Item | Value |
---|---|
geneid | 6801 |
ensemblid | ENSG00000115808.13 |
hgncid | 11424 |
symbol | STRN |
name | striatin |
refseq_nuc | NM_003162.4 |
refseq_prot | NP_003153.2 |
ensembl_nuc | ENST00000263918.9 |
ensembl_prot | ENSP00000263918.4 |
mane_status | MANE Select |
chr | chr2 |
start | 36837698 |
end | 36966536 |
strand | - |
ver | v1.2 |
region | chr2:36837698-36966536 |
region5000 | chr2:36832698-36971536 |
regionname0 | STRN_chr2_36837698_36966536 |
regionname5000 | STRN_chr2_36832698_36971536 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 780 | 295 | 75 | 49 | 122 | 13 | 34 | 87 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
a0002 | 0/0 | 780 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
a0003 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
a0004 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
a0005 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
a0006 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | MDEQA others(775): Show |
chr2 | 36832698 | 36971536 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2340 | 293 | 74 | 49 | 121 | 13 | 34 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0001c0003 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0001c0005 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0002c0002 | 0/0 | 2340 | 3 | 0 | 0 | 1 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0003c0007 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0004c0004 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0005c0006 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 | ||
a0006c0008 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | ATGGA others(2335): Show |
chr2 | 36832698 | 36971536 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 14173 | 60 | 6 | 11 | 32 | 4 | 7 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0002 | 0/0 | 14173 | 42 | 0 | 5 | 33 | 1 | 3 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0003 | 0/0 | 14173 | 30 | 4 | 5 | 8 | 4 | 9 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0004 | 0/0 | 14174 | 13 | 0 | 0 | 12 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0005 | 0/0 | 14176 | 8 | 4 | 0 | 2 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0006 | 0/0 | 14171 | 9 | 5 | 3 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14166): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0007 | 1/0 | 14174 | 9 | 8 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0008 | 0/0 | 14174 | 7 | 5 | 2 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0009 | 0/0 | 14173 | 5 | 0 | 0 | 5 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0010 | 0/0 | 14174 | 5 | 2 | 2 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0011 | 0/0 | 14173 | 4 | 0 | 1 | 0 | 2 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0012 | 0/0 | 14174 | 4 | 4 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0013 | 0/0 | 14175 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14170): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0014 | 0/0 | 14173 | 3 | 0 | 0 | 3 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0015 | 0/0 | 14173 | 3 | 2 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0016 | 0/0 | 14169 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14164): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0017 | 0/0 | 14176 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0018 | 0/0 | 14174 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0019 | 0/0 | 14174 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0020 | 0/0 | 14174 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0021 | 0/0 | 14174 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0022 | 0/0 | 14173 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0023 | 0/0 | 14173 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0024 | 0/0 | 14172 | 2 | 0 | 0 | 1 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0025 | 0/0 | 14173 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0026 | 0/0 | 14171 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14166): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0027 | 0/0 | 14173 | 2 | 1 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0028 | 0/0 | 14172 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0029 | 0/0 | 14173 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0030 | 0/0 | 14174 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0031 | 0/0 | 14173 | 2 | 0 | 2 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0032 | 0/0 | 14172 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0033 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0034 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0035 | 0/0 | 14176 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0036 | 0/0 | 14174 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0037 | 0/0 | 14176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0038 | 0/0 | 14176 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0039 | 0/0 | 14174 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0040 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0041 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14164): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0042 | 0/0 | 14174 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0044 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0045 | 0/0 | 14175 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14170): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0046 | 0/0 | 14175 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14170): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0047 | 0/0 | 14174 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0048 | 0/0 | 14174 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0049 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0050 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0051 | 0/1 | 14151 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14146): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0052 | 0/0 | 14174 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0053 | 0/0 | 14174 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0054 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0055 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0056 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0057 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0058 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0059 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0060 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0061 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0062 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0063 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0064 | 0/0 | 14172 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0065 | 0/0 | 14174 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0066 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0067 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0068 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0069 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0070 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0071 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0072 | 0/0 | 14140 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14135): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0073 | 0/0 | 14139 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14134): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0074 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0075 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14166): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0076 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0077 | 0/0 | 14174 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14169): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0078 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0079 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0080 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0081 | 0/0 | 14172 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0082 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0083 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0084 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0085 | 0/0 | 14172 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14167): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0086 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0001t0087 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0001c0003t0005 | 0/0 | 14176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0001c0005t0006 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14166): Show |
chr2 | 36832698 | 36971536 |
a0002c0002t0005 | 0/0 | 14176 | 2 | 0 | 0 | 1 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0002c0002t0043 | 0/0 | 14176 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14171): Show |
chr2 | 36832698 | 36971536 |
a0003c0007t0001 | 0/0 | 14173 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0004c0004t0002 | 0/0 | 14173 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0005c0006t0003 | 0/0 | 14173 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
a0006c0008t0003 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | GAGGC others(14168): Show |
chr2 | 36832698 | 36971536 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0010g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0012g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0014g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0015g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0015g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0015g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0016g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0016g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0017g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0017g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0018g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0018g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0020g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0020g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0021g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0022g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0023g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0023g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0024g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0024g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0025g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0025g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0026g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0026g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0027g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0028g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0028g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0029g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0029g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0030g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0030g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0031g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0031g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0033g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0034g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0035g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0036g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0037g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0038g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0039g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0040g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0041g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0042g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0044g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0045g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0046g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0047g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0048g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0049g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0050g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0051g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0052g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0053g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0054g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0055g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0056g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0057g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0058g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0059g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0060g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0061g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0062g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0063g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0064g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0065g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0066g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0067g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0068g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0069g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0070g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0071g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0072g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0073g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0074g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0075g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0076g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0077g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0078g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0079g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0080g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0081g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0082g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0083g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0084g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0085g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0086g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0001t0087g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0003t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0001c0005t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0002c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0002c0002t0043g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0003c0007t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0004c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0005c0006t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
a0006c0008t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0086 | g0055 | EUR | GBR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00099 | hp2 | a0001 | c0001 | t0011 | g0189 | EUR | GBR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0035 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0147 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00423 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0125 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00597 | hp1 | a0001 | c0001 | t0030 | g0016 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00621 | hp2 | a0001 | c0001 | t0032 | g0001 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00639 | hp1 | a0001 | c0001 | t0062 | g0167 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00673 | hp1 | a0001 | c0001 | t0085 | g0142 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00673 | hp2 | a0001 | c0001 | t0010 | g0301 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00735 | hp2 | a0001 | c0001 | t0066 | g0240 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00738 | hp1 | a0001 | c0001 | t0055 | g0179 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00738 | hp2 | a0001 | c0001 | t0048 | g0234 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG00741 | hp2 | a0001 | c0001 | t0082 | g0032 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01070 | hp2 | a0001 | c0001 | t0031 | g0031 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01106 | hp1 | a0001 | c0001 | t0028 | g0246 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01106 | hp2 | a0001 | c0001 | t0037 | g0244 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01168 | hp1 | a0001 | c0001 | t0054 | g0100 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01168 | hp2 | a0001 | c0001 | t0064 | g0182 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01175 | hp1 | a0001 | c0001 | t0010 | g0242 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0299 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01243 | hp2 | a0001 | c0001 | t0015 | g0237 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01255 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01261 | hp1 | a0001 | c0001 | t0031 | g0013 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01261 | hp2 | a0001 | c0001 | t0023 | g0153 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0211 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01346 | hp2 | a0001 | c0001 | t0050 | g0102 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01361 | hp2 | a0001 | c0001 | t0026 | g0155 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0298 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01496 | hp2 | a0001 | c0001 | t0073 | g0041 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0261 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0262 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0276 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0201 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01934 | hp2 | a0003 | c0007 | t0001 | g0168 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01952 | hp2 | a0001 | c0001 | t0022 | g0173 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02004 | hp2 | a0001 | c0001 | t0072 | g0044 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02015 | hp1 | a0001 | c0001 | t0027 | g0175 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02040 | hp2 | a0001 | c0001 | t0017 | g0226 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02055 | hp1 | a0001 | c0001 | t0021 | g0233 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02055 | hp2 | a0001 | c0001 | t0058 | g0116 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02056 | hp1 | a0001 | c0001 | t0009 | g0204 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02080 | hp2 | a0001 | c0001 | t0078 | g0006 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02083 | hp2 | a0001 | c0003 | t0005 | g0216 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02135 | hp2 | a0004 | c0004 | t0002 | g0048 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0269 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02155 | hp2 | a0001 | c0001 | t0029 | g0034 | EAS | CDX | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02273 | hp1 | a0001 | c0001 | t0069 | g0036 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0292 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0300 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0297 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02602 | hp2 | a0001 | c0001 | t0083 | g0117 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0283 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0198 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0288 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0270 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02647 | hp2 | a0001 | c0001 | t0010 | g0252 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02683 | hp2 | a0002 | c0002 | t0043 | g0219 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02698 | hp1 | a0001 | c0001 | t0077 | g0064 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02723 | hp2 | a0001 | c0001 | t0045 | g0232 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0289 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02886 | hp1 | a0001 | c0005 | t0006 | g0230 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02886 | hp2 | a0001 | c0001 | t0041 | g0202 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02896 | hp1 | a0001 | c0001 | t0012 | g0286 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02896 | hp2 | a0001 | c0001 | t0027 | g0136 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0285 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0287 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02965 | hp1 | a0001 | c0001 | t0047 | g0235 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02965 | hp2 | a0001 | c0001 | t0068 | g0255 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02970 | hp1 | a0001 | c0001 | t0016 | g0281 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0296 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02976 | hp1 | a0001 | c0001 | t0035 | g0257 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02976 | hp2 | a0001 | c0001 | t0016 | g0280 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03195 | hp1 | a0001 | c0001 | t0018 | g0291 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03195 | hp2 | a0001 | c0001 | t0042 | g0205 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0229 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03239 | hp2 | a0001 | c0001 | t0024 | g0165 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03453 | hp1 | a0001 | c0001 | t0044 | g0290 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0284 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03486 | hp1 | a0001 | c0001 | t0019 | g0206 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0197 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03490 | hp1 | a0001 | c0001 | t0022 | g0146 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0215 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03540 | hp1 | a0001 | c0001 | t0028 | g0238 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03540 | hp2 | a0001 | c0001 | t0075 | g0208 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03579 | hp1 | a0001 | c0001 | t0040 | g0203 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03669 | hp2 | a0001 | c0001 | t0039 | g0217 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03831 | hp1 | a0001 | c0001 | t0038 | g0220 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03834 | hp2 | a0001 | c0001 | t0011 | g0190 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03942 | hp2 | a0001 | c0001 | t0023 | g0115 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04184 | hp1 | a0001 | c0001 | t0076 | g0050 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04184 | hp2 | a0001 | c0001 | t0059 | g0111 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0212 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04204 | hp2 | a0001 | c0001 | t0067 | g0259 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG04228 | hp2 | a0002 | c0002 | t0005 | g0213 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0209 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18522 | hp2 | a0001 | c0001 | t0019 | g0207 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18906 | hp1 | a0001 | c0001 | t0046 | g0231 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18940 | hp2 | a0001 | c0001 | t0053 | g0127 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18941 | hp1 | a0001 | c0001 | t0025 | g0187 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18943 | hp2 | a0001 | c0001 | t0061 | g0110 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18959 | hp1 | a0001 | c0001 | t0063 | g0193 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18959 | hp2 | a0001 | c0001 | t0080 | g0053 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18961 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18963 | hp2 | a0001 | c0001 | t0057 | g0148 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18968 | hp2 | a0001 | c0001 | t0060 | g0133 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18982 | hp1 | a0001 | c0001 | t0014 | g0171 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18985 | hp1 | a0001 | c0001 | t0024 | g0109 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18986 | hp2 | a0002 | c0002 | t0005 | g0224 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19000 | hp1 | a0001 | c0001 | t0079 | g0049 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19000 | hp2 | a0001 | c0001 | t0052 | g0104 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19002 | hp2 | a0001 | c0001 | t0029 | g0015 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19006 | hp1 | a0001 | c0001 | t0017 | g0227 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19012 | hp1 | a0001 | c0001 | t0030 | g0089 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19012 | hp2 | a0001 | c0001 | t0014 | g0108 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19043 | hp1 | a0001 | c0001 | t0020 | g0277 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19043 | hp2 | a0001 | c0001 | t0036 | g0275 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19060 | hp1 | a0001 | c0001 | t0009 | g0139 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19063 | hp2 | a0001 | c0001 | t0081 | g0018 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19070 | hp2 | a0001 | c0001 | t0014 | g0135 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19086 | hp2 | a0001 | c0001 | t0056 | g0112 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19090 | hp1 | a0001 | c0001 | t0025 | g0151 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19090 | hp2 | a0001 | c0001 | t0087 | g0020 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19091 | hp1 | a0001 | c0001 | t0084 | g0061 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19240 | hp1 | a0001 | c0001 | t0049 | g0192 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20129 | hp1 | a0001 | c0001 | t0033 | g0243 | AFR | ASW | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20129 | hp2 | a0001 | c0001 | t0026 | g0159 | AFR | ASW | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20752 | hp1 | a0005 | c0006 | t0003 | g0253 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20905 | hp1 | a0001 | c0001 | t0034 | g0068 | SAS | GIH | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | GIH | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01123 | hp1 | a0001 | c0001 | t0070 | g0263 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0272 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02109 | hp2 | a0001 | c0001 | t0065 | g0293 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0236 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0282 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG03471 | hp2 | a0001 | c0001 | t0074 | g0278 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG06807 | hp1 | a0001 | c0001 | t0071 | g0241 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0295 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20300 | hp1 | a0001 | c0001 | t0020 | g0274 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA20300 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
NA21309 | hp2 | a0006 | c0008 | t0003 | g0266 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
homoSapiens | chm13v2 | a0001 | c0001 | t0051 | g0099 | REF | REF | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0154 | REF | REF | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:36855307 | C | G | 1 | a0004 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1883G>C | p.Ser628Thr | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/18 | 1956/14174 | 1883/2343 | 628/780 | chr2 | 36855307 | |||
chr2:36877898 | G | A | 1 | a0005 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1316C>T | p.Thr439Ile | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/18 | 1389/14174 | 1316/2343 | 439/780 | chr2 | 36877898 | |||
chr2:36877976 | G | C | 1 | a0003 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1238C>G | p.Ala413Gly | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/18 | 1311/14174 | 1238/2343 | 413/780 | chr2 | 36877976 | |||
chr2:36883980 | G | A | 1 | a0002 | 3 | HG02683.hp2 HG04228.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.1138C>T | p.Pro380Ser | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/18 | 1211/14174 | 1138/2343 | 380/780 | chr2 | 36883980 | |||
chr2:36902653 | T | C | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.590A>G | p.Glu197Gly | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/18 | 663/14174 | 590/2343 | 197/780 | chr2 | 36902653 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:36849510 | G | C | 1 | a0001c0005 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2289C>G | p.Ser763Ser | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2362/14174 | 2289/2343 | 763/780 | chr2 | 36849510 | |||
chr2:36905574 | A | G | 1 | a0001c0003 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.457T>C | p.Leu153Leu | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/18 | 530/14174 | 457/2343 | 153/780 | chr2 | 36905574 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:36837812 | A | G | 1 | a0001c0001t0009 | 5 | HG00423.hp2 HG00438.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11644T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11644 | chr2 | 36837812 | ||||||
chr2:36837861 | C | T | 10 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0019 others(7): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*11595G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11595 | chr2 | 36837861 | ||||||
chr2:36837995 | T | G | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*11461A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11461 | chr2 | 36837995 | ||||||
chr2:36838011 | G | A | 8 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0037 others(5): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11445C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11445 | chr2 | 36838011 | ||||||
chr2:36838148 | T | C | 3 | a0001c0001t0011 a0001c0001t0023 a0001c0001t0069 |
7 | HG00099.hp2 HG00323.hp1 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11308A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11308 | chr2 | 36838148 | ||||||
chr2:36838177 | G | A | 10 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0019 others(7): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*11279C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11279 | chr2 | 36838177 | ||||||
chr2:36838264 | C | G | 1 | a0001c0001t0076 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11192G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11192 | chr2 | 36838264 | ||||||
chr2:36838335 | T | C | 1 | a0001c0001t0063 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11121A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11121 | chr2 | 36838335 | ||||||
chr2:36838351 | G | T | 1 | a0001c0001t0045 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11105C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11105 | chr2 | 36838351 | ||||||
chr2:36838413 | G | C | 1 | a0001c0001t0079 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11043C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11043 | chr2 | 36838413 | ||||||
chr2:36838549 | C | T | 68 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(65): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*10907G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10907 | chr2 | 36838549 | ||||||
chr2:36838647 | G | T | 86 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(83): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*10809C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10809 | chr2 | 36838647 | ||||||
chr2:36838821 | G | T | 1 | a0001c0001t0077 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10635C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10635 | chr2 | 36838821 | ||||||
chr2:36838875 | T | G | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*10581A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10581 | chr2 | 36838875 | ||||||
chr2:36838878 | T | C | 1 | a0001c0001t0085 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10578A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10578 | chr2 | 36838878 | ||||||
chr2:36838904 | A | C | 1 | a0001c0001t0038 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10552T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10552 | chr2 | 36838904 | ||||||
chr2:36838943 | T | C | 1 | a0001c0001t0019 | 2 | HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10513A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10513 | chr2 | 36838943 | ||||||
chr2:36839020 | C | T | 90 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(87): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*10436G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10436 | chr2 | 36839020 | ||||||
chr2:36839043 | A | G | 1 | a0001c0001t0031 | 2 | HG01070.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10413T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10413 | chr2 | 36839043 | ||||||
chr2:36839103 | G | A | 1 | a0001c0001t0058 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10353C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10353 | chr2 | 36839103 | ||||||
chr2:36839354 | A | C | 1 | a0001c0001t0067 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10102T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10102 | chr2 | 36839354 | ||||||
chr2:36839365 | T | C | 2 | a0001c0001t0044 a0001c0001t0080 |
2 | HG03453.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10091A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10091 | chr2 | 36839365 | ||||||
chr2:36839388 | G | A | 1 | a0001c0001t0023 | 2 | HG01261.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10068C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10068 | chr2 | 36839388 | ||||||
chr2:36839781 | C | T | 1 | a0001c0001t0056 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9675G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9675 | chr2 | 36839781 | ||||||
chr2:36839782 | G | A | 1 | a0001c0001t0059 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9674C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9674 | chr2 | 36839782 | ||||||
chr2:36839795 | T | C | 2 | a0001c0001t0019 a0001c0001t0042 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9661A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9661 | chr2 | 36839795 | ||||||
chr2:36839975 | A | G | 1 | a0001c0001t0055 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9481T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9481 | chr2 | 36839975 | ||||||
chr2:36839994 | A | G | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(37): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*9462T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9462 | chr2 | 36839994 | ||||||
chr2:36840339 | C | A | 1 | a0001c0001t0060 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9117G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9117 | chr2 | 36840339 | ||||||
chr2:36840356 | C | T | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(72): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*9100G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9100 | chr2 | 36840356 | ||||||
chr2:36840456 | T | C | 3 | a0001c0001t0013 a0001c0001t0045 a0001c0001t0046 |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9000A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9000 | chr2 | 36840456 | ||||||
chr2:36840538 | A | ATT | 7 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0037 others(4): Show |
16 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8916_*8917dupAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8917 | chr2 | 36840538 | ||||||
chr2:36840538 | AT | A | 10 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(7): Show |
36 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8917delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8917 | chr2 | 36840538 | ||||||
chr2:36840538 | ATT | A | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*8916_*8917delAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8916 | chr2 | 36840538 | ||||||
chr2:36840538 | ATTT | A | 7 | a0001c0001t0024 a0001c0001t0028 a0001c0001t0032 others(4): Show |
9 | HG00621.hp2 HG01106.hp1 HG01496.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8915_*8917delAAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8915 | chr2 | 36840538 | ||||||
chr2:36841129 | C | A | 79 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(76): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*8327G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8327 | chr2 | 36841129 | ||||||
chr2:36841129 | C | T | 1 | a0001c0001t0037 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8327G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8327 | chr2 | 36841129 | ||||||
chr2:36841164 | C | CT | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(13): Show |
34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*8291dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8291 | chr2 | 36841164 | ||||||
chr2:36841164 | CT | C | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(10): Show |
33 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*8291delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8291 | chr2 | 36841164 | ||||||
chr2:36841279 | T | A | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8177A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8177 | chr2 | 36841279 | ||||||
chr2:36841285 | C | T | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
133 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*8171G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8171 | chr2 | 36841285 | ||||||
chr2:36841369 | T | C | 1 | a0001c0001t0070 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8087A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8087 | chr2 | 36841369 | ||||||
chr2:36841532 | G | A | 2 | a0001c0001t0061 a0001c0001t0065 |
2 | HG02109.hp2 NA18943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7924C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7924 | chr2 | 36841532 | ||||||
chr2:36841712 | A | G | 90 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(87): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*7744T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7744 | chr2 | 36841712 | ||||||
chr2:36841928 | G | A | 1 | a0001c0001t0041 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7528C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7528 | chr2 | 36841928 | ||||||
chr2:36842031 | T | C | 1 | a0001c0001t0083 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7425A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7425 | chr2 | 36842031 | ||||||
chr2:36842177 | C | T | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(64): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*7279G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7279 | chr2 | 36842177 | ||||||
chr2:36842507 | C | T | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(70): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*6949G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6949 | chr2 | 36842507 | ||||||
