 | a0001c0001t0077 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4224A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 4224 | chr12 | 108783764 | ||||||
chr12:108783793 | AGAT | A | 2 | a0001c0001t0031 a0001c0001t0079 |
3 | HG02976.hp1 HG03195.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4192_*4194delATC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 4192 | chr12 | 108783793 | ||||||
chr12:108783889 | A | G | 1 | a0001c0001t0079 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 4099 | chr12 | 108783889 | ||||||
chr12:108783979 | T | G | 1 | a0001c0001t0054 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4009A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 4009 | chr12 | 108783979 | ||||||
chr12:108784227 | C | A | 14 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0022 others(11): Show |
44 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3761G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3761 | chr12 | 108784227 | ||||||
chr12:108784250 | G | T | 1 | a0001c0002t0019 | 2 | HG02040.hp2 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3738C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3738 | chr12 | 108784250 | ||||||
chr12:108784397 | C | T | 1 | a0001c0001t0026 | 2 | NA18945.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3591G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3591 | chr12 | 108784397 | ||||||
chr12:108784437 | G | A | 2 | a0001c0008t0036 a0001c0008t0037 |
2 | HG02257.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3551C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3551 | chr12 | 108784437 | ||||||
chr12:108784585 | C | A | 3 | a0001c0003t0039 a0001c0009t0049 a0001c0009t0050 |
3 | HG01884.hp2 HG02965.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3403G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 3403 | chr12 | 108784585 | ||||||
chr12:108785016 | G | A | 1 | a0001c0002t0078 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2972C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2972 | chr12 | 108785016 | ||||||
chr12:108785017 | G | A | 3 | a0001c0003t0039 a0001c0009t0049 a0001c0009t0050 |
3 | HG01884.hp2 HG02965.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2971 | chr12 | 108785017 | ||||||
chr12:108785032 | C | T | 19 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0026 others(16): Show |
63 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2956G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2956 | chr12 | 108785032 | ||||||
chr12:108785082 | G | A | 2 | a0001c0008t0036 a0001c0008t0037 |
2 | HG02257.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2906C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2906 | chr12 | 108785082 | ||||||
chr12:108785197 | T | G | 40 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(37): Show |
115 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2791A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2791 | chr12 | 108785197 | ||||||
chr12:108785294 | G | A | 1 | a0001c0002t0051 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2694C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2694 | chr12 | 108785294 | ||||||
chr12:108785373 | C | T | 1 | a0001c0001t0026 | 2 | NA18945.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2615G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2615 | chr12 | 108785373 | ||||||
chr12:108785374 | G | A | 1 | a0001c0002t0088 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2614C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2614 | chr12 | 108785374 | ||||||
chr12:108785411 | C | T | 1 | a0001c0001t0025 | 2 | NA20752.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2577G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2577 | chr12 | 108785411 | ||||||
chr12:108785506 | C | T | 1 | a0001c0001t0008 | 7 | HG01099.hp1 HG01255.hp1 HG01433.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2482G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2482 | chr12 | 108785506 | ||||||
chr12:108785608 | A | G | 2 | a0001c0001t0012 a0001c0008t0036 |
6 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2380T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2380 | chr12 | 108785608 | ||||||
chr12:108785647 | C | T | 1 | a0001c0001t0024 | 2 | HG03453.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2341G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2341 | chr12 | 108785647 | ||||||
chr12:108785742 | CATACAT | C | 3 | a0001c0001t0012 a0001c0008t0036 a0001c0008t0037 |
7 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2240_*2245delATGT others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2240 | chr12 | 108785742 | ||||||
chr12:108785759 | A | T | 1 | a0003c0004t0016 | 4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2229T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 2229 | chr12 | 108785759 | ||||||
chr12:108786271 | G | C | 1 | a0001c0002t0052 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1717C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1717 | chr12 | 108786271 | ||||||
chr12:108786339 | G | T | 17 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(14): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1649C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1649 | chr12 | 108786339 | ||||||
chr12:108786370 | G | A | 1 | a0001c0001t0054 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1618 | chr12 | 108786370 | ||||||
chr12:108786391 | C | T | 1 | a0001c0001t0035 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1597G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1597 | chr12 | 108786391 | ||||||
chr12:108786616 | T | A | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG02071.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1372A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1372 | chr12 | 108786616 | ||||||
chr12:108786628 | G | T | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG02071.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1360C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1360 | chr12 | 108786628 | ||||||
chr12:108786831 | C | T | 1 | a0001c0002t0040 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1157G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 1157 | chr12 | 108786831 | ||||||
chr12:108787011 | C | T | 27 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0019 others(24): Show |
82 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*977G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 977 | chr12 | 108787011 | ||||||
chr12:108787055 | G | C | 1 | a0001c0001t0089 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*933C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 933 | chr12 | 108787055 | ||||||
chr12:108787118 | C | T | 1 | a0001c0003t0039 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 870 | chr12 | 108787118 | ||||||
chr12:108787160 | A | G | 1 | a0001c0001t0038 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 828 | chr12 | 108787160 | ||||||
chr12:108787179 | A | G | 5 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0035 others(2): Show |
14 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*809T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 809 | chr12 | 108787179 | ||||||
chr12:108787288 | CG | C | 1 | a0003c0004t0016 | 4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*699delC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 699 | chr12 | 108787288 | ||||||
chr12:108787295 | A | C | 1 | a0001c0001t0034 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 693 | chr12 | 108787295 | ||||||
chr12:108787311 | G | T | 2 | a0001c0002t0032 a0001c0002t0033 |
2 | HG02602.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 677 | chr12 | 108787311 | ||||||
chr12:108787463 | T | C | 1 | a0001c0001t0090 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*525A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 525 | chr12 | 108787463 | ||||||
chr12:108787546 | G | A | 1 | a0001c0001t0091 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 442 | chr12 | 108787546 | ||||||
chr12:108787969 | T | C | 1 | a0001c0001t0092 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 15/15 | 19 | chr12 | 108787969 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108789276 | C | T | 1 | a0001c0002t0001g0004 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1894-32G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789276 | |||||||
chr12:108789368 | C | CT | 71 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(68): Show |
76 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1894-125dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789368 | |||||||
chr12:108789425 | C | G | 70 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(67): Show |
75 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1894-181G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789425 | |||||||
chr12:108789429 | T | C | 16 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1894-185A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789429 | |||||||
chr12:108789601 | G | T | 1 | a0001c0002t0044g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1894-357C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789601 | |||||||
chr12:108789665 | G | A | 1 | a0001c0001t0004g0206 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1894-421C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789665 | |||||||
chr12:108789697 | G | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1894-453C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789697 | |||||||
chr12:108789784 | C | G | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1894-540G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789784 | |||||||
chr12:108789803 | C | T | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1894-559G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108789803 | |||||||
chr12:108790130 | T | A | 1 | a0001c0001t0004g0168 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1894-886A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790130 | |||||||
chr12:108790153 | G | GT | 73 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(70): Show |
78 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1894-910dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790153 | |||||||
chr12:108790187 | G | A | 1 | a0001c0001t0035g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1894-943C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790187 | |||||||
chr12:108790295 | C | T | 2 | a0001c0001t0004g0187 a0001c0001t0092g0189 |
2 | HG00438.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1894-1051G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790295 | |||||||
chr12:108790318 | T | C | 1 | a0001c0001t0004g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1894-1074A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790318 | |||||||
chr12:108790410 | A | G | 2 | a0001c0001t0007g0009 a0001c0001t0007g0132 |
3 | HG01109.hp1 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1894-1166T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790410 | |||||||
chr12:108790573 | T | C | 266 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(263): Show |
287 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.1894-1329A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790573 | |||||||
chr12:108790595 | C | G | 5 | a0001c0001t0012g0215 a0001c0001t0012g0293 a0001c0001t0012g0295 others(2): Show |
5 | HG01884.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-1351G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790595 | |||||||
chr12:108790748 | G | A | 1 | a0003c0004t0016g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1894-1504C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790748 | |||||||
chr12:108790788 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1893+1498G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790788 | |||||||
chr12:108790824 | G | A | 1 | a0001c0002t0003g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1893+1462C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790824 | |||||||
chr12:108790887 | G | A | 1 | a0001c0002t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1893+1399C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790887 | |||||||
chr12:108790964 | A | G | 1 | a0001c0001t0063g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1893+1322T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790964 | |||||||
chr12:108790988 | T | C | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1893+1298A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108790988 | |||||||
chr12:108791133 | G | A | 1 | a0006c0022t0003g0265 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1893+1153C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791133 | |||||||
chr12:108791220 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1893+1066C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791220 | |||||||
chr12:108791325 | G | A | 1 | a0001c0001t0004g0202 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1893+961C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791325 | |||||||
chr12:108791400 | G | A | 3 | a0001c0002t0003g0272 a0001c0002t0003g0273 a0001c0002t0076g0271 |
3 | HG00140.hp1 HG01074.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1893+886C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791400 | |||||||
chr12:108791632 | G | A | 5 | a0001c0001t0012g0215 a0001c0001t0012g0293 a0001c0001t0012g0295 others(2): Show |
5 | HG01884.hp1 HG02572.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+654C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791632 | |||||||
chr12:108791698 | G | A | 24 | a0001c0001t0006g0008 a0001c0001t0006g0103 a0001c0001t0006g0107 others(21): Show |
27 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1893+588C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108791698 | |||||||
chr12:108792035 | T | C | 1 | a0001c0001t0008g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1893+251A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108792035 | |||||||
chr12:108792247 | G | T | 1 | a0001c0002t0003g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1893+39C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 14/14 | chr12 | 108792247 | |||||||
chr12:108792840 | A | G | 4 | a0001c0001t0006g0008 a0001c0001t0006g0107 a0001c0001t0006g0130 others(1): Show |
5 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350-11T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108792840 | |||||||
chr12:108793011 | C | T | 15 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(12): Show |
17 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1350-182G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793011 | |||||||
chr12:108793027 | G | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1350-198C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793027 | |||||||
chr12:108793149 | G | A | 1 | a0001c0002t0045g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1350-320C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793149 | |||||||
chr12:108793261 | C | T | 1 | a0001c0001t0006g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1350-432G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793261 | |||||||
chr12:108793363 | T | C | 9 | a0001c0001t0072g0025 a0001c0002t0003g0019 a0001c0002t0003g0158 others(6): Show |
10 | HG01074.hp1 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1350-534A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793363 | |||||||
chr12:108793398 | CT | C | 74 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(71): Show |
79 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1350-570delA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793398 | |||||||
chr12:108793761 | C | T | 1 | a0008c0020t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1350-932G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793761 | |||||||
chr12:108793804 | G | A | 3 | a0001c0001t0006g0103 a0001c0001t0009g0101 a0001c0001t0009g0102 |
3 | HG01891.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1350-975C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793804 | |||||||
chr12:108793869 | C | T | 7 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(4): Show |
7 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1350-1040G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793869 | |||||||
chr12:108793912 | C | T | 2 | a0001c0001t0015g0120 a0001c0001t0081g0121 |
2 | HG01168.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1350-1083G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793912 | |||||||
chr12:108793936 | C | T | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-1107G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793936 | |||||||
chr12:108793962 | T | C | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-1133A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793962 | |||||||
chr12:108793968 | C | T | 11 | a0001c0001t0012g0215 a0001c0001t0012g0293 a0001c0001t0012g0295 others(8): Show |
11 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1350-1139G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793968 | |||||||
chr12:108793969 | G | A | 4 | a0001c0003t0001g0233 a0001c0003t0001g0234 a0001c0003t0020g0231 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1140C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108793969 | |||||||
chr12:108794055 | G | A | 2 | a0001c0001t0014g0221 a0001c0013t0014g0023 |
2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1350-1226C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794055 | |||||||
chr12:108794139 | G | A | 72 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(69): Show |
78 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1350-1310C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794139 | |||||||
chr12:108794182 | C | T | 4 | a0003c0004t0016g0227 a0003c0004t0016g0228 a0003c0004t0016g0229 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350-1353G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794182 | |||||||
chr12:108794254 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1350-1425C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794254 | |||||||
chr12:108794473 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1350-1644C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794473 | |||||||
chr12:108794722 | C | A | 2 | a0001c0001t0005g0002 a0001c0001t0005g0032 |
3 | NA18982.hp2 NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1350-1893G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794722 | |||||||
chr12:108794855 | A | G | 18 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1350-2026T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794855 | |||||||
chr12:108794860 | G | T | 6 | a0001c0001t0012g0215 a0001c0001t0012g0293 a0001c0001t0012g0295 others(3): Show |
6 | HG01884.hp1 HG02572.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1350-2031C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794860 | |||||||