chr2:36842654 | T | C | 1 | a0001c0001t0062 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6802A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6802 | chr2 | 36842654 | ||||||
chr2:36842695 | T | C | 2 | a0001c0001t0025 a0001c0001t0032 |
3 | HG00621.hp2 NA18941.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6761A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6761 | chr2 | 36842695 | ||||||
chr2:36842714 | TTA | T | 4 | a0001c0001t0006 a0001c0001t0041 a0001c0001t0075 others(1): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6740_*6741delTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6740 | chr2 | 36842714 | ||||||
chr2:36842742 | A | G | 68 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(65): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*6714T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6714 | chr2 | 36842742 | ||||||
chr2:36842906 | C | T | 1 | a0001c0001t0018 | 2 | HG02451.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6550G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6550 | chr2 | 36842906 | ||||||
chr2:36842920 | T | C | 4 | a0001c0001t0006 a0001c0001t0041 a0001c0001t0075 others(1): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6536A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6536 | chr2 | 36842920 | ||||||
chr2:36843169 | G | A | 1 | a0001c0001t0008 | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6287C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6287 | chr2 | 36843169 | ||||||
chr2:36843210 | G | A | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6246C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6246 | chr2 | 36843210 | ||||||
chr2:36843693 | A | G | 1 | a0001c0001t0078 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5763T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5763 | chr2 | 36843693 | ||||||
chr2:36843813 | C | T | 1 | a0001c0001t0074 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5643G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5643 | chr2 | 36843813 | ||||||
chr2:36843944 | T | C | 3 | a0001c0001t0028 a0001c0001t0033 a0001c0001t0071 |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5512A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5512 | chr2 | 36843944 | ||||||
chr2:36844321 | T | G | 1 | a0001c0001t0036 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5135A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5135 | chr2 | 36844321 | ||||||
chr2:36844355 | G | C | 1 | a0001c0001t0016 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5101C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5101 | chr2 | 36844355 | ||||||
chr2:36844402 | T | A | 1 | a0001c0001t0066 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5054A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5054 | chr2 | 36844402 | ||||||
chr2:36844403 | A | C | 1 | a0001c0001t0066 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5053T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5053 | chr2 | 36844403 | ||||||
chr2:36844455 | T | C | 1 | a0001c0001t0063 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5001A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5001 | chr2 | 36844455 | ||||||
chr2:36844701 | A | G | 3 | a0001c0001t0021 a0001c0001t0047 a0001c0001t0048 |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4755T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4755 | chr2 | 36844701 | ||||||
chr2:36845123 | C | G | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*4333G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4333 | chr2 | 36845123 | ||||||
chr2:36845357 | AT | A | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0045 others(3): Show |
11 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4098delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4098 | chr2 | 36845357 | ||||||
chr2:36845545 | A | C | 3 | a0001c0001t0013 a0001c0001t0045 a0001c0001t0046 |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3911T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3911 | chr2 | 36845545 | ||||||
chr2:36845674 | C | G | 1 | a0001c0001t0014 | 3 | NA18982.hp1 NA19012.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3782G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3782 | chr2 | 36845674 | ||||||
chr2:36845769 | A | G | 1 | a0001c0001t0075 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3687T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3687 | chr2 | 36845769 | ||||||
chr2:36845883 | AAACACAC others(26): Show |
A | 2 | a0001c0001t0072 a0001c0001t0073 |
2 | HG01496.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3540_*3572delGCAT others(29): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3540 | chr2 | 36845883 | ||||||
chr2:36845884 | AAC | A | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(41): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3570_*3571delGT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3570 | chr2 | 36845884 | ||||||
chr2:36845884 | AACACACA others(24): Show |
A | 1 | a0001c0001t0081 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3541_*3571delCATG others(27): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845884 | ||||||
chr2:36845884 | AACACACA others(25): Show |
A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
71 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3540_*3571delGCAT others(28): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3540 | chr2 | 36845884 | ||||||
chr2:36845884 | AACACACA others(27): Show |
A | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0054 |
12 | HG00323.hp2 HG01168.hp1 HG01952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3538_*3571delGTGC others(30): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3538 | chr2 | 36845884 | ||||||
chr2:36845884 | AACACACA others(35): Show |
A | 1 | a0001c0001t0002 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3530_*3571delGTGT others(38): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3530 | chr2 | 36845884 | ||||||
chr2:36845884 | AACACACA others(37): Show |
A | 1 | a0001c0001t0007 | 3 | HG01891.hp2 HG02109.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3528_*3571delGTGT others(40): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3528 | chr2 | 36845884 | ||||||
chr2:36845885 | ACACACAC others(23): Show |
A | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(10): Show |
51 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3541_*3570delCATG others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845885 | ||||||
chr2:36845887 | ACACACAC others(21): Show |
A | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(1): Show |
5 | HG01175.hp1 HG02647.hp2 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3541_*3568delCATG others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845887 | ||||||
chr2:36845889 | ACACACAC others(19): Show |
A | 1 | a0001c0001t0085 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3541_*3566delCATG others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845889 | ||||||
chr2:36845907 | G | A | 2 | a0001c0001t0020 a0001c0001t0064 |
3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3549C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3549 | chr2 | 36845907 | ||||||
chr2:36845910 | T | C | 2 | a0001c0001t0020 a0001c0001t0064 |
3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3546A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3546 | chr2 | 36845910 | ||||||
chr2:36845915 | GCA | G | 8 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(5): Show |
10 | HG00738.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3539_*3540delTG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3539 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACA | G | 9 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(6): Show |
14 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3537_*3540delTGTG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3537 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACA | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3535_*3540delTGTG others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3535 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACAC others(1): Show |
G | 7 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0026 others(4): Show |
9 | HG01361.hp2 HG02886.hp1 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3533_*3540delTGTG others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3533 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACAC others(3): Show |
G | 2 | a0001c0001t0001 a0001c0001t0016 |
4 | HG00558.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3531_*3540delTGTG others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3531 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACAC others(5): Show |
G | 4 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0019 others(1): Show |
7 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3529_*3540delTGTG others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3529 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3527_*3540delTGTG others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3527 | chr2 | 36845915 | ||||||
chr2:36845915 | GCACACAC others(9): Show |
G | 3 | a0001c0001t0019 a0001c0001t0042 a0001c0001t0074 |
3 | HG03195.hp2 HG03471.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3525_*3540delTGTG others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3525 | chr2 | 36845915 | ||||||
chr2:36845920 | C | T | 2 | a0001c0001t0020 a0001c0001t0064 |
3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3536G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3536 | chr2 | 36845920 | ||||||
chr2:36845921 | A | G | 2 | a0001c0001t0020 a0001c0001t0064 |
3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3535T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3535 | chr2 | 36845921 | ||||||
chr2:36845986 | A | AC | 4 | a0001c0001t0030 a0001c0001t0052 a0001c0001t0053 others(1): Show |
5 | HG00597.hp1 HG02698.hp1 NA18940.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3469dupG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3469 | chr2 | 36845986 | ||||||
chr2:36845987 | C | A | 1 | a0001c0001t0048 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3469G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3469 | chr2 | 36845987 | ||||||
chr2:36845990 | C | G | 1 | a0001c0001t0029 | 2 | HG02155.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3466G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3466 | chr2 | 36845990 | ||||||
chr2:36846029 | A | AT | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*3426dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | ||||||
chr2:36846029 | A | ATT | 7 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0035 others(4): Show |
12 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3425_*3426dupAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | ||||||
chr2:36846029 | AT | A | 6 | a0001c0001t0006 a0001c0001t0026 a0001c0001t0040 others(3): Show |
15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3426delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | ||||||
chr2:36846301 | G | A | 2 | a0001c0001t0019 a0001c0001t0042 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3155C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3155 | chr2 | 36846301 | ||||||
chr2:36846387 | T | TTA | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
24 | HG00673.hp1 HG00738.hp2 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3067_*3068dupTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATA | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(9): Show |
21 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3065_*3068dupTATA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATA | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
27 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3063_*3068dupTATA others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(1): Show |
18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
25 | HG01070.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3061_*3068dupTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(3): Show |
11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
21 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3059_*3068dupTATA others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(5): Show |
7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(4): Show |
15 | HG00280.hp1 HG00621.hp1 HG02071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3068dupTATA others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(7): Show |
4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0087 others(1): Show |
5 | HG01433.hp2 HG02135.hp2 HG03942.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3055_*3068dupTATA others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(9): Show |
1 | a0001c0001t0002 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3053_*3068dupTATA others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(11): Show |
2 | a0001c0001t0004 a0001c0001t0016 |
3 | HG00544.hp2 NA18954.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3051_*3068dupTATA others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTATATAT others(13): Show |
1 | a0001c0001t0003 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3049_*3068dupTATA others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | T | TTTTATAT others(1): Show |
1 | a0001c0001t0003 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3068_*3069insTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | ||||||
chr2:36846387 | TTA | T | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(5): Show |
16 | HG01891.hp1 HG01891.hp2 HG02056.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3067_*3068delTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3067 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATA | T | 2 | a0001c0001t0020 a0002c0002t0043 |
3 | HG02683.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3063_*3068delTATA others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3063 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0041 |
5 | HG00423.hp2 HG00438.hp1 HG02155.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3061_*3068delTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3061 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(3): Show |
T | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(2): Show |
10 | HG00544.hp1 HG01256.hp1 HG01993.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3059_*3068delTATA others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3059 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(5): Show |
T | 7 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0032 others(4): Show |
19 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3068delTATA others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3057 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(7): Show |
T | 20 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(17): Show |
65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3055_*3068delTATA others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3055 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(9): Show |
T | 5 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0029 others(2): Show |
8 | HG00735.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3053_*3068delTATA others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3053 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(13): Show |
T | 1 | a0001c0001t0005 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3049_*3068delTATA others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3049 | chr2 | 36846387 | ||||||
chr2:36846387 | TTATATAT others(17): Show |
T | 2 | a0001c0001t0010 a0002c0002t0005 |
2 | HG00639.hp2 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3045_*3068delTATA others(20): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3045 | chr2 | 36846387 | ||||||
chr2:36846430 | G | A | 1 | a0001c0001t0086 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3026C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3026 | chr2 | 36846430 | ||||||
chr2:36846430 | G | T | 2 | a0001c0001t0012 a0001c0001t0021 |
5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3026C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3026 | chr2 | 36846430 | ||||||
chr2:36846432 | T | A | 1 | a0001c0001t0086 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3024A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3024 | chr2 | 36846432 | ||||||
chr2:36846519 | CATT | C | 1 | a0001c0001t0016 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2934_*2936delAAT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2934 | chr2 | 36846519 | ||||||
chr2:36846666 | T | C | 89 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(86): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*2790A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2790 | chr2 | 36846666 | ||||||
chr2:36846698 | A | C | 1 | a0001c0001t0050 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2758T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2758 | chr2 | 36846698 | ||||||
chr2:36846749 | T | A | 1 | a0001c0001t0026 | 2 | HG01361.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2707A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2707 | chr2 | 36846749 | ||||||
chr2:36846965 | C | T | 1 | a0001c0001t0015 | 3 | HG01243.hp2 HG02615.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2491G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2491 | chr2 | 36846965 | ||||||
chr2:36846980 | T | C | 2 | a0001c0001t0019 a0001c0001t0042 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2476A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2476 | chr2 | 36846980 | ||||||
chr2:36847114 | C | T | 1 | a0001c0001t0049 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2342G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2342 | chr2 | 36847114 | ||||||
chr2:36847185 | T | C | 1 | a0001c0001t0020 | 2 | NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2271A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2271 | chr2 | 36847185 | ||||||
chr2:36847808 | G | A | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1648 | chr2 | 36847808 | ||||||
chr2:36847825 | A | G | 1 | a0001c0001t0017 | 2 | HG02040.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1631T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1631 | chr2 | 36847825 | ||||||
chr2:36847870 | T | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(37): Show |
144 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1586A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1586 | chr2 | 36847870 | ||||||
chr2:36847978 | T | C | 1 | a0002c0002t0043 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1478 | chr2 | 36847978 | ||||||
chr2:36848254 | T | G | 74 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(71): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*1202A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1202 | chr2 | 36848254 | ||||||
chr2:36848735 | G | C | 1 | a0001c0001t0074 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 721 | chr2 | 36848735 | ||||||
chr2:36848798 | A | G | 1 | a0001c0001t0035 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*658T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 658 | chr2 | 36848798 | ||||||
chr2:36849208 | C | T | 1 | a0001c0001t0034 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 248 | chr2 | 36849208 | ||||||
chr2:36849331 | T | C | 3 | a0001c0001t0006 a0001c0001t0075 a0001c0005t0006 |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*125A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 125 | chr2 | 36849331 | ||||||
chr2:36849344 | C | G | 1 | a0001c0001t0076 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 112 | chr2 | 36849344 | ||||||
chr2:36849353 | G | C | 1 | a0001c0001t0087 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 103 | chr2 | 36849353 | ||||||
chr2:36849355 | A | C | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0029 others(16): Show |
75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*101T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 101 | chr2 | 36849355 | ||||||
chr2:36849430 | C | G | 1 | a0001c0001t0033 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 26 | chr2 | 36849430 | ||||||
chr2:36849451 | T | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(17): Show |
82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5 | chr2 | 36849451 | ||||||
chr2:36966519 | G | T | 1 | a0001c0001t0032 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/18 | 56 | chr2 | 36966519 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:36849872 | C | A | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.2087-72G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849872 | |||||||
chr2:36849894 | C | G | 4 | a0001c0001t0003g0043 a0001c0001t0003g0067 a0001c0001t0003g0071 others(1): Show |
4 | HG00323.hp2 HG01168.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2087-94G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849894 | |||||||
chr2:36849979 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2087-179A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849979 | |||||||
chr2:36850033 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2087-233C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850033 | |||||||
chr2:36850272 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2087-472A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850272 | |||||||
chr2:36850316 | A | C | 24 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(21): Show |
24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2087-516T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850316 | |||||||
chr2:36850690 | A | C | 1 | a0001c0001t0073g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2086+310T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850690 | |||||||
chr2:36850867 | G | C | 1 | a0001c0003t0005g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2086+133C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850867 | |||||||
chr2:36850952 | A | AT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2086+47dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850952 | |||||||
chr2:36850952 | A | ATT | 139 | a0001c0001t0001g0145 a0001c0001t0001g0186 a0001c0001t0002g0007 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2086+46_2086+47dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850952 | |||||||
chr2:36851189 | A | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1979-82T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851189 | |||||||
chr2:36851206 | C | T | 1 | a0001c0001t0021g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1979-99G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851206 | |||||||
chr2:36851211 | G | A | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1979-104C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851211 | |||||||
chr2:36851245 | G | A | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1979-138C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851245 | |||||||
chr2:36851446 | G | A | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1979-339C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851446 | |||||||
chr2:36851483 | AAAAAAAG others(5): Show |
A | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1979-388_1979-377d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851483 | |||||||
chr2:36851562 | C | T | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1979-455G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851562 | |||||||
chr2:36851592 | G | A | 2 | a0001c0001t0045g0232 a0001c0001t0046g0231 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1979-485C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851592 | |||||||
chr2:36851617 | T | C | 1 | a0001c0001t0008g0298 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1979-510A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851617 | |||||||
chr2:36851651 | C | T | 1 | a0001c0001t0087g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1979-544G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851651 | |||||||
chr2:36851696 | A | G | 139 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1979-589T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851696 | |||||||
chr2:36851929 | C | T | 1 | a0001c0001t0011g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1979-822G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851929 | |||||||
chr2:36852053 | T | A | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1979-946A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852053 | |||||||
chr2:36852055 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1979-948A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852055 | |||||||
chr2:36852275 | A | G | 12 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0218 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1979-1168T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852275 | |||||||
chr2:36852363 | C | A | 1 | a0001c0001t0012g0287 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1979-1256G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852363 | |||||||
chr2:36852440 | T | C | 140 | a0001c0001t0001g0164 a0001c0001t0001g0200 a0001c0001t0002g0007 others(137): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1979-1333A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852440 | |||||||
chr2:36852517 | G | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1979-1410C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852517 | |||||||
chr2:36852698 | C | T | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1979-1591G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852698 | |||||||
chr2:36852773 | T | A | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1979-1666A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852773 | |||||||
chr2:36852933 | G | T | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1979-1826C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852933 | |||||||
chr2:36852963 | C | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1979-1856G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852963 | |||||||
chr2:36853019 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1979-1912A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853019 | |||||||
chr2:36853101 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1979-1994T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853101 | |||||||
chr2:36853112 | G | A | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1979-2005C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853112 | |||||||
chr2:36853156 | C | CA | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1979-2050dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853156 | |||||||
chr2:36853156 | C | CAA | 7 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1979-2051_1979-205 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853156 | |||||||
chr2:36853195 | T | A | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1978+2017A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853195 | |||||||
chr2:36853201 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1978+2011C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853201 | |||||||
chr2:36853547 | A | T | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1978+1665T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853547 | |||||||
chr2:36853556 | A | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1978+1656T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853556 | |||||||
chr2:36853568 | C | T | 1 | a0001c0001t0025g0151 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1978+1644G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853568 | |||||||
chr2:36853609 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1978+1603G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853609 | |||||||
chr2:36854069 | T | TA | 140 | a0001c0001t0001g0164 a0001c0001t0001g0200 a0001c0001t0002g0007 others(137): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1978+1142dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854069 | |||||||
chr2:36854380 | A | G | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1978+832T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854380 | |||||||
chr2:36854506 | G | A | 15 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0214 others(12): Show |
15 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1978+706C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854506 | |||||||
chr2:36854674 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1978+538A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854674 | |||||||
chr2:36854700 | A | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1978+512T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854700 | |||||||
chr2:36854820 | A | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1978+392T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854820 | |||||||
chr2:36854891 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1978+321C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854891 | |||||||
chr2:36854904 | T | C | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1978+308A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854904 | |||||||
chr2:36855099 | TAA | T | 15 | a0001c0001t0003g0040 a0001c0001t0003g0042 a0001c0001t0003g0043 others(12): Show |
15 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1978+111_1978+112d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36855099 | |||||||
chr2:36855136 | A | C | 1 | a0001c0001t0009g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1978+76T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36855136 | |||||||
chr2:36855552 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1838-200G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855552 | |||||||
chr2:36855764 | T | C | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1838-412A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855764 | |||||||
chr2:36855772 | A | T | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1838-420T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855772 | |||||||
chr2:36855787 | C | T | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1838-435G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855787 | |||||||
chr2:36855909 | T | G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0067 a0001c0001t0003g0071 |
3 | HG00323.hp2 HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1838-557A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855909 | |||||||
chr2:36855987 | A | AC | 3 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp1 HG02155.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1838-636_1838-635i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855987 | |||||||
chr2:36855988 | A | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1838-636T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855988 | |||||||
chr2:36855999 | G | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1838-647C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855999 | |||||||
chr2:36856163 | T | C | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1838-811A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856163 | |||||||
chr2:36856247 | T | C | 1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1838-895A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856247 | |||||||
chr2:36856546 | C | T | 1 | a0001c0001t0053g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1838-1194G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856546 | |||||||
chr2:36856820 | T | C | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837+1036A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856820 | |||||||
chr2:36856999 | G | A | 1 | a0001c0001t0007g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1837+857C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856999 | |||||||
chr2:36857087 | C | CT | 14 | a0001c0001t0011g0147 a0001c0001t0011g0189 a0001c0001t0011g0190 others(11): Show |
14 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1837+768dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857087 | |||||||
chr2:36857087 | C | CTT | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1837+767_1837+768d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857087 | |||||||
chr2:36857116 | C | T | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1837+740G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857116 | |||||||
chr2:36857134 | C | T | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1837+722G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857134 | |||||||
chr2:36857163 | G | A | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1837+693C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857163 | |||||||
chr2:36857226 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1837+630A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857226 | |||||||
chr2:36857294 | T | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837+562A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857294 | |||||||
chr2:36857574 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1837+282A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857574 | |||||||
chr2:36857651 | C | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0126 a0001c0001t0001g0145 others(4): Show |
7 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+205G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857651 | |||||||
chr2:36857655 | G | A | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1837+201C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857655 | |||||||
chr2:36857663 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837+183_1837+192d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857663 | |||||||
chr2:36857663 | AAAAACAA others(8): Show |
A | 6 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(3): Show |
6 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837+178_1837+192d others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857663 | |||||||
chr2:36857738 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0130 a0001c0001t0027g0175 |
3 | HG02015.hp1 NA19007.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1837+118C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857738 | |||||||
chr2:36858148 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1670-125G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858148 | |||||||
chr2:36858217 | A | T | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1670-194T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858217 | |||||||
chr2:36858331 | G | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1670-308C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858331 | |||||||
chr2:36858622 | C | T | 1 | a0001c0001t0013g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1670-599G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858622 | |||||||
chr2:36858692 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1670-669A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858692 | |||||||
chr2:36858797 | C | G | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1670-774G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858797 | |||||||
chr2:36858851 | C | A | 1 | a0001c0001t0019g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1670-828G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858851 | |||||||
chr2:36858918 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1670-895C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858918 | |||||||
chr2:36858953 | T | G | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1670-930A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858953 | |||||||
chr2:36859054 | G | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1670-1031C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859054 | |||||||
chr2:36859088 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1670-1065A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859088 | |||||||
chr2:36859197 | C | T | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1670-1174G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859197 | |||||||
chr2:36859261 | T | C | 3 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0066g0240 |
3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1670-1238A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859261 | |||||||
chr2:36859277 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1670-1254T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859277 | |||||||
chr2:36859337 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1670-1314T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859337 | |||||||
chr2:36859473 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1670-1450T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859473 | |||||||
chr2:36859762 | C | T | 1 | a0002c0002t0005g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1669+1370G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859762 | |||||||
chr2:36859794 | A | C | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669+1338T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859794 | |||||||
chr2:36859887 | T | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1669+1245A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859887 | |||||||
chr2:36860100 | T | C | 1 | a0001c0001t0019g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1669+1032A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860100 | |||||||
chr2:36860302 | C | A | 1 | a0001c0001t0063g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1669+830G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860302 | |||||||
chr2:36860310 | G | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1669+822C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860310 | |||||||
chr2:36860447 | C | G | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+685G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860447 | |||||||
chr2:36860520 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1669+612G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860520 | |||||||
chr2:36860625 | T | C | 1 | a0001c0001t0019g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1669+507A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860625 | |||||||
chr2:36860690 | T | A | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1669+442A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860690 | |||||||
chr2:36860797 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1669+335T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860797 | |||||||
chr2:36860940 | C | T | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1669+192G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860940 | |||||||
chr2:36860949 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1669+183A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860949 | |||||||
chr2:36860973 | T | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669+159A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860973 | |||||||
chr2:36860974 | A | G | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1669+158T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860974 | |||||||
chr2:36861332 | T | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-79A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861332 | |||||||
chr2:36861486 | C | T | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-233G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861486 | |||||||
chr2:36861490 | A | G | 1 | a0001c0001t0019g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1548-237T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861490 | |||||||
chr2:36861640 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1548-387T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861640 | |||||||
chr2:36861728 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1548-475A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861728 | |||||||
chr2:36861731 | GCA | G | 3 | a0001c0001t0007g0289 a0001c0001t0032g0001 a0001c0001t0044g0290 |
3 | HG00621.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1548-480_1548-479d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861731 | GCACA | G | 23 | a0001c0001t0001g0120 a0001c0001t0002g0054 a0001c0001t0003g0264 others(20): Show |
23 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1548-482_1548-479d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861731 | GCACACA | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1548-484_1548-479d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861731 | GCACACAC others(1): Show |
G | 3 | a0001c0001t0001g0164 a0001c0001t0002g0094 a0001c0001t0076g0050 |
3 | HG02280.hp1 HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1548-486_1548-479d others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861731 | GCACACAC others(5): Show |
G | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1548-490_1548-479d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861731 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1548-492_1548-479d others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | |||||||
chr2:36861931 | T | C | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1548-678A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861931 | |||||||
chr2:36861964 | C | G | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1548-711G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861964 | |||||||
chr2:36862017 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1548-764T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862017 | |||||||
chr2:36862085 | G | T | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1548-832C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862085 | |||||||
chr2:36862147 | T | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-894A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862147 | |||||||
chr2:36862167 | A | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1548-914T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862167 | |||||||
chr2:36862182 | G | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1548-929C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862182 | |||||||
chr2:36862239 | A | G | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1548-986T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862239 | |||||||
chr2:36862298 | G | C | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1548-1045C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862298 | |||||||
chr2:36862542 | GTCT | G | 3 | a0001c0001t0028g0246 a0001c0001t0033g0243 a0001c0001t0071g0241 |
3 | HG01106.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1548-1292_1548-129 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862542 | |||||||
chr2:36862560 | T | G | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1548-1307A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862560 | |||||||
chr2:36862667 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1548-1414G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862667 | |||||||
chr2:36862740 | C | CT | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1548-1488dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862740 | |||||||
chr2:36862740 | CT | C | 22 | a0001c0001t0003g0261 a0001c0001t0005g0090 a0001c0001t0005g0091 others(19): Show |
22 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548-1488delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862740 | |||||||
chr2:36862797 | C | T | 1 | a0001c0001t0064g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1548-1544G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862797 | |||||||
chr2:36862815 | A | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-1562T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862815 | |||||||
chr2:36862828 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1548-1575C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862828 | |||||||
chr2:36862885 | A | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.1548-1632T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862885 | |||||||
chr2:36862937 | G | A | 1 | a0001c0001t0009g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1548-1684C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862937 | |||||||
chr2:36863090 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1548-1837A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863090 | |||||||
chr2:36863134 | G | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1548-1881C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863134 | |||||||
chr2:36863306 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1548-2053A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863306 | |||||||
chr2:36863426 | T | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-2173A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863426 | |||||||
chr2:36863472 | G | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0132 a0001c0001t0001g0149 others(4): Show |
7 | HG01346.hp2 HG02698.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-2219C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863472 | |||||||
chr2:36863556 | A | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1548-2303T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863556 | |||||||
chr2:36863565 | T | C | 1 | a0001c0001t0063g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1548-2312A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863565 | |||||||
chr2:36863651 | C | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1548-2398G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863651 | |||||||
chr2:36863754 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1548-2501C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863754 | |||||||
chr2:36863833 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-2580C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863833 | |||||||
chr2:36863969 | G | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1548-2716C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863969 | |||||||
chr2:36864066 | T | C | 1 | a0001c0001t0034g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1548-2813A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864066 | |||||||
chr2:36864121 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1548-2868G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864121 | |||||||
chr2:36864163 | G | C | 7 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0051 others(4): Show |
7 | HG00621.hp1 HG00642.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-2910C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864163 | |||||||
chr2:36864248 | C | A | 1 | a0001c0001t0002g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1548-2995G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864248 | |||||||
chr2:36864291 | T | C | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-3038A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864291 | |||||||
chr2:36864317 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1548-3064C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864317 | |||||||
chr2:36864336 | C | A | 12 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0218 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1548-3083G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864336 | |||||||
chr2:36864383 | G | A | 4 | a0001c0001t0020g0274 a0001c0001t0020g0277 a0001c0001t0040g0203 others(1): Show |
4 | HG02886.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-3130C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864383 | |||||||
chr2:36864563 | T | C | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1547+3251A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864563 | |||||||
chr2:36864598 | A | T | 2 | a0001c0001t0003g0239 a0001c0001t0003g0251 |
2 | NA18943.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1547+3216T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864598 | |||||||
chr2:36864807 | G | C | 1 | a0001c0003t0005g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+3007C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864807 | |||||||
chr2:36864822 | C | T | 4 | a0001c0001t0008g0296 a0001c0001t0008g0298 a0001c0001t0008g0299 others(1): Show |
4 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547+2992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864822 | |||||||
chr2:36865042 | T | C | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1547+2772A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865042 | |||||||
chr2:36865073 | C | T | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1547+2741G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865073 | |||||||
chr2:36865472 | T | C | 1 | a0001c0001t0006g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1547+2342A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865472 | |||||||
chr2:36865603 | C | A | 2 | a0001c0001t0028g0246 a0001c0001t0071g0241 |
2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1547+2211G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865603 | |||||||
chr2:36865608 | T | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1547+2206A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865608 | |||||||
chr2:36865680 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+2134C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865680 | |||||||
chr2:36865717 | G | A | 1 | a0001c0001t0016g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1547+2097C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865717 | |||||||
chr2:36865767 | G | A | 1 | a0001c0003t0005g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+2047C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865767 | |||||||
chr2:36865802 | C | T | 1 | a0001c0001t0019g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1547+2012G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865802 | |||||||
chr2:36865813 | A | C | 1 | a0001c0001t0029g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1547+2001T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865813 | |||||||
chr2:36865859 | G | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1547+1955C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865859 | |||||||
chr2:36865954 | A | G | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1547+1860T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865954 | |||||||
chr2:36865973 | T | G | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1547+1841A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865973 | |||||||
chr2:36866106 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1547+1708C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866106 | |||||||
chr2:36866115 | C | G | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1547+1699G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866115 | |||||||
chr2:36866252 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+1562C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866252 | |||||||
chr2:36866384 | C | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1547+1430G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866384 | |||||||
chr2:36866407 | T | C | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547+1407A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866407 | |||||||
chr2:36866520 | T | C | 1 | a0001c0001t0008g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1547+1294A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866520 | |||||||
chr2:36866544 | C | T | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1547+1270G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866544 | |||||||
chr2:36866581 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1547+1233G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866581 | |||||||
chr2:36866831 | A | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+983T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866831 | |||||||
chr2:36866851 | C | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1547+963G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866851 | |||||||
chr2:36866859 | T | G | 1 | a0001c0001t0002g0010 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1547+955A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866859 | |||||||
chr2:36866875 | G | C | 1 | a0001c0001t0002g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1547+939C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866875 | |||||||
chr2:36866984 | C | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+830G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866984 | |||||||
chr2:36866985 | C | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+829G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866985 | |||||||
chr2:36866986 | A | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+828T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866986 | |||||||
chr2:36867103 | T | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+711A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867103 | |||||||
chr2:36867193 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+621A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867193 | |||||||
chr2:36867240 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+574C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867240 | |||||||
chr2:36867248 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+566A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867248 | |||||||
chr2:36867359 | C | A | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+455G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867359 | |||||||
chr2:36867410 | C | T | 2 | a0001c0001t0028g0246 a0001c0001t0071g0241 |
2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1547+404G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867410 | |||||||
chr2:36867470 | T | C | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1547+344A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867470 | |||||||
chr2:36867496 | G | A | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1547+318C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867496 | |||||||
chr2:36867556 | A | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+258T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867556 | |||||||
chr2:36867609 | T | C | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1547+205A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867609 | |||||||
chr2:36867661 | C | T | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+153G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867661 | |||||||
chr2:36867686 | A | T | 1 | a0001c0001t0022g0173 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1547+128T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867686 | |||||||
chr2:36867754 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1547+60A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867754 | |||||||
chr2:36867754 | T | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1547+60A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867754 | |||||||
chr2:36867802 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1547+12T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867802 | |||||||
chr2:36867870 | G | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1500-9C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867870 | |||||||
chr2:36867983 | G | A | 1 | a0001c0001t0044g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1500-122C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867983 | |||||||
chr2:36867996 | G | C | 140 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0143 others(137): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1500-135C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867996 | |||||||
chr2:36868025 | G | T | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1500-164C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868025 | |||||||
chr2:36868054 | A | G | 1 | a0001c0001t0031g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1500-193T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868054 | |||||||
chr2:36868055 | T | C | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500-194A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868055 | |||||||
chr2:36868063 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1500-202A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868063 | |||||||
chr2:36868246 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1500-385T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868246 | |||||||
chr2:36868254 | G | GA | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1500-394dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868254 | |||||||
chr2:36868341 | T | C | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1500-480A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868341 | |||||||
chr2:36868375 | C | T | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1500-514G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868375 | |||||||
chr2:36868651 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1500-790G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868651 | |||||||
chr2:36868708 | T | A | 1 | a0001c0001t0052g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1499+846A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868708 | |||||||
chr2:36868752 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+802A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868752 | |||||||
chr2:36868804 | C | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1499+750G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868804 | |||||||
chr2:36868869 | G | T | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1499+685C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868869 | |||||||
chr2:36868872 | C | CT | 27 | a0001c0001t0001g0105 a0001c0001t0001g0174 a0001c0001t0004g0083 others(24): Show |
27 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1499+681dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868872 | |||||||
chr2:36868935 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1499+619C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868935 | |||||||
chr2:36869029 | T | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1499+525A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869029 | |||||||
chr2:36869062 | T | C | 1 | a0001c0001t0002g0009 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1499+492A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869062 | |||||||
chr2:36869069 | G | A | 1 | a0001c0001t0066g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1499+485C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869069 | |||||||
chr2:36869115 | C | A | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+439G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869115 | |||||||
chr2:36869258 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+296A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869258 | |||||||
chr2:36869369 | C | G | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1499+185G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869369 | |||||||
chr2:36869483 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0172 |
2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1499+71A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869483 | |||||||
chr2:36869775 | T | C | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1324-46A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869775 | |||||||
chr2:36869827 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1324-98G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869827 | |||||||
chr2:36869866 | T | C | 135 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(132): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1324-137A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869866 | |||||||
chr2:36869880 | C | T | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1324-151G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869880 | |||||||
chr2:36869941 | A | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-212T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869941 | |||||||
chr2:36870028 | T | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1324-299A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870028 | |||||||
chr2:36870238 | C | T | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-509G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870238 | |||||||
chr2:36870239 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1324-510T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870239 | |||||||
chr2:36870252 | AAC | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1324-525_1324-524d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870252 | |||||||
chr2:36870296 | G | GA | 19 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(16): Show |
19 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1324-568dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870296 | |||||||
chr2:36870296 | GA | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1324-568delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870296 | |||||||
chr2:36870458 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1324-729G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870458 | |||||||
chr2:36870502 | A | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-773T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870502 | |||||||
chr2:36870667 | T | G | 1 | a0001c0001t0003g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324-938A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870667 | |||||||
chr2:36870720 | T | C | 2 | a0001c0001t0002g0062 a0001c0001t0082g0032 |
2 | HG00741.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1324-991A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870720 | |||||||
chr2:36870810 | G | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-1081C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870810 | |||||||
chr2:36870845 | G | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1324-1116C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870845 | |||||||
chr2:36870902 | A | T | 15 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1324-1173T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870902 | |||||||
chr2:36871176 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1324-1447T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871176 | |||||||
chr2:36871200 | T | G | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1324-1471A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871200 | |||||||
chr2:36871277 | C | T | 1 | a0001c0001t0056g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1324-1548G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871277 | |||||||
chr2:36871475 | C | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1324-1746G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871475 | |||||||
chr2:36871947 | G | A | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1324-2218C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871947 | |||||||
chr2:36871986 | G | A | 1 | a0002c0002t0005g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1324-2257C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871986 | |||||||
chr2:36872196 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1324-2467A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872196 | |||||||
chr2:36872327 | C | T | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-2598G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872327 | |||||||
chr2:36872368 | C | T | 21 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1324-2639G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872368 | |||||||
chr2:36872491 | C | T | 1 | a0001c0001t0082g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1324-2762G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872491 | |||||||
chr2:36872743 | T | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-3014A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872743 | |||||||
chr2:36872792 | T | C | 6 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0031g0013 others(3): Show |
6 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-3063A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872792 | |||||||
chr2:36872915 | G | A | 1 | a0001c0001t0050g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1324-3186C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872915 | |||||||
chr2:36873003 | T | G | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-3274A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873003 | |||||||
chr2:36873055 | G | A | 16 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1324-3326C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873055 | |||||||
chr2:36873062 | GGGCTCAG others(3): Show |
G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1324-3343_1324-333 others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873062 | |||||||
chr2:36873240 | C | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-3511G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873240 | |||||||
chr2:36873273 | T | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1324-3544A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873273 | |||||||
chr2:36873491 | C | G | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-3762G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873491 | |||||||
chr2:36873521 | T | C | 1 | a0001c0001t0080g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1324-3792A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873521 | |||||||
chr2:36873623 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1324-3894A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873623 | |||||||
chr2:36873673 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0018g0291 a0001c0001t0018g0292 |
3 | HG01934.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1324-3944C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873673 | |||||||
chr2:36873809 | G | GGCATGTG others(19): Show |
1 | a0001c0001t0002g0009 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1323+4056_1323+408 others(30): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873809 | |||||||
chr2:36873836 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0149 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1323+4055C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873836 | |||||||
chr2:36873855 | A | G | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1323+4036T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873855 | |||||||
chr2:36873892 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+3999C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873892 | |||||||
chr2:36873923 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1323+3968G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873923 | |||||||
chr2:36873941 | CA | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1323+3949delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873941 | |||||||
chr2:36874024 | G | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1323+3867C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874024 | |||||||
chr2:36874047 | A | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1323+3844T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874047 | |||||||
chr2:36874075 | G | A | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1323+3816C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874075 | |||||||
chr2:36874181 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+3710C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874181 | |||||||
chr2:36874221 | G | A | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1323+3670C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874221 | |||||||
chr2:36874263 | C | CA | 8 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0012g0282 others(5): Show |
8 | HG00735.hp2 HG01256.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1323+3627dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874263 | |||||||
chr2:36874274 | A | C | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3617T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874274 | |||||||
chr2:36874317 | C | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0066 others(2): Show |
5 | NA18945.hp2 NA18968.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3574G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874317 | |||||||
chr2:36874574 | A | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1323+3317T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874574 | |||||||
chr2:36874717 | T | TA | 16 | a0001c0001t0001g0143 a0001c0001t0002g0062 a0001c0001t0002g0075 others(13): Show |
16 | HG01891.hp1 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.1323+3173dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874717 | |||||||
chr2:36874717 | TA | T | 41 | a0001c0001t0001g0076 a0001c0001t0001g0103 a0001c0001t0001g0105 others(38): Show |
41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+3173delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874717 | |||||||
chr2:36874728 | A | C | 26 | a0001c0001t0002g0245 a0001c0001t0003g0096 a0001c0001t0003g0097 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1323+3163T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874728 | |||||||
chr2:36874730 | A | AAAC | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0214 others(17): Show |
20 | HG00438.hp2 HG00738.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+3160_1323+316 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874730 | |||||||
chr2:36874730 | A | C | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1323+3161T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874730 | |||||||
chr2:36874731 | A | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1323+3160T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874731 | |||||||
chr2:36874732 | A | C | 2 | a0001c0001t0002g0245 a0001c0001t0003g0247 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1323+3159T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874732 | |||||||
chr2:36874767 | G | A | 2 | a0001c0001t0009g0139 a0001c0001t0009g0140 |
2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1323+3124C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874767 | |||||||
chr2:36874774 | C | T | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1323+3117G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874774 | |||||||
chr2:36874835 | T | TG | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3055_1323+305 others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874835 | |||||||
chr2:36874889 | G | T | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1323+3002C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874889 | |||||||
chr2:36874986 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1323+2905C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874986 | |||||||
chr2:36875106 | A | G | 135 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(132): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1323+2785T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875106 | |||||||
chr2:36875121 | A | G | 15 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1323+2770T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875121 | |||||||
chr2:36875224 | C | A | 1 | a0001c0001t0077g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1323+2667G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875224 | |||||||
chr2:36875477 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1323+2414A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875477 | |||||||
chr2:36875505 | C | CA | 8 | a0001c0001t0005g0215 a0001c0001t0007g0272 a0001c0001t0013g0197 others(5): Show |
8 | HG02109.hp1 HG02723.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1323+2385dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875505 | |||||||
chr2:36875505 | CA | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1323+2385delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875505 | |||||||
chr2:36875532 | T | C | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+2359A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875532 | |||||||
chr2:36875572 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1323+2319G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875572 | |||||||
chr2:36875573 | CA | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1323+2317delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875573 | |||||||
chr2:36875659 | A | AT | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1323+2231dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875659 | |||||||
chr2:36875711 | C | T | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+2180G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875711 | |||||||
chr2:36875726 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0057 a0004c0004t0002g0048 |
3 | HG00408.hp2 HG02135.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1323+2165C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875726 | |||||||
chr2:36875729 | T | C | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+2162A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875729 | |||||||
chr2:36875807 | C | A | 1 | a0001c0001t0005g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1323+2084G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875807 | |||||||
chr2:36875813 | T | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+2078A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875813 | |||||||
chr2:36875920 | G | A | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323+1971C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875920 | |||||||
chr2:36875964 | AT | A | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+1926delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875964 | |||||||
chr2:36875972 | T | A | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+1919A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875972 | |||||||
chr2:36875996 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1323+1895C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875996 | |||||||
chr2:36876063 | G | C | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+1828C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876063 | |||||||
chr2:36876090 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1323+1801C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876090 | |||||||
chr2:36876144 | C | G | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+1747G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876144 | |||||||
chr2:36876175 | T | TGGGAGGA others(17): Show |
2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1692_1323+171 others(28): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876175 | |||||||
chr2:36876218 | C | T | 10 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0126 others(7): Show |
10 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1323+1673G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876218 | |||||||
chr2:36876270 | TA | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1323+1620delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876270 | |||||||
chr2:36876285 | A | T | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1606T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876285 | |||||||
chr2:36876364 | T | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+1527A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876364 | |||||||
chr2:36876433 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1458A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876433 | |||||||
chr2:36876547 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1323+1344C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876547 | |||||||
chr2:36876652 | G | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1323+1239C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876652 | |||||||
chr2:36876751 | AT | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1323+1139delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876751 | |||||||
chr2:36876770 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0072g0044 |
2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1323+1121G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876770 | |||||||
chr2:36876876 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323+1015A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876876 | |||||||
chr2:36876893 | G | A | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+998C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876893 | |||||||
chr2:36876937 | A | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+954T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876937 | |||||||
chr2:36876969 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1323+922G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876969 | |||||||
chr2:36876995 | G | A | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1323+896C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876995 | |||||||
chr2:36877265 | C | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1323+626G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877265 | |||||||
chr2:36877354 | C | T | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+537G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877354 | |||||||
chr2:36877372 | C | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1323+519G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877372 | |||||||
chr2:36877579 | A | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1323+312T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877579 | |||||||
chr2:36877660 | CT | C | 14 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(11): Show |
14 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1323+230delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877660 | |||||||
chr2:36877666 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1323+225C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877666 | |||||||
chr2:36877667 | C | A | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+224G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877667 | |||||||