chr12:108794995 | T | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1350-2166A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108794995 | |||||||
chr12:108795022 | T | G | 1 | a0001c0002t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1350-2193A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795022 | |||||||
chr12:108795057 | T | C | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1350-2228A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795057 | |||||||
chr12:108795263 | T | A | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1350-2434A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795263 | |||||||
chr12:108795286 | C | G | 40 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0014 others(37): Show |
43 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1350-2457G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795286 | |||||||
chr12:108795416 | A | AT | 5 | a0001c0001t0002g0152 a0001c0001t0012g0293 a0001c0001t0012g0295 others(2): Show |
5 | HG01884.hp1 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1350-2588dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795416 | |||||||
chr12:108795638 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1350-2809A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795638 | |||||||
chr12:108795798 | G | A | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-2969C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795798 | |||||||
chr12:108795944 | G | C | 1 | a0001c0001t0009g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1349+3056C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795944 | |||||||
chr12:108795957 | G | T | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1349+3043C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108795957 | |||||||
chr12:108796235 | G | A | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+2765C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796235 | |||||||
chr12:108796354 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1349+2646G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796354 | |||||||
chr12:108796457 | T | C | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1349+2543A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796457 | |||||||
chr12:108796509 | G | A | 1 | a0001c0001t0029g0015 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1349+2491C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796509 | |||||||
chr12:108796557 | A | G | 4 | a0001c0001t0013g0170 a0001c0001t0013g0171 a0001c0001t0013g0172 others(1): Show |
4 | NA18966.hp2 NA18968.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349+2443T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796557 | |||||||
chr12:108796671 | T | C | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1349+2329A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796671 | |||||||
chr12:108796727 | T | C | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1349+2273A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796727 | |||||||
chr12:108796811 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1349+2189G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796811 | |||||||
chr12:108796931 | G | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1349+2069C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108796931 | |||||||
chr12:108797122 | TTTTG | T | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1349+1874_1349+187 others(8): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797122 | |||||||
chr12:108797153 | G | A | 50 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(47): Show |
55 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1349+1847C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797153 | |||||||
chr12:108797283 | C | T | 2 | a0001c0002t0003g0021 a0001c0002t0003g0283 |
3 | HG01069.hp2 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1349+1717G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797283 | |||||||
chr12:108797312 | T | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+1688A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797312 | |||||||
chr12:108797542 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+1458G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797542 | |||||||
chr12:108797617 | A | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+1383T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797617 | |||||||
chr12:108797675 | G | A | 1 | a0001c0001t0056g0211 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1349+1325C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797675 | |||||||
chr12:108797837 | C | G | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1349+1163G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797837 | |||||||
chr12:108797926 | C | T | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1349+1074G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108797926 | |||||||
chr12:108798049 | C | T | 1 | a0001c0002t0003g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1349+951G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798049 | |||||||
chr12:108798089 | G | A | 1 | a0001c0001t0063g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1349+911C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798089 | |||||||
chr12:108798132 | G | A | 3 | a0002c0005t0017g0010 a0002c0005t0017g0141 a0002c0005t0065g0140 |
4 | HG02015.hp1 HG02132.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349+868C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798132 | |||||||
chr12:108798149 | C | T | 2 | a0001c0001t0011g0017 a0001c0001t0011g0291 |
3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1349+851G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798149 | |||||||
chr12:108798229 | A | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+771T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798229 | |||||||
chr12:108798230 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1349+770G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798230 | |||||||
chr12:108798249 | G | A | 2 | a0001c0001t0024g0261 a0001c0001t0024g0262 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1349+751C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798249 | |||||||
chr12:108798276 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1349+724G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798276 | |||||||
chr12:108798314 | C | T | 1 | a0004c0011t0005g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1349+686G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798314 | |||||||
chr12:108798350 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1349+650A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798350 | |||||||
chr12:108798556 | GCTTGCCC others(3): Show |
G | 105 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0014 others(102): Show |
115 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1349+434_1349+443d others(12): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798556 | |||||||
chr12:108798870 | G | A | 104 | a0001c0001t0004g0012 a0001c0001t0004g0013 a0001c0001t0004g0014 others(101): Show |
114 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1349+130C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798870 | |||||||
chr12:108798975 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1349+25G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 13/14 | chr12 | 108798975 | |||||||
chr12:108799329 | AC | A | 5 | a0001c0001t0004g0012 a0001c0001t0004g0169 a0001c0001t0004g0196 others(2): Show |
6 | NA18947.hp1 NA18948.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149-130delG | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799329 | |||||||
chr12:108799396 | C | T | 1 | a0001c0001t0079g0246 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1149-196G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799396 | |||||||
chr12:108799397 | C | T | 7 | a0001c0001t0011g0017 a0001c0001t0011g0250 a0001c0001t0011g0291 others(4): Show |
8 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-197G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799397 | |||||||
chr12:108799562 | C | T | 1 | a0001c0001t0004g0168 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1149-362G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799562 | |||||||
chr12:108799565 | A | G | 264 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(261): Show |
284 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.1149-365T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799565 | |||||||
chr12:108799778 | C | T | 2 | a0001c0001t0007g0111 a0001c0002t0001g0048 |
2 | NA18999.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1149-578G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799778 | |||||||
chr12:108799852 | T | C | 1 | a0001c0001t0004g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1149-652A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799852 | |||||||
chr12:108799954 | C | T | 1 | a0001c0001t0005g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1149-754G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108799954 | |||||||
chr12:108800215 | A | G | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1148+565T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800215 | |||||||
chr12:108800284 | C | T | 1 | a0001c0001t0071g0251 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1148+496G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800284 | |||||||
chr12:108800470 | A | G | 5 | a0001c0002t0003g0247 a0001c0002t0003g0257 a0001c0002t0003g0259 others(2): Show |
5 | HG02572.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148+310T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800470 | |||||||
chr12:108800632 | A | ACTCCCAC others(38): Show |
1 | a0001c0002t0003g0260 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1148+103_1148+147d others(47): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800632 | |||||||
chr12:108800632 | A | G | 164 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(161): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1148+148T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800632 | |||||||
chr12:108800673 | TC | T | 104 | a0001c0001t0002g0088 a0001c0001t0002g0145 a0001c0001t0004g0014 others(101): Show |
112 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.1148+106delG | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800673 | |||||||
chr12:108800767 | T | G | 1 | a0001c0001t0005g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1148+13A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 12/14 | chr12 | 108800767 | |||||||
chr12:108800943 | A | G | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1002-17T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108800943 | |||||||
chr12:108800956 | T | C | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1002-30A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108800956 | |||||||
chr12:108801159 | A | T | 17 | a0001c0001t0006g0103 a0001c0001t0009g0100 a0001c0001t0009g0101 others(14): Show |
17 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1002-233T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801159 | |||||||
chr12:108801209 | C | T | 209 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(206): Show |
223 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1002-283G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801209 | |||||||
chr12:108801248 | A | G | 181 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(178): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1002-322T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801248 | |||||||
chr12:108801371 | T | C | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1002-445A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801371 | |||||||
chr12:108801620 | C | T | 4 | a0001c0002t0001g0061 a0001c0002t0001g0066 a0001c0002t0001g0067 others(1): Show |
4 | HG01099.hp2 HG01106.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1002-694G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801620 | |||||||
chr12:108801736 | T | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1001+586A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801736 | |||||||
chr12:108801736 | TA | T | 148 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(145): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1001+585delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801736 | |||||||
chr12:108801736 | TAA | T | 6 | a0001c0001t0014g0219 a0001c0001t0018g0030 a0001c0002t0001g0042 others(3): Show |
6 | HG01256.hp2 HG02015.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001+584_1001+585d others(4): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108801736 | |||||||
chr12:108802146 | C | A | 4 | a0001c0002t0001g0068 a0001c0002t0001g0079 a0001c0002t0001g0081 others(1): Show |
4 | HG02523.hp1 NA18949.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+176G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 11/14 | chr12 | 108802146 | |||||||
chr12:108802649 | C | T | 1 | a0001c0001t0008g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.955-281G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108802649 | |||||||
chr12:108802681 | G | C | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.955-313C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108802681 | |||||||
chr12:108802816 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.955-448G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108802816 | |||||||
chr12:108803063 | T | TAA | 94 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(91): Show |
98 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.955-697_955-696dup others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803063 | |||||||
chr12:108803098 | C | T | 2 | a0001c0001t0011g0017 a0001c0001t0011g0291 |
3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.955-730G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803098 | |||||||
chr12:108803122 | G | T | 28 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 others(25): Show |
28 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.955-754C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803122 | |||||||
chr12:108803219 | T | C | 1 | a0001c0002t0003g0286 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.955-851A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803219 | |||||||
chr12:108803262 | T | G | 1 | a0001c0002t0003g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.955-894A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803262 | |||||||
chr12:108803364 | G | GA | 92 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(89): Show |
96 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.955-997dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803364 | |||||||
chr12:108803488 | AG | A | 80 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(77): Show |
84 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.955-1121delC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803488 | |||||||
chr12:108803542 | G | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955-1174C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803542 | |||||||
chr12:108803653 | C | T | 1 | a0001c0001t0014g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.955-1285G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803653 | |||||||
chr12:108803690 | T | G | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.955-1322A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108803690 | |||||||
chr12:108804099 | T | C | 80 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(77): Show |
84 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.954+957A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804099 | |||||||
chr12:108804210 | T | C | 1 | a0001c0002t0003g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.954+846A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804210 | |||||||
chr12:108804309 | G | A | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.954+747C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804309 | |||||||
chr12:108804408 | T | A | 7 | a0001c0001t0006g0008 a0001c0001t0006g0107 a0001c0001t0006g0130 others(4): Show |
10 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.954+648A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804408 | |||||||
chr12:108804466 | T | C | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.954+590A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804466 | |||||||
chr12:108804791 | G | T | 2 | a0001c0001t0014g0220 a0001c0002t0001g0222 |
2 | HG02129.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.954+265C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804791 | |||||||
chr12:108804792 | C | T | 2 | a0001c0001t0014g0220 a0001c0002t0001g0222 |
2 | HG02129.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.954+264G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804792 | |||||||
chr12:108804854 | C | T | 1 | a0001c0001t0004g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.954+202G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804854 | |||||||
chr12:108804975 | C | T | 1 | a0001c0001t0053g0203 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.954+81G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 10/14 | chr12 | 108804975 | |||||||
chr12:108805330 | C | T | 7 | a0001c0001t0008g0027 a0001c0001t0008g0174 a0001c0001t0008g0180 others(4): Show |
7 | HG01099.hp1 HG01255.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.826-146G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805330 | |||||||
chr12:108805475 | T | C | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.826-291A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805475 | |||||||
chr12:108805510 | TTCTA | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(6): Show |
11 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.826-330_826-327del others(4): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805510 | |||||||
chr12:108805546 | T | C | 1 | a0001c0001t0018g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.826-362A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805546 | |||||||
chr12:108805694 | T | TA | 162 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0001 others(159): Show |
173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.826-511dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805694 | |||||||
chr12:108805694 | TA | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(7): Show |
12 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.826-511delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805694 | |||||||
chr12:108805721 | A | G | 1 | a0001c0002t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.826-537T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805721 | |||||||
chr12:108805755 | A | G | 3 | a0001c0001t0018g0026 a0001c0001t0018g0029 a0001c0001t0018g0030 |