chr2:36877787 | C | T | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+104G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877787 | |||||||
chr2:36878035 | G | A | 24 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(21): Show |
24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1187-8C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878035 | |||||||
chr2:36878119 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1187-92C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878119 | |||||||
chr2:36878185 | T | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-158A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878185 | |||||||
chr2:36878632 | C | T | 8 | a0001c0001t0002g0019 a0001c0001t0006g0209 a0001c0001t0006g0210 others(5): Show |
8 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187-605G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878632 | |||||||
chr2:36878858 | T | C | 2 | a0001c0001t0008g0298 a0001c0001t0008g0299 |
2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1187-831A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878858 | |||||||
chr2:36878865 | G | A | 1 | a0001c0001t0086g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187-838C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878865 | |||||||
chr2:36878973 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1187-946C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878973 | |||||||
chr2:36879184 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-1157G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879184 | |||||||
chr2:36879268 | C | T | 1 | a0004c0004t0002g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1187-1241G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879268 | |||||||
chr2:36879285 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1187-1258T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879285 | |||||||
chr2:36879315 | C | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1187-1288G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879315 | |||||||
chr2:36879417 | C | CTG | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-1392_1187-139 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879417 | |||||||
chr2:36879487 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1187-1460A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879487 | |||||||
chr2:36879510 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0149 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1187-1483G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879510 | |||||||
chr2:36879839 | G | C | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187-1812C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879839 | |||||||
chr2:36879931 | A | G | 2 | a0001c0001t0031g0013 a0001c0001t0031g0031 |
2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1187-1904T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879931 | |||||||
chr2:36879941 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1187-1914C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879941 | |||||||
chr2:36880151 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1187-2124G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880151 | |||||||
chr2:36880205 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1187-2178G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880205 | |||||||
chr2:36880831 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1187-2804A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880831 | |||||||
chr2:36880856 | T | C | 1 | a0001c0001t0017g0226 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1187-2829A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880856 | |||||||
chr2:36880957 | T | C | 1 | a0001c0001t0021g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1187-2930A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880957 | |||||||
chr2:36881068 | A | AAAAAC | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1186+2859_1186+286 others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881068 | |||||||
chr2:36881118 | CT | C | 36 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0105 others(33): Show |
36 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1186+2813delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | |||||||
chr2:36881118 | CTT | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1186+2812_1186+281 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | |||||||
chr2:36881118 | CTTT | C | 29 | a0001c0001t0001g0132 a0001c0001t0002g0014 a0001c0001t0002g0017 others(26): Show |
29 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1186+2811_1186+281 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | |||||||
chr2:36881118 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1186+2804_1186+281 others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | |||||||
chr2:36881265 | C | A | 1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1186+2667G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881265 | |||||||
chr2:36881328 | A | C | 1 | a0001c0001t0056g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1186+2604T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881328 | |||||||
chr2:36881331 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+2601A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881331 | |||||||
chr2:36881332 | T | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1186+2600A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881332 | |||||||
chr2:36881347 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0149 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1186+2585A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881347 | |||||||
chr2:36881348 | G | C | 1 | a0001c0001t0077g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1186+2584C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881348 | |||||||
chr2:36881399 | A | G | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1186+2533T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881399 | |||||||
chr2:36881436 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1186+2496G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881436 | |||||||
chr2:36881494 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1186+2438A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881494 | |||||||
chr2:36881530 | A | G | 1 | a0001c0001t0007g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1186+2402T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881530 | |||||||
chr2:36881750 | G | A | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1186+2182C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881750 | |||||||
chr2:36881854 | T | C | 1 | a0001c0001t0026g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1186+2078A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881854 | |||||||
chr2:36881937 | T | C | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1186+1995A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881937 | |||||||
chr2:36882120 | T | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1186+1812A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882120 | |||||||
chr2:36882138 | G | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1186+1794C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882138 | |||||||
chr2:36882199 | GA | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+1732delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882199 | |||||||
chr2:36882206 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1186+1726T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882206 | |||||||
chr2:36882281 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1186+1651A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882281 | |||||||
chr2:36882307 | A | G | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1625T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882307 | |||||||
chr2:36882385 | G | A | 5 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(2): Show |
5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1547C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882385 | |||||||
chr2:36882571 | A | G | 3 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0066g0240 |
3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1186+1361T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882571 | |||||||
chr2:36882601 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1186+1331A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882601 | |||||||
chr2:36882696 | G | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1186+1236C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882696 | |||||||
chr2:36883300 | CA | C | 20 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1186+631delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883300 | |||||||
chr2:36883323 | G | A | 1 | a0001c0001t0068g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1186+609C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883323 | |||||||
chr2:36883379 | C | A | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1186+553G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883379 | |||||||
chr2:36883541 | G | C | 1 | a0001c0001t0003g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1186+391C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883541 | |||||||
chr2:36883603 | A | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1186+329T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883603 | |||||||
chr2:36883631 | A | G | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1186+301T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883631 | |||||||
chr2:36883778 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | NA19006.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1186+154G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883778 | |||||||
chr2:36883902 | T | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1186+30A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883902 | |||||||
chr2:36884111 | A | G | 1 | a0001c0001t0003g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1043-36T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884111 | |||||||
chr2:36884205 | T | G | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-130A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884205 | |||||||
chr2:36884266 | T | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-191A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884266 | |||||||
chr2:36884289 | G | T | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1043-214C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884289 | |||||||
chr2:36884314 | A | G | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-239T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884314 | |||||||
chr2:36884479 | T | C | 1 | a0001c0001t0077g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1043-404A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884479 | |||||||
chr2:36884741 | T | C | 6 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043-666A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884741 | |||||||
chr2:36884823 | T | C | 16 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(13): Show |
16 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1043-748A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884823 | |||||||
chr2:36884837 | T | A | 1 | a0002c0002t0005g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1043-762A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884837 | |||||||
chr2:36884867 | A | T | 2 | a0001c0001t0002g0245 a0001c0001t0003g0247 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1043-792T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884867 | |||||||
chr2:36884920 | T | C | 2 | a0001c0001t0003g0097 a0001c0001t0003g0098 |
2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1043-845A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884920 | |||||||
chr2:36885215 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1043-1140G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885215 | |||||||
chr2:36885636 | G | T | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042+1080C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885636 | |||||||
chr2:36885640 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp1 HG02155.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+1076C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885640 | |||||||
chr2:36885656 | T | C | 2 | a0001c0001t0007g0289 a0001c0001t0044g0290 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1042+1060A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885656 | |||||||
chr2:36885666 | G | C | 2 | a0001c0001t0045g0232 a0001c0001t0046g0231 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1042+1050C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885666 | |||||||
chr2:36885676 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1042+1040G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885676 | |||||||
chr2:36885779 | C | T | 1 | a0001c0001t0081g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1042+937G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885779 | |||||||
chr2:36885817 | T | G | 4 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 others(1): Show |
4 | HG02071.hp2 HG02965.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+899A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885817 | |||||||
chr2:36886013 | T | C | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1042+703A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886013 | |||||||
chr2:36886132 | C | T | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+584G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886132 | |||||||
chr2:36886233 | T | C | 1 | a0001c0001t0007g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1042+483A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886233 | |||||||
chr2:36886271 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1042+445A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886271 | |||||||
chr2:36886314 | T | C | 1 | a0001c0001t0002g0017 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1042+402A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886314 | |||||||
chr2:36886478 | GATTT | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | NA18940.hp2 NA18955.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+234_1042+237d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886478 | |||||||
chr2:36887040 | A | AAGAC | 5 | a0001c0001t0005g0215 a0001c0001t0005g0225 a0001c0001t0039g0217 others(2): Show |
5 | HG02083.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-218_932-215dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887040 | |||||||
chr2:36887042 | G | GAC | 3 | a0001c0001t0007g0270 a0001c0001t0007g0288 a0001c0001t0044g0290 |
3 | HG02630.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.932-218_932-217dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | G | GACAGAC | 3 | a0001c0001t0017g0226 a0001c0001t0038g0220 a0002c0002t0043g0219 |
3 | HG02040.hp2 HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.932-217_932-216ins others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACAC | G | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-220_932-217del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACACAC | G | 3 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0045g0232 |
3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.932-222_932-217del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACACACA others(1): Show |
G | 3 | a0001c0001t0046g0231 a0001c0001t0049g0192 a0001c0001t0057g0148 |
3 | NA18906.hp1 NA18963.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.932-224_932-217del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACACACA others(3): Show |
G | 22 | a0001c0001t0001g0101 a0001c0001t0001g0141 a0001c0001t0001g0164 others(19): Show |
22 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.932-226_932-217del others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACACACA others(5): Show |
G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.932-228_932-217del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887042 | GACACACA others(7): Show |
G | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-230_932-217del others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | |||||||
chr2:36887044 | C | CAG | 6 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0214 others(3): Show |
6 | HG00438.hp2 HG01106.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-219_932-218ins others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887044 | |||||||
chr2:36887046 | C | G | 6 | a0001c0001t0019g0207 a0001c0001t0021g0233 a0001c0001t0021g0236 others(3): Show |
6 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-220G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887046 | |||||||
chr2:36887052 | C | G | 2 | a0001c0001t0005g0092 a0001c0001t0005g0093 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.932-226G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887052 | |||||||
chr2:36887084 | C | CACAT | 4 | a0001c0001t0006g0211 a0001c0001t0006g0222 a0001c0001t0006g0223 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-259_932-258ins others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887084 | |||||||
chr2:36887084 | C | T | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0228 others(4): Show |
7 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-258G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887084 | |||||||
chr2:36887086 | C | T | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.932-260G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887086 | |||||||
chr2:36887266 | A | AAAAT | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-444_932-441dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887266 | A | AAAATAAA others(1): Show |
26 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0131 others(23): Show |
26 | HG00280.hp1 HG01168.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.932-448_932-441dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887266 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.932-452_932-441dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887266 | AAAAT | A | 25 | a0001c0001t0001g0156 a0001c0001t0003g0043 a0001c0001t0003g0239 others(22): Show |
25 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-444_932-441del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887266 | AAAATAAA others(1): Show |
A | 3 | a0001c0001t0029g0034 a0001c0001t0031g0013 a0001c0001t0031g0031 |
3 | HG01070.hp2 HG01261.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.932-448_932-441del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887266 | AAAATAAA others(5): Show |
A | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-452_932-441del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | |||||||
chr2:36887316 | C | T | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.932-490G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887316 | |||||||
chr2:36887326 | C | T | 2 | a0001c0001t0003g0250 a0001c0001t0003g0258 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.932-500G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887326 | |||||||
chr2:36887367 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.932-541C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887367 | |||||||
chr2:36887431 | T | C | 15 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.932-605A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887431 | |||||||
chr2:36887487 | C | CA | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.932-662dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887487 | |||||||
chr2:36887671 | G | C | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-845C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887671 | |||||||
chr2:36887703 | T | A | 1 | a0001c0001t0023g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-877A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887703 | |||||||
chr2:36887832 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.932-1006T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887832 | |||||||
chr2:36888093 | C | A | 1 | a0001c0001t0044g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-1267G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888093 | |||||||
chr2:36888253 | T | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.932-1427A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888253 | |||||||
chr2:36888321 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.932-1495A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888321 | |||||||
chr2:36888639 | A | ATG | 55 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0030 others(52): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.932-1815_932-1814d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTG | 24 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0024 others(21): Show |
24 | HG00323.hp2 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.932-1817_932-1814d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTGTG | 37 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(34): Show |
37 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.932-1819_932-1814d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTGTGT others(1): Show |
16 | a0001c0001t0002g0012 a0001c0001t0002g0028 a0001c0001t0002g0052 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.932-1821_932-1814d others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTGTGT others(3): Show |
9 | a0001c0001t0002g0011 a0001c0001t0002g0245 a0001c0001t0003g0247 others(6): Show |
9 | HG00673.hp2 HG01256.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.932-1823_932-1814d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.932-1825_932-1814d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.932-1827_932-1814d others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0086g0055 |
2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.932-1813T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | ATG | A | 23 | a0001c0001t0001g0118 a0001c0001t0001g0164 a0001c0001t0001g0170 others(20): Show |
23 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.932-1815_932-1814d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | ATGTG | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.932-1817_932-1814d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | ATGTGTG | A | 15 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0124 others(12): Show |
15 | HG00621.hp2 HG01934.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.932-1819_932-1814d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888639 | ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-1823_932-1814d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | |||||||
chr2:36888949 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-2123C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888949 | |||||||
chr2:36889270 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.932-2444C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889270 | |||||||
chr2:36889419 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.932-2593T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889419 | |||||||
chr2:36889460 | G | T | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.932-2634C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889460 | |||||||
chr2:36889468 | A | AG | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.932-2643_932-2642i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889468 | |||||||
chr2:36889554 | G | C | 1 | a0001c0001t0003g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.932-2728C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889554 | |||||||
chr2:36889610 | C | CT | 4 | a0001c0001t0002g0066 a0001c0001t0003g0040 a0001c0001t0003g0251 others(1): Show |
4 | HG00741.hp1 NA18952.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-2785dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889610 | |||||||
chr2:36889619 | G | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.932-2793C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889619 | |||||||
chr2:36889625 | G | A | 1 | a0001c0001t0003g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.932-2799C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889625 | |||||||
chr2:36889741 | T | A | 1 | a0001c0001t0005g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.932-2915A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889741 | |||||||
chr2:36889930 | C | T | 128 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.932-3104G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889930 | |||||||
chr2:36889939 | A | G | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-3113T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889939 | |||||||
chr2:36890136 | G | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.932-3310C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890136 | |||||||
chr2:36890299 | A | T | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-3473T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890299 | |||||||
chr2:36890353 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.932-3527C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890353 | |||||||
chr2:36890359 | G | C | 130 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(127): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.932-3533C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890359 | |||||||
chr2:36890477 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+3421G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | |||||||
chr2:36890477 | C | CT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0105 others(32): Show |
35 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.931+3420dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | |||||||
chr2:36890477 | CT | C | 18 | a0001c0001t0002g0017 a0001c0001t0002g0038 a0001c0001t0003g0247 others(15): Show |
18 | HG00099.hp2 HG02040.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.931+3420delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | |||||||
chr2:36890478 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+3420A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890478 | |||||||
chr2:36890710 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.931+3188G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890710 | |||||||
chr2:36890782 | C | T | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+3116G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890782 | |||||||
chr2:36890987 | G | T | 1 | a0001c0001t0053g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.931+2911C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890987 | |||||||
chr2:36891145 | T | G | 1 | a0001c0005t0006g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.931+2753A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891145 | |||||||
chr2:36891383 | G | A | 1 | a0001c0001t0042g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+2515C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891383 | |||||||
chr2:36891385 | G | A | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.931+2513C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891385 | |||||||
chr2:36891516 | C | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0071 |
2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.931+2382G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891516 | |||||||
chr2:36891522 | C | CA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.931+2375dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891522 | |||||||
chr2:36891577 | C | T | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2321G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891577 | |||||||
chr2:36891603 | G | C | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2295C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891603 | |||||||
chr2:36891626 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.931+2272T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891626 | |||||||
chr2:36891798 | C | G | 1 | a0001c0001t0040g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.931+2100G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891798 | |||||||
chr2:36891918 | T | C | 2 | a0001c0001t0045g0232 a0001c0001t0046g0231 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.931+1980A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891918 | |||||||
chr2:36891935 | C | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1963G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891935 | |||||||
chr2:36892027 | T | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.931+1871A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892027 | |||||||
chr2:36892094 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.931+1804G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892094 | |||||||
chr2:36892113 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.931+1785G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892113 | |||||||
chr2:36892208 | C | T | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.931+1690G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892208 | |||||||
chr2:36892262 | G | A | 1 | a0001c0001t0068g0255 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.931+1636C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892262 | |||||||
chr2:36892342 | A | G | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1556T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892342 | |||||||
chr2:36892636 | T | C | 1 | a0001c0001t0023g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.931+1262A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892636 | |||||||
chr2:36892662 | G | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.931+1236C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892662 | |||||||
chr2:36892709 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.931+1189A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892709 | |||||||
chr2:36892793 | G | C | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.931+1105C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892793 | |||||||
chr2:36893061 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.931+837G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893061 | |||||||
chr2:36893294 | C | CA | 5 | a0001c0001t0001g0131 a0001c0001t0001g0145 a0001c0001t0008g0295 others(2): Show |
5 | HG02300.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+603dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893294 | |||||||
chr2:36893303 | C | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.931+595G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893303 | |||||||
chr2:36893311 | C | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.931+587G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893311 | |||||||
chr2:36893312 | G | A | 1 | a0001c0001t0038g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+586C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893312 | |||||||
chr2:36893443 | A | AT | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.931+454dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893443 | |||||||
chr2:36893582 | T | C | 6 | a0001c0001t0001g0200 a0001c0001t0002g0019 a0001c0001t0002g0029 others(3): Show |
6 | HG00408.hp2 HG02135.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+316A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893582 | |||||||
chr2:36893593 | A | G | 1 | a0001c0001t0025g0187 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.931+305T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893593 | |||||||
chr2:36893654 | G | A | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.931+244C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893654 | |||||||
chr2:36893750 | A | G | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.931+148T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893750 | |||||||
chr2:36894103 | T | C | 1 | a0001c0001t0014g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.796-70A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894103 | |||||||
chr2:36894512 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.796-479T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894512 | |||||||
chr2:36894751 | T | C | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-718A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894751 | |||||||
chr2:36894809 | A | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-776T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894809 | |||||||
chr2:36894942 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-909C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894942 | |||||||
chr2:36894993 | C | T | 24 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(21): Show |
24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.796-960G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894993 | |||||||
chr2:36895055 | C | T | 17 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-1022G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895055 | |||||||
chr2:36895243 | C | T | 1 | a0001c0001t0083g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.796-1210G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895243 | |||||||
chr2:36895325 | T | TA | 9 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0003g0249 others(6): Show |
9 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.796-1293dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895325 | |||||||
chr2:36895381 | T | C | 1 | a0002c0002t0043g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.796-1348A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895381 | |||||||
chr2:36895402 | T | C | 1 | a0001c0001t0030g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.796-1369A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895402 | |||||||
chr2:36895409 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.796-1376T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895409 | |||||||
chr2:36895432 | T | A | 2 | a0001c0001t0023g0115 a0001c0001t0023g0153 |
2 | HG01261.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.796-1399A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895432 | |||||||
chr2:36895596 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.796-1563A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895596 | |||||||
chr2:36895631 | G | A | 73 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(70): Show |
73 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.796-1598C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895631 | |||||||
chr2:36895756 | CA | C | 152 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(149): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.796-1724delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895756 | |||||||
chr2:36895756 | CAA | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
100 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.796-1725_796-1724d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895756 | |||||||
chr2:36895873 | G | A | 2 | a0001c0001t0018g0291 a0001c0001t0018g0292 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.796-1840C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895873 | |||||||
chr2:36895987 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.796-1954C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895987 | |||||||
chr2:36895994 | A | G | 25 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(22): Show |
25 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.796-1961T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895994 | |||||||
chr2:36896153 | T | A | 76 | a0001c0001t0001g0184 a0001c0001t0001g0200 a0001c0001t0002g0007 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.796-2120A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896153 | |||||||
chr2:36896156 | A | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-2123T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896156 | |||||||
chr2:36896228 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.796-2195A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896228 | |||||||
chr2:36896240 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.796-2207A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896240 | |||||||
chr2:36896293 | A | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-2260T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896293 | |||||||
chr2:36896549 | A | C | 1 | a0001c0001t0003g0040 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.796-2516T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896549 | |||||||
chr2:36896665 | G | A | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.796-2632C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896665 | |||||||
chr2:36896711 | T | C | 17 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.796-2678A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896711 | |||||||
chr2:36896933 | C | T | 12 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(9): Show |
12 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.795+2590G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896933 | |||||||
chr2:36897006 | A | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2517T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897006 | |||||||
chr2:36897060 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.795+2463C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897060 | |||||||
chr2:36897122 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.795+2401T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897122 | |||||||
chr2:36897310 | C | A | 2 | a0001c0001t0045g0232 a0001c0001t0046g0231 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.795+2213G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897310 | |||||||
chr2:36897316 | C | A | 15 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.795+2207G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897316 | |||||||
chr2:36897330 | G | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.795+2193C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897330 | |||||||
chr2:36897400 | G | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+2123C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897400 | |||||||
chr2:36897429 | T | TAA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.795+2092_795+2093d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897429 | |||||||
chr2:36897434 | A | T | 14 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(11): Show |
14 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.795+2089T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897434 | |||||||
chr2:36897435 | AT | A | 4 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+2087delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897435 | |||||||
chr2:36897436 | T | A | 180 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(177): Show |
180 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.795+2087A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897436 | |||||||
chr2:36897438 | T | A | 69 | a0001c0001t0001g0047 a0001c0001t0002g0054 a0001c0001t0002g0073 others(66): Show |
69 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.795+2085A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897438 | |||||||
chr2:36897443 | A | AT | 9 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(6): Show |
9 | HG00738.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.795+2079dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897443 | |||||||
chr2:36897443 | A | T | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.795+2080T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897443 | |||||||
chr2:36897445 | A | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.795+2078T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897445 | |||||||
chr2:36897447 | T | A | 3 | a0001c0001t0007g0272 a0001c0001t0020g0274 a0001c0001t0020g0277 |
3 | HG02109.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2076A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897447 | |||||||
chr2:36897462 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.795+2061C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897462 | |||||||
chr2:36897485 | G | A | 6 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+2038C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897485 | |||||||
chr2:36897497 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2026C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897497 | |||||||
chr2:36897517 | GCTCTGCC others(77): Show |
G | 1 | a0001c0001t0033g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.795+1922_795+2005d others(86): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897517 | |||||||
chr2:36897612 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.795+1911A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897612 | |||||||
chr2:36897683 | C | T | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.795+1840G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897683 | |||||||
chr2:36897747 | A | C | 1 | a0001c0001t0002g0019 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.795+1776T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897747 | |||||||
chr2:36897960 | G | C | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.795+1563C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897960 | |||||||
chr2:36897972 | C | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0183 a0001c0001t0001g0184 others(3): Show |
6 | NA18940.hp2 NA18955.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+1551G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897972 | |||||||
chr2:36897985 | G | A | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.795+1538C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897985 | |||||||
chr2:36898092 | T | C | 4 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
4 | HG01433.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+1431A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898092 | |||||||
chr2:36898299 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.795+1224C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898299 | |||||||
chr2:36898350 | G | A | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.795+1173C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898350 | |||||||
chr2:36898379 | T | C | 4 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 others(1): Show |
4 | HG03195.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+1144A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898379 | |||||||
chr2:36898394 | T | C | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.795+1129A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898394 | |||||||
chr2:36898503 | C | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.795+1020G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898503 | |||||||
chr2:36898826 | T | C | 1 | a0001c0001t0010g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.795+697A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898826 | |||||||
chr2:36899016 | C | G | 28 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(25): Show |
28 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.795+507G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899016 | |||||||
chr2:36899043 | C | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.795+480G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899043 | |||||||
chr2:36899417 | G | T | 1 | a0001c0001t0004g0060 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.795+106C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899417 | |||||||
chr2:36899508 | A | C | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.795+15T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899508 | |||||||
chr2:36899881 | C | T | 2 | a0001c0001t0042g0205 a0001c0001t0044g0290 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.660-223G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36899881 | |||||||
chr2:36900132 | G | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.660-474C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900132 | |||||||
chr2:36900250 | G | A | 7 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0143 others(4): Show |
7 | HG00621.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.660-592C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900250 | |||||||
chr2:36900414 | T | C | 4 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 others(1): Show |
4 | HG03195.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.660-756A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900414 | |||||||
chr2:36900801 | C | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.660-1143G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900801 | |||||||
chr2:36900848 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.660-1190C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900848 | |||||||
chr2:36901003 | G | GA | 18 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0002g0030 others(15): Show |
18 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.660-1346dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901003 | |||||||
chr2:36901169 | A | G | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.659+1415T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901169 | |||||||
chr2:36901272 | G | C | 1 | a0001c0003t0005g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.659+1312C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901272 | |||||||
chr2:36901294 | G | A | 1 | a0001c0001t0022g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.659+1290C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901294 | |||||||
chr2:36901449 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+1135C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901449 | |||||||
chr2:36901551 | CA | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.659+1032delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901551 | |||||||
chr2:36901563 | A | C | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.659+1021T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901563 | |||||||
chr2:36901567 | AAAC | A | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.659+1014_659+1016d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901567 | |||||||
chr2:36901571 | A | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.659+1013T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901571 | |||||||
chr2:36901663 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659+921C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901663 | |||||||
chr2:36901674 | T | A | 21 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.659+910A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901674 | |||||||
chr2:36901711 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+873A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901711 | |||||||
chr2:36901783 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+801C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901783 | |||||||
chr2:36901915 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.659+669C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901915 | |||||||
chr2:36901916 | T | C | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.659+668A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901916 | |||||||
chr2:36901941 | T | A | 1 | a0001c0001t0003g0258 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.659+643A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901941 | |||||||
chr2:36901978 | A | T | 21 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.659+606T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901978 | |||||||
chr2:36902044 | T | C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp1 HG02155.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.659+540A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902044 | |||||||
chr2:36902245 | C | T | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+339G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902245 | |||||||
chr2:36902414 | T | A | 1 | a0001c0001t0002g0012 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.659+170A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902414 | |||||||
chr2:36902475 | A | ATAAT | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.659+108_659+109ins others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902475 | |||||||
chr2:36902960 | G | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.492-209C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36902960 | |||||||
chr2:36903010 | G | C | 1 | a0001c0001t0007g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492-259C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903010 | |||||||
chr2:36903108 | T | A | 2 | a0001c0001t0026g0155 a0001c0001t0026g0159 |
2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.492-357A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903108 | |||||||
chr2:36903180 | C | T | 1 | a0001c0001t0007g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.492-429G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903180 | |||||||
chr2:36903199 | G | A | 2 | a0001c0001t0026g0155 a0001c0001t0026g0159 |
2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.492-448C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903199 | |||||||
chr2:36903227 | T | C | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.492-476A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903227 | |||||||
chr2:36903230 | T | C | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.492-479A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903230 | |||||||
chr2:36903283 | G | A | 1 | a0002c0002t0005g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.492-532C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903283 | |||||||
chr2:36903515 | A | C | 57 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0002g0245 others(54): Show |
57 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.492-764T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903515 | |||||||
chr2:36903515 | A | T | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.492-764T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903515 | |||||||
chr2:36903581 | A | G | 25 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(22): Show |
25 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.492-830T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903581 | |||||||
chr2:36903619 | G | A | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.492-868C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903619 | |||||||
chr2:36903637 | C | T | 3 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 |
3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.492-886G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903637 | |||||||
chr2:36903738 | G | C | 1 | a0001c0001t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.492-987C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903738 | |||||||
chr2:36903738 | G | T | 6 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(3): Show |
6 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-987C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903738 | |||||||
chr2:36903758 | G | T | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.492-1007C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903758 | |||||||
chr2:36903854 | C | T | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-1103G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903854 | |||||||
chr2:36904148 | A | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.491+1392T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904148 | |||||||
chr2:36904288 | G | A | 1 | a0001c0001t0039g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.491+1252C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904288 | |||||||
chr2:36904322 | T | A | 6 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(3): Show |
6 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+1218A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904322 | |||||||
chr2:36904328 | C | T | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.491+1212G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904328 | |||||||
chr2:36904403 | G | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.491+1137C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904403 | |||||||
chr2:36904548 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.491+992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904548 | |||||||
chr2:36904549 | G | A | 1 | a0001c0001t0007g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.491+991C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904549 | |||||||
chr2:36904554 | T | C | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.491+986A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904554 | |||||||
chr2:36904557 | T | C | 1 | a0001c0001t0040g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.491+983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904557 | |||||||
chr2:36904669 | T | C | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.491+871A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904669 | |||||||
chr2:36904686 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.491+854C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904686 | |||||||
chr2:36904720 | C | T | 47 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0002g0245 others(44): Show |
47 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.491+820G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904720 | |||||||
chr2:36904734 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.491+806T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904734 | |||||||
chr2:36904747 | G | C | 21 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.491+793C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904747 | |||||||
chr2:36904829 | A | G | 1 | a0001c0001t0060g0133 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.491+711T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904829 | |||||||
chr2:36904838 | C | A | 3 | a0001c0001t0029g0015 a0001c0001t0029g0034 a0001c0001t0059g0111 |
3 | HG02155.hp2 HG04184.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.491+702G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904838 | |||||||
chr2:36904838 | C | CTGAA | 79 | a0001c0001t0001g0122 a0001c0001t0002g0007 a0001c0001t0002g0009 others(76): Show |
79 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.491+698_491+701dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904838 | |||||||
chr2:36904952 | T | C | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.491+588A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904952 | |||||||
chr2:36904969 | CT | C | 166 | a0001c0001t0001g0047 a0001c0001t0001g0122 a0001c0001t0001g0138 others(163): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.491+570delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904969 | |||||||
chr2:36905031 | G | A | 8 | a0001c0001t0011g0190 a0001c0001t0012g0282 a0001c0001t0012g0285 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.491+509C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905031 | |||||||
chr2:36905032 | C | T | 45 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(42): Show |
45 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.491+508G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905032 | |||||||
chr2:36905038 | C | A | 1 | a0001c0001t0002g0012 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.491+502G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905038 | |||||||
chr2:36905096 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.491+444T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905096 | |||||||
chr2:36905104 | G | A | 1 | a0001c0001t0010g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.491+436C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905104 | |||||||
chr2:36905117 | G | A | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.491+423C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905117 | |||||||
chr2:36905358 | G | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.491+182C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905358 | |||||||
chr2:36905663 | T | G | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.413-45A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36905663 | |||||||
chr2:36905984 | C | T | 201 | a0001c0001t0001g0047 a0001c0001t0001g0122 a0001c0001t0002g0007 others(198): Show |
201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.413-366G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36905984 | |||||||
chr2:36906137 | T | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413-519A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906137 | |||||||
chr2:36906209 | A | G | 2 | a0001c0001t0006g0222 a0001c0001t0006g0223 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.413-591T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906209 | |||||||
chr2:36906293 | T | C | 1 | a0001c0001t0002g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.413-675A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906293 | |||||||
chr2:36906392 | G | A | 1 | a0001c0001t0029g0015 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413-774C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906392 | |||||||
chr2:36906463 | C | CAATGAAT others(1): Show |
32 | a0001c0001t0002g0022 a0001c0001t0002g0033 a0001c0001t0002g0054 others(29): Show |
32 | HG00099.hp1 HG01243.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.413-853_413-846dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | |||||||
chr2:36906463 | C | CAATGAAT others(5): Show |
102 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(99): Show |
102 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.413-857_413-846dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | |||||||
chr2:36906463 | C | CAATGAAT others(9): Show |
8 | a0001c0001t0002g0075 a0001c0001t0003g0067 a0001c0001t0003g0071 others(5): Show |
8 | HG00280.hp1 HG00735.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-861_413-846dup others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | |||||||
chr2:36906463 | C | CAATGAAT others(13): Show |
2 | a0001c0001t0002g0037 a0001c0001t0003g0043 |
2 | HG00323.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.413-865_413-846dup others(20): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | |||||||
chr2:36906463 | C | CAATGAAT others(17): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0066 |
2 | NA18985.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.413-869_413-846dup others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | |||||||
chr2:36906493 | G | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0030 a0001c0001t0002g0058 others(2): Show |
5 | HG02135.hp1 HG02135.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-875C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906493 | |||||||
chr2:36906514 | T | A | 33 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(30): Show |
33 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.413-896A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906514 | |||||||
chr2:36906538 | C | A | 11 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-920G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906538 | |||||||
chr2:36906694 | A | G | 56 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(53): Show |
56 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-1076T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906694 | |||||||
chr2:36906696 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.413-1078G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906696 | |||||||
chr2:36906704 | T | C | 4 | a0001c0001t0012g0285 a0001c0001t0012g0286 a0001c0001t0015g0283 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-1086A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906704 | |||||||
chr2:36906740 | A | C | 1 | a0001c0001t0003g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.413-1122T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906740 | |||||||
chr2:36906868 | C | G | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.413-1250G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906868 | |||||||
chr2:36906938 | A | AAAC | 6 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0031g0013 others(3): Show |
6 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-1321_413-1320i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906938 | |||||||
chr2:36906938 | A | AAC | 69 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.413-1321_413-1320i others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906938 | |||||||
chr2:36906939 | C | A | 75 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413-1321G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906939 | |||||||
chr2:36906939 | C | CA | 73 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0129 others(70): Show |
73 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.413-1322dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906939 | |||||||
chr2:36906949 | C | A | 156 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0129 others(153): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.413-1331G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906949 | |||||||
chr2:36906968 | T | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-1350A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906968 | |||||||
chr2:36907071 | C | T | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-1453G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907071 | |||||||
chr2:36907142 | G | A | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.413-1524C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907142 | |||||||
chr2:36907190 | T | G | 1 | a0001c0001t0003g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.413-1572A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907190 | |||||||
chr2:36907516 | C | G | 1 | a0001c0001t0003g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.413-1898G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907516 | |||||||
chr2:36907617 | T | C | 2 | a0001c0001t0026g0155 a0001c0001t0026g0159 |
2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-1999A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907617 | |||||||
chr2:36907637 | A | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0086g0055 |
3 | HG00099.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.413-2019T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907637 | |||||||
chr2:36907718 | G | A | 1 | a0001c0001t0026g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.413-2100C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907718 | |||||||
chr2:36907869 | G | A | 2 | a0001c0001t0003g0239 a0001c0001t0003g0251 |
2 | NA18943.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.413-2251C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907869 | |||||||
chr2:36907960 | C | T | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.413-2342G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907960 | |||||||
chr2:36908074 | C | T | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.413-2456G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908074 | |||||||
chr2:36908301 | G | C | 1 | a0001c0001t0002g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.413-2683C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908301 | |||||||
chr2:36908314 | A | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0037 a0001c0001t0002g0038 others(1): Show |
4 | NA18940.hp1 NA18985.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-2696T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908314 | |||||||
chr2:36908357 | C | G | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-2739G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908357 | |||||||
chr2:36908426 | T | G | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-2808A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908426 | |||||||
chr2:36908571 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-2953A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908571 | |||||||
chr2:36908748 | C | T | 1 | a0001c0001t0085g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.413-3130G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908748 | |||||||
chr2:36908844 | G | A | 1 | a0001c0001t0040g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413-3226C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908844 | |||||||
chr2:36908893 | A | C | 158 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(155): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.413-3275T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908893 | |||||||
chr2:36908964 | G | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-3346C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908964 | |||||||
chr2:36908998 | G | GA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0169 a0001c0001t0006g0209 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-3381dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | |||||||
chr2:36908998 | G | GAA | 16 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.413-3382_413-3381d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | |||||||
chr2:36908998 | G | GAAA | 138 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.413-3383_413-3381d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | |||||||
chr2:36908998 | G | GAAAA | 12 | a0001c0001t0002g0033 a0001c0001t0002g0113 a0001c0001t0003g0040 others(9): Show |
12 | HG00741.hp1 HG01255.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-3384_413-3381d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | |||||||
chr2:36909002 | A | AAAC | 12 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0218 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-3385_413-3384i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909002 | |||||||
chr2:36909013 | G | C | 2 | a0001c0001t0045g0232 a0001c0001t0046g0231 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.413-3395C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909013 | |||||||
chr2:36909031 | G | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-3413C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909031 | |||||||
chr2:36909157 | C | CA | 14 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-3540dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909157 | |||||||
chr2:36909157 | CA | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0120 others(58): Show |
61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.413-3540delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909157 | |||||||
chr2:36909217 | A | T | 1 | a0001c0001t0009g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413-3599T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909217 | |||||||
chr2:36909255 | T | C | 75 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413-3637A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909255 | |||||||
chr2:36909374 | A | G | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-3756T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909374 | |||||||
chr2:36909492 | C | T | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-3874G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909492 | |||||||
chr2:36909495 | T | C | 189 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(186): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.413-3877A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909495 | |||||||
chr2:36909617 | T | C | 190 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(187): Show |
190 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.413-3999A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909617 | |||||||
chr2:36909669 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0061g0110 |
2 | NA18943.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.413-4051A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909669 | |||||||
chr2:36909746 | A | G | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-4128T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909746 | |||||||
chr2:36909764 | T | C | 5 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0228 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-4146A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909764 | |||||||
chr2:36909877 | TAAAG | T | 3 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0066g0240 |
3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.413-4263_413-4260d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909877 | |||||||
chr2:36909946 | G | T | 1 | a0001c0001t0002g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.413-4328C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909946 | |||||||
chr2:36909980 | C | G | 58 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0002g0245 others(55): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.413-4362G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909980 | |||||||
chr2:36910110 | C | T | 201 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(198): Show |
201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.413-4492G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910110 | |||||||
chr2:36910122 | G | A | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.413-4504C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910122 | |||||||
chr2:36910127 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.413-4509G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910127 | |||||||
chr2:36910152 | G | T | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-4534C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910152 | |||||||
chr2:36910161 | G | A | 52 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(49): Show |
52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.413-4543C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910161 | |||||||
chr2:36910173 | C | CA | 53 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0123 others(50): Show |
53 | HG00438.hp2 HG00597.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.413-4556dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | |||||||
chr2:36910173 | C | CAA | 7 | a0001c0001t0005g0092 a0001c0001t0007g0270 a0001c0001t0021g0233 others(4): Show |
7 | HG00738.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-4557_413-4556d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | |||||||
chr2:36910173 | CA | C | 10 | a0001c0001t0002g0009 a0001c0001t0006g0209 a0001c0001t0006g0210 others(7): Show |
10 | HG02886.hp1 HG02895.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.413-4556delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | |||||||
chr2:36910173 | CAAAAAAA others(4): Show |
C | 58 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0002g0245 others(55): Show |
58 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.413-4566_413-4556d others(13): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | |||||||
chr2:36910237 | T | G | 1 | a0001c0001t0056g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413-4619A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910237 | |||||||
chr2:36910252 | C | T | 48 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(45): Show |
48 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.413-4634G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910252 | |||||||
chr2:36910497 | T | C | 16 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.413-4879A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910497 | |||||||
chr2:36910705 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.413-5087A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910705 | |||||||
chr2:36910903 | C | A | 181 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(178): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.412+5175G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910903 | |||||||
chr2:36910944 | T | C | 1 | a0001c0001t0048g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.412+5134A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910944 | |||||||
chr2:36911203 | A | G | 3 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0066g0240 |
3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.412+4875T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911203 | |||||||
chr2:36911207 | G | C | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.412+4871C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911207 | |||||||
chr2:36911243 | C | T | 2 | a0001c0001t0004g0080 a0001c0001t0065g0293 |
2 | HG00544.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.412+4835G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911243 | |||||||
chr2:36911322 | C | G | 155 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(152): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.412+4756G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911322 | |||||||
chr2:36911421 | G | A | 5 | a0001c0001t0009g0125 a0001c0001t0009g0139 a0001c0001t0009g0140 others(2): Show |
5 | HG00423.hp2 HG00438.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+4657C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911421 | |||||||
chr2:36911511 | T | C | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412+4567A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911511 | |||||||
chr2:36911554 | A | T | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.412+4524T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911554 | |||||||
chr2:36911690 | T | C | 3 | a0001c0001t0020g0274 a0001c0001t0020g0277 a0001c0001t0040g0203 |
3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+4388A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911690 | |||||||
chr2:36912014 | A | G | 17 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.412+4064T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912014 | |||||||
chr2:36912113 | T | G | 1 | a0001c0001t0002g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.412+3965A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912113 | |||||||
chr2:36912236 | G | A | 1 | a0001c0001t0007g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.412+3842C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912236 | |||||||
chr2:36912253 | C | T | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.412+3825G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912253 | |||||||
chr2:36912260 | G | A | 7 | a0001c0001t0002g0014 a0001c0001t0002g0023 a0001c0001t0002g0051 others(4): Show |
7 | HG00621.hp1 HG00642.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+3818C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912260 | |||||||
chr2:36912273 | T | C | 1 | a0001c0001t0085g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.412+3805A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912273 | |||||||
chr2:36912345 | C | G | 1 | a0001c0001t0019g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+3733G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912345 | |||||||
chr2:36912384 | T | C | 26 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(23): Show |
26 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+3694A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912384 | |||||||
chr2:36912392 | T | A | 55 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(52): Show |
55 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+3686A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912392 | |||||||
chr2:36912403 | T | A | 1 | a0001c0001t0029g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.412+3675A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912403 | |||||||
chr2:36912580 | T | C | 1 | a0001c0001t0039g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.412+3498A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912580 | |||||||
chr2:36912701 | G | T | 1 | a0001c0001t0006g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.412+3377C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912701 | |||||||
chr2:36912704 | T | C | 1 | a0001c0001t0002g0019 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.412+3374A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912704 | |||||||
chr2:36912996 | A | G | 1 | a0001c0001t0067g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.412+3082T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912996 | |||||||
chr2:36913072 | G | A | 1 | a0001c0001t0026g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.412+3006C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913072 | |||||||
chr2:36913228 | T | C | 1 | a0001c0001t0011g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+2850A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913228 | |||||||
chr2:36913449 | T | C | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+2629A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913449 | |||||||
chr2:36913482 | G | A | 1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.412+2596C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913482 | |||||||
chr2:36913557 | G | A | 47 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(44): Show |
47 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.412+2521C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913557 | |||||||
chr2:36913570 | A | C | 187 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(184): Show |
187 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.412+2508T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913570 | |||||||
chr2:36913580 | CA | C | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.412+2497delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913580 | |||||||
chr2:36913693 | A | G | 1 | a0001c0001t0019g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+2385T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913693 | |||||||
chr2:36913942 | C | T | 156 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(153): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.412+2136G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913942 | |||||||
chr2:36913943 | G | A | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.412+2135C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913943 | |||||||
chr2:36914017 | C | A | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.412+2061G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914017 | |||||||