3 | NA18942.hp2 NA18960.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.825+546T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805755 | |||||||
chr12:108805836 | T | G | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.825+465A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108805836 | |||||||
chr12:108806000 | C | T | 1 | a0001c0002t0001g0003 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.825+301G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108806000 | |||||||
chr12:108806005 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.825+296G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108806005 | |||||||
chr12:108806075 | C | A | 1 | a0001c0001t0008g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.825+226G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108806075 | |||||||
chr12:108806186 | C | T | 1 | a0001c0001t0007g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.825+115G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 9/14 | chr12 | 108806186 | |||||||
chr12:108806491 | C | T | 27 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(24): Show |
29 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.732-97G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108806491 | |||||||
chr12:108806606 | C | G | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.732-212G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108806606 | |||||||
chr12:108806615 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.732-221G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108806615 | |||||||
chr12:108806649 | A | G | 1 | a0001c0001t0008g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.732-255T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108806649 | |||||||
chr12:108807022 | T | C | 82 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(79): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.731+611A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807022 | |||||||
chr12:108807026 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.731+607C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807026 | |||||||
chr12:108807061 | G | A | 1 | a0001c0001t0005g0123 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.731+572C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807061 | |||||||
chr12:108807069 | G | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.731+564C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807069 | |||||||
chr12:108807338 | A | G | 1 | a0001c0002t0003g0274 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.731+295T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807338 | |||||||
chr12:108807384 | G | A | 80 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(77): Show |
84 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.731+249C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807384 | |||||||
chr12:108807418 | AT | A | 180 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0002g0161 others(177): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.731+214delA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807418 | |||||||
chr12:108807418 | ATT | A | 116 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0001 others(113): Show |
125 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.731+213_731+214del others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807418 | |||||||
chr12:108807550 | T | C | 66 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(63): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.731+83A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 8/14 | chr12 | 108807550 | |||||||
chr12:108807835 | G | A | 1 | a0001c0002t0074g0264 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.537-8C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108807835 | |||||||
chr12:108808057 | C | T | 1 | a0001c0007t0002g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.537-230G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808057 | |||||||
chr12:108808074 | A | G | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.537-247T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808074 | |||||||
chr12:108808152 | G | C | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.537-325C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808152 | |||||||
chr12:108808208 | G | A | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.537-381C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808208 | |||||||
chr12:108808282 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(33): Show |
41 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-455G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808282 | |||||||
chr12:108808285 | A | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.537-458T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808285 | |||||||
chr12:108808309 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.537-482A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808309 | |||||||
chr12:108808821 | C | CT | 33 | a0001c0001t0002g0138 a0001c0001t0002g0145 a0001c0001t0002g0151 others(30): Show |
34 | HG00423.hp2 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.536+871dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808821 | |||||||
chr12:108808821 | CT | C | 109 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0004g0191 others(106): Show |
115 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.536+871delA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808821 | |||||||
chr12:108808821 | CTTTTTTT others(4): Show |
C | 1 | a0004c0011t0005g0218 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.536+861_536+871del others(11): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808821 | |||||||
chr12:108808825 | T | G | 4 | a0001c0001t0015g0007 a0001c0001t0015g0120 a0001c0001t0015g0124 others(1): Show |
5 | HG00099.hp1 HG01168.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.536+868A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808825 | |||||||
chr12:108808844 | T | G | 4 | a0001c0001t0012g0305 a0001c0001t0089g0306 a0001c0008t0036g0308 others(1): Show |
4 | HG02257.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+849A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808844 | |||||||
chr12:108808844 | T | TG | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.536+848_536+849ins others(1): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108808844 | |||||||
chr12:108809046 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.536+647G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809046 | |||||||
chr12:108809125 | C | T | 4 | a0001c0001t0007g0009 a0001c0001t0007g0117 a0001c0001t0007g0132 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.536+568G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809125 | |||||||
chr12:108809207 | GGGA | G | 90 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(87): Show |
94 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.536+483_536+485del others(3): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809207 | |||||||
chr12:108809314 | G | A | 1 | a0001c0001t0005g0032 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.536+379C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809314 | |||||||
chr12:108809360 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.536+333C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809360 | |||||||
chr12:108809456 | C | CA | 87 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(84): Show |
91 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.536+236dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809456 | |||||||
chr12:108809576 | C | T | 1 | a0001c0002t0003g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.536+117G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 7/14 | chr12 | 108809576 | |||||||
chr12:108809837 | G | A | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.471-79C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108809837 | |||||||
chr12:108809910 | C | T | 1 | a0001c0002t0051g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.471-152G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108809910 | |||||||
chr12:108810035 | G | A | 199 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(196): Show |
213 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.471-277C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810035 | |||||||
chr12:108810108 | T | G | 2 | a0001c0001t0002g0193 a0001c0001t0008g0224 |
2 | HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.471-350A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810108 | |||||||
chr12:108810262 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.471-504G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810262 | |||||||
chr12:108810471 | G | A | 1 | a0001c0001t0031g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.471-713C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810471 | |||||||
chr12:108810477 | G | A | 1 | a0001c0002t0003g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.471-719C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810477 | |||||||
chr12:108810530 | G | GA | 7 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.470+729dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810530 | |||||||
chr12:108810539 | A | G | 4 | a0001c0003t0001g0233 a0001c0003t0001g0234 a0001c0003t0020g0231 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+721T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810539 | |||||||
chr12:108810544 | T | C | 1 | a0001c0001t0035g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.470+716A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810544 | |||||||
chr12:108810568 | G | A | 16 | a0001c0001t0006g0103 a0001c0001t0009g0100 a0001c0001t0009g0101 others(13): Show |
16 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.470+692C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810568 | |||||||
chr12:108810582 | T | G | 40 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(37): Show |
46 | HG00099.hp1 HG00408.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.470+678A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810582 | |||||||
chr12:108810692 | C | G | 1 | a0001c0001t0072g0025 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.470+568G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810692 | |||||||
chr12:108810745 | G | A | 1 | a0001c0002t0003g0286 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.470+515C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810745 | |||||||
chr12:108810784 | C | A | 1 | a0001c0002t0001g0003 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.470+476G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108810784 | |||||||
chr12:108811101 | C | T | 1 | a0001c0001t0012g0296 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.470+159G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108811101 | |||||||
chr12:108811102 | G | A | 1 | a0001c0002t0003g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.470+158C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108811102 | |||||||
chr12:108811116 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.470+144C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 6/14 | chr12 | 108811116 | |||||||
chr12:108811336 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA18950.hp2 | splice_region_variant&intron_variant | LOW | c.402-8C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811336 | |||||||
chr12:108811413 | C | T | 76 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(73): Show |
80 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.402-85G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811413 | |||||||
chr12:108811474 | T | A | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.402-146A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811474 | |||||||
chr12:108811560 | G | A | 1 | a0001c0001t0029g0015 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402-232C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811560 | |||||||
chr12:108811564 | G | A | 24 | a0001c0001t0004g0238 a0001c0001t0006g0103 a0001c0001t0006g0212 others(21): Show |
26 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.402-236C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811564 | |||||||
chr12:108811642 | T | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.402-314A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811642 | |||||||
chr12:108811685 | T | G | 1 | a0003c0004t0016g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.402-357A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811685 | |||||||
chr12:108811692 | A | G | 264 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(261): Show |
285 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.402-364T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811692 | |||||||
chr12:108811701 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.402-373C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811701 | |||||||
chr12:108811712 | G | A | 1 | a0001c0002t0003g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.402-384C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811712 | |||||||
chr12:108811718 | G | A | 3 | a0001c0001t0010g0240 a0001c0001t0010g0241 a0001c0001t0010g0242 |
3 | HG02486.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.402-390C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108811718 | |||||||
chr12:108812186 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.402-858C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812186 | |||||||
chr12:108812220 | T | C | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.402-892A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812220 | |||||||
chr12:108812565 | G | T | 1 | a0001c0001t0004g0168 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.402-1237C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812565 | |||||||
chr12:108812581 | C | T | 1 | a0001c0001t0018g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402-1253G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812581 | |||||||
chr12:108812845 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.402-1517C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812845 | |||||||
chr12:108812864 | CT | C | 181 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(178): Show |
197 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.402-1537delA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812864 | |||||||
chr12:108812864 | CTT | C | 75 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(72): Show |
80 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.402-1538_402-1537d others(4): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812864 | |||||||
chr12:108812948 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0205 |
3 | HG00733.hp1 HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.402-1620C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812948 | |||||||
chr12:108812989 | A | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.402-1661T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108812989 | |||||||
chr12:108813039 | A | C | 1 | a0001c0002t0021g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.402-1711T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813039 | |||||||
chr12:108813099 | C | A | 2 | a0001c0001t0012g0215 a0001c0001t0056g0211 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.402-1771G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813099 | |||||||
chr12:108813130 | A | C | 68 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(65): Show |
72 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.402-1802T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813130 | |||||||
chr12:108813406 | C | A | 1 | a0001c0002t0011g0290 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402-2078G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813406 | |||||||
chr12:108813506 | G | T | 1 | a0001c0001t0002g0137 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.402-2178C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813506 | |||||||
chr12:108813526 | C | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.402-2198G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813526 | |||||||
chr12:108813594 | C | T | 9 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.402-2266G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813594 | |||||||
chr12:108813710 | A | G | 4 | a0001c0003t0001g0233 a0001c0003t0001g0234 a0001c0003t0020g0231 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-2382T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813710 | |||||||
chr12:108813713 | TA | T | 23 | a0001c0001t0002g0128 a0001c0001t0004g0194 a0001c0001t0004g0205 others(20): Show |
23 | HG00558.hp1 HG01069.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.402-2386delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813713 | |||||||
chr12:108813744 | A | AAGGGG | 3 | a0001c0003t0001g0226 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.402-2421_402-2417d others(7): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813744 | |||||||
chr12:108813764 | G | GAGGGGAA others(9): Show |
4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-2452_402-2437d others(18): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813764 | |||||||
chr12:108813779 | G | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.402-2451C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813779 | |||||||
chr12:108813980 | A | G | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.402-2652T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108813980 | |||||||
chr12:108814270 | G | A | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.401+2768C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814270 | |||||||
chr12:108814322 | C | T | 1 | a0001c0002t0003g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.401+2716G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814322 | |||||||
chr12:108814349 | C | CT | 35 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(32): Show |
40 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.401+2688dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814349 | |||||||
chr12:108814426 | T | G | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.401+2612A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814426 | |||||||
chr12:108814501 | G | C | 1 | a0001c0001t0081g0121 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.401+2537C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814501 | |||||||
chr12:108814518 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.401+2520G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814518 | |||||||
chr12:108814711 | T | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.401+2327A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814711 | |||||||