chr2:36914104 | C | T | 1 | a0001c0001t0064g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.412+1974G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914104 | |||||||
chr2:36914156 | A | G | 4 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+1922T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914156 | |||||||
chr2:36914193 | A | G | 185 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(182): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.412+1885T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914193 | |||||||
chr2:36914269 | T | C | 3 | a0001c0001t0020g0274 a0001c0001t0020g0277 a0001c0001t0040g0203 |
3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+1809A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914269 | |||||||
chr2:36914352 | C | T | 185 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(182): Show |
185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.412+1726G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914352 | |||||||
chr2:36914426 | A | G | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1652T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914426 | |||||||
chr2:36914904 | A | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.412+1174T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914904 | |||||||
chr2:36914966 | G | C | 2 | a0001c0001t0005g0090 a0001c0001t0005g0091 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.412+1112C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914966 | |||||||
chr2:36914967 | G | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.412+1111C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914967 | |||||||
chr2:36915135 | T | C | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+943A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915135 | |||||||
chr2:36915172 | G | A | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+906C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915172 | |||||||
chr2:36915228 | CATAAAT | C | 3 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 |
3 | HG02572.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.412+844_412+849del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915228 | |||||||
chr2:36915232 | A | AAT | 26 | a0001c0001t0001g0106 a0001c0001t0001g0124 a0001c0001t0001g0130 others(23): Show |
26 | HG00621.hp2 HG01070.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+844_412+845dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATAT | 15 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0164 others(12): Show |
15 | HG00438.hp1 HG00673.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+842_412+845dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATAT | 18 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0145 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+840_412+845dup others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(1): Show |
15 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(12): Show |
15 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+838_412+845dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(3): Show |
18 | a0001c0001t0001g0077 a0001c0001t0001g0129 a0001c0001t0001g0158 others(15): Show |
18 | HG00099.hp1 HG01993.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+836_412+845dup others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(5): Show |
15 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0002g0023 others(12): Show |
15 | HG00621.hp1 HG00642.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+834_412+845dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(7): Show |
13 | a0001c0001t0001g0123 a0001c0001t0001g0160 a0001c0001t0002g0014 others(10): Show |
13 | HG01993.hp2 HG02055.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+832_412+845dup others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(9): Show |
3 | a0001c0001t0001g0003 a0001c0001t0002g0113 a0001c0001t0004g0081 |
3 | HG00408.hp1 NA18955.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.412+830_412+845dup others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(11): Show |
1 | a0001c0001t0008g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.412+828_412+845dup others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(15): Show |
1 | a0001c0001t0002g0024 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.412+824_412+845dup others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | A | AATATATA others(19): Show |
1 | a0001c0001t0004g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.412+820_412+845dup others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AAT | A | 9 | a0001c0001t0001g0141 a0001c0001t0001g0178 a0001c0001t0003g0239 others(6): Show |
9 | HG00544.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+844_412+845del others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATAT | A | 7 | a0001c0001t0003g0069 a0001c0001t0003g0249 a0001c0001t0003g0258 others(4): Show |
7 | HG01256.hp2 HG02602.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+842_412+845del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATAT | A | 11 | a0001c0001t0003g0072 a0001c0001t0003g0251 a0001c0001t0003g0260 others(8): Show |
11 | HG00639.hp2 HG01433.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+840_412+845del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(1): Show |
A | 34 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0002g0245 others(31): Show |
34 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.412+838_412+845del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(3): Show |
A | 1 | a0001c0001t0013g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412+836_412+845del others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(5): Show |
A | 5 | a0001c0001t0001g0180 a0001c0001t0004g0199 a0001c0001t0013g0198 others(2): Show |
5 | HG01517.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+834_412+845del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(9): Show |
A | 14 | a0001c0001t0005g0090 a0001c0001t0007g0269 a0001c0001t0007g0270 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+830_412+845del others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(11): Show |
A | 33 | a0001c0001t0005g0091 a0001c0001t0005g0092 a0001c0001t0005g0093 others(30): Show |
33 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.412+828_412+845del others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915232 | AATATATA others(19): Show |
A | 18 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(15): Show |
18 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+820_412+845del others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | |||||||
chr2:36915259 | A | ATATATAT others(16): Show |
1 | a0001c0001t0087g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.412+818_412+819ins others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915259 | |||||||
chr2:36915274 | A | T | 1 | a0004c0004t0002g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.412+804T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915274 | |||||||
chr2:36915334 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+744C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915334 | |||||||
chr2:36915399 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+679A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915399 | |||||||
chr2:36915460 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.412+618A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915460 | |||||||
chr2:36915526 | A | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+552T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915526 | |||||||
chr2:36915583 | C | A | 1 | a0001c0001t0029g0015 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.412+495G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915583 | |||||||
chr2:36915611 | A | G | 40 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(37): Show |
40 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.412+467T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915611 | |||||||
chr2:36915661 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0174 |
2 | HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.412+417C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915661 | |||||||
chr2:36915683 | G | A | 1 | a0001c0001t0072g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.412+395C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915683 | |||||||
chr2:36915765 | T | C | 2 | a0001c0001t0019g0206 a0001c0001t0042g0205 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.412+313A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915765 | |||||||
chr2:36915786 | C | G | 1 | a0001c0001t0082g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.412+292G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915786 | |||||||
chr2:36915946 | A | G | 4 | a0001c0001t0002g0024 a0001c0001t0002g0037 a0001c0001t0002g0038 others(1): Show |
4 | NA18940.hp1 NA18985.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+132T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915946 | |||||||
chr2:36915997 | A | G | 52 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(49): Show |
52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.412+81T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915997 | |||||||
chr2:36916005 | T | C | 1 | a0001c0001t0006g0221 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+73A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36916005 | |||||||
chr2:36916230 | T | C | 1 | a0001c0001t0002g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.339-79A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916230 | |||||||
chr2:36916412 | A | C | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.339-261T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916412 | |||||||
chr2:36916496 | TA | T | 6 | a0001c0001t0003g0247 a0001c0001t0016g0279 a0001c0001t0016g0280 others(3): Show |
6 | HG02040.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.339-346delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916496 | |||||||
chr2:36916554 | A | T | 1 | a0001c0001t0003g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.339-403T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916554 | |||||||
chr2:36916772 | T | C | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.339-621A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916772 | |||||||
chr2:36916780 | C | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339-629G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916780 | |||||||
chr2:36917044 | T | TA | 6 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(3): Show |
6 | HG02970.hp1 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-894dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917044 | |||||||
chr2:36917051 | AT | A | 29 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(26): Show |
29 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.339-901delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917051 | |||||||
chr2:36917052 | T | A | 162 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(159): Show |
162 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339-901A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917052 | |||||||
chr2:36917053 | A | T | 12 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0218 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.339-902T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917053 | |||||||
chr2:36917056 | A | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.339-905T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917056 | |||||||
chr2:36917069 | T | TA | 12 | a0001c0001t0003g0249 a0001c0001t0006g0209 a0001c0001t0006g0210 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-919dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917069 | |||||||
chr2:36917103 | C | CAAT | 50 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0214 others(47): Show |
50 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-955_339-953dup others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917103 | |||||||
chr2:36917162 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.339-1011A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917162 | |||||||
chr2:36917173 | T | C | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-1022A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917173 | |||||||
chr2:36917195 | T | C | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1044A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917195 | |||||||
chr2:36917213 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339-1062C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917213 | |||||||
chr2:36917213 | G | GT | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-1063dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917213 | |||||||
chr2:36917249 | C | A | 52 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(49): Show |
52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.339-1098G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917249 | |||||||
chr2:36917390 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.339-1239C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917390 | |||||||
chr2:36917471 | C | T | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-1320G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917471 | |||||||
chr2:36917529 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0003g0040 a0001c0001t0014g0135 |
2 | HG00741.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.339-1394_339-1379d others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917529 | |||||||
chr2:36917532 | A | T | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.339-1381T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917532 | |||||||
chr2:36917538 | G | GA | 47 | a0001c0001t0001g0163 a0001c0001t0003g0096 a0001c0001t0005g0090 others(44): Show |
47 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.339-1388dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917538 | |||||||
chr2:36917656 | C | T | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1505G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917656 | |||||||
chr2:36917830 | GA | G | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1680delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917830 | |||||||
chr2:36917903 | T | C | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.339-1752A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917903 | |||||||
chr2:36917950 | C | T | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1799G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917950 | |||||||
chr2:36917964 | T | C | 3 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0066 |
3 | NA18985.hp2 NA19054.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.339-1813A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917964 | |||||||
chr2:36918083 | T | C | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1932A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918083 | |||||||
chr2:36918213 | A | G | 1 | a0001c0001t0078g0006 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.339-2062T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918213 | |||||||
chr2:36918249 | C | T | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.339-2098G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918249 | |||||||
chr2:36918609 | T | C | 5 | a0001c0001t0001g0144 a0001c0001t0003g0043 a0001c0001t0003g0067 others(2): Show |
5 | HG00323.hp2 HG01168.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-2458A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918609 | |||||||
chr2:36918810 | C | T | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-2659G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918810 | |||||||
chr2:36918931 | G | C | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-2780C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918931 | |||||||
chr2:36918981 | A | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339-2830T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918981 | |||||||
chr2:36919197 | T | C | 1 | a0001c0001t0003g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.339-3046A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919197 | |||||||
chr2:36919231 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.339-3080G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919231 | |||||||
chr2:36919279 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0185 others(2): Show |
5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-3128A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919279 | |||||||
chr2:36919549 | G | A | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-3398C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919549 | |||||||
chr2:36919562 | A | C | 1 | a0001c0001t0067g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.339-3411T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919562 | |||||||
chr2:36919621 | A | G | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-3470T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919621 | |||||||
chr2:36919634 | C | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.339-3483G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919634 | |||||||
chr2:36919681 | C | T | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.339-3530G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919681 | |||||||
chr2:36919878 | T | C | 1 | a0001c0001t0005g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.339-3727A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919878 | |||||||
chr2:36920065 | T | C | 1 | a0001c0001t0063g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.339-3914A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920065 | |||||||
chr2:36920085 | GAATT | G | 171 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(168): Show |
171 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.339-3938_339-3935d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920085 | |||||||
chr2:36920179 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.339-4028C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920179 | |||||||
chr2:36920426 | G | A | 1 | a0001c0001t0017g0227 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.339-4275C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920426 | |||||||
chr2:36920437 | G | A | 1 | a0001c0005t0006g0230 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339-4286C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920437 | |||||||
chr2:36920492 | G | C | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.339-4341C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920492 | |||||||
chr2:36920638 | C | CA | 9 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0002g0094 others(6): Show |
9 | HG00099.hp1 HG01255.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.338+4466dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920638 | |||||||
chr2:36920776 | T | TA | 5 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0228 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+4328dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920776 | |||||||
chr2:36920829 | C | T | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.338+4276G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920829 | |||||||
chr2:36920832 | T | G | 181 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(178): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.338+4273A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920832 | |||||||
chr2:36920947 | C | T | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+4158G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920947 | |||||||
chr2:36920973 | A | G | 1 | a0001c0001t0080g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.338+4132T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920973 | |||||||
chr2:36921087 | T | A | 119 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0129 others(116): Show |
119 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.338+4018A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921087 | |||||||
chr2:36921090 | T | A | 3 | a0001c0001t0003g0250 a0001c0001t0003g0258 a0001c0001t0066g0240 |
3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.338+4015A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921090 | |||||||
chr2:36921122 | T | C | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.338+3983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921122 | |||||||
chr2:36921398 | CCTT | C | 12 | a0001c0001t0002g0059 a0001c0001t0002g0087 a0001c0001t0004g0078 others(9): Show |
12 | HG00423.hp1 HG00544.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.338+3704_338+3706d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921398 | |||||||
chr2:36921503 | G | A | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+3602C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921503 | |||||||
chr2:36921712 | G | GTC | 186 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(183): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.338+3391_338+3392d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921712 | |||||||
chr2:36921760 | C | T | 1 | a0001c0001t0002g0019 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.338+3345G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921760 | |||||||
chr2:36921865 | A | T | 17 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.338+3240T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921865 | |||||||
chr2:36922073 | G | C | 1 | a0001c0001t0038g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.338+3032C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922073 | |||||||
chr2:36922175 | T | C | 1 | a0001c0001t0054g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.338+2930A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922175 | |||||||
chr2:36922355 | T | C | 188 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(185): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.338+2750A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922355 | |||||||
chr2:36922389 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.338+2716A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922389 | |||||||
chr2:36922458 | G | A | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+2647C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922458 | |||||||
chr2:36922482 | G | A | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+2623C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922482 | |||||||
chr2:36922518 | C | CA | 11 | a0001c0001t0001g0145 a0001c0001t0002g0054 a0001c0001t0004g0079 others(8): Show |
11 | HG00099.hp1 HG02109.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+2586dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922518 | |||||||
chr2:36922518 | CA | C | 97 | a0001c0001t0001g0047 a0001c0001t0001g0183 a0001c0001t0001g0188 others(94): Show |
97 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.338+2586delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922518 | |||||||
chr2:36922540 | A | AT | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0223 others(1): Show |
4 | HG01071.hp2 HG01123.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+2564_338+2565i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922540 | |||||||
chr2:36922540 | A | T | 1 | a0001c0001t0006g0222 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.338+2565T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922540 | |||||||
chr2:36922567 | A | G | 17 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.338+2538T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922567 | |||||||
chr2:36922621 | C | T | 1 | a0001c0001t0007g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.338+2484G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922621 | |||||||
chr2:36922630 | C | T | 5 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+2475G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922630 | |||||||
chr2:36922639 | GTCA | G | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+2463_338+2465d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922639 | |||||||
chr2:36922668 | A | G | 1 | a0001c0001t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.338+2437T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922668 | |||||||
chr2:36922816 | T | TA | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+2288dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922816 | |||||||
chr2:36922926 | G | A | 2 | a0001c0001t0015g0237 a0002c0002t0043g0219 |
2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.338+2179C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922926 | |||||||
chr2:36922998 | T | A | 1 | a0001c0001t0040g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.338+2107A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922998 | |||||||
chr2:36923013 | G | A | 1 | a0001c0001t0008g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.338+2092C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923013 | |||||||
chr2:36923072 | G | T | 32 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(29): Show |
32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.338+2033C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923072 | |||||||
chr2:36923140 | G | GA | 18 | a0001c0001t0002g0195 a0001c0001t0005g0090 a0001c0001t0005g0091 others(15): Show |
18 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.338+1964dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923140 | |||||||
chr2:36923162 | A | C | 1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.338+1943T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923162 | |||||||
chr2:36923207 | T | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+1898A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923207 | |||||||
chr2:36923280 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.338+1825G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923280 | |||||||
chr2:36923344 | G | A | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+1761C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923344 | |||||||
chr2:36923388 | T | C | 136 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(133): Show |
136 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.338+1717A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923388 | |||||||
chr2:36923399 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.338+1706G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923399 | |||||||
chr2:36923445 | C | CA | 38 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0001g0145 others(35): Show |
38 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.338+1659dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923445 | |||||||
chr2:36923445 | C | CAA | 10 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0212 others(7): Show |
10 | HG01071.hp2 HG01123.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.338+1658_338+1659d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923445 | |||||||
chr2:36923465 | C | A | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+1640G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923465 | |||||||
chr2:36923507 | T | TCTTTCCA others(24): Show |
1 | a0001c0001t0053g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.338+1567_338+1597d others(33): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923507 | |||||||
chr2:36923593 | T | A | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+1512A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923593 | |||||||
chr2:36923650 | A | G | 135 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(132): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.338+1455T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923650 | |||||||
chr2:36923895 | A | G | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.338+1210T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923895 | |||||||
chr2:36924026 | T | C | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+1079A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924026 | |||||||
chr2:36924061 | A | C | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+1044T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924061 | |||||||
chr2:36924104 | C | A | 2 | a0001c0001t0028g0246 a0001c0001t0071g0241 |
2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.338+1001G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924104 | |||||||
chr2:36924133 | G | C | 12 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0121 others(9): Show |
12 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+972C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924133 | |||||||
chr2:36924355 | C | CA | 33 | a0001c0001t0003g0042 a0001c0001t0006g0209 a0001c0001t0006g0210 others(30): Show |
33 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.338+749dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924355 | |||||||
chr2:36924355 | C | CAA | 150 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0009 others(147): Show |
150 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.338+748_338+749dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924355 | |||||||
chr2:36924535 | G | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+570C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924535 | |||||||
chr2:36924545 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0172 |
2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.338+560A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924545 | |||||||
chr2:36924652 | A | G | 1 | a0001c0001t0009g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.338+453T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924652 | |||||||
chr2:36924683 | C | T | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.338+422G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924683 | |||||||
chr2:36924796 | C | A | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.338+309G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924796 | |||||||
chr2:36924862 | G | C | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+243C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924862 | |||||||
chr2:36924876 | G | T | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+229C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924876 | |||||||
chr2:36924946 | C | T | 1 | a0001c0001t0030g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.338+159G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924946 | |||||||
chr2:36924995 | G | A | 75 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.338+110C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924995 | |||||||
chr2:36925018 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.338+87A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36925018 | |||||||
chr2:36925028 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+77G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36925028 | |||||||
chr2:36925229 | A | C | 52 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(49): Show |
52 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.235-21T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925229 | |||||||
chr2:36925282 | T | C | 52 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(49): Show |
52 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.235-74A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925282 | |||||||
chr2:36925309 | A | C | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-101T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925309 | |||||||
chr2:36925434 | A | G | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-226T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925434 | |||||||
chr2:36925756 | G | C | 132 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(129): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.235-548C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925756 | |||||||
chr2:36925824 | A | C | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-616T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925824 | |||||||
chr2:36925977 | T | G | 1 | a0001c0001t0053g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.235-769A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925977 | |||||||
chr2:36926106 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235-898G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926106 | |||||||
chr2:36926389 | C | T | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-1181G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926389 | |||||||
chr2:36926583 | T | C | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-1375A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926583 | |||||||
chr2:36926753 | G | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-1545C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926753 | |||||||
chr2:36926772 | A | G | 16 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-1564T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926772 | |||||||
chr2:36926986 | T | C | 1 | a0001c0001t0071g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235-1778A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926986 | |||||||
chr2:36927026 | A | T | 5 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-1818T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927026 | |||||||
chr2:36927041 | T | G | 1 | a0001c0001t0005g0092 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235-1833A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927041 | |||||||
chr2:36927080 | C | T | 2 | a0001c0001t0001g0176 a0003c0007t0001g0168 |
2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.235-1872G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927080 | |||||||
chr2:36927282 | T | A | 207 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0129 others(204): Show |
207 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.235-2074A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927282 | |||||||
chr2:36927315 | CTGTGCAA | C | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-2114_235-2108d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927315 | |||||||
chr2:36927325 | T | C | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-2117A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927325 | |||||||
chr2:36927381 | T | C | 11 | a0001c0001t0001g0119 a0001c0001t0001g0137 a0001c0001t0001g0144 others(8): Show |
11 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.235-2173A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927381 | |||||||
chr2:36927476 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.235-2268A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927476 | |||||||
chr2:36927524 | A | AG | 51 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0101 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.235-2317dupC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | |||||||
chr2:36927524 | A | AGG | 40 | a0001c0001t0001g0103 a0001c0001t0001g0118 a0001c0001t0001g0145 others(37): Show |
40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.235-2318_235-2317d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | |||||||
chr2:36927524 | A | AGGG | 28 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0014 others(25): Show |
28 | HG00621.hp1 HG00642.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.235-2319_235-2317d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | |||||||
chr2:36927524 | AG | A | 46 | a0001c0001t0001g0129 a0001c0001t0001g0158 a0001c0001t0001g0174 others(43): Show |
46 | HG00323.hp2 HG00597.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.235-2317delC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | |||||||
chr2:36927524 | AGG | A | 17 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-2318_235-2317d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | |||||||
chr2:36927526 | G | T | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.235-2318C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927526 | |||||||
chr2:36927528 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.235-2320C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927528 | |||||||
chr2:36927536 | G | T | 9 | a0001c0001t0005g0215 a0001c0001t0005g0225 a0001c0001t0012g0282 others(6): Show |
9 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-2328C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927536 | |||||||
chr2:36927597 | G | A | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2389C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927597 | |||||||
chr2:36927723 | A | G | 3 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0086g0055 |
3 | HG00099.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.235-2515T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927723 | |||||||
chr2:36927838 | T | C | 4 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
4 | HG01433.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2630A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927838 | |||||||
chr2:36927870 | T | C | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-2662A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927870 | |||||||
chr2:36927875 | T | C | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-2667A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927875 | |||||||
chr2:36927911 | G | T | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-2703C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927911 | |||||||
chr2:36927920 | G | A | 1 | a0001c0001t0019g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-2712C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927920 | |||||||
chr2:36928097 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.235-2889A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928097 | |||||||
chr2:36928097 | T | G | 1 | a0001c0001t0003g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.235-2889A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928097 | |||||||
chr2:36928106 | G | C | 116 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-2898C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928106 | |||||||
chr2:36928133 | T | TA | 7 | a0001c0001t0002g0024 a0001c0001t0003g0096 a0001c0001t0003g0097 others(4): Show |
7 | HG02056.hp1 HG02071.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-2926dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928133 | |||||||
chr2:36928172 | G | A | 32 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(29): Show |
32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-2964C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928172 | |||||||
chr2:36928227 | A | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3019T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928227 | |||||||
chr2:36928228 | G | C | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3020C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928228 | |||||||
chr2:36928274 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0185 others(2): Show |
5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-3066A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928274 | |||||||