chr12:108814868 | G | A | 1 | a0001c0007t0002g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.401+2170C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814868 | |||||||
chr12:108814884 | C | T | 2 | a0001c0001t0013g0177 a0001c0001t0058g0178 |
2 | HG00673.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.401+2154G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814884 | |||||||
chr12:108814925 | C | T | 1 | a0001c0001t0014g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401+2113G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814925 | |||||||
chr12:108814975 | T | A | 1 | a0001c0002t0003g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.401+2063A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108814975 | |||||||
chr12:108815126 | G | A | 74 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(71): Show |
78 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.401+1912C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815126 | |||||||
chr12:108815166 | G | A | 2 | a0001c0010t0002g0108 a0001c0010t0002g0135 |
2 | NA18971.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.401+1872C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815166 | |||||||
chr12:108815181 | G | A | 4 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | NA18993.hp2 NA19057.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.401+1857C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815181 | |||||||
chr12:108815315 | A | T | 1 | a0001c0001t0013g0170 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.401+1723T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815315 | |||||||
chr12:108815418 | T | C | 91 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(88): Show |
95 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.401+1620A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815418 | |||||||
chr12:108815474 | C | A | 1 | a0001c0003t0001g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.401+1564G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815474 | |||||||
chr12:108815541 | G | A | 30 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(27): Show |
32 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.401+1497C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815541 | |||||||
chr12:108815581 | C | T | 1 | a0001c0008t0037g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.401+1457G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815581 | |||||||
chr12:108815834 | C | T | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+1204G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108815834 | |||||||
chr12:108816159 | G | A | 1 | a0001c0001t0006g0008 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.401+879C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816159 | |||||||
chr12:108816352 | G | A | 7 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.401+686C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816352 | |||||||
chr12:108816432 | T | C | 4 | a0001c0001t0015g0007 a0001c0001t0015g0120 a0001c0001t0015g0124 others(1): Show |
5 | HG00099.hp1 HG01168.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.401+606A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816432 | |||||||
chr12:108816716 | T | G | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.401+322A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816716 | |||||||
chr12:108816809 | T | C | 1 | a0001c0001t0007g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.401+229A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816809 | |||||||
chr12:108816823 | A | ACT | 298 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(295): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.401+213_401+214dup others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 5/14 | chr12 | 108816823 | |||||||
chr12:108817255 | T | C | 123 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(120): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.280-96A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817255 | |||||||
chr12:108817366 | G | C | 1 | a0001c0002t0073g0270 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-207C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817366 | |||||||
chr12:108817443 | C | T | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280-284G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817443 | |||||||
chr12:108817467 | CAG | C | 123 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(120): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.280-310_280-309del others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817467 | |||||||
chr12:108817472 | G | C | 1 | a0001c0001t0009g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.280-313C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817472 | |||||||
chr12:108817486 | A | T | 1 | a0001c0024t0021g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.280-327T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817486 | |||||||
chr12:108817531 | T | C | 90 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(87): Show |
94 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.280-372A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817531 | |||||||
chr12:108817532 | GCCA | G | 56 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(53): Show |
59 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.280-376_280-374del others(3): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817532 | |||||||
chr12:108817564 | G | A | 7 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-405C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817564 | |||||||
chr12:108817592 | C | CAAAACAC others(3): Show |
1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.280-443_280-434dup others(10): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817592 | |||||||
chr12:108817672 | G | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0152 |
2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.280-513C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817672 | |||||||
chr12:108817693 | G | T | 2 | a0001c0001t0004g0206 a0001c0001t0004g0207 |
2 | NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.280-534C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817693 | |||||||
chr12:108817749 | C | T | 1 | a0001c0002t0051g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.279+500G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817749 | |||||||
chr12:108817776 | C | T | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.279+473G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817776 | |||||||
chr12:108817827 | T | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+422A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108817827 | |||||||
chr12:108818048 | A | T | 1 | a0001c0001t0005g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.279+201T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108818048 | |||||||
chr12:108818208 | A | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+41T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108818208 | |||||||
chr12:108818217 | T | A | 3 | a0001c0001t0038g0126 a0001c0002t0003g0019 a0001c0002t0003g0260 |
3 | HG01943.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279+32A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108818217 | |||||||
chr12:108818218 | T | G | 1 | a0001c0001t0006g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.279+31A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 4/14 | chr12 | 108818218 | |||||||
chr12:108818326 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.215-13A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818326 | |||||||
chr12:108818402 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.215-89T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818402 | |||||||
chr12:108818470 | G | C | 2 | a0001c0002t0001g0003 a0001c0002t0001g0054 |
3 | HG01081.hp1 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.215-157C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818470 | |||||||
chr12:108818505 | G | A | 4 | a0001c0001t0009g0110 a0001c0001t0009g0208 a0001c0001t0031g0245 others(1): Show |
4 | HG02615.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-192C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818505 | |||||||
chr12:108818625 | A | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(3): Show |
8 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.215-312T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818625 | |||||||
chr12:108818817 | G | C | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215-504C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818817 | |||||||
chr12:108818874 | C | T | 1 | a0001c0001t0029g0015 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.215-561G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818874 | |||||||
chr12:108818953 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.215-640G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108818953 | |||||||
chr12:108819189 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.215-876G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819189 | |||||||
chr12:108819358 | G | A | 1 | a0001c0001t0026g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.215-1045C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819358 | |||||||
chr12:108819361 | C | T | 2 | a0001c0002t0003g0285 a0001c0002t0003g0286 |
2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.215-1048G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819361 | |||||||
chr12:108819458 | T | C | 1 | a0001c0002t0003g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.215-1145A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819458 | |||||||
chr12:108819533 | G | A | 87 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(84): Show |
91 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-1220C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819533 | |||||||
chr12:108819538 | G | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1225C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819538 | |||||||
chr12:108819594 | C | A | 3 | a0001c0002t0003g0272 a0001c0002t0003g0273 a0001c0002t0076g0271 |
3 | HG00140.hp1 HG01074.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.215-1281G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819594 | |||||||
chr12:108819613 | G | C | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215-1300C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819613 | |||||||
chr12:108819777 | A | G | 1 | a0001c0001t0004g0198 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.215-1464T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819777 | |||||||
chr12:108819872 | T | C | 1 | a0001c0001t0008g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.215-1559A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108819872 | |||||||
chr12:108820006 | A | C | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.215-1693T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820006 | |||||||
chr12:108820060 | T | C | 93 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(90): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.215-1747A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820060 | |||||||
chr12:108820113 | A | T | 1 | a0001c0001t0002g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.215-1800T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820113 | |||||||
chr12:108820146 | G | A | 1 | a0001c0002t0003g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.215-1833C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820146 | |||||||
chr12:108820235 | T | A | 1 | a0001c0002t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.215-1922A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820235 | |||||||
chr12:108820402 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.215-2089G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820402 | |||||||
chr12:108820521 | T | C | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.215-2208A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820521 | |||||||
chr12:108820681 | C | A | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.215-2368G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820681 | |||||||
chr12:108820716 | A | G | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.215-2403T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820716 | |||||||
chr12:108820746 | G | C | 1 | a0001c0001t0004g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-2433C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820746 | |||||||
chr12:108820795 | A | C | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.214+2463T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820795 | |||||||
chr12:108820851 | G | A | 81 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(78): Show |
85 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.214+2407C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108820851 | |||||||
chr12:108821016 | A | G | 1 | a0001c0002t0003g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.214+2242T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821016 | |||||||
chr12:108821035 | C | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2223G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821035 | |||||||
chr12:108821038 | G | T | 1 | a0001c0001t0008g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+2220C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821038 | |||||||
chr12:108821152 | G | A | 1 | a0001c0002t0003g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214+2106C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821152 | |||||||
chr12:108821216 | T | TAC | 10 | a0001c0001t0005g0127 a0001c0001t0012g0305 a0001c0001t0028g0115 others(7): Show |
10 | HG01169.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+2040_214+2041d others(4): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821216 | |||||||
chr12:108821216 | TAC | T | 228 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(225): Show |
249 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.214+2040_214+2041d others(4): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821216 | |||||||
chr12:108821270 | T | A | 1 | a0001c0001t0010g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.214+1988A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821270 | |||||||
chr12:108821459 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.214+1799G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821459 | |||||||
chr12:108821471 | G | A | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.214+1787C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821471 | |||||||
chr12:108821590 | A | C | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+1668T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821590 | |||||||
chr12:108821647 | T | C | 81 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(78): Show |
85 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.214+1611A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108821647 | |||||||
chr12:108822322 | T | C | 1 | a0001c0002t0003g0257 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214+936A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108822322 | |||||||
chr12:108822348 | A | G | 90 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(87): Show |
94 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.214+910T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108822348 | |||||||
chr12:108822456 | T | C | 2 | a0001c0001t0002g0134 a0001c0001t0062g0133 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.214+802A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108822456 | |||||||
chr12:108822524 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.214+734C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108822524 | |||||||
chr12:108822919 | C | T | 6 | a0001c0001t0007g0009 a0001c0001t0007g0011 a0001c0001t0007g0111 others(3): Show |
8 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+339G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108822919 | |||||||
chr12:108823099 | C | G | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+159G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108823099 | |||||||
chr12:108823128 | A | G | 26 | a0001c0001t0004g0238 a0001c0001t0006g0103 a0001c0001t0006g0107 others(23): Show |
28 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+130T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108823128 | |||||||
chr12:108823147 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.214+111G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108823147 | |||||||
chr12:108823231 | G | GT | 68 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(65): Show |
72 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.214+26dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 3/14 | chr12 | 108823231 | |||||||
chr12:108823403 | G | T | 2 | a0001c0001t0004g0162 a0001c0001t0004g0173 |
2 | NA18979.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.111-42C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823403 | |||||||
chr12:108823652 | T | C | 12 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 others(9): Show |
12 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.111-291A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823652 | |||||||
chr12:108823666 | T | C | 1 | a0001c0002t0044g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.111-305A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823666 | |||||||
chr12:108823824 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.111-463A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823824 | |||||||
chr12:108823827 | C | T | 35 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(32): Show |
40 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-466G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823827 | |||||||
chr12:108823960 | A | G | 90 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(87): Show |
94 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.111-599T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823960 | |||||||
chr12:108823988 | C | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-627G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108823988 | |||||||
chr12:108824299 | C | A | 2 | a0001c0001t0006g0212 a0001c0001t0030g0016 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111-938G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824299 | |||||||
chr12:108824402 | C | T | 17 | a0001c0001t0002g0001 a0001c0001t0002g0136 a0001c0001t0002g0144 others(14): Show |
21 | HG00408.hp2 HG02165.hp1 NA18612.hp1 others(18): Show |
intron_variant | MODIFIER | c.111-1041G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824402 | |||||||
chr12:108824454 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0002g0001 others(12): Show |
21 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.111-1094dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824454 | |||||||