chr2:36928310 | A | C | 1 | a0001c0001t0003g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-3102T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928310 | |||||||
chr2:36928685 | C | T | 3 | a0001c0001t0020g0274 a0001c0001t0020g0277 a0001c0001t0040g0203 |
3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3477G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928685 | |||||||
chr2:36928745 | C | T | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-3537G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928745 | |||||||
chr2:36928805 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.235-3597G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928805 | |||||||
chr2:36928806 | G | A | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-3598C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928806 | |||||||
chr2:36928831 | C | T | 1 | a0001c0001t0064g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.235-3623G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928831 | |||||||
chr2:36928856 | C | G | 32 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(29): Show |
32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-3648G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928856 | |||||||
chr2:36928931 | G | C | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-3723C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928931 | |||||||
chr2:36928947 | C | CA | 19 | a0001c0001t0002g0028 a0001c0001t0002g0033 a0001c0001t0002g0066 others(16): Show |
19 | HG00673.hp2 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.235-3740dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928947 | |||||||
chr2:36928947 | CA | C | 35 | a0001c0001t0003g0249 a0001c0001t0005g0090 a0001c0001t0005g0091 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-3740delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928947 | |||||||
chr2:36929048 | C | T | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-3840G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929048 | |||||||
chr2:36929074 | A | G | 1 | a0001c0001t0059g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-3866T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929074 | |||||||
chr2:36929095 | T | A | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-3887A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929095 | |||||||
chr2:36929118 | G | A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.235-3910C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929118 | |||||||
chr2:36929183 | T | C | 1 | a0001c0001t0086g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.235-3975A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929183 | |||||||
chr2:36929415 | G | A | 1 | a0001c0001t0032g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.235-4207C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929415 | |||||||
chr2:36929477 | A | T | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-4269T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929477 | |||||||
chr2:36929483 | G | C | 1 | a0001c0001t0003g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.235-4275C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929483 | |||||||
chr2:36929506 | T | G | 1 | a0002c0002t0043g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235-4298A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929506 | |||||||
chr2:36929738 | C | A | 1 | a0001c0001t0003g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235-4530G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929738 | |||||||
chr2:36929790 | T | C | 22 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(19): Show |
22 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.235-4582A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929790 | |||||||
chr2:36929824 | C | T | 2 | a0001c0001t0015g0283 a0001c0001t0015g0284 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-4616G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929824 | |||||||
chr2:36930000 | T | A | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-4792A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930000 | |||||||
chr2:36930251 | A | G | 1 | a0001c0001t0073g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.235-5043T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930251 | |||||||
chr2:36930431 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.235-5223G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930431 | |||||||
chr2:36930529 | C | A | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.235-5321G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930529 | |||||||
chr2:36930787 | C | T | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-5579G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930787 | |||||||
chr2:36930979 | G | C | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-5771C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930979 | |||||||
chr2:36930984 | G | C | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-5776C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930984 | |||||||
chr2:36931011 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-5803A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931011 | |||||||
chr2:36931024 | T | C | 115 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(112): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.235-5816A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931024 | |||||||
chr2:36931030 | C | CA | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-5823dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931030 | |||||||
chr2:36931200 | C | T | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-5992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931200 | |||||||
chr2:36931241 | G | T | 161 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(158): Show |
161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.235-6033C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931241 | |||||||
chr2:36931450 | A | G | 1 | a0001c0001t0072g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.235-6242T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931450 | |||||||
chr2:36931599 | G | C | 1 | a0001c0001t0010g0242 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.235-6391C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931599 | |||||||
chr2:36931673 | A | G | 1 | a0001c0001t0053g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.235-6465T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931673 | |||||||
chr2:36931851 | C | T | 4 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 others(1): Show |
4 | HG02071.hp2 HG02965.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-6643G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931851 | |||||||
chr2:36931873 | G | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-6665C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931873 | |||||||
chr2:36932097 | T | A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.235-6889A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932097 | |||||||
chr2:36932165 | C | A | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-6957G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932165 | |||||||
chr2:36932175 | G | T | 2 | a0001c0001t0002g0245 a0001c0001t0003g0247 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.235-6967C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932175 | |||||||
chr2:36932232 | G | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-7024C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932232 | |||||||
chr2:36932241 | A | G | 35 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-7033T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932241 | |||||||
chr2:36932247 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235-7039G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932247 | |||||||
chr2:36932647 | G | A | 1 | a0001c0001t0038g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-7439C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932647 | |||||||
chr2:36932651 | G | C | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-7443C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932651 | |||||||
chr2:36932656 | A | G | 201 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(198): Show |
201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.235-7448T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932656 | |||||||
chr2:36932913 | T | C | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-7705A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932913 | |||||||
chr2:36933045 | AT | A | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-7838delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933045 | |||||||
chr2:36933054 | T | A | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-7846A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933054 | |||||||
chr2:36933059 | T | TAC | 95 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0200 others(92): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.235-7853_235-7852d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | |||||||
chr2:36933059 | T | TACAC | 44 | a0001c0001t0001g0047 a0001c0001t0002g0009 a0001c0001t0002g0014 others(41): Show |
44 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.235-7855_235-7852d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | |||||||
chr2:36933059 | TAC | T | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-7853_235-7852d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | |||||||
chr2:36933085 | CAT | C | 15 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(12): Show |
15 | HG00597.hp2 HG01884.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.235-7879_235-7878d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933085 | |||||||
chr2:36933087 | T | C | 7 | a0001c0001t0005g0214 a0001c0001t0017g0226 a0001c0001t0019g0206 others(4): Show |
7 | HG00438.hp2 HG02040.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-7879A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933087 | |||||||
chr2:36933185 | T | A | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-7977A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933185 | |||||||
chr2:36933191 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.235-7983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933191 | |||||||
chr2:36933378 | C | A | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-8170G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933378 | |||||||
chr2:36933630 | G | T | 1 | a0001c0001t0002g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.235-8422C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933630 | |||||||
chr2:36933657 | T | A | 75 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(72): Show |
75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.235-8449A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933657 | |||||||
chr2:36933883 | G | A | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-8675C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933883 | |||||||
chr2:36933927 | C | G | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-8719G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933927 | |||||||
chr2:36934025 | C | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-8817G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934025 | |||||||
chr2:36934111 | A | G | 6 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(3): Show |
6 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-8903T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934111 | |||||||
chr2:36934343 | T | C | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-9135A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934343 | |||||||
chr2:36934408 | T | G | 6 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-9200A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934408 | |||||||
chr2:36934480 | A | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-9272T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934480 | |||||||
chr2:36934480 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.235-9272T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934480 | |||||||
chr2:36934567 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-9359C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934567 | |||||||
chr2:36934570 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.235-9362A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934570 | |||||||
chr2:36934661 | T | G | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-9453A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934661 | |||||||
chr2:36934695 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.235-9487C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934695 | |||||||
chr2:36934708 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.235-9500G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934708 | |||||||
chr2:36934789 | C | T | 1 | a0001c0001t0009g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.235-9581G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934789 | |||||||
chr2:36934805 | G | A | 5 | a0001c0001t0012g0285 a0001c0001t0012g0286 a0001c0001t0016g0279 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-9597C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934805 | |||||||
chr2:36935149 | C | T | 1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235-9941G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935149 | |||||||
chr2:36935186 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.235-9978G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935186 | |||||||
chr2:36935289 | G | C | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-10081C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935289 | |||||||
chr2:36935463 | AT | A | 3 | a0001c0001t0020g0274 a0001c0001t0020g0277 a0001c0001t0040g0203 |
3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-10256delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935463 | |||||||
chr2:36935558 | A | C | 22 | a0001c0001t0001g0047 a0001c0001t0001g0118 a0001c0001t0002g0073 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.235-10350T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935558 | |||||||
chr2:36935752 | C | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-10544G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935752 | |||||||
chr2:36935820 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.235-10612C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935820 | |||||||
chr2:36935832 | T | C | 25 | a0001c0001t0002g0245 a0001c0001t0003g0096 a0001c0001t0003g0097 others(22): Show |
25 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.235-10624A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935832 | |||||||
chr2:36935948 | T | G | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-10740A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935948 | |||||||
chr2:36936233 | C | T | 34 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(31): Show |
34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.235-11025G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936233 | |||||||
chr2:36936244 | T | C | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-11036A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936244 | |||||||
chr2:36936272 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.235-11064C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936272 | |||||||
chr2:36936405 | A | T | 1 | a0001c0001t0015g0284 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-11197T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936405 | |||||||
chr2:36936446 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0149 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.235-11238C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936446 | |||||||
chr2:36936524 | T | C | 1 | a0001c0001t0067g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.235-11316A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936524 | |||||||
chr2:36936553 | G | T | 16 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.235-11345C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936553 | |||||||
chr2:36936634 | A | G | 2 | a0001c0001t0031g0013 a0001c0001t0031g0031 |
2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.235-11426T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936634 | |||||||
chr2:36936724 | G | A | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-11516C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936724 | |||||||
chr2:36936901 | T | G | 13 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0163 others(10): Show |
13 | HG01071.hp1 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-11693A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936901 | |||||||
chr2:36937040 | G | A | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-11832C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937040 | |||||||
chr2:36937041 | C | A | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-11833G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937041 | |||||||
chr2:36937100 | T | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-11892A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937100 | |||||||
chr2:36937144 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-11936C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937144 | |||||||
chr2:36937153 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-11945C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937153 | |||||||
chr2:36937342 | CA | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.235-12135delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937342 | |||||||
chr2:36937344 | A | G | 1 | a0001c0001t0036g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-12136T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937344 | |||||||
chr2:36937357 | AAG | A | 30 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(27): Show |
30 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.235-12151_235-1215 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937357 | |||||||
chr2:36937526 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0003g0095 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.235-12318C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937526 | |||||||
chr2:36937600 | T | G | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-12392A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937600 | |||||||
chr2:36937697 | A | G | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-12489T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937697 | |||||||
chr2:36937714 | T | G | 157 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(154): Show |
157 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.235-12506A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937714 | |||||||
chr2:36937768 | C | G | 151 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(148): Show |
151 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.235-12560G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937768 | |||||||
chr2:36937825 | C | T | 12 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-12617G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937825 | |||||||
chr2:36938276 | A | C | 17 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-13068T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938276 | |||||||
chr2:36938370 | G | T | 1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-13162C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938370 | |||||||
chr2:36938429 | T | TA | 9 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-13222dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938429 | |||||||
chr2:36938429 | TA | T | 9 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0003g0067 others(6): Show |
9 | HG01516.hp1 HG02015.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-13222delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938429 | |||||||
chr2:36938440 | A | G | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-13232T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938440 | |||||||
chr2:36938622 | C | T | 34 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(31): Show |
34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.235-13414G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938622 | |||||||
chr2:36938652 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.235-13444A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938652 | |||||||
chr2:36938703 | A | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-13495T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938703 | |||||||
chr2:36938828 | T | C | 2 | a0001c0001t0006g0222 a0001c0001t0006g0223 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.235-13620A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938828 | |||||||
chr2:36938981 | T | A | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-13773A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938981 | |||||||
chr2:36939152 | C | T | 1 | a0001c0001t0007g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.235-13944G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939152 | |||||||
chr2:36939178 | G | A | 19 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(16): Show |
19 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.235-13970C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939178 | |||||||
chr2:36939218 | G | A | 3 | a0001c0001t0005g0215 a0001c0001t0005g0225 a0001c0001t0011g0147 |
3 | HG00323.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235-14010C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939218 | |||||||
chr2:36939223 | G | A | 1 | a0001c0001t0003g0239 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.235-14015C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939223 | |||||||
chr2:36939262 | G | A | 14 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-14054C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939262 | |||||||
chr2:36939270 | G | A | 1 | a0001c0001t0007g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235-14062C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939270 | |||||||
chr2:36939289 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.235-14081C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939289 | |||||||
chr2:36939332 | C | A | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-14124G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939332 | |||||||
chr2:36939377 | C | T | 1 | a0001c0001t0019g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-14169G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939377 | |||||||
chr2:36939445 | T | C | 1 | a0001c0001t0003g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-14237A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939445 | |||||||
chr2:36939543 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235-14335A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939543 | |||||||
chr2:36939560 | T | A | 1 | a0001c0001t0052g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235-14352A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939560 | |||||||
chr2:36939774 | G | C | 3 | a0001c0001t0002g0073 a0001c0001t0003g0046 a0001c0001t0003g0070 |
3 | HG00642.hp1 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.235-14566C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939774 | |||||||
chr2:36939846 | A | G | 33 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(30): Show |
33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-14638T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939846 | |||||||
chr2:36940048 | T | C | 116 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-14840A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940048 | |||||||
chr2:36940120 | G | A | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-14912C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940120 | |||||||
chr2:36940208 | A | G | 7 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0143 others(4): Show |
7 | HG00621.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-15000T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940208 | |||||||
chr2:36940228 | AAAGT | A | 6 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0158 others(3): Show |
6 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-15024_235-1502 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940228 | |||||||
chr2:36940299 | T | C | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-15091A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940299 | |||||||
chr2:36940331 | G | T | 1 | a0001c0001t0078g0006 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.235-15123C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940331 | |||||||
chr2:36940354 | A | G | 33 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(30): Show |
33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-15146T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940354 | |||||||
chr2:36940502 | C | A | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-15294G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940502 | |||||||
chr2:36940603 | G | A | 19 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(16): Show |
19 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.235-15395C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940603 | |||||||
chr2:36940805 | G | C | 29 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(26): Show |
29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.235-15597C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940805 | |||||||
chr2:36940823 | C | G | 1 | a0001c0001t0039g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-15615G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940823 | |||||||
chr2:36940836 | C | CA | 57 | a0001c0001t0001g0106 a0001c0001t0001g0123 a0001c0001t0001g0126 others(54): Show |
57 | HG00099.hp1 HG00621.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.235-15629dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | |||||||
chr2:36940836 | CA | C | 8 | a0001c0001t0001g0120 a0001c0001t0002g0025 a0001c0001t0003g0267 others(5): Show |
8 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-15629delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | |||||||
chr2:36940836 | CAAAAAAA others(4): Show |
C | 33 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(30): Show |
33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-15639_235-1562 others(15): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | |||||||
chr2:36941098 | T | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235-15890A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941098 | |||||||
chr2:36941120 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.235-15912G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941120 | |||||||
chr2:36941321 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235-16113A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941321 | |||||||
chr2:36941581 | T | G | 1 | a0001c0001t0013g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235-16373A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941581 | |||||||
chr2:36941716 | A | AT | 6 | a0001c0001t0002g0066 a0001c0001t0003g0095 a0001c0001t0032g0001 others(3): Show |
6 | HG00621.hp2 HG02602.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-16509dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941716 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0019g0207 a0001c0001t0042g0205 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.235-16520_235-1650 others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941716 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-16521_235-1650 others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941716 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0006g0212 a0001c0001t0040g0203 a0001c0005t0006g0230 |
3 | HG02886.hp1 HG03579.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.235-16522_235-1650 others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941716 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0041g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-16523_235-1650 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941716 | ATTTT | A | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-16512_235-1650 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | |||||||
chr2:36941804 | C | T | 1 | a0001c0001t0087g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.235-16596G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941804 | |||||||
chr2:36941906 | G | A | 184 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(181): Show |
184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.235-16698C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941906 | |||||||
chr2:36942003 | T | C | 1 | a0001c0001t0005g0093 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.235-16795A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942003 | |||||||
chr2:36942325 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235-17117A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942325 | |||||||
chr2:36942328 | T | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-17120A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942328 | |||||||
chr2:36942446 | T | C | 1 | a0001c0001t0040g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-17238A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942446 | |||||||
chr2:36942593 | T | C | 1 | a0001c0001t0019g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.235-17385A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942593 | |||||||
chr2:36942600 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.235-17392A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942600 | |||||||
chr2:36942629 | T | C | 5 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0228 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-17421A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942629 | |||||||
chr2:36942826 | G | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235-17618C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942826 | |||||||
chr2:36942898 | G | GT | 118 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.235-17691dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942898 | |||||||
chr2:36942915 | C | T | 2 | a0001c0001t0026g0155 a0001c0001t0026g0159 |
2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.235-17707G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942915 | |||||||
chr2:36943262 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.235-18054C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943262 | |||||||
chr2:36943386 | CTA | C | 17 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-18180_235-1817 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943386 | |||||||
chr2:36943457 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-18249T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943457 | |||||||
chr2:36943533 | A | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-18325T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943533 | |||||||
chr2:36943557 | C | G | 1 | a0002c0002t0005g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-18349G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943557 | |||||||
chr2:36943579 | A | C | 17 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-18371T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943579 | |||||||
chr2:36943595 | G | C | 6 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-18387C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943595 | |||||||
chr2:36944038 | T | G | 1 | a0001c0001t0064g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.235-18830A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944038 | |||||||
chr2:36944088 | C | A | 2 | a0001c0001t0005g0092 a0001c0001t0005g0093 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.235-18880G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944088 | |||||||
chr2:36944124 | AAAAC | A | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-18920_235-1891 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944124 | |||||||
chr2:36944154 | A | G | 1 | a0001c0001t0060g0133 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.235-18946T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944154 | |||||||
chr2:36944165 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235-18957G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944165 | |||||||
chr2:36944244 | G | A | 1 | a0001c0001t0007g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.235-19036C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944244 | |||||||
chr2:36944254 | C | T | 3 | a0001c0001t0021g0233 a0001c0001t0047g0235 a0001c0001t0048g0234 |
3 | HG00738.hp2 HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235-19046G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944254 | |||||||
chr2:36944404 | T | C | 55 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(52): Show |
55 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.235-19196A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944404 | |||||||
chr2:36944495 | C | A | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.235-19287G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944495 | |||||||
chr2:36945147 | T | C | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-19939A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945147 | |||||||
chr2:36945357 | C | T | 7 | a0001c0001t0001g0105 a0001c0001t0001g0132 a0001c0001t0001g0149 others(4): Show |
7 | HG01346.hp2 HG02698.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-20149G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945357 | |||||||
chr2:36945388 | T | C | 149 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(146): Show |
149 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.235-20180A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945388 | |||||||
chr2:36945482 | G | A | 116 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-20274C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945482 | |||||||
chr2:36945549 | C | T | 82 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.235-20341G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945549 | |||||||
chr2:36945602 | T | G | 2 | a0001c0001t0017g0226 a0001c0001t0017g0227 |
2 | HG02040.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.235-20394A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945602 | |||||||
chr2:36945764 | T | C | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.234+20466A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945764 | |||||||
chr2:36945807 | C | T | 1 | a0001c0001t0057g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.234+20423G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945807 | |||||||
chr2:36945889 | T | C | 139 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0009 others(136): Show |
139 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234+20341A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945889 | |||||||
chr2:36946152 | TAAATATT others(64): Show |
T | 5 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0228 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+20007_234+2007 others(75): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36946152 | |||||||
chr2:36946578 | C | T | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+19652G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36946578 | |||||||
chr2:36947160 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+19070A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947160 | |||||||
chr2:36947410 | T | C | 2 | a0001c0001t0004g0082 a0001c0001t0022g0146 |
2 | HG03490.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.234+18820A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947410 | |||||||
chr2:36947540 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.234+18690G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947540 | |||||||
chr2:36947544 | AACATATA others(8): Show |
A | 1 | a0001c0001t0010g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.234+18671_234+1868 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947544 | |||||||
chr2:36947569 | T | TTATA | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+18657_234+1866 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947569 | |||||||
chr2:36947570 | T | A | 18 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(15): Show |
18 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.234+18660A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947570 | |||||||
chr2:36947571 | A | T | 31 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
31 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.234+18659T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947571 | |||||||
chr2:36947658 | A | G | 1 | a0001c0001t0031g0031 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234+18572T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947658 | |||||||
chr2:36947854 | G | T | 1 | a0001c0001t0029g0015 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.234+18376C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947854 | |||||||
chr2:36948040 | T | C | 1 | a0004c0004t0002g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+18190A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948040 | |||||||
chr2:36948081 | C | CT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0103 others(55): Show |
58 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.234+18148dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0101 others(17): Show |
20 | HG00408.hp1 HG01123.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+18147_234+1814 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0007g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.234+18138_234+1814 others(15): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0013g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+18134_234+1814 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0074g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+18131_234+1814 others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0046g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+18130_234+1814 others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+18129_234+1814 others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0016g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+18127_234+1814 others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0045g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+18120_234+1814 others(33): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0016g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234+18115_234+1814 others(38): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0022g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.234+18136_234+1814 others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0016g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234+18134_234+1814 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(10): Show |
C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0023 a0001c0001t0002g0030 others(5): Show |
8 | HG00621.hp1 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+18132_234+1814 others(21): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(11): Show |