chr12:108824464 | A | AAAAG | 27 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(24): Show |
29 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.111-1107_111-1104d others(6): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824464 | |||||||
chr12:108824468 | G | A | 1 | a0001c0001t0018g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.111-1107C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824468 | |||||||
chr12:108824469 | A | G | 1 | a0001c0001t0018g0029 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.111-1108T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824469 | |||||||
chr12:108824747 | C | T | 2 | a0001c0001t0010g0241 a0001c0001t0010g0242 |
2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.111-1386G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108824747 | |||||||
chr12:108825119 | A | G | 81 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(78): Show |
85 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.111-1758T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108825119 | |||||||
chr12:108825256 | G | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-1895C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108825256 | |||||||
chr12:108825283 | A | G | 1 | a0001c0002t0003g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.111-1922T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108825283 | |||||||
chr12:108825594 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.111-2233T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108825594 | |||||||
chr12:108826031 | G | C | 2 | a0001c0002t0003g0021 a0001c0002t0003g0283 |
3 | HG01069.hp2 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.111-2670C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826031 | |||||||
chr12:108826048 | G | C | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.111-2687C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826048 | |||||||
chr12:108826085 | A | G | 1 | a0001c0002t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.111-2724T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826085 | |||||||
chr12:108826127 | C | G | 93 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(90): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.111-2766G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826127 | |||||||
chr12:108826206 | A | G | 34 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(31): Show |
36 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.111-2845T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826206 | |||||||
chr12:108826450 | G | A | 1 | a0001c0002t0003g0285 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.111-3089C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826450 | |||||||
chr12:108826613 | T | C | 66 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(63): Show |
70 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.111-3252A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826613 | |||||||
chr12:108826753 | C | A | 1 | a0001c0001t0005g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111-3392G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826753 | |||||||
chr12:108826800 | T | C | 1 | a0001c0001t0027g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.111-3439A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108826800 | |||||||
chr12:108827003 | TA | T | 89 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(86): Show |
93 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.111-3643delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827003 | |||||||
chr12:108827020 | G | A | 1 | a0001c0001t0084g0106 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.111-3659C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827020 | |||||||
chr12:108827093 | G | C | 1 | a0001c0002t0044g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.111-3732C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827093 | |||||||
chr12:108827135 | T | C | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-3774A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827135 | |||||||
chr12:108827237 | C | A | 88 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(85): Show |
92 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.111-3876G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827237 | |||||||
chr12:108827243 | A | G | 1 | a0001c0002t0021g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.111-3882T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827243 | |||||||
chr12:108827293 | A | C | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.111-3932T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827293 | |||||||
chr12:108827698 | TG | T | 8 | a0001c0002t0001g0041 a0001c0002t0001g0051 a0001c0002t0001g0052 others(5): Show |
8 | HG02602.hp2 HG02683.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.111-4338delC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827698 | |||||||
chr12:108827732 | C | T | 82 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(79): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.111-4371G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827732 | |||||||
chr12:108827793 | A | G | 1 | a0001c0002t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.111-4432T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827793 | |||||||
chr12:108827954 | C | T | 3 | a0001c0001t0013g0170 a0001c0001t0013g0171 a0001c0001t0013g0172 |
3 | NA18968.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.111-4593G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108827954 | |||||||
chr12:108828035 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-4674G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828035 | |||||||
chr12:108828134 | G | C | 20 | a0001c0001t0002g0001 a0001c0001t0002g0136 a0001c0001t0002g0137 others(17): Show |
24 | HG00408.hp2 HG02165.hp1 NA18612.hp1 others(21): Show |
intron_variant | MODIFIER | c.111-4773C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828134 | |||||||
chr12:108828256 | C | T | 68 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(65): Show |
72 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.111-4895G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828256 | |||||||
chr12:108828354 | A | G | 1 | a0001c0002t0003g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.111-4993T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828354 | |||||||
chr12:108828527 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.111-5166C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828527 | |||||||
chr12:108828550 | C | T | 2 | a0001c0001t0004g0012 a0001c0001t0023g0167 |
3 | NA18952.hp1 NA18990.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.111-5189G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828550 | |||||||
chr12:108828555 | G | A | 26 | a0001c0001t0004g0238 a0001c0001t0006g0103 a0001c0001t0006g0107 others(23): Show |
28 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.111-5194C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828555 | |||||||
chr12:108828582 | G | A | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-5221C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828582 | |||||||
chr12:108828625 | G | A | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-5264C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828625 | |||||||
chr12:108828754 | T | C | 1 | a0001c0001t0038g0126 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.111-5393A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828754 | |||||||
chr12:108828960 | G | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-5599C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828960 | |||||||
chr12:108828965 | C | G | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.111-5604G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828965 | |||||||
chr12:108828966 | A | G | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-5605T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108828966 | |||||||
chr12:108829020 | G | A | 2 | a0001c0001t0024g0261 a0001c0001t0024g0262 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.111-5659C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829020 | |||||||
chr12:108829028 | A | G | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-5667T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829028 | |||||||
chr12:108829068 | C | T | 7 | a0001c0001t0004g0012 a0001c0001t0004g0168 a0001c0001t0004g0169 others(4): Show |
8 | NA18947.hp1 NA18948.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-5707G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829068 | |||||||
chr12:108829102 | T | C | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-5741A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829102 | |||||||
chr12:108829131 | T | C | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-5770A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829131 | |||||||
chr12:108829441 | G | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.111-6080C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829441 | |||||||
chr12:108829478 | G | C | 87 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(84): Show |
91 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.111-6117C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829478 | |||||||
chr12:108829493 | G | A | 1 | a0001c0001t0005g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111-6132C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829493 | |||||||
chr12:108829606 | T | C | 35 | a0001c0001t0002g0001 a0001c0001t0002g0088 a0001c0001t0002g0128 others(32): Show |
40 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.111-6245A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829606 | |||||||
chr12:108829881 | C | G | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111-6520G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829881 | |||||||
chr12:108829931 | A | G | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-6570T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829931 | |||||||
chr12:108829935 | C | A | 1 | a0001c0001t0007g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.111-6574G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108829935 | |||||||
chr12:108830134 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-6773G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108830134 | |||||||
chr12:108830190 | G | A | 4 | a0001c0001t0007g0009 a0001c0001t0007g0117 a0001c0001t0007g0132 others(1): Show |
5 | HG01109.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-6829C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108830190 | |||||||
chr12:108830360 | G | A | 3 | a0001c0001t0022g0199 a0001c0001t0022g0200 a0001c0001t0060g0201 |
3 | NA18960.hp1 NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.111-6999C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108830360 | |||||||
chr12:108830892 | G | A | 2 | a0001c0001t0027g0276 a0001c0002t0027g0275 |
2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.111-7531C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108830892 | |||||||
chr12:108831084 | T | C | 2 | a0001c0002t0001g0004 a0001c0002t0001g0039 |
3 | HG00735.hp2 HG01109.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.111-7723A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831084 | |||||||
chr12:108831147 | G | C | 1 | a0001c0001t0004g0196 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.111-7786C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831147 | |||||||
chr12:108831316 | T | G | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.111-7955A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831316 | |||||||
chr12:108831340 | A | T | 1 | a0001c0002t0003g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.111-7979T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831340 | |||||||
chr12:108831421 | T | C | 1 | a0001c0001t0077g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.111-8060A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831421 | |||||||
chr12:108831447 | A | G | 1 | a0001c0001t0070g0249 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.111-8086T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831447 | |||||||
chr12:108831617 | C | G | 1 | a0001c0002t0001g0057 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.111-8256G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108831617 | |||||||
chr12:108832000 | T | C | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.111-8639A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832000 | |||||||
chr12:108832142 | C | T | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111-8781G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832142 | |||||||
chr12:108832256 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-8895G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832256 | |||||||
chr12:108832306 | C | T | 1 | a0001c0001t0005g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.111-8945G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832306 | |||||||
chr12:108832409 | T | C | 1 | a0001c0002t0003g0286 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.111-9048A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832409 | |||||||
chr12:108832492 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-9131G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832492 | |||||||
chr12:108832869 | C | G | 1 | a0001c0001t0053g0203 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.111-9508G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108832869 | |||||||
chr12:108833074 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.111-9713C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833074 | |||||||
chr12:108833135 | C | A | 4 | a0003c0004t0016g0227 a0003c0004t0016g0228 a0003c0004t0016g0229 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-9774G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833135 | |||||||
chr12:108833153 | C | CT | 6 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0009g0101 others(3): Show |
6 | HG01891.hp1 NA18944.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-9793dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833153 | |||||||
chr12:108833174 | A | G | 67 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(64): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.111-9813T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833174 | |||||||
chr12:108833180 | G | A | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.111-9819C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833180 | |||||||
chr12:108833811 | A | G | 1 | a0001c0002t0040g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.111-10450T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833811 | |||||||
chr12:108833835 | G | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-10474C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833835 | |||||||
chr12:108833989 | A | G | 79 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(76): Show |
83 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.111-10628T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108833989 | |||||||
chr12:108834041 | G | C | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-10680C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834041 | |||||||
chr12:108834138 | T | C | 93 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(90): Show |
97 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.111-10777A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834138 | |||||||
chr12:108834140 | T | G | 1 | a0001c0001t0006g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.111-10779A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834140 | |||||||
chr12:108834146 | TA | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-10786delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834146 | |||||||
chr12:108834155 | A | C | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-10794T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834155 | |||||||
chr12:108834201 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.111-10840C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834201 | |||||||
chr12:108834325 | T | C | 1 | a0001c0001t0015g0007 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.111-10964A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834325 | |||||||
chr12:108834326 | C | T | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111-10965G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834326 | |||||||
chr12:108834379 | C | G | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-11018G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834379 | |||||||
chr12:108834482 | G | A | 3 | a0001c0001t0006g0212 a0001c0001t0029g0015 a0001c0001t0030g0016 |
5 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-11121C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834482 | |||||||
chr12:108834561 | G | A | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.111-11200C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834561 | |||||||
chr12:108834568 | C | T | 7 | a0001c0001t0035g0304 a0001c0001t0089g0306 a0001c0002t0003g0020 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-11207G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834568 | |||||||
chr12:108834891 | G | T | 1 | a0001c0001t0007g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.111-11530C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834891 | |||||||
chr12:108834915 | C | G | 1 | a0001c0001t0067g0209 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.111-11554G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834915 | |||||||
chr12:108834950 | TC | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-11590delG | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108834950 | |||||||
chr12:108835232 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-11871G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835232 | |||||||
chr12:108835420 | G | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.111-12059C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835420 | |||||||
chr12:108835449 | A | G | 6 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.111-12088T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835449 | |||||||
chr12:108835557 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.111-12196G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835557 | |||||||
chr12:108835645 | TA | T | 184 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0002g0001 others(181): Show |
201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.111-12285delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835645 | |||||||
chr12:108835660 | G | A | 175 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0002g0001 others(172): Show |
192 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.111-12299C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835660 | |||||||
chr12:108835697 | G | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.111-12336C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835697 | |||||||
chr12:108835710 | A | G | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.111-12349T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835710 | |||||||
chr12:108835798 | G | A | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.111-12437C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835798 | |||||||
chr12:108835859 | T | C | 1 | a0001c0003t0001g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111-12498A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835859 | |||||||
chr12:108835862 | CAT | C | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-12503_111-1250 others(6): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835862 | |||||||
chr12:108835878 | A | G | 3 | a0001c0001t0006g0008 a0001c0001t0006g0130 a0001c0001t0006g0131 |
4 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.111-12517T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835878 | |||||||
chr12:108835879 | T | TTAATTAA others(59): Show |
54 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(51): Show |
55 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.111-12519_111-1251 others(70): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835879 | |||||||
chr12:108835879 | T | TTAATTAA others(83): Show |
3 | a0001c0001t0069g0024 a0001c0002t0001g0004 a0001c0002t0045g0053 |
4 | HG00735.hp2 HG00738.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12519_111-1251 others(94): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835879 | |||||||
chr12:108835881 | A | AATTAATT others(33): Show |
4 | a0001c0002t0001g0003 a0001c0002t0001g0040 a0001c0002t0001g0048 others(1): Show |
5 | HG01081.hp1 HG01257.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.111-12521_111-1252 others(44): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835881 | |||||||
chr12:108835884 | T | TAATTTAT others(83): Show |
1 | a0001c0002t0021g0083 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.111-12524_111-1252 others(94): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835884 | |||||||
chr12:108835884 | T | TAATTTAT others(107): Show |
3 | a0001c0002t0001g0006 a0001c0002t0001g0089 a0001c0023t0001g0093 |
4 | HG00621.hp1 HG01346.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12524_111-1252 others(118): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835884 | |||||||
chr12:108835884 | T | TAATTTAT others(107): Show |
11 | a0001c0001t0002g0088 a0001c0002t0001g0084 a0001c0002t0001g0085 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-12524_111-1252 others(118): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835884 | |||||||
chr12:108835884 | T | TAATTTAT others(131): Show |
2 | a0001c0001t0066g0086 a0001c0002t0001g0052 |
2 | HG03704.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.111-12524_111-1252 others(142): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835884 | |||||||
chr12:108835885 | A | AATTTATA others(107): Show |
1 | a0001c0002t0048g0096 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.111-12525_111-1252 others(118): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835885 | |||||||
chr12:108835885 | A | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12524T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835885 | |||||||
chr12:108835887 | T | TTTATAAT others(35): Show |
2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-12527_111-1252 others(46): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835887 | |||||||
chr12:108835888 | T | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12527A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835888 | |||||||
chr12:108835888 | T | TTATAATA others(9): Show |
3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-12528_111-1252 others(20): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835888 | |||||||
chr12:108835889 | A | ATATAGTT others(5): Show |
4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12529_111-1252 others(16): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835889 | |||||||
chr12:108835889 | A | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.111-12528T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835889 | |||||||
chr12:108835892 | A | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-12531T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835892 | |||||||
chr12:108835893 | C | T | 9 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-12532G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835893 | |||||||
chr12:108835894 | T | A | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-12533A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835894 | |||||||
chr12:108835905 | A | G | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12544T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835905 | |||||||
chr12:108835908 | T | C | 25 | a0001c0001t0002g0088 a0001c0001t0004g0197 a0001c0001t0026g0160 others(22): Show |
27 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.111-12547A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835908 | |||||||
chr12:108835909 | A | G | 9 | a0001c0001t0066g0086 a0001c0002t0001g0004 a0001c0002t0001g0006 others(6): Show |
11 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.111-12548T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835909 | |||||||
chr12:108835916 | A | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12555T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835916 | |||||||
chr12:108835917 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12556G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835917 | |||||||
chr12:108835918 | T | TTA | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12558_111-1255 others(6): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835918 | |||||||
chr12:108835932 | C | T | 9 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-12571G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835932 | |||||||
chr12:108835933 | A | AATTATAA others(41): Show |
1 | a0001c0001t0004g0205 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.111-12620_111-1257 others(52): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835933 | |||||||
chr12:108835933 | A | G | 27 | a0001c0001t0002g0088 a0001c0001t0002g0134 a0001c0001t0006g0008 others(24): Show |
30 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.111-12572T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835933 | |||||||
chr12:108835936 | T | TATAACTA others(14): Show |
1 | a0001c0001t0012g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.111-12596_111-1257 others(25): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835936 | |||||||
chr12:108835946 | T | C | 1 | a0001c0002t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.111-12585A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835946 | |||||||
chr12:108835956 | C | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12595G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835956 | |||||||
chr12:108835957 | G | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12596C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835957 | |||||||
chr12:108835957 | G | T | 1 | a0001c0001t0031g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.111-12596C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835957 | |||||||
chr12:108835980 | C | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12619G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835980 | |||||||
chr12:108835981 | G | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-12620C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835981 | |||||||
chr12:108835990 | T | TATATTAA others(41): Show |
1 | a0001c0001t0001g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.111-12677_111-1263 others(52): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835990 | |||||||
chr12:108835990 | T | TATATTAA others(17): Show |
3 | a0001c0001t0007g0036 a0001c0001t0012g0295 a0001c0001t0090g0297 |
3 | HG02818.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.111-12630_111-1262 others(28): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835990 | |||||||
chr12:108835990 | T | TATATTAA others(41): Show |
1 | a0001c0001t0024g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.111-12630_111-1262 others(52): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835990 | |||||||
chr12:108835990 | T | TATATTAA others(38): Show |
1 | a0001c0001t0014g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.111-12630_111-1262 others(49): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108835990 | |||||||
chr12:108836005 | G | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-12644C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836005 | |||||||
chr12:108836012 | A | T | 14 | a0001c0001t0007g0036 a0001c0001t0012g0295 a0001c0001t0014g0219 others(11): Show |
16 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.111-12651T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836012 | |||||||
chr12:108836012 | ACTATATT others(17): Show |
A | 1 | a0001c0001t0005g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111-12675_111-1265 others(28): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836012 | |||||||
chr12:108836013 | C | T | 45 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(42): Show |
49 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.111-12652G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836013 | |||||||
chr12:108836014 | T | A | 14 | a0001c0001t0007g0036 a0001c0001t0012g0295 a0001c0001t0014g0219 others(11): Show |
16 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.111-12653A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(65): Show |
7 | a0001c0001t0069g0024 a0001c0002t0001g0003 a0001c0002t0001g0041 others(4): Show |
8 | HG01257.hp1 HG01358.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.111-12654_111-1265 others(76): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(89): Show |
1 | a0001c0002t0074g0264 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.111-12654_111-1265 others(100): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(41): Show |
50 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0054g0080 others(47): Show |
51 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.111-12654_111-1265 others(52): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(65): Show |
9 | a0001c0001t0055g0116 a0001c0001t0083g0112 a0001c0002t0001g0042 others(6): Show |
10 | HG01255.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.111-12654_111-1265 others(76): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(17): Show |
14 | a0001c0001t0002g0088 a0001c0001t0006g0237 a0001c0001t0009g0100 others(11): Show |
14 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.111-12677_111-1265 others(28): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(41): Show |
182 | a0001c0001t0001g0018 a0001c0001t0002g0001 a0001c0001t0002g0128 others(179): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.111-12654_111-1265 others(52): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(65): Show |
9 | a0001c0001t0004g0198 a0001c0001t0010g0028 a0001c0001t0010g0240 others(6): Show |
9 | HG01243.hp1 HG01256.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.111-12654_111-1265 others(76): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(113): Show |
2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-12654_111-1265 others(124): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836014 | T | TATATTAA others(89): Show |
2 | a0001c0001t0004g0238 a0001c0001t0006g0239 |
2 | HG00642.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.111-12654_111-1265 others(100): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836014 | |||||||
chr12:108836036 | T | A | 5 | a0001c0001t0002g0046 a0001c0002t0001g0039 a0001c0002t0001g0044 others(2): Show |
5 | HG01070.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-12675A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836036 | |||||||
chr12:108836037 | T | C | 5 | a0001c0001t0002g0046 a0001c0002t0001g0039 a0001c0002t0001g0044 others(2): Show |
5 | HG01070.hp1 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-12676A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836037 | |||||||
chr12:108836038 | A | T | 6 | a0001c0001t0002g0046 a0001c0001t0005g0118 a0001c0002t0001g0039 others(3): Show |
6 | HG01070.hp1 HG01928.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.111-12677T>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836038 | |||||||
chr12:108836378 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-13017G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836378 | |||||||
chr12:108836474 | G | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.111-13113C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836474 | |||||||
chr12:108836476 | T | C | 2 | a0001c0001t0006g0212 a0001c0001t0030g0016 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.111-13115A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836476 | |||||||
chr12:108836540 | C | A | 1 | a0001c0024t0021g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.111-13179G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836540 | |||||||
chr12:108836699 | G | A | 1 | a0001c0023t0001g0093 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.111-13338C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836699 | |||||||
chr12:108836771 | G | T | 1 | a0001c0001t0025g0299 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.111-13410C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836771 | |||||||
chr12:108836794 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111-13433G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836794 | |||||||
chr12:108836941 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111-13580G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108836941 | |||||||
chr12:108837089 | G | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.111-13728C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837089 | |||||||
chr12:108837147 | G | A | 1 | a0001c0001t0010g0242 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.111-13786C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837147 | |||||||
chr12:108837462 | G | T | 2 | a0001c0001t0015g0120 a0001c0001t0081g0121 |
2 | HG01168.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.111-14101C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837462 | |||||||
chr12:108837581 | T | C | 1 | a0001c0001t0005g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.111-14220A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837581 | |||||||
chr12:108837628 | C | T | 33 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(30): Show |
35 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.111-14267G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837628 | |||||||
chr12:108837753 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.111-14392T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837753 | |||||||
chr12:108837768 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.111-14407G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837768 | |||||||
chr12:108837788 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.111-14427A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837788 | |||||||
chr12:108837854 | C | T | 1 | a0009c0014t0004g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.111-14493G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108837854 | |||||||
chr12:108838075 | T | C | 99 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(96): Show |
103 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.110+14563A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838075 | |||||||
chr12:108838139 | G | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.110+14499C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838139 | |||||||
chr12:108838221 | T | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+14417A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838221 | |||||||
chr12:108838249 | C | T | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.110+14389G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838249 | |||||||
chr12:108838307 | G | A | 3 | a0001c0001t0022g0199 a0001c0001t0022g0200 a0001c0001t0060g0201 |
3 | NA18960.hp1 NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.110+14331C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838307 | |||||||
chr12:108838377 | C | T | 11 | a0001c0001t0077g0279 a0001c0002t0003g0021 a0001c0002t0003g0248 others(8): Show |
12 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.110+14261G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838377 | |||||||
chr12:108838470 | C | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.110+14168G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838470 | |||||||
chr12:108838690 | C | A | 3 | a0004c0011t0005g0217 a0004c0011t0005g0218 a0005c0015t0085g0129 |
3 | HG02280.hp2 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.110+13948G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838690 | |||||||
chr12:108838744 | C | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+13894G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838744 | |||||||
chr12:108838849 | A | G | 1 | a0001c0002t0003g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110+13789T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838849 | |||||||
chr12:108838906 | G | A | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.110+13732C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838906 | |||||||
chr12:108838943 | T | C | 6 | a0001c0002t0003g0158 a0001c0002t0003g0247 a0001c0002t0003g0257 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+13695A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108838943 | |||||||
chr12:108839263 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(6): Show |
11 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.110+13375C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839263 | |||||||
chr12:108839405 | G | T | 1 | a0001c0002t0003g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110+13233C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839405 | |||||||
chr12:108839513 | A | G | 10 | a0001c0002t0003g0257 a0001c0003t0001g0226 a0001c0003t0001g0233 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+13125T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839513 | |||||||
chr12:108839690 | G | GA | 15 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(12): Show |
17 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.110+12947dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839690 | |||||||
chr12:108839730 | A | G | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+12908T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839730 | |||||||