C | 124 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(121): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+18131_234+1814 others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(12): Show |
C | 20 | a0001c0001t0002g0026 a0001c0001t0005g0090 a0001c0001t0005g0091 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+18130_234+1814 others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0003g0040 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234+18128_234+1814 others(25): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948081 | CTTTTTTT others(15): Show |
C | 15 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0042 others(12): Show |
15 | HG00323.hp2 HG00642.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+18127_234+1814 others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | |||||||
chr2:36948119 | T | G | 1 | a0001c0001t0077g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234+18111A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948119 | |||||||
chr2:36948167 | T | G | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+18063A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948167 | |||||||
chr2:36948280 | T | G | 12 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.234+17950A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948280 | |||||||
chr2:36948301 | T | C | 182 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(179): Show |
182 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.234+17929A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948301 | |||||||
chr2:36948627 | T | C | 4 | a0001c0001t0028g0238 a0001c0001t0028g0246 a0001c0001t0033g0243 others(1): Show |
4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+17603A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948627 | |||||||
chr2:36948648 | T | C | 1 | a0001c0001t0066g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+17582A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948648 | |||||||
chr2:36948689 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+17541A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948689 | |||||||
chr2:36948820 | G | C | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+17410C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948820 | |||||||
chr2:36949067 | T | A | 1 | a0001c0001t0076g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.234+17163A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949067 | |||||||
chr2:36949070 | G | A | 186 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0009 others(183): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.234+17160C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949070 | |||||||
chr2:36949426 | TAAAC | T | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16800_234+1680 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949426 | |||||||
chr2:36949641 | G | A | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16589C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949641 | |||||||
chr2:36949780 | T | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.234+16450A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949780 | |||||||
chr2:36950019 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.234+16211T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950019 | |||||||
chr2:36950031 | A | G | 1 | a0001c0001t0044g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.234+16199T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950031 | |||||||
chr2:36950096 | G | A | 1 | a0001c0001t0030g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+16134C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950096 | |||||||
chr2:36950115 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.234+16115T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950115 | |||||||
chr2:36950212 | T | G | 1 | a0001c0001t0017g0227 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.234+16018A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950212 | |||||||
chr2:36950213 | G | GT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0123 a0001c0001t0001g0126 others(56): Show |
59 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.234+16016dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | |||||||
chr2:36950213 | G | GTT | 54 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(51): Show |
54 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.234+16015_234+1601 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | |||||||
chr2:36950213 | G | GTTT | 20 | a0001c0001t0002g0007 a0001c0001t0002g0030 a0001c0001t0002g0037 others(17): Show |
20 | HG00423.hp1 HG00642.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+16014_234+1601 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | |||||||
chr2:36950213 | G | T | 5 | a0001c0001t0001g0200 a0001c0001t0002g0113 a0001c0001t0016g0279 others(2): Show |
5 | HG02970.hp1 HG02976.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+16017C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | |||||||
chr2:36950213 | GT | G | 21 | a0001c0001t0001g0047 a0001c0001t0001g0077 a0001c0001t0001g0183 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16016delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | |||||||
chr2:36950292 | C | T | 4 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+15938G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950292 | |||||||
chr2:36950418 | G | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0185 others(2): Show |
5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+15812C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950418 | |||||||
chr2:36950589 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+15641A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950589 | |||||||
chr2:36951112 | C | T | 152 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(149): Show |
152 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.234+15118G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951112 | |||||||
chr2:36951168 | A | C | 1 | a0001c0001t0003g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.234+15062T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951168 | |||||||
chr2:36951276 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+14954C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951276 | |||||||
chr2:36951480 | G | C | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+14750C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951480 | |||||||
chr2:36951596 | T | C | 1 | a0001c0001t0011g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.234+14634A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951596 | |||||||
chr2:36951728 | T | C | 51 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(48): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.234+14502A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951728 | |||||||
chr2:36951906 | G | C | 21 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(18): Show |
21 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.234+14324C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951906 | |||||||
chr2:36951958 | C | T | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+14272G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951958 | |||||||
chr2:36952063 | A | G | 1 | a0001c0001t0087g0020 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.234+14167T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952063 | |||||||
chr2:36952290 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
295 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.234+13940C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952290 | |||||||
chr2:36952449 | GAA | G | 51 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(48): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.234+13779_234+1378 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952449 | |||||||
chr2:36952534 | T | C | 1 | a0001c0001t0086g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+13696A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952534 | |||||||
chr2:36953064 | C | A | 49 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(46): Show |
49 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+13166G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953064 | |||||||
chr2:36953188 | A | T | 1 | a0001c0001t0037g0244 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.234+13042T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953188 | |||||||
chr2:36953402 | C | CT | 27 | a0001c0001t0001g0114 a0001c0001t0001g0126 a0001c0001t0002g0007 others(24): Show |
27 | HG01255.hp1 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+12827dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953402 | |||||||
chr2:36953518 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0003g0095 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.234+12712A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953518 | |||||||
chr2:36953545 | G | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.234+12685C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953545 | |||||||
chr2:36954126 | G | T | 4 | a0001c0001t0021g0233 a0001c0001t0021g0236 a0001c0001t0047g0235 others(1): Show |
4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+12104C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954126 | |||||||
chr2:36954175 | T | A | 1 | a0001c0001t0086g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+12055A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954175 | |||||||
chr2:36954236 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.234+11994G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954236 | |||||||
chr2:36954310 | A | T | 1 | a0001c0001t0007g0269 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.234+11920T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954310 | |||||||
chr2:36954340 | G | C | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.234+11890C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954340 | |||||||
chr2:36954466 | T | G | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+11764A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954466 | |||||||
chr2:36954515 | C | A | 24 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(21): Show |
24 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.234+11715G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954515 | |||||||
chr2:36954520 | G | GA | 16 | a0001c0001t0001g0107 a0001c0001t0001g0123 a0001c0001t0001g0145 others(13): Show |
16 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+11709dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954520 | |||||||
chr2:36954521 | A | G | 40 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(37): Show |
40 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.234+11709T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954521 | |||||||
chr2:36954522 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0045 |
2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.234+11708T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954522 | |||||||
chr2:36954828 | G | A | 1 | a0005c0006t0003g0253 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.234+11402C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954828 | |||||||
chr2:36955036 | G | A | 3 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 |
3 | HG01433.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.234+11194C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955036 | |||||||
chr2:36955170 | A | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0059 |
2 | NA19081.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.234+11060T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955170 | |||||||
chr2:36955174 | G | C | 1 | a0001c0001t0003g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.234+11056C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955174 | |||||||
chr2:36955199 | C | T | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+11031G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955199 | |||||||
chr2:36955376 | G | A | 11 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+10854C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955376 | |||||||
chr2:36955468 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234+10762C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955468 | |||||||
chr2:36955621 | G | A | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+10609C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955621 | |||||||
chr2:36955642 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.234+10588A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955642 | |||||||
chr2:36955843 | A | G | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+10387T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955843 | |||||||
chr2:36955896 | T | C | 1 | a0001c0003t0005g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.234+10334A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955896 | |||||||
chr2:36955905 | T | C | 1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.234+10325A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955905 | |||||||
chr2:36955910 | A | G | 1 | a0001c0001t0014g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.234+10320T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955910 | |||||||
chr2:36955921 | G | C | 1 | a0001c0001t0008g0294 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234+10309C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955921 | |||||||
chr2:36956098 | T | G | 2 | a0001c0001t0012g0285 a0001c0001t0012g0286 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.234+10132A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956098 | |||||||
chr2:36956146 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.234+10084T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956146 | |||||||
chr2:36956160 | G | T | 112 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(109): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.234+10070C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956160 | |||||||
chr2:36956213 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.234+10017G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956213 | |||||||
chr2:36956344 | C | A | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+9886G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956344 | |||||||
chr2:36956468 | C | A | 1 | a0001c0001t0050g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+9762G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956468 | |||||||
chr2:36956649 | T | C | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+9581A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956649 | |||||||
chr2:36956652 | C | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+9578G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956652 | |||||||
chr2:36956920 | C | T | 1 | a0001c0001t0073g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.234+9310G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956920 | |||||||
chr2:36956955 | T | C | 1 | a0001c0001t0066g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+9275A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956955 | |||||||
chr2:36956979 | G | A | 1 | a0001c0001t0072g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.234+9251C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956979 | |||||||
chr2:36957209 | C | A | 2 | a0001c0001t0005g0092 a0001c0001t0005g0093 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.234+9021G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957209 | |||||||
chr2:36957273 | A | G | 2 | a0001c0001t0002g0245 a0001c0001t0003g0247 |
2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.234+8957T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957273 | |||||||
chr2:36957342 | C | T | 196 | a0001c0001t0001g0047 a0001c0001t0001g0141 a0001c0001t0001g0200 others(193): Show |
196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.234+8888G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957342 | |||||||
chr2:36957446 | G | T | 1 | a0001c0001t0075g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.234+8784C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957446 | |||||||
chr2:36957538 | A | G | 1 | a0001c0001t0009g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.234+8692T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957538 | |||||||
chr2:36957611 | C | T | 156 | a0001c0001t0001g0141 a0001c0001t0001g0200 a0001c0001t0002g0007 others(153): Show |
156 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.234+8619G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957611 | |||||||
chr2:36957613 | C | T | 7 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0221 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+8617G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957613 | |||||||
chr2:36957654 | TAAAAAAC | T | 4 | a0001c0001t0012g0285 a0001c0001t0012g0286 a0001c0001t0015g0283 others(1): Show |
4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+8569_234+8575d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957654 | |||||||
chr2:36957672 | C | CA | 24 | a0001c0001t0001g0124 a0001c0001t0002g0019 a0001c0001t0003g0098 others(21): Show |
24 | HG00438.hp2 HG00597.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.234+8557dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957672 | |||||||
chr2:36957676 | A | C | 1 | a0001c0001t0002g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.234+8554T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957676 | |||||||
chr2:36957742 | G | GT | 4 | a0001c0001t0003g0268 a0001c0001t0015g0237 a0001c0001t0071g0241 others(1): Show |
4 | HG01243.hp2 HG02897.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+8487dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | |||||||
chr2:36957742 | G | GTT | 11 | a0001c0001t0003g0258 a0001c0001t0003g0260 a0001c0001t0003g0262 others(8): Show |
11 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+8487_234+8488i others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | |||||||
chr2:36957742 | G | GTTT | 14 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 others(11): Show |
14 | HG00673.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+8487_234+8488i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | |||||||
chr2:36957742 | G | GTTTT | 3 | a0001c0001t0002g0245 a0001c0001t0003g0247 a0001c0001t0067g0259 |
3 | HG02040.hp1 HG02129.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.234+8487_234+8488i others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | |||||||
chr2:36957744 | C | CT | 32 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(29): Show |
32 | HG00323.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.234+8485dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | C | CTTT | 37 | a0001c0001t0001g0200 a0001c0001t0002g0011 a0001c0001t0002g0012 others(34): Show |
37 | HG00280.hp1 HG01993.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.234+8483_234+8485d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | C | CTTTT | 31 | a0001c0001t0001g0141 a0001c0001t0002g0007 a0001c0001t0002g0009 others(28): Show |
31 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.234+8482_234+8485d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | C | CTTTTT | 6 | a0001c0001t0002g0019 a0001c0001t0002g0054 a0001c0001t0002g0196 others(3): Show |
6 | HG00099.hp1 HG02129.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+8481_234+8485d others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | C | T | 34 | a0001c0001t0002g0245 a0001c0001t0003g0096 a0001c0001t0003g0097 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+8486G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | CT | C | 6 | a0001c0001t0001g0003 a0001c0001t0003g0071 a0001c0001t0009g0139 others(3): Show |
6 | HG00099.hp2 HG00408.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+8485delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | CTTTTTTT | C | 27 | a0001c0001t0005g0091 a0001c0001t0005g0092 a0001c0001t0005g0093 others(24): Show |
27 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.234+8479_234+8485d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957744 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0008g0295 a0001c0001t0008g0296 a0001c0001t0008g0297 others(3): Show |
6 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+8476_234+8485d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | |||||||
chr2:36957810 | G | A | 1 | a0001c0001t0010g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.234+8420C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957810 | |||||||
chr2:36957876 | G | A | 1 | a0001c0001t0009g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.234+8354C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957876 | |||||||
chr2:36957905 | G | A | 1 | a0001c0001t0002g0014 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.234+8325C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957905 | |||||||
chr2:36957914 | C | A | 1 | a0001c0001t0030g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+8316G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957914 | |||||||
chr2:36957917 | A | AT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0105 others(35): Show |
38 | HG00408.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.234+8312dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957917 | |||||||
chr2:36957988 | T | C | 156 | a0001c0001t0001g0141 a0001c0001t0001g0200 a0001c0001t0002g0007 others(153): Show |
156 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.234+8242A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957988 | |||||||
chr2:36958092 | A | G | 13 | a0001c0001t0006g0209 a0001c0001t0006g0210 a0001c0001t0006g0211 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+8138T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958092 | |||||||
chr2:36958147 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.234+8083C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958147 | |||||||
chr2:36958461 | C | T | 2 | a0001c0001t0003g0261 a0001c0001t0003g0262 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.234+7769G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958461 | |||||||
chr2:36958550 | T | G | 1 | a0001c0001t0085g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.234+7680A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958550 | |||||||
chr2:36958579 | T | A | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+7651A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958579 | |||||||
chr2:36958649 | G | A | 7 | a0001c0001t0012g0282 a0001c0001t0012g0285 a0001c0001t0012g0286 others(4): Show |
7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+7581C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958649 | |||||||
chr2:36958722 | T | C | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+7508A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958722 | |||||||
chr2:36958895 | G | T | 1 | a0001c0001t0052g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.234+7335C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958895 | |||||||
chr2:36958940 | C | G | 1 | a0001c0001t0032g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.234+7290G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958940 | |||||||
chr2:36959016 | T | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.234+7214A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959016 | |||||||
chr2:36959029 | T | C | 1 | a0001c0001t0039g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+7201A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959029 | |||||||
chr2:36959092 | G | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+7138C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959092 | |||||||
chr2:36959146 | A | C | 2 | a0001c0001t0002g0025 a0001c0001t0030g0016 |
2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.234+7084T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959146 | |||||||
chr2:36959293 | T | A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6937A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959293 | |||||||
chr2:36959437 | G | A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6793C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959437 | |||||||
chr2:36959551 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.234+6679A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959551 | |||||||
chr2:36959635 | AC | A | 4 | a0001c0001t0006g0211 a0001c0001t0006g0212 a0001c0001t0006g0222 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+6594delG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959635 | |||||||
chr2:36959681 | G | A | 3 | a0001c0001t0013g0197 a0001c0001t0013g0198 a0001c0001t0013g0201 |
3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6549C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959681 | |||||||
chr2:36959845 | T | C | 2 | a0001c0001t0019g0206 a0001c0001t0042g0205 |
2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.234+6385A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959845 | |||||||
chr2:36959976 | T | C | 1 | a0001c0001t0016g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+6254A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959976 | |||||||
chr2:36960160 | C | A | 1 | a0001c0001t0035g0257 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.234+6070G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960160 | |||||||
chr2:36960614 | T | C | 1 | a0001c0001t0002g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.234+5616A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960614 | |||||||
chr2:36960650 | A | C | 29 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(26): Show |
29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+5580T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960650 | |||||||
chr2:36960651 | G | A | 16 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(13): Show |
16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+5579C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960651 | |||||||
chr2:36960997 | A | C | 52 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.234+5233T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960997 | |||||||
chr2:36961039 | G | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+5191C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961039 | |||||||
chr2:36961115 | C | CT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0076 a0001c0001t0001g0103 others(78): Show |
81 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.234+5114dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961115 | C | CTTTT | 11 | a0001c0001t0003g0072 a0001c0001t0007g0271 a0001c0001t0007g0272 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+5111_234+5114d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961115 | C | CTTTTT | 17 | a0001c0001t0003g0040 a0001c0001t0003g0042 a0001c0001t0003g0043 others(14): Show |
17 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.234+5110_234+5114d others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961115 | CT | C | 20 | a0001c0001t0002g0039 a0001c0001t0003g0258 a0001c0001t0005g0090 others(17): Show |
20 | HG00597.hp2 HG01256.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+5114delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961115 | CTT | C | 21 | a0001c0001t0005g0091 a0001c0001t0005g0092 a0001c0001t0005g0093 others(18): Show |
21 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.234+5113_234+5114d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961115 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0049g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.234+5105_234+5114d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | |||||||
chr2:36961285 | AT | A | 27 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(24): Show |
27 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+4944delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961285 | |||||||
chr2:36961290 | T | A | 27 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(24): Show |
27 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+4940A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961290 | |||||||
chr2:36961472 | C | T | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4758G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961472 | |||||||
chr2:36961485 | C | T | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4745G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961485 | |||||||
chr2:36961718 | G | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+4512C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961718 | |||||||
chr2:36961802 | T | C | 1 | a0001c0001t0067g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.234+4428A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961802 | |||||||
chr2:36961980 | T | C | 66 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(63): Show |
66 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.234+4250A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961980 | |||||||
chr2:36962034 | A | C | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+4196T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962034 | |||||||
chr2:36962047 | A | C | 4 | a0001c0001t0016g0279 a0001c0001t0016g0280 a0001c0001t0016g0281 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4183T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962047 | |||||||
chr2:36962145 | G | A | 1 | a0001c0001t0063g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.234+4085C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962145 | |||||||
chr2:36962153 | T | C | 193 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(190): Show |
193 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.234+4077A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962153 | |||||||
chr2:36962411 | C | T | 2 | a0001c0001t0040g0203 a0001c0001t0041g0202 |
2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+3819G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962411 | |||||||
chr2:36962481 | A | C | 55 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(52): Show |
55 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.234+3749T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962481 | |||||||
chr2:36962531 | C | CT | 50 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(47): Show |
50 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.234+3698dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962531 | |||||||
chr2:36962550 | T | C | 1 | a0001c0001t0009g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.234+3680A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962550 | |||||||
chr2:36962573 | C | A | 2 | a0001c0001t0007g0289 a0001c0001t0044g0290 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.234+3657G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962573 | |||||||
chr2:36962627 | A | G | 6 | a0001c0001t0007g0269 a0001c0001t0007g0270 a0001c0001t0007g0271 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+3603T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962627 | |||||||
chr2:36962758 | T | C | 21 | a0001c0001t0001g0047 a0001c0001t0002g0073 a0001c0001t0003g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+3472A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962758 | |||||||
chr2:36962882 | G | A | 29 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(26): Show |
29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+3348C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962882 | |||||||
chr2:36962911 | G | T | 1 | a0001c0001t0036g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234+3319C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962911 | |||||||
chr2:36963249 | G | C | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2981C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963249 | |||||||
chr2:36963273 | C | G | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2957G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963273 | |||||||
chr2:36963286 | T | C | 1 | a0004c0004t0002g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+2944A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963286 | |||||||
chr2:36963390 | G | A | 2 | a0001c0001t0018g0291 a0001c0001t0018g0292 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.234+2840C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963390 | |||||||
chr2:36963430 | A | G | 1 | a0001c0001t0028g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.234+2800T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963430 | |||||||
chr2:36963431 | T | C | 31 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2799A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963431 | |||||||
chr2:36963552 | A | G | 29 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(26): Show |
29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+2678T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963552 | |||||||
chr2:36963583 | C | T | 126 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.234+2647G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963583 | |||||||
chr2:36963618 | T | G | 5 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2612A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963618 | |||||||
chr2:36963783 | C | G | 2 | a0001c0001t0020g0274 a0001c0001t0020g0277 |
2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.234+2447G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963783 | |||||||
chr2:36963836 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.234+2394T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963836 | |||||||
chr2:36963845 | T | TACTTGGG others(25): Show |
1 | a0001c0001t0079g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.234+2353_234+2384d others(34): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963845 | |||||||
chr2:36963845 | TACTTGGG others(25): Show |
T | 1 | a0001c0001t0050g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+2353_234+2384d others(34): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963845 | |||||||
chr2:36964014 | T | A | 1 | a0001c0001t0005g0218 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.234+2216A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964014 | |||||||
chr2:36964067 | T | C | 5 | a0001c0001t0003g0265 a0001c0001t0003g0267 a0001c0001t0003g0268 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2163A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964067 | |||||||
chr2:36964176 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.234+2054C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964176 | |||||||
chr2:36964180 | C | CG | 31 | a0001c0001t0001g0200 a0001c0001t0002g0051 a0001c0001t0002g0052 others(28): Show |
31 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2049dupC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | |||||||
chr2:36964180 | C | CGG | 55 | a0001c0001t0001g0047 a0001c0001t0002g0017 a0001c0001t0002g0019 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.234+2048_234+2049d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | |||||||
chr2:36964180 | C | CGGG | 31 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2047_234+2049d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | |||||||
chr2:36964183 | GGC | G | 43 | a0001c0001t0002g0245 a0001c0001t0003g0096 a0001c0001t0003g0097 others(40): Show |
43 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.234+2045_234+2046d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964183 | |||||||
chr2:36964185 | C | G | 145 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0002g0007 others(142): Show |
145 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.234+2045G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964185 | |||||||
chr2:36964186 | G | A | 11 | a0001c0001t0002g0087 a0001c0001t0004g0078 a0001c0001t0004g0079 others(8): Show |
11 | HG00423.hp1 HG00544.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+2044C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964186 | |||||||
chr2:36964193 | A | C | 3 | a0001c0001t0019g0206 a0001c0001t0019g0207 a0001c0001t0042g0205 |
3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+2037T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964193 | |||||||
chr2:36964217 | T | G | 1 | a0001c0001t0065g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+2013A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964217 | |||||||
chr2:36964243 | T | C | 1 | a0001c0001t0030g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+1987A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964243 | |||||||
chr2:36964272 | G | GT | 16 | a0001c0001t0001g0162 a0001c0001t0002g0022 a0001c0001t0006g0209 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+1957dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964272 | |||||||
chr2:36964568 | T | C | 1 | a0001c0001t0010g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+1662A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964568 | |||||||
chr2:36964694 | T | C | 7 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+1536A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964694 | |||||||
chr2:36965083 | A | G | 1 | a0001c0001t0015g0237 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.234+1147T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965083 | |||||||
chr2:36965107 | CTCT | C | 30 | a0001c0001t0005g0090 a0001c0001t0005g0091 a0001c0001t0005g0092 others(27): Show |
30 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.234+1120_234+1122d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965107 | |||||||
chr2:36965262 | T | C | 1 | a0001c0001t0010g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+968A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965262 | |||||||
chr2:36965352 | T | C | 195 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(192): Show |
195 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.234+878A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965352 | |||||||
chr2:36965362 | T | A | 2 | a0001c0001t0002g0094 a0001c0001t0003g0095 |
2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.234+868A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965362 | |||||||
chr2:36965464 | T | C | 74 | a0001c0001t0002g0245 a0001c0001t0003g0096 a0001c0001t0003g0097 others(71): Show |
74 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.234+766A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965464 | |||||||
chr2:36965625 | A | G | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.234+605T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965625 | |||||||
chr2:36965723 | C | T | 91 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(88): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.234+507G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965723 | |||||||
chr2:36965824 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.234+406C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965824 | |||||||
chr2:36965932 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(1): Show |
4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+298C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965932 |