chr12:108839793 | G | A | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110+12845C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108839793 | |||||||
chr12:108840013 | G | A | 1 | a0001c0001t0029g0015 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.110+12625C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840013 | |||||||
chr12:108840034 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.110+12604C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840034 | |||||||
chr12:108840226 | G | A | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.110+12412C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840226 | |||||||
chr12:108840368 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110+12270G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840368 | |||||||
chr12:108840488 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.110+12150C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840488 | |||||||
chr12:108840688 | A | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+11950T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840688 | |||||||
chr12:108840695 | C | T | 262 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0094 others(259): Show |
283 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.110+11943G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840695 | |||||||
chr12:108840802 | A | G | 1 | a0001c0002t0088g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.110+11836T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840802 | |||||||
chr12:108840816 | G | A | 3 | a0001c0001t0005g0033 a0001c0001t0005g0035 a0001c0001t0082g0034 |
3 | HG00423.hp1 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.110+11822C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840816 | |||||||
chr12:108840927 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(6): Show |
11 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.110+11711T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840927 | |||||||
chr12:108840959 | G | A | 1 | a0001c0002t0003g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.110+11679C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108840959 | |||||||
chr12:108841113 | G | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+11525C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841113 | |||||||
chr12:108841152 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+11486G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841152 | |||||||
chr12:108841175 | T | C | 1 | a0001c0001t0077g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.110+11463A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841175 | |||||||
chr12:108841241 | C | T | 2 | a0001c0001t0011g0017 a0001c0001t0011g0291 |
3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.110+11397G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841241 | |||||||
chr12:108841309 | T | A | 1 | a0001c0001t0004g0202 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110+11329A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841309 | |||||||
chr12:108841414 | C | T | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.110+11224G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841414 | |||||||
chr12:108841546 | G | A | 1 | a0010c0012t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.110+11092C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841546 | |||||||
chr12:108841582 | T | C | 1 | a0001c0002t0001g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.110+11056A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841582 | |||||||
chr12:108841610 | C | T | 17 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(14): Show |
19 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.110+11028G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841610 | |||||||
chr12:108841677 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.110+10961G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841677 | |||||||
chr12:108841729 | A | G | 1 | a0001c0003t0001g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110+10909T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841729 | |||||||
chr12:108841736 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.110+10902C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841736 | |||||||
chr12:108841801 | C | T | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110+10837G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841801 | |||||||
chr12:108841811 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+10827G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841811 | |||||||
chr12:108841814 | C | A | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+10824G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841814 | |||||||
chr12:108841842 | GTA | G | 46 | a0001c0001t0001g0292 a0001c0001t0002g0001 a0001c0001t0002g0134 others(43): Show |
52 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.110+10794_110+1079 others(6): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841842 | |||||||
chr12:108841842 | GTATA | G | 208 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(205): Show |
222 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.110+10792_110+1079 others(8): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841842 | |||||||
chr12:108841844 | A | G | 3 | a0001c0001t0001g0018 a0001c0008t0036g0308 a0001c0008t0037g0307 |
4 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+10794T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841844 | |||||||
chr12:108841846 | A | G | 1 | a0001c0001t0031g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.110+10792T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108841846 | |||||||
chr12:108842281 | A | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+10357T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108842281 | |||||||
chr12:108842305 | G | T | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+10333C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108842305 | |||||||
chr12:108842569 | G | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+10069C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108842569 | |||||||
chr12:108842815 | C | T | 7 | a0001c0001t0002g0046 a0001c0002t0001g0039 a0001c0002t0001g0043 others(4): Show |
7 | HG01070.hp1 HG01928.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+9823G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108842815 | |||||||
chr12:108843472 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+9166G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843472 | |||||||
chr12:108843496 | T | C | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110+9142A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843496 | |||||||
chr12:108843683 | C | T | 1 | a0001c0001t0072g0025 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110+8955G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843683 | |||||||
chr12:108843722 | A | G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+8916T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843722 | |||||||
chr12:108843781 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.110+8857G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843781 | |||||||
chr12:108843815 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.110+8823C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108843815 | |||||||
chr12:108844020 | C | T | 1 | a0001c0002t0001g0043 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.110+8618G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844020 | |||||||
chr12:108844041 | T | C | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+8597A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844041 | |||||||
chr12:108844099 | G | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+8539C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844099 | |||||||
chr12:108844133 | C | A | 3 | a0001c0001t0006g0212 a0001c0001t0029g0015 a0001c0001t0030g0016 |
5 | HG02896.hp1 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.110+8505G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844133 | |||||||
chr12:108844183 | C | G | 67 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(64): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.110+8455G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844183 | |||||||
chr12:108844251 | C | T | 1 | a0001c0001t0070g0249 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.110+8387G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844251 | |||||||
chr12:108844315 | G | C | 2 | a0004c0011t0005g0217 a0004c0011t0005g0218 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.110+8323C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844315 | |||||||
chr12:108844376 | G | C | 1 | a0001c0001t0012g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.110+8262C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844376 | |||||||
chr12:108844460 | A | G | 1 | a0001c0001t0077g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.110+8178T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844460 | |||||||
chr12:108844474 | C | T | 1 | a0001c0001t0004g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.110+8164G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844474 | |||||||
chr12:108844616 | C | T | 1 | a0001c0002t0003g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.110+8022G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844616 | |||||||
chr12:108844633 | T | C | 1 | a0001c0001t0007g0011 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.110+8005A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844633 | |||||||
chr12:108844952 | TACAAAAA others(48): Show |
T | 4 | a0001c0001t0010g0240 a0001c0001t0089g0306 a0001c0008t0036g0308 others(1): Show |
4 | HG02257.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+7631_110+7685d others(57): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844952 | |||||||
chr12:108844965 | A | G | 2 | a0001c0001t0061g0195 a0001c0003t0020g0232 |
2 | HG02970.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.110+7673T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108844965 | |||||||
chr12:108845007 | G | A | 1 | a0001c0001t0066g0086 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.110+7631C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845007 | |||||||
chr12:108845197 | GA | G | 32 | a0001c0001t0002g0128 a0001c0001t0005g0002 a0001c0001t0005g0031 others(29): Show |
34 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.110+7440delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845197 | |||||||
chr12:108845294 | C | T | 1 | a0001c0002t0001g0040 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.110+7344G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845294 | |||||||
chr12:108845298 | G | A | 2 | a0001c0001t0004g0014 a0001c0001t0004g0205 |
3 | HG00733.hp1 HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.110+7340C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845298 | |||||||
chr12:108845385 | C | T | 1 | a0001c0003t0001g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110+7253G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845385 | |||||||
chr12:108845399 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(6): Show |
11 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.110+7239C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845399 | |||||||
chr12:108845413 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.110+7225G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845413 | |||||||
chr12:108845505 | T | C | 1 | a0001c0006t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110+7133A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845505 | |||||||
chr12:108845595 | G | A | 1 | a0001c0001t0006g0239 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.110+7043C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845595 | |||||||
chr12:108845718 | A | C | 3 | a0001c0001t0038g0126 a0001c0002t0003g0019 a0001c0002t0003g0260 |
4 | HG01943.hp2 HG02723.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+6920T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845718 | |||||||
chr12:108845732 | T | C | 1 | a0001c0001t0026g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.110+6906A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845732 | |||||||
chr12:108845753 | G | T | 1 | a0001c0002t0001g0039 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.110+6885C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845753 | |||||||
chr12:108845797 | C | T | 1 | a0001c0001t0064g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110+6841G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845797 | |||||||
chr12:108845909 | G | A | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110+6729C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108845909 | |||||||
chr12:108846409 | G | A | 1 | a0001c0002t0003g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.110+6229C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108846409 | |||||||
chr12:108846498 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+6140G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108846498 | |||||||
chr12:108846855 | C | T | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110+5783G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108846855 | |||||||
chr12:108847006 | C | G | 3 | a0001c0002t0003g0257 a0001c0002t0003g0259 a0001c0002t0078g0258 |
3 | HG02572.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.110+5632G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847006 | |||||||
chr12:108847037 | C | T | 17 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(14): Show |
19 | HG00099.hp1 HG00423.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.110+5601G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847037 | |||||||
chr12:108847124 | A | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+5514T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847124 | |||||||
chr12:108847469 | A | G | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+5169T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847469 | |||||||
chr12:108847495 | G | A | 8 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+5143C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847495 | |||||||
chr12:108847559 | A | G | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+5079T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847559 | |||||||
chr12:108847648 | G | A | 1 | a0001c0001t0080g0223 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.110+4990C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108847648 | |||||||
chr12:108848028 | G | C | 1 | a0001c0001t0012g0296 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.110+4610C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848028 | |||||||
chr12:108848074 | T | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+4564A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848074 | |||||||
chr12:108848093 | G | A | 58 | a0001c0001t0002g0161 a0001c0001t0002g0175 a0001c0001t0002g0176 others(55): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.110+4545C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848093 | |||||||
chr12:108848188 | A | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+4450T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848188 | |||||||
chr12:108848210 | A | G | 9 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.110+4428T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848210 | |||||||
chr12:108848221 | G | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+4417C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848221 | |||||||
chr12:108848246 | G | T | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.110+4392C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848246 | |||||||
chr12:108848339 | G | A | 1 | a0001c0023t0001g0093 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.110+4299C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848339 | |||||||
chr12:108848441 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.110+4197C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848441 | |||||||
chr12:108848471 | A | G | 1 | a0001c0002t0001g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.110+4167T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848471 | |||||||
chr12:108848602 | G | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+4036C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848602 | |||||||
chr12:108848634 | C | T | 2 | a0001c0001t0007g0117 a0001c0001t0055g0116 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.110+4004G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848634 | |||||||
chr12:108848862 | C | T | 1 | a0001c0002t0019g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.110+3776G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848862 | |||||||
chr12:108848963 | T | A | 1 | a0001c0002t0042g0095 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.110+3675A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848963 | |||||||
chr12:108848964 | C | T | 2 | a0001c0006t0003g0254 a0001c0006t0003g0255 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.110+3674G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848964 | |||||||
chr12:108848967 | C | A | 1 | a0001c0002t0048g0096 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.110+3671G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108848967 | |||||||
chr12:108849127 | G | A | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+3511C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849127 | |||||||
chr12:108849426 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110+3212C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849426 | |||||||
chr12:108849527 | G | A | 15 | a0001c0001t0077g0279 a0001c0002t0003g0021 a0001c0002t0003g0248 others(12): Show |
16 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.110+3111C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849527 | |||||||
chr12:108849643 | A | G | 1 | a0001c0002t0003g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.110+2995T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849643 | |||||||
chr12:108849675 | T | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+2963A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849675 | |||||||
chr12:108849692 | C | T | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+2946G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849692 | |||||||
chr12:108849713 | T | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.110+2925A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849713 | |||||||
chr12:108849728 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.110+2910A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849728 | |||||||
chr12:108849905 | C | CTGGGGGA others(8): Show |
1 | a0001c0002t0003g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110+2718_110+2732d others(17): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849905 | |||||||
chr12:108849918 | ACATGGGG others(8): Show |
A | 2 | a0001c0001t0004g0206 a0001c0001t0004g0207 |
2 | NA18983.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.110+2705_110+2719d others(17): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849918 | |||||||
chr12:108849997 | A | G | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.110+2641T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108849997 | |||||||
chr12:108850014 | G | A | 24 | a0001c0001t0004g0238 a0001c0001t0006g0103 a0001c0001t0006g0107 others(21): Show |
26 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.110+2624C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850014 | |||||||
chr12:108850056 | G | A | 1 | a0001c0001t0007g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.110+2582C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850056 | |||||||
chr12:108850068 | GGAGATGG others(20): Show |
G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+2543_110+2569d others(29): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850068 | |||||||
chr12:108850095 | T | TGAGCTGG others(33): Show |
1 | a0001c0001t0004g0014 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.110+2503_110+2542d others(42): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850095 | |||||||
chr12:108850103 | G | C | 1 | a0001c0025t0011g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.110+2535C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850103 | |||||||
chr12:108850110 | GAGATGGG others(113): Show |
G | 13 | a0001c0001t0006g0103 a0001c0001t0006g0107 a0001c0001t0009g0100 others(10): Show |
13 | HG01167.hp1 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.110+2408_110+2527d others(2): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850110 | |||||||
chr12:108850161 | G | C | 1 | a0001c0002t0001g0082 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.110+2477C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850161 | |||||||
chr12:108850179 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+2459G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850179 | |||||||
chr12:108850190 | A | G | 1 | a0001c0002t0003g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110+2448T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850190 | |||||||
chr12:108850190 | AAGATGGG others(33): Show |
G | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+2408_110+2448d others(47): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850190 | |||||||
chr12:108850218 | G | C | 2 | a0004c0011t0005g0217 a0004c0011t0005g0218 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.110+2420C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850218 | |||||||
chr12:108850230 | C | G | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.110+2408G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850230 | |||||||
chr12:108850230 | CAGATGGG others(33): Show |
C | 1 | a0001c0002t0003g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110+2368_110+2407d others(42): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850230 | |||||||
chr12:108850259 | C | CTGGGGGA others(113): Show |
1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.110+2378_110+2379i others(122): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850259 | |||||||
chr12:108850259 | C | CTGGGGGA others(73): Show |
8 | a0001c0001t0025g0299 a0001c0001t0025g0300 a0001c0001t0035g0304 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.110+2378_110+2379i others(82): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850259 | |||||||
chr12:108850259 | C | T | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.110+2379G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850259 | |||||||
chr12:108850384 | TGGGGAGG others(7): Show |
T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0292 a0001c0001t0011g0017 others(6): Show |
11 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.110+2240_110+2253d others(16): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850384 | |||||||
chr12:108850396 | A | C | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2242T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850396 | |||||||
chr12:108850398 | G | T | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.110+2240C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850398 | |||||||
chr12:108850486 | T | A | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+2152A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850486 | |||||||
chr12:108850571 | G | C | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110+2067C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850571 | |||||||
chr12:108850785 | G | A | 4 | a0001c0003t0001g0233 a0001c0003t0001g0234 a0001c0003t0020g0231 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+1853C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850785 | |||||||
chr12:108850893 | C | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+1745G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850893 | |||||||
chr12:108850906 | C | T | 1 | a0001c0001t0007g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110+1732G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850906 | |||||||
chr12:108850944 | C | T | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.110+1694G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850944 | |||||||
chr12:108850981 | T | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+1657A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850981 | |||||||
chr12:108850995 | C | G | 1 | a0001c0002t0046g0037 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.110+1643G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108850995 | |||||||
chr12:108851021 | A | G | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.110+1617T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851021 | |||||||
chr12:108851123 | G | A | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+1515C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851123 | |||||||
chr12:108851172 | C | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+1466G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851172 | |||||||
chr12:108851255 | C | T | 3 | a0001c0001t0025g0299 a0001c0001t0025g0300 a0001c0003t0039g0301 |
3 | NA20300.hp1 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.110+1383G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851255 | |||||||
chr12:108851307 | G | A | 3 | a0001c0001t0089g0306 a0001c0008t0036g0308 a0001c0008t0037g0307 |
3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.110+1331C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851307 | |||||||
chr12:108851349 | T | G | 1 | a0001c0002t0003g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110+1289A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851349 | |||||||
chr12:108851554 | G | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.110+1084C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851554 | |||||||
chr12:108851855 | T | C | 2 | a0001c0001t0012g0215 a0001c0001t0056g0211 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.110+783A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108851855 | |||||||
chr12:108852094 | G | A | 1 | a0001c0002t0001g0098 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.110+544C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852094 | |||||||
chr12:108852101 | T | C | 3 | a0001c0001t0010g0028 a0001c0001t0010g0243 a0001c0001t0010g0244 |
3 | HG01243.hp1 HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.110+537A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852101 | |||||||
chr12:108852121 | C | A | 2 | a0001c0001t0006g0212 a0001c0001t0030g0016 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.110+517G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852121 | |||||||
chr12:108852238 | C | CT | 15 | a0001c0001t0006g0103 a0001c0001t0006g0107 a0001c0001t0009g0100 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.110+399dupA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852238 | |||||||
chr12:108852238 | CT | C | 9 | a0001c0001t0002g0213 a0001c0001t0004g0214 a0001c0001t0008g0216 others(6): Show |
9 | HG01978.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.110+399delA | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852238 | |||||||
chr12:108852259 | C | T | 1 | a0001c0002t0003g0248 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110+379G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852259 | |||||||
chr12:108852446 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110+192C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852446 | |||||||
chr12:108852635 | T | A | 1 | a0001c0001t0012g0215 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.110+3A>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 2/14 | chr12 | 108852635 | |||||||
chr12:108853010 | C | T | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-332G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853010 | |||||||
chr12:108853214 | T | TA | 7 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0001t0089g0306 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-537dupT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853214 | |||||||
chr12:108853219 | A | G | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-541T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853219 | |||||||
chr12:108853307 | G | A | 6 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0008t0036g0308 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-629C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853307 | |||||||
chr12:108853411 | G | A | 4 | a0001c0001t0012g0305 a0001c0001t0035g0304 a0001c0009t0049g0302 others(1): Show |
4 | HG01884.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-733C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853411 | |||||||
chr12:108853419 | G | A | 10 | a0001c0001t0069g0024 a0001c0003t0001g0226 a0001c0003t0001g0233 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-741C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853419 | |||||||
chr12:108853547 | G | A | 1 | a0001c0002t0011g0290 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.70-869C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853547 | |||||||
chr12:108853550 | G | C | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.70-872C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853550 | |||||||
chr12:108853851 | GAGGCGGA others(25): Show |
G | 1 | a0001c0002t0003g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70-1205_70-1174del others(32): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853851 | |||||||
chr12:108853858 | A | G | 1 | a0001c0001t0007g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-1180T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853858 | |||||||
chr12:108853872 | C | T | 3 | a0001c0001t0035g0304 a0001c0009t0049g0302 a0001c0009t0050g0303 |
3 | HG01884.hp2 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.70-1194G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853872 | |||||||
chr12:108853907 | A | G | 68 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0046 others(65): Show |
72 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.70-1229T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853907 | |||||||
chr12:108853922 | CA | C | 16 | a0001c0001t0002g0138 a0001c0001t0012g0305 a0001c0001t0025g0299 others(13): Show |
16 | HG00438.hp2 HG01884.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-1245delT | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853922 | |||||||
chr12:108853923 | A | C | 1 | a0001c0001t0008g0027 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.70-1245T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853923 | |||||||
chr12:108853939 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70-1261G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108853939 | |||||||
chr12:108854120 | G | A | 5 | a0001c0003t0001g0226 a0003c0004t0016g0227 a0003c0004t0016g0228 others(2): Show |
5 | HG02145.hp2 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-1442C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854120 | |||||||
chr12:108854157 | T | C | 1 | a0001c0001t0011g0291 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.70-1479A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854157 | |||||||
chr12:108854493 | G | A | 1 | a0001c0001t0008g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70-1815C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854493 | |||||||
chr12:108854500 | A | G | 1 | a0001c0001t0008g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70-1822T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854500 | |||||||
chr12:108854501 | G | A | 1 | a0001c0001t0008g0216 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70-1823C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854501 | |||||||
chr12:108854654 | G | A | 1 | a0001c0001t0012g0305 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70-1976C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854654 | |||||||
chr12:108854655 | G | A | 2 | a0004c0011t0005g0217 a0004c0011t0005g0218 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.70-1977C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854655 | |||||||
chr12:108854710 | A | C | 1 | a0001c0003t0039g0301 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-2032T>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854710 | |||||||
chr12:108854746 | T | C | 7 | a0001c0001t0008g0224 a0001c0001t0014g0219 a0001c0001t0014g0220 others(4): Show |
7 | HG02129.hp2 HG02273.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-2068A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854746 | |||||||
chr12:108854846 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.70-2168C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854846 | |||||||
chr12:108854991 | T | C | 1 | a0001c0002t0001g0225 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.70-2313A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854991 | |||||||
chr12:108854994 | G | A | 4 | a0001c0001t0012g0293 a0001c0001t0012g0295 a0001c0001t0012g0296 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2316C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108854994 | |||||||
chr12:108855258 | T | C | 4 | a0001c0003t0001g0233 a0001c0003t0001g0234 a0001c0003t0020g0231 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+2170A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855258 | |||||||
chr12:108855359 | G | C | 10 | a0001c0001t0069g0024 a0001c0003t0001g0226 a0001c0003t0001g0233 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+2069C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855359 | |||||||
chr12:108855429 | TTGCACAA others(24): Show |
T | 1 | a0010c0012t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.69+1968_69+1998del others(31): Show |
SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855429 | |||||||
chr12:108855467 | G | A | 1 | a0001c0002t0087g0235 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.69+1961C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855467 | |||||||
chr12:108855511 | A | G | 9 | a0001c0001t0005g0002 a0001c0001t0005g0031 a0001c0001t0005g0032 others(6): Show |
10 | HG00423.hp1 NA18942.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+1917T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855511 | |||||||
chr12:108855696 | G | A | 3 | a0001c0001t0004g0238 a0001c0001t0006g0237 a0001c0001t0006g0239 |
3 | HG00642.hp2 HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.69+1732C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855696 | |||||||
chr12:108855835 | A | G | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+1593T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855835 | |||||||
chr12:108855859 | C | A | 1 | a0001c0001t0089g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+1569G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855859 | |||||||
chr12:108855939 | T | G | 6 | a0001c0001t0010g0028 a0001c0001t0010g0240 a0001c0001t0010g0241 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1489A>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108855939 | |||||||
chr12:108856085 | T | C | 2 | a0001c0001t0031g0245 a0001c0001t0079g0246 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.69+1343A>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856085 | |||||||
chr12:108856216 | G | T | 1 | a0010c0012t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.69+1212C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856216 | |||||||
chr12:108856444 | G | A | 1 | a0001c0001t0090g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+984C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856444 | |||||||
chr12:108856568 | G | A | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+860C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856568 | |||||||
chr12:108856580 | A | G | 249 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0002g0001 others(246): Show |
268 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.69+848T>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856580 | |||||||
chr12:108856669 | C | CG | 4 | a0001c0001t0004g0298 a0001c0001t0008g0027 a0001c0001t0010g0028 others(1): Show |
4 | HG01243.hp1 HG01255.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+758dupC | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856669 | |||||||
chr12:108856762 | C | G | 1 | a0001c0001t0072g0025 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.69+666G>C | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856762 | |||||||
chr12:108856900 | G | T | 2 | a0001c0001t0025g0299 a0001c0001t0025g0300 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.69+528C>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108856900 | |||||||
chr12:108857106 | C | A | 1 | a0001c0001t0004g0298 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.69+322G>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857106 | |||||||
chr12:108857108 | C | T | 1 | a0001c0001t0069g0024 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.69+320G>A | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857108 | |||||||
chr12:108857246 | G | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+182C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857246 | |||||||
chr12:108857320 | G | C | 10 | a0001c0001t0012g0305 a0001c0001t0025g0299 a0001c0001t0025g0300 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+108C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857320 | |||||||
chr12:108857371 | G | A | 1 | a0001c0002t0003g0021 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.69+57C>T | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857371 | |||||||
chr12:108857411 | G | C | 2 | a0001c0008t0036g0308 a0001c0008t0037g0307 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.69+17C>G | SSH1 | ENSG00000084112.15 | transcript | ENST00000326495.10 | protein_coding | 1/14 | chr12 | 108857411 |